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资源简介：
Gene Expression Changes in Nemaline Myopathy
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创建时间：
2015-09-01
相关数据集
Gene expression profiles using microarrays in mdx and mdx/MMP-2-/- mice at 1 and 3 months of age. Mus musculus
Matrix metalloprotease (MMP) -2 has been reported to be up-regulated in skeletal muscle in the lethal X-linked muscle disorder Duchenne muscular dystrophy (DMD), which is caused by loss of dystrophin.
NIAID Data Ecosystem70
Temporal expression profiling of beta- and gamma-sarcoglycan deficient mice. Mus musculus
Temporal expression profiling of hindlimb muscle of beta- and gamma-sarcoglycan deficient mice aged 1, 2.5, 4, 6, 8, 10, 12, 14 and 20 weeks. Keywords: time course Overall design: 4 closed loop-design
NIAID Data Ecosystem40
Canine skeletal muscle RNAscope raw data and analysis
Raw image data, imageJ macros used for analysis, and analysis of healthy and dystrophic canine muscle probed with dystrophin multiplex ISH RNAscope probes. Data used for manuscriptSingle-transcript mu
NIAID Data Ecosystem40
Increased Systemic HSP70B Levels in Spinal Muscular Atrophy Infants. Increased Systemic HSP70B Levels in Spinal Muscular Atrophy Infants
RNA sequencing in whole blood from spinal muscular atrophy patients and healthy control infants Overall design: Here, we performed whole-blood RNA sequencing and differential expression analyses in SM
NIAID Data Ecosystem60
SMCHD1 activates the expression of genes required for the expansion of human myoblasts (RNA-seq). SMCHD1 activates the expression of genes required for the expansion of human myoblasts (RNA-seq)
In human muscle, SMCHD1 mutations are associated with the onset of FSHD2, but the mechanism driving the disease onset remains unclear. A commonly accepted explanation is the loss of SMCHD1 binding to
NIAID Data Ecosystem40
