(Q37543845)

20 August 2017

1 reference

title

Aneuploidy: from a physiological mechanism of variance to Down syndrome (English)

1 reference

Xavier Estivill i Pallejà

20 August 2017

author

series ordinal

3

1 reference

20 August 2017

Yann Herault

2

0 references

Mara Dierssen Sotos

object named as

Mara Dierssen

series ordinal

1

0 references

publication date

1 July 2009

1 reference

20 August 2017

published in

Physiological Reviews

1 reference

20 August 2017

volume

89

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20 August 2017

issue

3

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20 August 2017

page(s)

887-920

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Adult neurogenesis: from precursors to network and physiology

20 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Kinetic properties of a MNB/DYRK1A mutant suitable for the elucidation of biochemical pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

DYRK1A BAC transgenic mice show altered synaptic plasticity with learning and memory defects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Classification of human chromosome 21 gene-expression variations in Down syndrome: impact on disease phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

DYRK1A autophosphorylation on serine residue 520 modulates its kinase activity via 14-3-3 binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Dosage-dependent over-expression of genes in the trisomic region of Ts1Cje mouse model for Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The three-dimensional organization of the hippocampal formation: a review of anatomical data

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The challenge of Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Chromosome 21 and down syndrome: from genomics to pathophysiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Actin-binding protein, drebrin, accumulates in submembranous regions in parallel with neuronal differentiation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Combined ultrasound biometry, serum markers and age for Down syndrome risk estimation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Recent segmental duplications in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The selectivity of protein kinase inhibitors: a further update

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Dendritic atrophy in children with Down's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Synaptic and cognitive abnormalities in mouse models of Down syndrome: exploring genotype-phenotype relationships

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Synaptic structural abnormalities in the Ts65Dn mouse model of Down Syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Alterations in the phenotype of neocortical pyramidal cells in the Dyrk1A+/- mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Modeling the monosomy for the telomeric part of human chromosome 21 reveals haploinsufficient genes modulating the inflammatory and airway responses.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Ts65Dn, a mouse model of Down syndrome, exhibits increased GABAB-induced potassium current.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

A retroviral strategy that efficiently creates chromosomal deletions in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The role of genes in the etiology of specific language impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Continuity in mental development from infancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Modeling chromosomes in mouse to explore the function of genes, genomic disorders, and chromosomal organization

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Spatial representation and attention in toddlers with Williams syndrome and Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Dementia in adults with Down syndrome: diagnostic challenges.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Risk factors for dementia in people with down syndrome: issues in assessment and diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Reading, language and memory skills: a comparative longitudinal study of children with Down syndrome and their mainstream peers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Elevated gene expression levels distinguish human from non-human primate brains

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

National estimates and race/ethnic-specific variation of selected birth defects in the United States, 1999-2001.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Mapping heritability and molecular genetic associations with cortical features using probabilistic brain atlases: methods and applications to schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Depolarization of neural cells induces transcription of the Down syndrome critical region 1 isoform 4 via a calcineurin/nuclear factor of activated T cells-dependent pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

DYRK1A-dosage imbalance perturbs NRSF/REST levels, deregulating pluripotency and embryonic stem cell fate in Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Long-term memory in mental retardation: evidence for a specific impairment in subjects with Down's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Methods and strategies for analyzing copy number variation using DNA microarrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Predicting longitudinal change in language production and comprehension in individuals with Down syndrome: hierarchical linear modeling.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Predicting language production in children and adolescents with Down syndrome: the role of comprehension.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The mouse brain transcriptome by SAGE: differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normals

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Cell cycle elongation impairs proliferation of cerebellar granule cell precursors in the Ts65Dn mouse, an animal model for Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Choline acetyltransferase activity at different ages in brain of Ts65Dn mice, an animal model for Down's syndrome and related neurodegenerative diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Cell cycle alteration and decreased cell proliferation in the hippocampal dentate gyrus and in the neocortical germinal matrix of fetuses with Down syndrome and in Ts65Dn mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Copy-number variations associated with neuropsychiatric conditions

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Failed retrograde transport of NGF in a mouse model of Down's syndrome: reversal of cholinergic neurodegenerative phenotypes following NGF infusion

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Object and spatial visual working memory activate separate neural systems in human cortex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Genes coding for sensitivity to interferon (IfRec) and soluble superoxide dismutase (SOD-1) are linked in mouse and man and map to mouse chromosome 16

