Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Wai Yan Fung"'
Publikováno v:
Archives of Plastic Surgery, Vol 42, Iss 03, Pp 278-281 (2015)
Open release remains the gold standard in the treatment of carpal tunnel syndrome in cases where conservative treatment fails. However, the efficacy of carpal tunnel release in the elderly has been debated in the literature throughout the years. This
Externí odkaz:
https://doaj.org/article/b334a685b12749418cccf0b9c80430a1
Publikováno v:
PLoS ONE, Vol 8, Iss 4, p e61805 (2013)
Myopia is the most common ocular disease worldwide. We investigated the association of high myopia with the common single nucleotide polymorphisms (SNPs) of five candidate genes - early growth response 1 (EGR1), v-fos FBJ murine osteosarcoma viral on
Externí odkaz:
https://doaj.org/article/4bd5806fa8c74501bf222829095dd850
Publikováno v:
PLoS ONE, Vol 7, Iss 6, p e40238 (2012)
BackgroundMyopia is the most common ocular disorder worldwide and imposes tremendous burden on the society. It is a complex disease. The MYP6 locus at 22 q12 is of particular interest because many studies have detected linkage signals at this interva
Externí odkaz:
https://doaj.org/article/48fe2a0afd57444ca0c97036aed326be
Autor:
Bo Jiang, Maurice K H Yap, Kim Hung Leung, Po Wah Ng, Wai Yan Fung, Wai Wa Lam, Yang-Shun Gu, Shea Ping Yip
Publikováno v:
PLoS ONE, Vol 6, Iss 5, p e19587 (2011)
The paired box 6 (PAX6) gene is considered as a master gene for eye development. Linkage of myopia to the PAX6 region on chromosome 11p13 was shown in several studies, but the results for association between myopia and PAX6 were inconsistent so far.W
Externí odkaz:
https://doaj.org/article/8a9bde2655b347a48ef28e90b8401104
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e26119 (2011)
Whole genome amplification can faithfully amplify genomic DNA (gDNA) with minimal bias and substantial genome coverage. Whole genome amplified DNA (wgaDNA) has been tested to be workable for high-throughput genotyping arrays. However, issues about wh
Externí odkaz:
https://doaj.org/article/12e87087011743b4b23e81d151f2b39f
Publikováno v:
Archives of Plastic Surgery, Vol 42, Iss 3, Pp 278-281 (2015)
Archives of Plastic Surgery
Archives of Plastic Surgery
Open release remains the gold standard in the treatment of carpal tunnel syndrome in cases where conservative treatment fails. However, the efficacy of carpal tunnel release in the elderly has been debated in the literature throughout the years. This
Autor:
Henry H. L. Chan, Po Wah Ng, Bo Jiang, Wing Hong Hung, Man Chi Lai, Wai Wa Lam, Patrick H W Chu, Wai Chi Yiu, Choi Chu Li, Maurice Yap, Wai Yan Fung, Shea Ping Yip
Publikováno v:
Ophthalmic and Physiological Optics. 33:346-353
Purpose Myopia is a complex eye disorder. The X-linked form of complete congenital stationary night blindness (CSNB1A) is usually associated with moderate to high myopia, and is caused by mutations in the NYX gene. We explored if NYX mutations could
Publikováno v:
PLoS ONE
PLoS ONE, Vol 8, Iss 4, p e61805 (2013)
PLoS ONE, Vol 8, Iss 4, p e61805 (2013)
Myopia is the most common ocular disease worldwide. We investigated the association of high myopia with the common single nucleotide polymorphisms (SNPs) of five candidate genes - early growth response 1 (EGR1), v-fos FBJ murine osteosarcoma viral on
Autor:
Yang-shun Gu, Maurice Yap, Daniel W.H. Ho, Wai Yan Fung, Miao-miao Zhu, Po Wah Ng, Shea Ping Yip
Publikováno v:
BMC Medical Genetics, Vol 13, Iss 1, p 64 (2012)
BMC Medical Genetics
BMC Medical Genetics
Background The UMODL1 gene was found to be associated with high myopia in Japanese. This study aimed to investigate this gene for association with high myopia in Chinese. Methods Two groups of unrelated Han Chinese from Hong Kong were recruited using
Publikováno v:
Archives of ophthalmology (Chicago, Ill. : 1960). 130(2)
To investigate the association of high myopia with common single-nucleotide polymorphisms (SNPs) in the IGF1, IGFBP3, and IGFBP4 genes in a Chinese population.For our case-control study, we recruited 600 unrelated participants: 300 case participants