Zobrazeno 1 - 9
of 9
pro vyhledávání: '"RACHEL KWOK"'
Autor:
KINGA SUBA, YATEEN S. PATEL, ANNA ROBERTS, JED V. SHREWSBURY, SHIQIAN CHEN, RACHEL KWOK, VASILIKI KALOGIANNI, XIAOXUAN LIU, GUY A. RUTTER, BEN JONES, TRICIA M. TAN, BRYN OWEN, DANIEL J. DRUCKER, STEPHEN BLOOM, KEVIN MURPHY, VICTORIA SALEM
Publikováno v:
Diabetes. 71
Background: Type 2 diabetes (T2D) is characterised by the loss of pulsatile insulin secretion. We studied mice with β-cell specific loss of the glucagon receptor (GCGRflox/flox X Ins-1 cre) , to investigate the role of intra-islet glucagon signallin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89583c31d6ef2cf4eb9f1ab0d03e844f
https://doi.org/10.2337/db22-362-or
https://doi.org/10.2337/db22-362-or
Publikováno v:
The Journal of hand surgery, European volume. 47(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d4fd82ec8c085ab9292b06b760519c2
https://pubmed.ncbi.nlm.nih.gov/34278812
https://pubmed.ncbi.nlm.nih.gov/34278812
Publikováno v:
F1000Research
Lichen sclerosus (LS), or balanitis xerotica obliterans as it was previously known, is a chronic inflammatory lymphocyte-mediated scarring dermatosis that often affects the preputial skin and glans, leading to phimosis and urethral strictures if left
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7163e347f10249a9c7129940ff483454
http://europepmc.org/articles/PMC7233179
http://europepmc.org/articles/PMC7233179
Autor:
Hang Yee Wong, Jiayu Tan, Christopher Kiu Choong Syn, Zi Gui Lim, Wilson Wen Xiang Lim, Rachel Kwok
Publikováno v:
Forensic Science International: Genetics Supplement Series. 7:597-599
Advances in forensic DNA profiling have facilitated the generation of DNA profiles from trace (touch/contact) articles. This pilot study aimed to examine the DNA profiling success of such articles which may be unique to our local scene, as well as to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d05adcee80a46d975e89ed4848d8f032
https://doi.org/10.1016/j.fsigss.2019.10.104
https://doi.org/10.1016/j.fsigss.2019.10.104
Publikováno v:
Optometry and vision science : official publication of the American Academy of Optometry. 94(3)
Purpose To report an atypical case of contact lens-related Acanthamoeba keratitis. Case report A 15-year-old secondary school female student with a history of soft contact lens wear was referred to our hospital by a private general practitioner for m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afea0d81835bfa45c23ad1218f701b4a
https://pubmed.ncbi.nlm.nih.gov/27870779
https://pubmed.ncbi.nlm.nih.gov/27870779
Autor:
Clive S. Cockram, Morris H. L. Tai, Xiaoqiang Yao, Nelson L.S. Tang, Chung-Mo Chow, Gary T. C. Ko, Rachel Kwok
Publikováno v:
Clinical Endocrinology. 66:229-234
Summary Objective Thyrotoxic periodic paralysis (TTP) has been associated with genetic variations in the gene encoding the alpha 1 subunit of the L-type calcium channel (CACNA1S). Mutations in CACNA1S are known to account for the majority of cases of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d7a3a82716b2412902901c0be9e5626
https://doi.org/10.1111/j.1365-2265.2006.02713.x
https://doi.org/10.1111/j.1365-2265.2006.02713.x
Autor:
Bobby K. W. Ng, Hiu-Yan Yeung, Catherine Sill-King Cheung, Xia Guo, Jack C. Y. Cheng, Ling Qin, Nelson L.S. Tang, Rachel Kwok, Kwong-Man Lee, Vivian Wing-Yin Hung
Publikováno v:
Spine. 31:2463-2468
Study design A genetic association study of estrogen receptor-[alpha] gene (ESR1) with adolescent idiopathic scoliosis (AIS) in Chinese. Objectives To investigate whether: 1) PvuII and XbaI polymorphisms in ESR1 are predisposition factor for AIS and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9f18902dc2e85f51552ed71ab2c6b9f
https://doi.org/10.1097/01.brs.0000239179.81596.2b
https://doi.org/10.1097/01.brs.0000239179.81596.2b
Autor:
Xiaoqiang Yao, Gary T. C. Ko, Chung-Mo Chow, Morris H. L. Tai, Nelson L.S. Tang, Rachel Kwok, Clive S. Cockram
Publikováno v:
Clinical Endocrinology. 61:109-112
Summary objectives Mutation in KCNE3 gene (Isk-related family potassium voltage-gated channel member 3 gene) was recently associated with the aetiology of thyrotoxic periodic paralysis (TPP). We studied 79 Chinese TPP patients by DNA sequencing of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d037940938a039b148bee76c5f2017d5
https://doi.org/10.1111/j.1365-2265.2004.02079.x
https://doi.org/10.1111/j.1365-2265.2004.02079.x
Autor:
Hiu Yan Yeung, Xu Sheng Qiu, Suk Ling Ma, Yong Qiu, Lin Qin, Vivian Wing-Yin Hung, Jack C. Y. Cheng, Rachel Kwok, Kwong-Man Lee, Nelson L.S. Tang, Bobby K. W. Ng
Publikováno v:
Spine. 32(16)
Study Design. A genetic association study to comprehensively investigate variations of melatonin receptor 1B gene polymorphism by a set of tagging single nucleotide polymorphisms (tagSNPs) derived from the International Hapmap project. Objectives. To
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc99d9f9f92a619df1f5116083b22b5a
https://pubmed.ncbi.nlm.nih.gov/17632395
https://pubmed.ncbi.nlm.nih.gov/17632395