Hepatocyte-Specific Deletion of Mouse Lamin A/C Leads to Male-Selective Steatohepatitis.
about
Nuclear lamina genetic variants, including a truncated LAP2, in twins and siblings with nonalcoholic fatty liver disease.Lamin Deficiency in the Liver Sets the Stage for Nonalcoholic Steatohepatitis Development in Males.Lamin A/C Maintains Exocrine Pancreas Homeostasis by Regulating Stability of RB and Activity of E2F.Changes at the nuclear lamina alter binding of pioneer factor Foxa2 in aged liver.Potential association of LMNA-associated generalized lipodystrophy with juvenile dermatomyositis.
P2860
Hepatocyte-Specific Deletion of Mouse Lamin A/C Leads to Male-Selective Steatohepatitis.
description
2017 nî lūn-bûn
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2017年論文
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2017年論文
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2017年論文
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name
Hepatocyte-Specific Deletion of Mouse Lamin A/C Leads to Male-Selective Steatohepatitis.
@en
type
label
Hepatocyte-Specific Deletion of Mouse Lamin A/C Leads to Male-Selective Steatohepatitis.
@en
prefLabel
Hepatocyte-Specific Deletion of Mouse Lamin A/C Leads to Male-Selective Steatohepatitis.
@en
P2093
P2860
P1476
Hepatocyte-Specific Deletion of Mouse Lamin A/C Leads to Male-Selective Steatohepatitis.
@en
P2093
Colin L Stewart
Graham F Brady
Hope Martin
Makayla J Brunt
Maria Brzozowski
Min-Jung Park
Ram K Menon
Raymond Kwan
Sujith V Weerasinghe
P2860
P304
P356
10.1016/J.JCMGH.2017.06.005
P50
P577
2017-07-06T00:00:00Z