Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Yuan-Yuan Ho"'
Autor:
Jun-Wei Zhou, Stephen K W Tsui, Maggie C Y Ng, Hua Geng, Sai-Kam Li, Wing-Yee So, Ronald C Ma, Ying Wang, Qian Tao, Zhen-Yu Chen, Juliana C N Chan, Yuan-Yuan Ho
Publikováno v:
PLoS ONE, Vol 6, Iss 2, p e17324 (2011)
This study aimed at substantiating the associations of the apolipoproein M gene (APOM) with type 2 diabetes (T2D) as well as with metabolic traits in Hong Kong Chinese. In addition, APOM gene function was further characterized to elucidate its activi
Externí odkaz:
https://doaj.org/article/560cd0378460496f907cb8bce1a40156
Autor:
Hua Geng, Peggy P Y Law, Maggie C Y Ng, Ting Li, Li-Yun Liang, Tian-Fang Ge, Kam-Bo Wong, Chun Liang, Ronald C Ma, Wing-Yee So, Juliana C N Chan, Yuan-Yuan Ho
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e24669 (2011)
The apolipoprotein E gene (APOE) coding polymorphism modifies the risks of Alzheimer's disease, type 2 diabetes, and coronary heart disease. Aside from the coding variants, single nucleotide polymorphism (SNP) of the APOE promoter has also been shown
Externí odkaz:
https://doaj.org/article/ef154d4f200e423e9e30eb7f0908133a
Autor:
Rachel Harte, Michele Cargill, Yuan-Yuan Ho, Shan Yang, Laura Murillo, Nicole Faulkner, Daniel Beltran, Xu Li, Robert L. Nussbaum, K. Robinson
Publikováno v:
Molecular Genetics and Metabolism. 129:S135-S136
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6196e853ef3e2b60a89db6a43872550e
https://doi.org/10.1016/j.ymgme.2019.11.356
https://doi.org/10.1016/j.ymgme.2019.11.356
Autor:
Keith Nykamp, Michael Anderson, Martin Powers, John Garcia, Blanca Herrera, Yuan-Yuan Ho, Yuya Kobayashi, Nila Patil, Janita Thusberg, Marjorie Westbrook, Scott Topper, Sienna Aguilar, Swaroop Aradhya, Daniel Beltran, Brandon Bunker, Amy Daly, Anne Deucher, Tali Ekstein, Ali Entezam, Karl Erhard, Ed Esplin, Jennifer Fulbright, Amy Fuller, Kristen McDonald Gibson, Tina Hambuch, Rachel Harte, Christy Hartshorne, Eden Haverfield, Nastaran Heidari, Michelle Hogue, Daniela Iacoboni, Britt Johnson, Hio Chung Kang, Rachel Lewis, Shiloh Martin, Sarah McCalmon, Scott Michalski, Cindy Morgan, Laura Murillo, Piper Nicolosi, Karen Ouyang, Carolina Pardo, Rita Quintana, Marina Rabideau, Darlene Riethmaier, Amanda Stafford, Jackie Tahiliani, Chris Tan, S. Paige Taylor, Shu-Huei Wang, Hannah White, Ian Wilson, Tom Winder, Michelle K. Zeman
Publikováno v:
Genetics in Medicine
Purpose The 2015 American College of Medical Genetics and Genomics–Association for Molecular Pathology (ACMG–AMP) guidelines were a major step toward establishing a common framework for variant classification. In practice, however, several aspect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a146539648054315d9d756d7fc859d77
https://doi.org/10.1038/s41436-019-0624-9
https://doi.org/10.1038/s41436-019-0624-9
Autor:
Rachel Harte, Tom Winder, Yuan-Yuan Ho, Daniel Beltran, Michelle Fox, Britt Johnson, Stacey Wong, Laura Murillo, Hannah White
Publikováno v:
Molecular Genetics and Metabolism. 123:S101-S102
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7109a748c684634203257a4b5cb291a6
https://doi.org/10.1016/j.ymgme.2017.12.268
https://doi.org/10.1016/j.ymgme.2017.12.268
Autor:
Joannie Hui, John Wong, Joerg Klepper, Eva Lai-Wah Fung, Tzi Bun Ng, Yuan Yuan Ho, Nga-Yin Fion Fong, Kwok-Wing Stephen Tsui
Publikováno v:
Brain and Development. 33:170-173
Glucose transporter type 1 deficiency syndrome (GLUT1DS) is increasingly recognized as a cause of various neurological disorders but a high index of suspicion is important to make the diagnosis. We report two Chinese patients with GLUT1DS, one of whi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46c7da6302c652341fe5ea280f8c77e6
https://doi.org/10.1016/j.braindev.2010.03.009
https://doi.org/10.1016/j.braindev.2010.03.009
Autor:
Daniel Beltran, Stacey Wong, Tom Winder, Yuan-Yuan Ho, Laura Murillo, Michelle Fox, Rachel Harte, Hannah White, Britt Johnson
Publikováno v:
Molecular Genetics and Metabolism. 123:S64
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65c9dd5f2187affd1285c457b99cebf4
https://doi.org/10.1016/j.ymgme.2017.12.157
https://doi.org/10.1016/j.ymgme.2017.12.157
Autor:
Stacey Wong, Rachel Harte, Tom Winder, Michelle Fox, Hannah White, Laura Murillo, Britt Johnson, Yuan-Yuan Ho, Daniel Beltran
Publikováno v:
Molecular Genetics and Metabolism. 123:S148
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f28925c8af8b35856077674ddcc38559
https://doi.org/10.1016/j.ymgme.2017.12.411
https://doi.org/10.1016/j.ymgme.2017.12.411
Publikováno v:
European Journal of Pharmacology. 573:70-74
Gatifloxacin may induce life-threatening dysglycemia. The facilitated glucose transporter type 1 (GLUT1) protein is ubiquitously expressed in many tissues. Disturbed GLUT1 protein function weakens the systemic glycemic control and may cause dysglycem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d670ac62e9add856f5cc3cb5b192579
https://doi.org/10.1016/j.ejphar.2007.07.038
https://doi.org/10.1016/j.ejphar.2007.07.038
Autor:
Tomoko Miyajima, Yuan-Yuan Ho, Po-Ting Tsang, Dong Wang, Hei-Yi Wong, Yukiyoshi Shirasaka, Masatoshi Ito, Takashi Kudo, Darryl C. De Vivo, Tatsuya Fujii
Publikováno v:
Brain and Development. 29:92-97
We report three Japanese patients with glucose transporter type 1 deficiency syndrome (Glut1DS). Two patients had a normal erythrocyte 3- O -methylglucose (3OMG) uptake, one with a previously reported T295M substitution and the other with a novel 12-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0edfbc85c8c54611ca4d8e7374e78e9c
https://doi.org/10.1016/j.braindev.2006.07.007
https://doi.org/10.1016/j.braindev.2006.07.007