(Q37060646)

18 August 2017

1 reference

title

Imprinted genes and neuroendocrine function (English)

1 reference

18 August 2017

William Davies

1

1 reference

18 August 2017

Phoebe M Y Lynn

series ordinal

2

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18 August 2017

Dinko Relkovic

series ordinal

3

1 reference

18 August 2017

Lawrence S Wilkinson

series ordinal

4

1 reference

18 August 2017

publication date

10 December 2007

1 reference

Frontiers in Neuroendocrinology

18 August 2017

published in

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18 August 2017

volume

29

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18 August 2017

issue

3

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18 August 2017

page(s)

413-427

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Cerebrospinal fluid monoamines in Prader-Willi syndrome

18 August 2017

cites work

1 reference

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Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death

7 January 2021

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Regulation of placental efficiency for nutrient transport by imprinted genes

7 January 2021

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Imbalanced genomic imprinting in brain development: an evolutionary basis for the aetiology of autism

7 January 2021

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Sex differences in the brain: implications for explaining autism

7 January 2021

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The neuroscience of affiliation: forging links between basic and clinical research on neuropeptides and social behavior

7 January 2021

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Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Distinctive patterns of memory function in subgroups of females with Turner syndrome: evidence for imprinted loci on the X-chromosome affecting neurodevelopment.

7 January 2021

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Whole genome microarray analysis of gene expression in Prader-Willi syndrome.

7 January 2021

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The pseudoautosomal regions, SHOX and disease

7 January 2021

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Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy.

7 January 2021

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Care of girls and women with Turner syndrome: a guideline of the Turner Syndrome Study Group

7 January 2021

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Peripheral markers of the gamma-aminobutyric acid (GABA)ergic system in Angelman's syndrome

7 January 2021

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Possible parent-of-origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain.

7 January 2021

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Plasma obestatin and ghrelin levels in subjects with Prader-Willi syndrome.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Plasma peptide YY and ghrelin levels in infants and children with Prader-Willi syndrome

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Effects of growth hormone on body composition and bone metabolism

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

7 January 2021

Prader-Willi syndrome

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https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Prader-Willi and Angelman syndromes: sister imprinted disorders

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Differential activity of maternally and paternally derived chromosome regions in mice

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Epsilon-sarcoglycan immunoreactivity and mRNA expression in mouse brain.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Alternative Gnas gene products have opposite effects on glucose and lipid metabolism.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Increased density of ghrelin-expressing cells in the gastric fundus and body in Prader-Willi syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Midbrain expression of Delta-like 1 homologue is regulated by GDNF and is associated with dopaminergic differentiation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Increased body fat in mice with a targeted mutation of the paternally expressed imprinted gene Peg3.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Influence of X chromosome and hormones on human brain development: a magnetic resonance imaging and proton magnetic resonance spectroscopy study of Turner syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Serotonin 1B and 2C receptor interactions in the modulation of feeding behaviour in the mouse.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Growth hormone treatment of early growth failure in toddlers with Turner syndrome: a randomized, controlled, multicenter trial

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

X-linked imprinting: effects on brain and behaviour

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

What are imprinted genes doing in the brain?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Imprinted gene expression in the brain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Parent-of-origin effect and genomic imprinting of the HTR2A receptor gene T102C polymorphism in psychosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

High circulating ghrelin: a potential cause for hyperphagia and obesity in prader-willi syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Appetitive behavior, compulsivity, and neurochemistry in Prader-Willi syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Autistic-like symptomatology in Prader-Willi syndrome: a review of recent findings

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

SGCE missense mutations that cause myoclonus-dystonia syndrome impair epsilon-sarcoglycan trafficking to the plasma membrane: modulation by ubiquitination and torsinA

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Neuroendocrine secretory protein 55: a novel marker for the constitutive secretory pathway

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Imprinted genes, placental development and fetal growth

