Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.
about
Facioscapulohumeral dystrophy: the path to consensus on pathophysiologyEvidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD)STRP screening sets for the human genome at 5 cM densityChromosome 4 localization of a second gene for autosomal dominant polycystic kidney diseaseInfluence of Repressive Histone and DNA Methylation upon D4Z4 Transcription in Non-Myogenic CellsActinin-associated LIM protein-deficient mice maintain normal development and structure of skeletal muscleExclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1BChromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy[Facioscapulohumeral muscular dystrophy. Clinical picture, atypical forms, diagnostics, genetics].Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiationGenetic counselling in facioscapulohumeral muscular dystrophyMyogenic enhancers regulate expression of the facioscapulohumeral muscular dystrophy-associated DUX4 gene.Mouse Dux is myotoxic and shares partial functional homology with its human paralog DUX4.De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1).Improved molecular diagnosis of facioscapulohumeral muscular dystrophy (FSHD): validation of the differential double digestion for FSHDDiagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases.Chronic pain in persons with myotonic dystrophy and facioscapulohumeral dystrophy.The muscular dystrophies.Decreased proliferation kinetics of mouse myoblasts overexpressing FRG1.The D4Z4 repeat-mediated pathogenesis of facioscapulohumeral muscular dystrophyComprehensive expression analysis of FSHD candidate genes at the mRNA and protein level.Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortionIdentifying diagnostic DNA methylation profiles for facioscapulohumeral muscular dystrophy in blood and saliva using bisulfite sequencing.Molecular diagnosis of facioscapulohumeral muscular dystrophy.Facioscapulohumeral Muscular Dystrophy: More Complex than it Appears.DUX4 differentially regulates transcriptomes of human rhabdomyosarcoma and mouse C2C12 cellsFacioscapulohumeral muscular dystrophy and DUX4: breaking the silence.miRNA expression in control and FSHD fetal human muscle biopsiesLinkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD)Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD)DNA typing and genetic mapping with trimeric and tetrameric tandem repeatsAmerican Society of Human Genetics presidential address, October 18, 1990A new dosage test for subtelomeric 4;10 translocations improves conventional diagnosis of facioscapulohumeral muscular dystrophy (FSHD).FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients.Recent advances in understanding muscular dystrophyEmerging preclinical animal models for FSHD.Facioscapulohumeral muscular dystrophy as a model for epigenetic regulation and diseaseHigh proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy familiesAtypical onset in a series of 122 cases with FacioScapuloHumeral Muscular Dystrophy.
P2860
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P2860
Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.
description
1990 nî lūn-bûn
@nan
1990年の論文
@ja
1990年学术文章
@wuu
1990年学术文章
@zh-cn
1990年学术文章
@zh-hans
1990年学术文章
@zh-my
1990年学术文章
@zh-sg
1990年學術文章
@yue
1990年學術文章
@zh
1990年學術文章
@zh-hant
name
Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.
@en
Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.
@nl
type
label
Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.
@en
Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.
@nl
prefLabel
Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.
@en
Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.
@nl
P2093
P1433
P1476
Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.
@en
P2093
C Wijmenga
G W Padberg
O F Brouwer
R R Frants
P304
P356
10.1016/0140-6736(90)92148-B
P407
P577
1990-09-01T00:00:00Z