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Copy number variation at the 7q11.23 segmental duplications is a susceptibility factor for the Williams-Beuren syndrome deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Breaking the neuronal sphere: regulation of the actin cytoskeleton in neuritogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The cerebellar transcriptome during postnatal development of the Ts1Cje mouse, a segmental trisomy model for Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Impact of trisomy on fertility and meiosis in male mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Cooperation to amplify gene-dosage-imbalance effects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Developmental defects in trisomy 21 and mouse models.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Spatial memory deficits in segmental trisomic Ts65Dn mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Comparison of human chromosome 21 conserved nongenic sequences (CNGs) with the mouse and dog genomes shows that their selective constraint is independent of their genic environment

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Numerous potentially functional but non-genic conserved sequences on human chromosome 21

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Gene expression variation and expression quantitative trait mapping of human chromosome 21 genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Relation of EEG alpha background to cognitive function, brain atrophy, and cerebral metabolism in Down's syndrome. Age-specific changes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Alterations of neocortical pyramidal cell phenotype in the Ts65Dn mouse model of Down syndrome: effects of environmental enrichment

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

DYRK1A (dual-specificity tyrosine-phosphorylated and -regulated kinase 1A): a gene with dosage effect during development and neurogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Murine models for Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Pitfalls and hopes in Down syndrome therapeutic approaches: in the search for evidence-based treatments.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Alterations of central noradrenergic transmission in Ts65Dn mouse, a model for Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The actin cytoskeleton: integrating form and function at the synapse

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Microcell-mediated chromosome transfer (MMCT): small cells with huge potential

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Gene copy number variation spanning 60 million years of human and primate evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The hippocampus--what does it do?

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Functional organization of the hippocampal memory system

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The medial temporal lobe and recognition memory

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Completing the map of human genetic variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Intra- and interspecific variation in primate gene expression patterns

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

21 January 2018

Developmental genetics

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Specificity versus nonspecificity in the pathogenesis of aneuploid phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

A behavioral assessment of Ts65Dn mice: a putative Down syndrome model.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Impaired short- and long-term memory in Ts65Dn mice, a model for Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

A callosal transfer deficit in children with developmental language disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Minicolumnar organization within somatosensory cortical segregates: I. Development of afferent connections

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Minicolumnar organization within somatosensory cortical segregates: II. Emergent functional properties

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

A chromosome 8 gene-cluster polymorphism with low human beta-defensin 2 gene copy number predisposes to Crohn disease of the colon

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Education and children with Down syndrome: neuroscience, development, and intervention

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Transcriptional consequences of autosomal trisomy: primary gene dosage with complex downstream effects

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Dyrk1A haploinsufficiency affects viability and causes developmental delay and abnormal brain morphology in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Small planum temporale volume in Down's syndrome: a volumetric MRI study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Copy number variation: new insights in genome diversity

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The developmental cognitive neuroscience of language: a new research domain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Impairments in motor coordination without major changes in cerebellar plasticity in the Tc1 mouse model of Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Understanding mental retardation in Down's syndrome using trisomy 16 mouse models

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Gene-dosage effects in Down syndrome and trisomic mouse models

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

An integrative view of dynamic genomic elements influencing human brain evolution and individual neurodevelopment

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Neuroimaging endophenotypes: strategies for finding genes influencing brain structure and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Tc-99m HMPAO brain perfusion imaging in young Down's syndrome patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Development of the superior temporal neocortex is anomalous in trisomy 21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Triplicated alpha-globin loci in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Estrogen restores cognition and cholinergic phenotype in an animal model of Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Estrogen alters amyloid precursor protein as well as dendritic and cholinergic markers in a mouse model of Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Loss of cholinergic phenotype in basal forebrain coincides with cognitive decline in a mouse model of Down's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

A high-resolution map of segmental DNA copy number variation in the mouse genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The planum temporale as a computational hub.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Induced gene expression in human brain after the split from chimpanzee

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Distribution and functional impact of DNA copy number variation in the rat.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Expression patterns and subcellular localization of the Down syndrome candidate protein MNB/DYRK1A suggest a role in late neuronal differentiation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Mnb/Dyrk1A is transiently expressed and asymmetrically segregated in neural progenitor cells at the transition to neurogenic divisions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The functional nature of synaptic circuitry is altered in area CA3 of the hippocampus in a mouse model of Down's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Abnormal expression of the G-protein-activated inwardly rectifying potassium channel 2 (GIRK2) in hippocampus, frontal cortex, and substantia nigra of Ts65Dn mouse: a model of Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The hippocampus is required for short-term topographical memory in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Toward constructing an endophenotype strategy for bipolar disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The origin of human aneuploidy: where we have been, where we are going

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

To err (meiotically) is human: the genesis of human aneuploidy

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The DNA sequence of human chromosome 21

