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Additional file 1 of Use of constitutive and inducible oncogene-containing iPSCs as surrogates for transgenic mice to study breast oncogenesis

NIAID Data Ecosystem2026-03-12 收录

乳腺癌发生机制

iPSC疾病模型

数据链接：

https://figshare.com/articles/dataset/Additional_file_1_of_Use_of_constitutive_and_inducible_oncogene-containing_iPSCs_as_surrogates_for_transgenic_mice_to_study_breast_oncogenesis/14691729 数据链接链接失效反馈

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资源简介：

Additional file 1.

应用场景：

创建时间：

2021-05-27

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 Ecosystem110

Personalized genome sequencing coupled with iPSC technology identifies GTDC1 as a gene involved in Neurodevelopmental Disorders. Homo sapiens

神经发育障碍分子机制

iPSC疾病模型

The cellular and molecular mechanisms underlying neurodevelopmental conditions such as autism spectrum disorders have been studied intensively for decades. The ability to generate patient-specific ind

NIAID Data Ecosystem50

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

Gene expression data from human fibroblasts and induced Pluripotent Stem cells from amyotrophic lateral sclerosis patients. Homo sapiens

ALS分子机制

iPSC疾病模型

We have generated human induced Pluripotent Stem cells (hiPSc) from amyotrophic lateral sclerosis (ALS, motor neuron disease) patients, using Sendai virus-mediated delivery of reprogramming factors. h

NIAID Data Ecosystem60

Additional file 1: of Induced pluripotent stem cell models of Zellweger spectrum disorder show impaired peroxisome assembly and cell type-specific lipid abnormalities

iPSC疾病模型

Zellweger谱系障碍

Characterization of candidate iPSCs. A complete listing of the protein, genetic, epigenetic, and cell differentiation assays performed on the iPSCs generated in this study is provided. (XLSX 11 kb)

Figshare2016-12-15 更新50

Additional file 1 of Use of constitutive and inducible oncogene-containing iPSCs as surrogates for transgenic mice to study breast oncogenesis

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