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Modeling Fanconi Anemia pathogenesis and therapeutics using integration-free patient iPSCs. Modeling Fanconi Anemia pathogenesis and therapeutics using integration-free patient iPSCs

NIAID Data Ecosystem2026-05-26 收录

范可尼贫血建模

iPSC疾病模型

数据链接：

https://www.ncbi.nlm.nih.gov/bioproject/PRJNA248194 数据链接链接失效反馈

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资源简介：

This SuperSeries is composed of the SubSeries listed below. Overall design: Refer to individual Series

应用场景：

创建时间：

2014-05-20

ALS疾病分子机制

iPSC疾病模型

We established iPSCs from healthy donors, FUS-ALS and SOD1-ALS patients. Using our differentiation protocol originally developed by Reinhardt et al.,2013, we diferentiated these iPSCs toward spinal mo

NIAID Data Ecosystem100

Elucidating the role of miRNA in the modulation of Survival Motor Neuron (SMN) genes in both fibroblasts and firboblast-derived iPSCs.. Elucidating the role of miRNA in the modulation of Survival Motor Neuron (SMN) genes in both fibroblasts and firboblast-derived iPSCs.

脊髓性肌萎缩症分子机制

iPSC疾病模型

Spinal muscular atrophy (SMA) is a devastating neuromuscular disorder that affects the spinal motor neurons and leads to progressive muscle wasting and atrophy. It is caused by a reduction in SMN prot

NIAID Data Ecosystem40

Stage-specific human induced pluripotent stem cells map the progression of myeloid transformation to transplantable leukemia. Homo sapiens

iPSC疾病模型

MDS骨髓增生异常综合征

Comparison of disease stage transitions between a panel of iPSC clones derived from different MDS patients Overall design: RNA from CD34+ cells derived from in vitro hematopoietic differentiation of i

NIAID Data Ecosystem20

Batten's Disease proteomics using iTRAQ LC-MS/MS

神经退行性疾病蛋白质

iPSC疾病模型

Proteomic analysis using iTRAQ technique to identify global changes in Batten's disease samples using iPSCs derived from keratinocytes and differentiated to iNPCs Three separate mass spectrometry runs

NIAID Data Ecosystem50

RNA-seq profiling of MED patient-derived (MATN3 T195K) and unaffected iPSC-chondrogenesis

iPSC疾病模型

软骨分化转录组学

PBMCs from MED patients carrying the MATN3 T195K mutation and unaffected controls were reprogrammed into hiPSCs using Sendai virus. Data includes three differentiation stages: pluripotent hiPSCs, iMSC

NIAID Data Ecosystem30

Modeling Fanconi Anemia pathogenesis and therapeutics using integration-free patient iPSCs. Modeling Fanconi Anemia pathogenesis and therapeutics using integration-free patient iPSCs

资源简介：

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