Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Guanglan, Guo"'
Autor:
Anne Keogh, Robyn Otway, Diane Fatkin, Christopher S. Hayward, Changbaig Hyun, Aaron M. Zorn, Margaret Sunde, Michael P. Feneley, M. Leticia Castro, Orit Wolstein, Scott A. Rankin, Andrew D. Cole, Leigh B. Waddell, Gary F. Sholler, Lyn R. Griffiths, Edwin P. Kirk, Tanya L. Butler, David S. Winlaw, Joel P. Mackay, Peter S. Macdonald, Mauro W. Costa, Richard P. Harvey, Guanglan Guo
Publikováno v:
The American Journal of Human Genetics. 81(2):280-291
The T-box family transcription factor gene TBX20 acts in a conserved regulatory network, guiding heart formation and patterning in diverse species. Mouse Tbx20 is expressed in cardiac progenitor cells, differentiating cardiomyocytes, and developing v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0fadbf91db8b7acd1009a1b4338e5ae
Autor:
Joseph D. Terwilliger, Eric K. Moses, Madonna Grehan, Alan N. Wilton, Katy A. Freed, Robyn A. North, Guanglan Guo, Anthony J. Borg, Desmond W. Cooper, Jennifer A. Lade, Shaun P. Brennecke
Publikováno v:
The American Journal of Human Genetics. 67(6):1581-1585
Epidemiological studies have shown that genetic factors contribute to the etiology of the common and serious pregnancy-specific disorder pre-eclampsia (PE)/eclampsia (E). Candidate-gene studies have provided evidence (albeit controversial) of linkage
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8d46fd9acf237293cd5d3a0701ca3db
Autor:
Maria Leticia Castro, Diane Fatkin, Anne Keogh, Christopher S. Hayward, Jonathan G. Seidman, Libin Wang, Robert M. Graham, Orit Wolstein, Milena B. Furtado, Natalie Cochrane, Nadia Rosenthal, Robyn Otway, Peter Riek, Christopher Semsarian, Robert G. Weintraub, Richard P. Harvey, Peter S. Macdonald, Mauro W. Costa, Molly Vale, Christine E. Seidman, Guanglan Guo, Thomas Yeoh, Michael P. Feneley
Publikováno v:
Circulation. Cardiovascular genetics. 6(3)
Background— The transcription factor NKX2-5 is crucial for heart development, and mutations in this gene have been implicated in diverse congenital heart diseases and conduction defects in mouse models and humans. Whether NKX2-5 mutations have a ro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13e803b5818270c74898a44e4ab83725
https://pubmed.ncbi.nlm.nih.gov/23661673
https://pubmed.ncbi.nlm.nih.gov/23661673
Publikováno v:
Hypertension in Pregnancy. 14:251-260
Objective: To test the hypothesis that variants in the angiotensinogen gene are a major genetic cause of preeclampsia (PE).Methods: Ten families with a high incidence of PE were typed for alleles at a microsatellite repeat within the angiotensinogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2dc8ad426bc457c09d62e96777b7001e
https://doi.org/10.3109/10641959509009586
https://doi.org/10.3109/10641959509009586
Autor:
Monique Ohanian, Stefan A. Mann, Kathryn Stockhammer, Diane Fatkin, Angela Sheu, Poonam Zodgekar, Jamie I. Vandenberg, Guanglan Guo, Rajesh N. Subbiah, Maria Leticia Castro, Dennis L. Kuchar, Anu Aggarwal, David Playford, T. Thompson
Publikováno v:
Journal of the American College of Cardiology. 60(16)
Objectives Our aim was to characterize a variant in the SCN5A gene that encodes the alpha-subunit of the cardiac sodium channel, Nav1.5, which was identified in 1 large kindred with dilated cardiomyopathy (DCM) and multiple arrhythmias, including pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d17ddedd63f5d359fdb6ca806e0d2b1
https://pubmed.ncbi.nlm.nih.gov/22999724
https://pubmed.ncbi.nlm.nih.gov/22999724
Autor:
Robyn, Otway, Jamie I, Vandenberg, Guanglan, Guo, Anthony, Varghese, M Leticia, Castro, Jian, Liu, JingTing, Zhao, Jane A, Bursill, Ken R, Wyse, Haley, Crotty, Olivia, Baddeley, Bruce, Walker, Dennis, Kuchar, Charles, Thorburn, Diane, Fatkin
Publikováno v:
Journal of the American College of Cardiology. 49(5)
This study sought to evaluate mutations in genes encoding the slow component of the cardiac delayed rectifier K+ current (I(Ks)) channel in familial atrial fibrillation (AF).Although AF can have a genetic etiology, links between inherited gene defect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::eb2c82949ca76ed90a5a11ec7008e5f6
https://pubmed.ncbi.nlm.nih.gov/17276182
https://pubmed.ncbi.nlm.nih.gov/17276182
Autor:
Hongyu Qiu, Eric K. Moses, Yuliang Fu, Guanglan Guo, Alan N. Wilton, Shaun P. Brennecke, Jennifer A. Lade, Desmond W. Cooper, Madonna Grehan
Publikováno v:
Human genetics. 105(6)
Pre-eclampsia is the most common serious medical disorder of human pregnancy. The human endothelial cell nitric oxide synthase (eNOS) gene is a candidate for pre-eclampsia/eclampsia (PE/E) susceptibility. A linkage study was performed on Australian P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::490faf1686ff93c8df3ba42f638f83d1
https://pubmed.ncbi.nlm.nih.gov/10647900
https://pubmed.ncbi.nlm.nih.gov/10647900
Publikováno v:
Electrophoresis. 18(9)
Preeclampsia/eclampsia (PE/E) is a common disease of human pregnancy with a strong genetic component. The etiology of PE/E is unknown. Two recent reports indicated that the angiotensinogen gene (AGT) could be involved in susceptibility to PE/E. We pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6881c0024dd53cc062033f6164bafe52
https://pubmed.ncbi.nlm.nih.gov/9378138
https://pubmed.ncbi.nlm.nih.gov/9378138
Autor:
Diane Fatkin, Lina Karlsdotter, Lyn R. Griffiths, Robyn Otway, Monique Ohanian, Gunjan Trivedi, Bruce D. Walker, Prashanthan Sanders, Magdalena Soka, Robert A. Smith, Stefan A. Mann, Rajesh N. Subbiah, Dennis L. Kuchar, Merridee A. Wouters, Poonam Zodgekar, Jamie I. Vandenberg, Guanglan Guo
Publikováno v:
Journal of the American College of Cardiology. (11):1017-1025
ObjectivesThe aim of this study was to evaluate the role of cardiac K+ channel gene variants in families with atrial fibrillation (AF).BackgroundThe K+ channels play a major role in atrial repolarization but single mutations in cardiac K+ channel gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cb71305198982ccdd62d63c61c47b1e
Autor:
Guanglan Guo, Desmond W. Cooper, Shaun P. Brennecke, Eric K. Moses, Alan N. Wilton, Madonna Grehan, Jennifer A. Lade
Publikováno v:
Europe PubMed Central
To investigate the endothelial cell nitric oxide synthase (eNOS) gene as a candidate for susceptibility to preeclampsia.Twenty-six Australian families containing 11 eclamptics, 59 severe preeclamptics, and 27 mild preeclamptics were used to test for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e32a86c1dac7cdd42d5d52406fb249b9
http://europepmc.org/abstract/med/10464002
http://europepmc.org/abstract/med/10464002