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Monoallelic and unequal allelic expression of the HTR2A gene in human brain and peripheral lymphocytes.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Disruption of the mouse necdin gene results in early post-natal lethality

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Contributions of 5-HT(2C) receptors to multiple actions of central serotonin systems

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

APeg3, a novel paternally expressed gene 3 antisense RNA transcript specifically expressed in vasopressinergic magnocellular neurons in the rat supraoptic nucleus.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Prader-Willi syndrome: advances in genetics, pathophysiology and treatment

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Resting metabolic rate, plasma leptin concentrations, leptin receptor expression, and adipose tissue measured by whole-body magnetic resonance imaging in women with Prader-Willi syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Hypothalamic growth hormone-releasing hormone (GHRH) cell number is increased in human illness, but is not reduced in Prader-Willi syndrome or obesity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Analysis of the linkage of the Taq1A and Taq1B loci of the dopamine D2 receptor gene with schizophrenia in patients and their siblings.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Clinical practice in Turner syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

The disparate maternal aunt-uncle ratio in male transsexuals: an explanation invoking genomic imprinting.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Genomic imprinting and kinship: how good is the evidence?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Prader‐Willi syndrome and the evolution of human childhood

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Serotonergic drugs : effects on appetite expression and use for the treatment of obesity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Genomic imprinting in Turner syndrome: effects on response to growth hormone and on risk of sensorineural hearing loss.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Preferential transmission of paternal alleles at risk genes in attention-deficit/hyperactivity disorder

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Imprinting of the G(s)alpha gene GNAS1 in the pathogenesis of acromegaly

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

A comprehensive transcript map of the mouse Gnas imprinted complex

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Somatic mosaicism for maternal uniparental disomy 15 in a girl with Prader-Willi syndrome: confirmation by cell cloning and identification of candidate downstream genes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Peromysci, promiscuity and imprinting.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Growth effects of uniparental disomies and the conflict theory of genomic imprinting

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

A possible role for imprinted genes in inbreeding avoidance and dispersal from the natal area in mice.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Genomic imprinting and the social brain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Endocrine function in the Prader-Willi syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Neurons in the monoaminergic nuclei of the rat and human central nervous system express FA1/dlk

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Paternal imprinting of mouse serotonin receptor 2A gene Htr2 in embryonic eye: a conserved imprinting regulation on the RB/Rb locus.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Effects of X-monosomy and X-linked imprinting on superior temporal gyrus morphology in Turner syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Multifunction steroid receptor coactivator, E6-associated protein, is involved in development of the prostate gland

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Genetic and functional analysis of neuronatin in mice with maternal or paternal duplication of distal Chr 2.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Dlx5, the mouse homologue of the human-imprinted DLX5 gene, is biallelically expressed in the mouse brain.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Regulation of alternative splicing by snoRNAs

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

The snoRNA HBII-52 regulates alternative splicing of the serotonin receptor 2C

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Growth parameters in maternal uniparental disomy 7 and 14

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Changes in gene expression foreshadow diet-induced obesity in genetically identical mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

The imprinted gene Magel2 regulates normal circadian output.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Necdin downregulates CDC2 expression to attenuate neuronal apoptosis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Biased paternal transmission of SNAP-25 risk alleles in attention-deficit hyperactivity disorder

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Necdin promotes GABAergic neuron differentiation in cooperation with Dlx homeodomain proteins.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Cognitive abilities associated with the Silver-Russell syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Regulation of maternal behavior and offspring growth by paternally expressed Peg3.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

E6AP and calmodulin reciprocally regulate estrogen receptor stability.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

GABAA receptor beta3 subunit gene-deficient heterozygous mice show parent-of-origin and gender-related differences in beta3 subunit levels, EEG, and behavior

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Grb10: more than a simple adaptor protein

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Neuropeptidergic regulation of affiliative behavior and social bonding in animals

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

The effects of 5-HT1A and 5-HT2C receptor agonists on behavioral satiety sequence in rats