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Domain analysis of the actin-binding and actin-remodeling activities of drebrin

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The effect of scene context on episodic object recognition: parahippocampal cortex mediates memory encoding and retrieval success

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Transchromosomal mouse embryonic stem cell lines and chimeric mice that contain freely segregating segments of human chromosome 21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Effects of aneuploidy on skull growth in a mouse model of Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Direct and indirect behavioral effects of different genetic disorders of mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Measuring behavior in genetic disorders of mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Strengthening behavioral research on genetic mental retardation syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Psoriasis is associated with increased beta-defensin genomic copy number

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Developmental abnormalities and age-related neurodegeneration in a mouse model of Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Minocycline prevents cholinergic loss in a mouse model of Down's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Behavioral comparison of 4 and 6 month-old Ts65Dn mice: age-related impairments in working and reference memory

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Behavioral and neurobiological markers of Alzheimer's disease in Ts65Dn mice: effects of estrogen

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Regional alterations in amyloid precursor protein and nerve growth factor across age in a mouse model of Down's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Reactivity to object and spatial novelty is normal in older Ts65Dn mice that model Down syndrome and Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Motor learning in Ts65Dn mice, a model for Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Ts65Dn mice, a model for Down syndrome, have deficits in context discrimination learning suggesting impaired hippocampal function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Detection of large-scale variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

A morphometric CT study of Down's syndrome showing small posterior fossa and calcification of basal ganglia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Hippocampal volume and neuronal number in Ts65Dn mice: a murine model of Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

A haplotype map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Organization of intrahippocampal projections originating from CA3 pyramidal cells in the rat.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Cerebral morphologic distinctions between Williams and Down syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Gene-dosage effect on chromosome 21 transcriptome in trisomy 21: implication in Down syndrome cognitive disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Pathogenesis of chromosomal mosaicism and its effect on early human development

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Germline transmission of a transferred human chromosome 21 fragment in transchromosomal mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Magnetic resonance imaging analysis of age-related changes in the brains of individuals with Down's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Regional patterns of gene expression in human and chimpanzee brains

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

A neutral model of transcriptome evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Genome assembly comparison identifies structural variants in the human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Modality-specific retrograde amnesia of fear

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Putative therapeutic agents for the learning and memory deficits of people with Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Dual-task processing as a measure of executive function: a comparison between adults with Williams and Down syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Hippocampal long-term potentiation suppressed by increased inhibition in the Ts65Dn mouse, a genetic model of Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The effect of damage to the cerebellum on sensorimotor and cognitive function in children and adolescents.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Paired-end mapping reveals extensive structural variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Down syndrome phenotypes: the consequences of chromosomal imbalance

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Relation of medial temporal lobe volumes to age and memory function in nondemented adults with Down's syndrome: implications for the prodromal phase of Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Changes in explicit memory associated with early dementia in adults with Down's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Human chromosome 21-derived miRNAs are overexpressed in down syndrome brains and hearts

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Synaptic deficit in the temporal cortex of partial trisomy 16 (Ts65Dn) mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Deficits of neuronal density in CA1 and synaptic density in the dentate gyrus, CA3 and CA1, in a mouse model of Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Reduced cell number in the neocortical part of the human fetal brain in Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Working memory in children and adolescents with Down syndrome: evidence from a colour memory experiment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Analysis of copy number variation in the rhesus macaque genome identifies candidate loci for evolutionary and human disease studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Genome-wide atlas of gene expression in the adult mouse brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Duplication of the entire 22.9 Mb human chromosome 21 syntenic region on mouse chromosome 16 causes cardiovascular and gastrointestinal abnormalities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Overexpression of Dyrk1A contributes to neurofibrillary degeneration in Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Both increases in immature dentate neuron number and decreases of immobility time in the forced swim test occurred in parallel after environmental enrichment of mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The prenatal development of the human cerebellar field in Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Hippocampal hypocellularity in the Ts65Dn mouse originates early in development

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The concerted modulation of proliferation and migration contributes to the specification of the cytoarchitecture and dimensions of cortical areas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Actin cytoskeleton regulation in neuronal morphogenesis and structural plasticity

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Gene expression from the aneuploid chromosome in a trisomy mouse model of down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The effects of bilateral hippocampal damage on fMRI regional activations and interactions during memory retrieval.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Loss of neurones from cortical and subcortical areas in Down's syndrome patients at middle age. Quantitative comparisons with younger Down's patients and patients with Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Global up-regulation of chromosome 21 gene expression in the developing down syndrome brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Pyramidal cell abnormalities in the motor cortex of a child with Down's syndrome. A Golgi study

