Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death - Wikidata - awgldk - TriplyDB

Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death

Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death

http://www.wikidata.org/entity/Q24682020

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A highly conserved SOX6 double binding site mediates SOX6 gene downregulation in erythroid cells Sox6 regulation of cardiac myocyte development Control of cell fate and differentiation by Sry-related high-mobility-group box (Sox) transcription factors Sox6 directly silences epsilon globin expression in definitive erythropoiesis.MiR-499 regulates cell proliferation and apoptosis during late-stage cardiac differentiation via Sox6 and cyclin D1 SOX7 and GATA-4 are competitive activators of Fgf-3 transcription Sox6 is necessary for efficient erythropoiesis in adult mice under physiological and anemia-induced stress conditions SOX7 transcription factor: sequence, chromosomal localisation, expression, transactivation and interference with Wnt signalling Identification of a human glioma antigen, SOX6, recognized by patients' sera.Characterization of the chromosomal inversion associated with the Koa mutation in the mouse revealed the cause of skeletal abnormalities Uncoupling of expression of an intronic microRNA and its myosin host gene by exon skipping A direct role of SRY and SOX proteins in pre-mRNA splicing.Genome-wide mapping of Sox6 binding sites in skeletal muscle reveals both direct and indirect regulation of muscle terminal differentiation by Sox6.Sox6 overexpression causes cellular aggregation and the neuronal differentiation of P19 embryonic carcinoma cells in the absence of retinoic acid.Genomewide linkage and peakwide association analyses of carotid plaque in Caribbean Hispanics Repression of SOX6 transcriptional activity by SUMO modification.Sox6 up-regulation by macrophage migration inhibitory factor promotes survival and maintenance of mouse neural stem/progenitor cells.Regulation of Sox6 by cyclin dependent kinase 5 in brain Transcriptome Dynamics and Potential Roles of Sox6 in the Postnatal Heart.Trip12, a HECT domain E3 ubiquitin ligase, targets Sox6 for proteasomal degradation and affects fiber type-specific gene expression in muscle cells.Genetic analysis of tongue size and taste papillae number and size in recombinant inbred strains of mice.The SoxD transcription factors--Sox5, Sox6, and Sox13--are key cell fate modulators.A spectrum of gene regulatory phenomena at mammalian beta-globin gene loci.Advances in the understanding of haemoglobin switching.Sox6, jack of all trades: a versatile regulatory protein in vertebrate development Sox6 suppression induces RA-dependent apoptosis mediated by BMP-4 expression during neuronal differentiation in P19 cells.The transcription factor Sox5 modulates Sox10 function during melanocyte development.Suppression of Sox6 in P19 cells leads to failure of neuronal differentiation by retinoic acid and induces retinoic acid-dependent apoptosis.Inducing indel mutation in the SOX6 Gene by Zinc Finger Nuclease for gamma reactivation: An Approach towards Gene Therapy of Beta Thalassemia.Expression of Sox genes in tooth development.Electrical stimulation influences chronic intermittent hypoxia-hypercapnia induction of muscle fibre transformation by regulating the microRNA/Sox6 pathway Unravelling pathways downstream Sox6 induction in K562 erythroid cells by proteomic analysis.Sox13 functionally complements the related Sox5 and Sox6 as important developmental modulators in mouse spinal cord oligodendrocytes.SOX6 Downregulation Induces γ-Globin in Human β-Thalassemia Major Erythroid Cells.

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P2860

Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death

http://www.wikidata.org/entity/Q24682020

description

2000 nî lūn-bûn

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2000 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2000 թվականի ապրիլին հրատարակված գիտական հոդված

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2000年の論文

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2000年学术文章

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2000年学术文章

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2000年学术文章

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2000年学术文章

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2000年学术文章

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2000年學術文章

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Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death

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Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death

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Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death

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Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death

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Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death

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Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death

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Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death

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Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death

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Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death

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D T Erickson

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M F Lyon

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M H Brilliant

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N Hagiwara

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R A Samson

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S E Klewer

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P2860

The ancestral gene for transcribed, low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking, which is deficient in mice with neuromuscular and spermiogenic abnormalities

Congenital heart disease caused by mutations in the transcription factor NKX2-5

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome

Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model

Cloning and characterization of SOX5, a new member of the human SOX gene family

A new long form of Sox5 (L-Sox5), Sox6 and Sox9 are coexpressed in chondrogenesis and cooperatively activate the type II collagen gene

From head to toes: the multiple facets of Sox proteins

Molecular characterization of radiation- and chemically induced mutations associated with neuromuscular tremors, runting, juvenile lethality, and sperm defects in jdf2 mice

Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9

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1477144

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10.1073/PNAS.97.8.4180

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8

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97

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235609286

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10760285

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18189

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