Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ju-Chiat Tan"'
Autor:
Ze-Yan Yu, Ju-Chiat Tan, Aisling C McMahon, Siiri E Iismaa, Xiao-Hui Xiao, Scott H Kesteven, Melissa E Reichelt, Marion C Mohl, Nicola J Smith, Diane Fatkin, David Allen, Stewart I Head, Robert M Graham, Michael P Feneley
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e99024 (2014)
To determine the mechanisms by which the α1A-adrenergic receptor (AR) regulates cardiac contractility.We reported previously that transgenic mice with cardiac-restricted α1A-AR overexpression (α1A-TG) exhibit enhanced contractility but not hypertr
Externí odkaz:
https://doaj.org/article/7cf2975340e84d309efedf580a689349
Autor:
Xiao-Hui Xiao, Li Sze Yeo, Christiana Leimena, Qiuping Zhang, Arthur Carlton, Ju-Chiat Tan, Scott H. Kesteven, Catherine M. Shanahan, Vesna Nikolova-Krstevski, Ze-Yan Yu, Stewart I. Head, Michael P. Feneley, Diane Fatkin
Publikováno v:
Journal of Molecular and Cellular Cardiology. 50:479-486
Lamin A/C mutations are the most common cause of familial dilated cardiomyopathy (DCM) but the pathogenetic mechanisms are incompletely understood. Nesprins are spectrin repeat-containing proteins that interact with lamin A/C and are components of th
Autor:
Suchitra Chandar, Lina Karlsdotter, Vesna Nikolova-Krstevski, Arthur Carlton, Shweta Natarajan, S. Rainer, Diane Fatkin, Yoshinori Yasuoka, Li Sze Yeo, Christiana Leimena, Margaret Gardiner-Garden, Michael P. Feneley, Xiao-Hui Xiao, Scott H. Kesteven, Ju-Chiat Tan, Jianxin Wu
Publikováno v:
Circulation Research. 106:573-582
Rationale : Mutations in the LMNA gene, which encodes the nuclear lamina proteins lamin A and lamin C, are the most common cause of familial dilated cardiomyopathy (DCM). Mechanical stress-induced apoptosis has been proposed as the mechanism underpin
Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C–deficient mice
Autor:
Vesna Nikolova, Christiana Leimena, Aisling C. McMahon, Ju Chiat Tan, Suchitra Chandar, Dilesh Jogia, Scott H. Kesteven, Jan Michalicek, Robyn Otway, Fons Verheyen, Stephen Rainer, Colin L. Stewart, David Martin, Michael P. Feneley, Diane Fatkin
Laminopathies are a group of disorders caused by mutations in the LMNA gene that encodes the nuclear lamina proteins, lamin A and lamin C; their pathophysiological basis is unknown. We report that lamin A/C–deficient (Lmna–/–) mice develop rapi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f1fa873397907c21b599ee81e997e39
https://europepmc.org/articles/PMC324538/
https://europepmc.org/articles/PMC324538/
Autor:
Hutao Gong, Ze-Yan Yu, Stewart I. Head, Melissa E. Reichelt, Scott H. Kesteven, Ju-Chiat Tan, Xiao-Hui Xiao, Michael P. Feneley, Aisling C. McMahon, A Sketchley, David G. Allen, Yun Dai, L Yang, Diane Fatkin, Siiri E. Iismaa, Marion C. Mohl, Robert M. Graham
Publikováno v:
Heart, Lung and Circulation. 22:S59
Autor:
Chandar, Suchitra, Li Sze Yeo, Leimena, Christiana, Ju-Chiat Tan, Xiao-Hui Xiao, Nikolova-Krstevski, Vesna, Yasuoka, Yoshinori, Gardiner-Garden, Margaret, Jianxin Wu, Kesteven, Scott, Karisdotter, Lina, Natarajan, Shweta, Canton, Arthur, Rainer, Stephen, Feneley, Michael P., Fatkin, Diane
Publikováno v:
Circulation Research; 2/19/2010, Vol. 106 Issue 3, p573-582, 10p
Autor:
Nikolova, Vesna1, Leimena, Christiana1, McMahon, Aisling C.2, Ju Chiat Tan, Aisling C.2, Chandar, Suchitra1, Jogia, Dilesh3, Kesteven, Scott H.2, Michalicek, Jan1, Otway, Robyn1, Verheyen, Fons4, Rainer, Stephen5, Stewart, Colin L.6, Martin, David3, Feneley, Michael P.2, Fatkin, Diane1 d.fatkin@victorchang.unsw.edu.au
Publikováno v:
Journal of Clinical Investigation. Feb2004, Vol. 113 Issue 3, p357-369. 13p. 21 Color Photographs, 15 Black and White Photographs, 4 Charts, 6 Graphs.