Zobrazeno 1 - 6
of 6
pro vyhledávání: '"John E. A. COMMON"'
Autor:
Dilip Kumar, Kia Joo Puan, Anand Kumar Andiappan, Bernett Lee, Geertje H. A. Westerlaken, Doreen Haase, Rossella Melchiotti, Zhuang Li, Nurhashikin Yusof, Josephine Lum, Geraldine Koh, Shihui Foo, Joe Yeong, Alexessander Couto Alves, Juha Pekkanen, Liang Dan Sun, Astrid Irwanto, Benjamin P. Fairfax, Vivek Naranbhai, John E. A. Common, Mark Tang, Chin Keh Chuang, Marjo-Riitta Jarvelin, Julian C. Knight, Xuejun Zhang, Fook Tim Chew, Shyam Prabhakar, Liu Jianjun, De Yun Wang, Francesca Zolezzi, Michael Poidinger, E. Birgitte Lane, Linde Meyaard, Olaf Rötzschke
Publikováno v:
Genome Medicine, Vol 9, Iss 1, Pp 1-16 (2017)
Abstract Background Expression quantitative trait loci (eQTL) databases represent a valuable resource to link disease-associated SNPs to specific candidate genes whose gene expression is significantly modulated by the SNP under investigation. We prev
Externí odkaz:
https://doaj.org/article/5e11065b92e948459f1e77a7ba21067a
Autor:
Khek-Chian Tham, Rachel Lefferdink, Kaibo Duan, Seong Soo Lim, X.F. Colin C. Wong, Erin Ibler, Benedict Wu, Hajar Abu-Zayed, Stephanie M. Rangel, Ester Del Duca, Mashkura Chowdhury, Margot Chima, Hee Jee Kim, Bernett Lee, Emma Guttman-Yassky, Amy S. Paller, John E. A. Common
Publikováno v:
British Journal of Dermatology. 187:557-570
Background The ichthyoses are rare genetic keratinizing disorders that share the characteristics of an impaired epidermal barrier and increased risk of microbial infections. Although ichthyotic diseases share a T helper (Th) 17 cell immune signature,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d291a9a51948b68ad40630188db23348
https://doi.org/10.1111/bjd.21687
https://doi.org/10.1111/bjd.21687
Autor:
Kim S. ROBINSON, Gee Ann TOH, Muhammad Jasrie FIRDAUS, Khek Chian THAM, Pritisha ROZARIO, Chrissie LIM, Ying Xiu TOH, Zhi Heng LAU, Sophie Charlotte BINDER, Jacob MAYER, Carine BONNARD, Florian I. SCHMIDT, John E. A. COMMON, Franklin L. ZHONG
NLRP1 is an innate immune sensor protein that activates inflammasome-driven pyroptotic cell death. Recent work demonstrates that human NLRP1 has evolved to sense viral infections. Whether and how human NLRP1 responds to other infectious agents is unc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad76428c5948ff4f0a10289c3b7465b3
https://doi.org/10.1101/2023.01.16.524188
https://doi.org/10.1101/2023.01.16.524188
Autor:
Si En, Poh, Winston L C, Koh, