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Quantitative Analysis of Human Pluripotency and Neural Specification By In-Depth (Phospho)Proteomic Profiling

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干细胞蛋白质组学

神经分化转录调控

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Quantitative (Phospho)Proteomic Profiling of Human Pluripotency and Neural Specification

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创建时间：

2016-08-25

阿尔茨海默病模型

神经分化转录调控

Alzheimer’s disease (AD) is preceded by a long prodromal period of decades during which pathology accumulates in the brain prior to the onset of dementia. The molecular basis of these changes as well

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Additional file 7: Table S6. of A proteomic analysis of chondrogenic, osteogenic and tenogenic constructs from ageing mesenchymal stem cells

干细胞蛋白质组学

细胞分裂机制

Complete list of significantly expressed proteins and DAVID analysis of the expression patterns. (XLSX 297 kb)

Figshare2016-12-15 更新40

Diversification of posterior Hox patterning by graded ability to engage inaccessible chromatin [RNA-seq]. Diversification of posterior Hox patterning by graded ability to engage inaccessible chromatin [RNA-seq]

HOX基因功能

神经分化转录调控

While Hox genes encode for similar transcription factors (TFs), they induce different fates across body axes. We sought to understand how Hox TF genomic binding preferences relate to their patterning

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Proteomic profiling of human mesenchymal stem cells derived from umbilical cord or adipose tissue

干细胞蛋白质组学

组织来源比较

We performed a proteomic profiling of human mesenchymal stem cells (hMSCs) derived from adipose tissue or umbilical cord.

NIAID Data Ecosystem50

Quantitative subcellular proteomics using SILAC reveals enhanced metabolic buffering in ground state pluripotency

干细胞蛋白质组学

代谢功能调控

The ground state of pluripotency is defined as a minimal unrestricted state as present in the Inner Cell Mass (ICM). Mouse embryonic stem cells (ESCs) grown in a defined serum-free medium with two kin

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Quantitative Analysis of Human Pluripotency and Neural Specification By In-Depth (Phospho)Proteomic Profiling

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