Comparing ESC and iPSC-Based Models for Human Genetic Disorders
about
Pluripotent stem cells: the last 10 years.Functional Divergence of the Nuclear Receptor NR2C1 as a Modulator of Pluripotentiality During Hominid Evolution.Pluripotent stem cells in disease modelling and drug discovery.Epithelial-mesenchymal transition (EMT): A biological process in the development, stem cell differentiation, and tumorigenesis.Multiple roles of NF1 in the melanocyte lineage.Proteomics and molecular tools for unveiling missing links in the biochemical understanding of schizophrenia.Generation of Cholinergic and Dopaminergic Interneurons from Human Pluripotent Stem Cells as a Relevant Tool for In Vitro Modeling of Neurological Disorders Pathology and Therapy.Molecular Characterization of Down Syndrome Embryonic Stem Cells Reveals a Role for RUNX1 in Neural Differentiation.Combining Patient-Reprogrammed Neural Cells and Proteomics as a Model to Study Psychiatric Disorders.
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P2860
Comparing ESC and iPSC-Based Models for Human Genetic Disorders
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
Comparing ESC and iPSC-Based Models for Human Genetic Disorders
@ast
Comparing ESC and iPSC-Based Models for Human Genetic Disorders
@en
type
label
Comparing ESC and iPSC-Based Models for Human Genetic Disorders
@ast
Comparing ESC and iPSC-Based Models for Human Genetic Disorders
@en
prefLabel
Comparing ESC and iPSC-Based Models for Human Genetic Disorders
@ast
Comparing ESC and iPSC-Based Models for Human Genetic Disorders
@en
P2860
P356
P1476
Comparing ESC and iPSC-Based Models for Human Genetic Disorders
@en
P2093
Achia Urbach
Tomer Halevy
P2860
P304
P356
10.3390/JCM3041146
P577
2014-10-24T00:00:00Z