(Q48126436)

English

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

scientific article published on 25 June 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17591625

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

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17591625

haploinsufficiency

0 references

8

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17591625

object named as

Arnaud Duchon

3

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author name string

Vanessa Besson

1

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17591625

Véronique Brault

2

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17591625

Dieudonné Togbe

4

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17591625

Jean-Charles Bizot

5

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17591625

Valérie F J Quesniaux

6

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17591625

Bernard Ryffel

7

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17591625

publication date

25 June 2007

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17591625

Human Molecular Genetics

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17591625

16

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17591625

17

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17591625

2040-2052

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17591625

Deletion of chromosome 21 disturbs human brain morphogenesis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Mild phenotype in two unrelated patients with a partial deletion of 21q22.2-q22.3 defined by FISH and molecular studies.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Unbalanced 18q/21q translocation in a patient previously reported as monosomy 21.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Protein methyltransferase 2 inhibits NF-kappaB function and promotes apoptosis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

The arginine methyltransferase PRMT2 binds RB and regulates E2F function

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Glial protein S100B modulates long-term neuronal synaptic plasticity

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Proteins of the S100 family regulate the oligomerization of p53 tumor suppressor

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

S100B in neuropathologic states: the CRP of the brain?

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Primary cilia: putting sensors together

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Embryonic expression of pericentrin suggests universal roles in ciliogenesis.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Germinal center-associated nuclear protein contributes to affinity maturation of B cell antigen receptor in T cell-dependent responses.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Involvement of GANP in B cell activation in T cell-dependent antigen response

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Increased expression of germinal center-associated nuclear protein RNA-primase is associated with lymphomagenesis.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Collagen VI deficiency induces early onset myopathy in the mouse: an animal model for Bethlem myopathy.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Collagen VI related muscle disorders

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Dominant and recessive COL6A1 mutations in Ullrich scleroatonic muscular dystrophy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Lanosterol synthase mutations cause cholesterol deficiency-associated cataracts in the Shumiya cataract rat

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Formiminotransferase cyclodeaminase is an organ-specific autoantigen recognized by sera of patients with autoimmune hepatitis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

The molecular basis of glutamate formiminotransferase deficiency

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

A system for rapid generation of coat color-tagged knockouts and defined chromosomal rearrangements in mice

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

A new mouse embryonic stem cell line with good germ line contribution and gene targeting frequency

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Both hemopoietic and resident cells are required for MyD88-dependent pulmonary inflammatory response to inhaled endotoxin

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Toll-like receptors in innate immunity

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

A highly sensitive cell line, WEHI 164 clone 13, for measuring cytotoxic factor/tumor necrosis factor from human monocytes.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Inversion-induced disruption of the Hoxd cluster leads to the partition of regulatory landscapes.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Endothelium-derived Toll-like receptor-4 is the key molecule in LPS-induced neutrophil sequestration into lungs

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Primary and secondary transcriptional effects in the developing human Down syndrome brain and heart

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Detection of DNA copy number abnormality by microarray expression analysis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Global analysis of X-chromosome dosage compensation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Dosage compensation of the active X chromosome in mammals

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Mucociliary and long-term particle clearance in airways of patients with immotile cilia

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

The Ciliopathies: An Emerging Class of Human Genetic Disorders

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

S100: a multigenic family of calcium-modulated proteins of the EF-hand type with intracellular and extracellular functional roles

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Modulation of glial activation by astrocyte-derived protein S100B: differential responses of astrocyte and microglial cultures

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

S100B-stimulated NO production by BV-2 microglia is independent of RAGE transducing activity but dependent on RAGE extracellular domain

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

The astroglial-derived S100beta protein stimulates the expression of nitric oxide synthase in rodent macrophages through p38 MAP kinase activation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

High-mobility group box 1 protein (HMGB1): nuclear weapon in the immune arsenal

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Receptor for advanced glycation end products (RAGE) regulates sepsis but not the adaptive immune response

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Promotion of cell adherence and spreading: a novel function of RAGE, the highly selective differentiation marker of human alveolar epithelial type I cells.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Anti-inflammatory effects of the advanced glycation end product inhibitor LR-90 in human monocytes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Increased protein arginine methylation in chronic hypoxia: role of protein arginine methyltransferases

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Human subtelomeres are hot spots of interchromosomal recombination and segmental duplication

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Global variation in copy number in the human genome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Common deletions and SNPs are in linkage disequilibrium in the human genome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Common deletion polymorphisms in the human genome.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

SHIRPA, a protocol for behavioral assessment: validation for longitudinal study of neurological dysfunction in mice.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Development of SHIRPA to characterise the phenotype of gene-targeted mice

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Role of nitric oxide and cyclic GMP in the dizocilpine-induced impairment of spontaneous alternation behavior in mice.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Dual effects of p38 MAPK on TNF-dependent bronchoconstriction and TNF-independent neutrophil recruitment in lipopolysaccharide-induced acute respiratory distress syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

An advanced culture method for generating large quantities of highly pure dendritic cells from mouse bone marrow

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM152

21 January 2018

Identifiers

10.1093/HMG/DDM152

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17591625

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/17591625

ResearchGate publication ID

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