Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Alwin, Loh"'
Autor:
Xiubo Fan, Chin Teck Ng, Dianyang Guo, Frances Lim, Jia Chi Tan, Annie Law, Lim Hee Goh, Zhi Yong Poon, Alice Cheung, Say Li Kong, Michelle Tan, Shang Li, Alwin Loh, Anne James, Tony Lim, Jinmiao Chen, Julian Thumboo, William Hwang, Andrea Low
Publikováno v:
Arthritis & Rheumatology. 75:553-566
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21023613e8be5edc80dc6aa0eb77061e
https://doi.org/10.1002/art.42383
https://doi.org/10.1002/art.42383
Autor:
Liangjian, Lu, Yok-Chin, Yap, Duc Quang, Nguyen, Yiong-Huak, Chan, Jun-Li, Ng, Yao-Chun, Zhang, Chang-Yien, Chan, Mya, Than, Isaac Desheng, Liu, Sadaf, Asim, Khemchand, Moorani, Bilquis, Naeem, Iftikhar, Ijaz, Thi Minh Tan, Nguyen, Ming-Lee, Lee, Caroline, Eng, Syed Saimul, Huque, Yong-Hong, Ng, Indra, Ganesan, Sing-Ming, Chao, Siew-Le, Chong, Puay-Hoon, Tan, Alwin, Loh, Sonia, Davila, Vikrant, Kumar, Joanna Zhi-Jie, Ling, Rajesh Babu, Moorakonda, Karen Mei-Ling, Tan, Alvin Yu-Jin, Ng, Kok-Siong, Poon, Franz, Schaefer, Beata, Lipska-Zietkiewicz, Hui-Kim, Yap, Kar-Hui, Ng
Publikováno v:
Clinical geneticsREFERENCES. 101(5-6)
Multinational studies have reported monogenic etiologies in 25%-30% of children with steroid-resistant nephrotic syndrome. Such large studies are lacking in Asia. We established Deciphering Diversities: Renal Asian Genetics Network (DRAGoN) and aimed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad8e066c7c89daac4804864b4dad8fe2
https://pubmed.ncbi.nlm.nih.gov/35064937
https://pubmed.ncbi.nlm.nih.gov/35064937
Autor:
Suha Salim, Peter I. Benke, Friedhelm Hildebrandt, Khalid Alhasan, Stacey Kiat Hong Tay, Abdullah A. Alangari, Isaac Desheng Liu, Federico Torta, Nicole Weaver, Bonnie Sullivan, Karin Chen, Piming Zhao, Megan A. Cooper, Emily Tang, Alwin Loh, Markus R. Wenk, Jeffrey B. Hodgin, James A. Endrizzi, Weixing Ou, Jeremy Selva, Julie D. Saba, Olivia West, Austin Larson, Evren Gumus, Hui Kim Yap, Martin Zenker, Denise Li Meng Goh
Publikováno v:
J Inherit Metab Dis
Sphingosine-1-phosphate (S1P) lyase is a vitamin B6-dependent enzyme that degrades sphingosine-1-phosphate in the final step of sphingolipid metabolism. In 2017, a new inherited disorder was described caused by mutations in SGPL1, which encodes sphin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ebc6a97179986bd6bad6306c3e16592
https://pubmed.ncbi.nlm.nih.gov/32233035
https://pubmed.ncbi.nlm.nih.gov/32233035
Publikováno v:
Pathology; January 2014, Vol. 46 Issue: 1, Number 1 Supplement 1 pS66-S66, 1p