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Selective Death in Spinal Muscular Atrophy: Genome-Wide RNA-Seq Using Purified Patient-Derived Motor Neurons. Homo sapiens
Spinal Muscular Atrophy (SMA) is well-known to be caused by mutations in the gene Survival of Motor Neuron 1 (SMN1). Because this gene is ubiquitously expressed, it remains poorly understood why motor
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Depressed beta-adrenergic inotropic responsiveness and intracellular calcium handling abnormalities in Duchenne Muscular Dystrophy patients induced pluripotent stem cell-derived cardiomyocytes
Duchenne Muscular Dystrophy (DMD) caused by mutations in the dystrophin gene,is an X-linked disease affecting male and rarely adult heterozygous females, resulting in death by the late 20s early 30s.
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Data_Sheet_1_Dementia-related genetic variants in an Italian population of early-onset Alzheimer’s disease.docx
Early-onset Alzheimer’s disease (EOAD) is the most common form of early-onset dementia. Although three major genes have been identified as causative, the genetic contribution to the disease remains un
NIAID Data Ecosystem30
Spinal Muscular Atrophy Patient iPSC-Derived Motor Neurons Display Altered Proteomes at Early Stages of Differentiation
Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disorder characterized by loss of motor neurons (MN) in the spinal cord leading to progressive muscle atrophy and weakness. SM
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Additional file 5: of Dipeptide repeat proteins activate a heat shock response found in C9ORF72-ALS/FTLD patients
Table S3. Genes significantly changes in RNA-seq analysis from ALS patients. (XLSX 52 kb)
Figshare2018-07-05 更新40
