Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress.
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Attention to Background Strain Is Essential for Metabolic Research: C57BL/6 and the International Knockout Mouse ConsortiumThree-Dimensional Model of Human Nicotinamide Nucleotide Transhydrogenase (NNT) and Sequence-Structure Analysis of its Disease-Causing Variations.Adipogenic placenta-derived mesenchymal stem cells are not lineage restricted by withdrawing extrinsic factors: developing a novel visual angle in stem cell biology.Proton-Translocating Nicotinamide Nucleotide Transhydrogenase: A Structural Perspective.Glucocorticoid deficiency causes transcriptional and post-transcriptional reprogramming of glutamine metabolism
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Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress.
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Combined mineralocorticoid and ...... nd increases oxidative stress.
@en
Combined mineralocorticoid and ...... nd increases oxidative stress.
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type
label
Combined mineralocorticoid and ...... nd increases oxidative stress.
@en
Combined mineralocorticoid and ...... nd increases oxidative stress.
@nl
prefLabel
Combined mineralocorticoid and ...... nd increases oxidative stress.
@en
Combined mineralocorticoid and ...... nd increases oxidative stress.
@nl
P2093
P2860
P1476
Combined mineralocorticoid and ...... nd increases oxidative stress.
@en
P2093
Abdulsalam Abu-Libdeh
Ariella Weinberg-Shukron
Aviram Kogot-Levin
David Zangen
Fouad Zhadeh
Lara Kamal
Liran Carmel
Moien Kanaan
Paul Renbaum
Sharon Zeligson
P2860
P304
P356
10.1136/JMEDGENET-2015-103078
P407
P577
2015-06-12T00:00:00Z