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Mouse Models for Muscular Dystrophy
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创建时间：
2010-06-06
相关数据集
Data from: A family-based study into penetrance in facioscapulohumeral muscular dystrophy type 1
Objective: An observational cross-sectional study was conducted in a national facioscapulohumeral muscular dystrophy (FSHD) expertise center to estimate the penetrance of FSHD1 and to evaluate phenoty
DataONE2018-08-08 更新60
Additional file 3 of The nSMase2/Smpd3 gene modulates the severity of muscular dystrophy and the emotional stress response in mdx mice
Additional file 3 : Table S3. Oligonucleotide sequences for genotyping the nSMase2/Smpd3 and the dystrophin genes.
Figshare2020-11-19 更新50
Feminized behavior and gene expression in the BNST/POA in a novel mouse model of Klinefelter Syndrome. Mus musculus
Analysis of gene expression in the bed nucleus of the stria terminalis/preoptic area in a mouse model of Klinefelter Syndrome (the Sex Chromosome Trisomy model). The hypothesis tested was that feminiz
NIAID Data Ecosystem40
Inactivation of Pkd2 in adult mice results in delayed cyst formation and identifies sex as a major modifier of disease severity
Autosomal Dominant Polycystic Kidney Disease (ADPKD) is caused by mutations in PKD1 or PKD2 and is the most common single gene disorder resulting in end-stage kidney disease. Since deletion of either
NIAID Data Ecosystem60
Developmental Alterations in the Transcriptome of Three Distinct Rodent Models of Schizophrenia
Schizophrenia is a debilitating disorder affecting just under 1% of the population. While the symptoms of this disorder do not appear until late adolescence, pathological alterations likely occur earl
NIAID Data Ecosystem50
