Altered iPSC-derived neurons' sodium channel properties in subjects with Monge's disease.
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Senp1 drives hypoxia-induced polycythemia via GATA1 and Bcl-xL in subjects with Monge's disease.The translational potential of human induced pluripotent stem cells for clinical neurology : The translational potential of hiPSCs in neurology.The Na+/HCO3- co-transporter is protective during ischemia in astrocytes.Intracellular pH Regulation in iPSCs-derived Astrocytes from Subjects with Chronic Mountain Sickness.MITOCHONDRIAL DYSFUNCTION IN IPSC-DERIVED NEURONS OF SUBJECTS WITH CHRONIC MOUNTAIN SICKNESS.
P2860
Altered iPSC-derived neurons' sodium channel properties in subjects with Monge's disease.
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2015 nî lūn-bûn
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2015 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի հունվարին հրատարակված գիտական հոդված
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2015年の論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年论文
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name
Altered iPSC-derived neurons' sodium channel properties in subjects with Monge's disease.
@ast
Altered iPSC-derived neurons' sodium channel properties in subjects with Monge's disease.
@en
type
label
Altered iPSC-derived neurons' sodium channel properties in subjects with Monge's disease.
@ast
Altered iPSC-derived neurons' sodium channel properties in subjects with Monge's disease.
@en
prefLabel
Altered iPSC-derived neurons' sodium channel properties in subjects with Monge's disease.
@ast
Altered iPSC-derived neurons' sodium channel properties in subjects with Monge's disease.
@en
P2093
P2860
P1433
P1476
Altered iPSC-derived neurons' sodium channel properties in subjects with Monge's disease.
@en
P2093
A R Muotri
D Callacondo
G G Haddad
O Appenzeller
T Chailangkarn
P2860
P304
P356
10.1016/J.NEUROSCIENCE.2014.12.039
P407
P577
2015-01-03T00:00:00Z