(Q40596613)

English

DSCR1 gene expression is dependent on NFATc1 during cardiac valve formation and colocalizes with anomalous organ development in trisomy 16 mice

scientific article published on February 2004

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

DSCR1 gene expression is dependent on NFATc1 during cardiac valve formation and colocalizes with anomalous organ development in trisomy 16 mice (English)

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

1 reference

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Katherine E. Yutzey

object named as

Katherine E Yutzey

3

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Jeffery D. Molkentin

object named as

Jeffery D Molkentin

2

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author name string

Alexander W Lange

1

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Europe PubMed Central

PubMed publication ID

21 September 2017

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publication date

1 February 2004

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Europe PubMed Central

PubMed publication ID

21 September 2017

Developmental Biology

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Europe PubMed Central

PubMed publication ID

21 September 2017

266

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Europe PubMed Central

PubMed publication ID

21 September 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

346-360

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

Nuclear localization of NF-ATc by a calcineurin-dependent, cyclosporin-sensitive intramolecular interaction

1 reference

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Low copy number detection of herpes simplex virus type 1 mRNA and mouse Th1 type cytokine mRNAs by Light Cycler quantitative real-time PCR.

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Abnormal blood vessel development and lethality in embryos lacking a single VEGF allele

1 reference

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Dscr1, a novel endogenous inhibitor of calcineurin signaling, is expressed in the primitive ventricle of the heart and during neurogenesis.

1 reference

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Cardiac compartment-specific overexpression of a modified retinoic acid receptor produces dilated cardiomyopathy and congestive heart failure in transgenic mice

1 reference

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NFAT signaling: choreographing the social lives of cells

1 reference

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Ocular findings in Down's syndrome

1 reference

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Role of the NF-ATc transcription factor in morphogenesis of cardiac valves and septum

1 reference

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VEGF modulates early heart valve formation.

1 reference

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Lack of regulation in the heart forming region of avian embryos.

1 reference

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Genetic control of the survival of murine trisomy 16 fetuses

1 reference

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Mouse trisomy 16: an animal model of human trisomy 21 (Down syndrome)

1 reference

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Chronic overexpression of the calcineurin inhibitory gene DSCR1 (Adapt78) is associated with Alzheimer's disease

1 reference

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The DSCR1 (Adapt78) isoform 1 protein calcipressin 1 inhibits calcineurin and protects against acute calcium-mediated stress damage, including transient oxidative stress.

1 reference

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Heterozygous embryonic lethality induced by targeted inactivation of the VEGF gene

1 reference

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A new human gene from the Down syndrome critical region encodes a proline-rich protein highly expressed in fetal brain and heart

1 reference

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Genomic organization, alternative splicing, and expression patterns of the DSCR1 (Down syndrome candidate region 1) gene

1 reference

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DSCR1, overexpressed in Down syndrome, is an inhibitor of calcineurin-mediated signaling pathways

1 reference

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Nf1 has an essential role in endothelial cells

1 reference

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A gene expression map of human chromosome 21 orthologues in the mouse

1 reference

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NFAT signaling in vertebrate development

1 reference

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The DNA sequence of human chromosome 21

1 reference

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NFATc1 mediates vascular endothelial growth factor-induced proliferation of human pulmonary valve endothelial cells

1 reference

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7 January 2021

Down syndrome and mouse models.

1 reference

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Down syndrome phenotypes: the consequences of chromosomal imbalance

1 reference

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Nkx-2.5 gene induction in mice is mediated by a Smad consensus regulatory region.

1 reference

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Examination of the eyelid closure defect in trisomy 16 mice

1 reference

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The embryonic development of sensory organs and the skull in the trisomy 16 mouse, an animal model for Down's syndrome.

1 reference

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7 January 2021

Partners in transcription: NFAT and AP-1.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2003.10.036

7 January 2021

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

1 reference

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7 January 2021

Molecular cloning of a novel thyroid hormone-responsive gene, ZAKI-4, in human skin fibroblasts

1 reference

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A calcineurin-dependent transcriptional pathway for cardiac hypertrophy

1 reference

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A comparison of whole-genome shotgun-derived mouse chromosome 16 and the human genome.

1 reference

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7 January 2021

Identification of amino acid residues and protein kinases involved in the regulation of NFATc subcellular localization

1 reference

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7 January 2021

The transcription factor NF-ATc is essential for cardiac valve formation

1 reference

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7 January 2021

Transcription factors of the NFAT family: regulation and function

1 reference

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Too much of a good thing: mechanisms of gene action in Down syndrome.

1 reference

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Human chromosome 21 gene expression atlas in the mouse.

1 reference

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A protein encoded within the Down syndrome critical region is enriched in striated muscles and inhibits calcineurin signaling

1 reference

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Myocyte-enriched calcineurin-interacting protein, MCIP1, inhibits cardiac hypertrophy in vivo

1 reference

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The role of modulatory calcineurin-interacting proteins in calcineurin signaling

1 reference

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A new gene family including DSCR1 (Down Syndrome Candidate Region 1) and ZAKI-4: characterization from yeast to human and identification of DSCR1-like 2, a novel human member (DSCR1L2)

1 reference

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Dual roles of modulatory calcineurin-interacting protein 1 in cardiac hypertrophy

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Conotruncal anomalies in the trisomy 16 mouse: an immunohistochemical analysis with emphasis on the involvement of the neural crest

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Endocardial cushion development and heart loop architecture in the trisomy 16 mouse.

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Cardiac morphology at late fetal stages in the mouse with trisomy 16: consequences for different formation of the atrioventricular junction when compared to humans with trisomy 21

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Mechanisms of deficient cardiac septation in the mouse with trisomy 16.

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Occurrence of neuropathological changes and dementia of Alzheimer's disease in Down's syndrome.

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MEF2 responds to multiple calcium-regulated signals in the control of skeletal muscle fiber type

1 reference

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Independent signals control expression of the calcineurin inhibitory proteins MCIP1 and MCIP2 in striated muscles

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Abnormal pinna type and hearing loss correlations in Down's syndrome.

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10.1016/J.YDBIO.2003.10.036

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

ResearchGate publication ID

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