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Structural abnormalities of the cerebral cortex in human chromosomal aberrations: a Golgi study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Structural variation of chromosomes in autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Dyrk1A expression pattern supports specific roles of this kinase in the adult central nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The human angiotensin II type 1 receptor +1166 A/C polymorphism attenuates microRNA-155 binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Motor phenotypic alterations in TgDyrk1a transgenic mice implicate DYRK1A in Down syndrome motor dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Common deletion polymorphisms in the human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The manipulation of chromosomes by mankind: the uses of microcell-mediated chromosome transfer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

FMRI reveals brain regions mediating slow prosodic modulations in spoken sentences

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Visual recognition and recall after right temporal-lobe excision in man.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Trisomy 16 in the mouse fetus associated with generalized edema and cardiovascular and urinary tract anomalies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Down syndrome: a study of chromosomal mosaicism

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Down syndrome gene dosage imbalance on cerebellum development

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Cerebellar contribution to spatial event processing: right/left discrimination abilities in rats.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Postnatal lethality and cardiac anomalies in the Ts65Dn Down syndrome mouse model

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The effects of piracetam on cognitive performance in a mouse model of Down's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Preservation of long-term memory and synaptic plasticity despite short-term impairments in the Tc1 mouse model of Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The cognitive neuroscience of remote episodic, semantic and spatial memory

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Introduction. Computation in cortical columns.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Preduodenal position of the common bile duct associated with annular pancreas: case report and literature review

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Down's syndrome: a genetic disorder in biobehavioral perspective

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Memory consolidation, retrograde amnesia and the hippocampal complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Functional neuroanatomy of spatial working memory in children

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Mechanisms of verbal memory impairment in four neurodevelopmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Dendritic mechanisms in brain function and developmental disabilities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

New insights into human nondisjunction of chromosome 21 in oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

A chromosome 21 critical region does not cause specific Down syndrome phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Trisomy for the Down syndrome 'critical region' is necessary but not sufficient for brain phenotypes of trisomic mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Targeting Dyrk1A with AAVshRNA attenuates motor alterations in TgDyrk1A, a mouse model of Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The neurobiologic consequences of autosomal trisomy in mice and men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Microstructure of trabecular bone in a mouse model for Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

From single to multiple deficit models of developmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The neuropsychology of Down syndrome: evidence for hippocampal dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Hotspots for copy number variation in chimpanzees and humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Copy number variation and evolution in humans and chimpanzees

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Amygdala and hippocampal volumes in children with Down syndrome: a high-resolution MRI study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Neuroanatomy of Down's syndrome: a high-resolution MRI study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Transcriptional disruptions in Down syndrome: a case study in the Ts1Cje mouse cerebellum during post-natal development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Natural gene-expression variation in Down syndrome modulates the outcome of gene-dosage imbalance

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Down syndrome and the genes of human chromosome 21: current knowledge and future potentials

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Intersectin 2, a new multimodular protein involved in clathrin-mediated endocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Alu-splice cloning of human Intersectin (ITSN), a putative multivalent binding protein expressed in proliferating and differentiating neurons and overexpressed in Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Dendritic Spine "Dysgenesis" and Mental Retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Chromosome engineering in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Global variation in copy number in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Down syndrome mouse models are looking up.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

A mouse model for Down syndrome exhibits learning and behaviour deficits.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Chromosomal variation in neurons of the developing and adult mammalian nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Constitutional aneuploidy in the normal human brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Spatial memory dissociations in mice lacking GluR1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Nineteen additional unpredicted transcripts from human chromosome 21

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

From PREDs and open reading frames to cDNA isolation: revisiting the human chromosome 21 transcription map

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Human chromosome 21 gene expression atlas in the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Hair keratin associated proteins: characterization of a second high sulfur KAP gene domain on human chromosome 21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Defective cerebellar response to mitogenic Hedgehog signaling in Down [corrected] syndrome mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Understanding the basis for Down syndrome phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Down's syndrome: Is there a decreased population of neurons?