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

GABA A receptor abnormalities in Prader-Willi syndrome assessed with positron emission tomography and [11C]flumazenil

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Mutations in the Gs alpha gene causing hormone resistance

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Cerebrospinal fluid levels of oxytocin in Prader-Willi syndrome: a preliminary report.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Evidence against GRB10 as the gene responsible for Silver-Russell syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Evidence for uniparental, paternal expression of the human GABAA receptor subunit genes, using microcell-mediated chromosome transfer

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Regional distribution of the expression of a human stimulatory GTP-binding protein α-subunit in the human brain studied by in situ hybridization

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Conflicting reports of imprinting status of human GRB10 in developing brain: how reliable are somatic cell hybrids for predicting allelic origin of expression?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Haplotype analysis of SNAP-25 suggests a role in the aetiology of ADHD.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Sylvian fissure morphology in Prader-Willi syndrome and early-onset morbid obesity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient mice.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Limited evolutionary conservation of imprinting in the human placenta

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Mice lacking paternally expressed Pref-1/Dlk1 display growth retardation and accelerated adiposity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

A census of mammalian imprinting.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Dopamine D4 receptor and tyrosine hydroxylase genes in bipolar disorder: evidence for a role of DRD4.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

A genomewide scan of male sexual orientation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Leptin concentrations in Prader-Willi syndrome before and after growth hormone replacement

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Prader-Willi syndrome with elevated follicle stimulating hormone levels and diabetes mellitus.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

The Angelman syndrome-associated protein, E6-AP, is a coactivator for the nuclear hormone receptor superfamily

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

A survey of genetic and epigenetic variation affecting human gene expression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromosome 2

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

The imprinted signaling protein XL alpha s is required for postnatal adaptation to feeding.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Imprinted Nesp55 influences behavioral reactivity to novel environments

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Parental genomic imprinting in endocrinopathies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Identification of a cluster of X-linked imprinted genes in mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

The neurodevelopment of human sexual orientation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Genomic imprinting: parental influence on the genome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Cognition and the sex chromosomes: studies in Turner syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Clinical significance of the parental origin of the X chromosome in turner syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Staying awake for dinner: hypothalamic integration of sleep, feeding, and circadian rhythms

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Satiety dysfunction in Prader-Willi syndrome demonstrated by fMRI.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Tryptophan hydroxylase 2 (TPH2) gene variants associated with ADHD.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Identification and properties of imprinted genes and their control elements.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Association of GABA(A) receptors and alcohol dependence and the effects of genetic imprinting

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Hormonal and metabolic defects in a prader-willi syndrome mouse model with neonatal failure to thrive

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Imprinted genes in placental growth and obstetric disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Parental origin of normal X chromosomes in Turner syndrome patients with various karyotypes: implications for the mechanism leading to generation of a 45,X karyotype

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Molecular genetics of autism spectrum disorder.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Prader-Willi syndrome: atypical psychoses and motor dysfunctions

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

The ubiquitin-conjugating enzyme UBCH7 acts as a coactivator for steroid hormone receptors

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Minireview: GNAS: normal and abnormal functions.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

What good is genomic imprinting: the function of parent-specific gene expression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Genomic imprinting effects on brain development and function

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Angelman syndrome: mimicking conditions and phenotypes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Opposite imprinting of the mouse Igf2 and Igf2r genes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

The alternative stimulatory G protein alpha-subunit XLalphas is a critical regulator of energy and glucose metabolism and sympathetic nerve activity in adult mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Identification of cell-specific messenger ribonucleic acids in oxytocinergic and vasopressinergic magnocellular neurons in rat supraoptic nucleus by single-cell differential hybridization

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Myoclonus, motor deficits, alterations in emotional responses and monoamine metabolism in epsilon-sarcoglycan deficient mice.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

Prader-Willi syndrome and the hypothalamus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YFRNE.2007.12.001

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/J.YFRNE.2007.12.001

1 reference

18 August 2017

1 reference