Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Lane H. Wilson"'
Autor:
Lane H. Wilson, Jun‐Ho Cho, Ana Estrella, Joan A. Smyth, Rong Wu, Tayoot Chengsupanimit, Laurie M. Brown, David A. Weinstein, Young Mok Lee
Publikováno v:
Hepatology Communications, Vol 3, Iss 11, Pp 1544-1555 (2019)
Mutations in the liver glycogen phosphorylase (Pygl) gene are associated with the diagnosis of glycogen storage disease type VI (GSD‐VI). To understand the pathogenesis of GSD‐VI, we generated a mouse model with Pygl deficiency (Pygl−/−). Pyg
Externí odkaz:
https://doaj.org/article/eb094ee5286e491c88069ed9a8d697ac
Autor:
Yusuke Yamamoto, Xia Wang, Denis Bertrand, Florian Kern, Ting Zhang, Marcin Duleba, Supriya Srivastava, Chiea Chuen Khor, Yuanyu Hu, Lane H. Wilson, Hagen Blaszyk, Daniil Rolshud, Ming Teh, Jianjun Liu, Brooke E. Howitt, Matthew Vincent, Christopher P. Crum, Niranjan Nagarajan, Khek Yu Ho, Frank McKeon, Wa Xian
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-10 (2016)
Barrett’s oesophagus is a precancerous intestinal metaplasia that can progress to oesophageal adenocarcinoma. In this study, the authors isolate and characterize human Barrett’s stem cells and identify a specific genomic pedigree that supports th
Externí odkaz:
https://doaj.org/article/c0724ec3705f4b048002d0900b5ba0a1
Autor:
Charles J, Arends, Lane H, Wilson, Ana, Estrella, Oh Sung, Kwon, David A, Weinstein, Young Mok, Lee
Publikováno v:
International journal of molecular sciences. 23(17)
Glycogen storage disease type IX (GSD-IX) constitutes nearly a quarter of all GSDs. This ketotic form of GSD is caused by mutations in phosphorylase kinase (PhK), which is composed of four subunits (α, β, γ, δ). PhK is required for the activation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9c5b07e11bec93ebddb3666e8e621435
https://pubmed.ncbi.nlm.nih.gov/36077341
https://pubmed.ncbi.nlm.nih.gov/36077341
Autor:
Jun-Ho Cho, Tayoot Chengsupanimit, David A. Weinstein, Laurie M. Brown, Ana M. Estrella, Lane H. Wilson, Young Mok Lee, Rong Wu, Joan A. Smyth
Publikováno v:
Hepatology Communications
Hepatology Communications, Vol 3, Iss 11, Pp 1544-1555 (2019)
Hepatology Communications, Vol 3, Iss 11, Pp 1544-1555 (2019)
Mutations in the liver glycogen phosphorylase (Pygl) gene are associated with the diagnosis of glycogen storage disease type VI (GSD-VI). To understand the pathogenesis of GSD-VI, we generated a mouse model with Pygl deficiency (Pygl -/-). Pygl -/- m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82dae2e44eb7c0a2a2b15313199bbdad
https://pubmed.ncbi.nlm.nih.gov/31701076
https://pubmed.ncbi.nlm.nih.gov/31701076
Autor:
Janice Y. Chou, Chi-Jiunn Pan, Hyun Sik Jun, Young Mok Lee, Lane H. Wilson, Su-Ru Lin, Brian C. Mansfield
Publikováno v:
Hepatology (Baltimore, Md.). 56(5)
Glycogen storage disease type Ia (GSD-Ia), which is characterized by impaired glucose homeostasis and chronic risk of hepatocellular adenoma (HCA), is caused by deficiencies in the endoplasmic reticulum (ER)-associated glucose-6-phosphatase-α (G6Pas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24bc2e6c8546754e71435233981e4815
https://pubmed.ncbi.nlm.nih.gov/22706804
https://pubmed.ncbi.nlm.nih.gov/22706804