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Cognitive executive function in Down's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Chronic pentylenetetrazole but not donepezil treatment rescues spatial cognition in Ts65Dn mice, a model for Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Effects of chronic administration of SGS-111 during adulthood and during the pre- and post-natal periods on the cognitive deficits of Ts65Dn mice, a model of Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Cell proliferation is reduced in the dentate gyrus of aged but not young Ts65Dn mice, a model of Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Ts1Cje, a partial trisomy 16 mouse model for Down syndrome, exhibits learning and behavioral abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Increased App expression in a mouse model of Down's syndrome disrupts NGF transport and causes cholinergic neuron degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Global disruption of the cerebellar transcriptome in a Down syndrome mouse model.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The 22q11 deletion syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Regional cerebral blood flow in Down syndrome adults during the Wisconsin Card Sorting Test: exploring cognitive activation in the context of poor performance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Genetic influence on neurogenesis in the dentate gyrus of two strains of adult mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Restoration of spatial working memory by genetic rescue of GluR-A-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Strong association of de novo copy number mutations with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Large-scale copy number polymorphism in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Abnormal APP, cholinergic and cognitive function in Ts65Dn Down's model mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Human microRNA-155 on chromosome 21 differentially interacts with its polymorphic target in the AGTR1 3' untranslated region: a mechanism for functional single-nucleotide polymorphisms related to phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Segmental duplications and copy-number variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Characterization of a recurrent 15q24 microdeletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Comparative genomics of the keratin-associated protein (KAP) gene clusters in human, chimpanzee, and baboon

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Annotating gene function by combining expression data with a modular gene network

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Mice containing a human chromosome 21 model behavioral impairment and cardiac anomalies of Down's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Dynamics of postural control in the child with Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Altered signaling pathways underlying abnormal hippocampal synaptic plasticity in the Ts65Dn mouse model of Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

alpha-Synuclein locus triplication causes Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Dyrk1A potentiates steroid hormone-induced transcription via the chromatin remodeling factor Arip4

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

21 January 2018

The medial temporal lobe

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Molecular-evolutionary mechanisms for genomic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Experimental parameters affecting the Morris water maze performance of a mouse model of Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Relative impact of nucleotide and copy number variation on gene expression phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Spine distribution along the apical dendrites of the pyramidal neurons in Down's syndrome. A quantitative Golgi study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Gene expression variation in Down's syndrome mice allows prioritization of candidate genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Abnormal neuronal development in the visual cortex of the human fetus and infant with down's syndrome. A quantitative and qualitative Golgi study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Mapping genetic influences on human brain structure

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Genetic influences on brain structure

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Ethnic variation in the prevalence of echogenic intracardiac foci and the association with Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

New techniques to understand chromosome dosage: mouse models of aneuploidy

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Sister grouping of chimpanzees and humans as revealed by genome-wide phylogenetic analysis of brain gene expression profiles

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Hemisphere and gender differences in mental rotation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Segmental trisomy of chromosome 17: a mouse model of human aneuploidy syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

MRS quality assessment in a multicentre study on MRS-based classification of brain tumours

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Reading skills and phonological awareness acquisition in Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Evidence from two genetic syndromes for the independence of spatial and visual working memory.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Visual and spatial long-term memory: differential pattern of impairments in Williams and Down syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Verbal short-term memory in Down's syndrome: an articulatory loop deficit?

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Recurrent CNVs disrupt three candidate genes in schizophrenia patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Perinatal growth of prefrontal layer III pyramids in Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Stability of inbred mouse strain differences in behavior and brain size between laboratories and across decades

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Callosal morphology concurs with neurobehavioral and neuropathological findings in two neurodevelopmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Toward the genetics of mammalian reproduction: induction and mapping of gametogenesis mutants in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Initial sequencing and comparative analysis of the mouse genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Genomic copy number and expression variation within the C57BL/6J inbred mouse strain

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Association between microdeletion and microduplication at 16p11.2 and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Temporally graded retrograde amnesia following separate and combined lesions of the perirhinal cortex and fornix in the rat.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Copy number of FCGR3B, which is associated with systemic lupus erythematosus, correlates with protein expression and immune complex uptake

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Alzheimer's disease in Down's syndrome: clinicopathologic studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Copy number variant analysis of human embryonic stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Penetrance of craniofacial anomalies in mouse models of Smith-Magenis syndrome is modified by genomic sequence surrounding Rai1: not all null alleles are alike

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Reduced penetrance of craniofacial anomalies as a function of deletion size and genetic background in a chromosome engineered partial mouse model for Smith-Magenis syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Protein kinase Dyrk1 activates cAMP response element-binding protein during neuronal differentiation in hippocampal progenitor cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European A

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The variation of aneuploidy frequency in the developing and adult human brain revealed by an interphase FISH study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Aneuploidy and confined chromosomal mosaicism in the developing human brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

The primate hippocampal formation: evidence for a time-limited role in memory storage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

Congenital heart disease in mice deficient for the DiGeorge syndrome region

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSREV.00032.2007

10.1152/PHYSREV.00032.2007

21 January 2018

Identifiers

DOI

1 reference

20 August 2017

1 reference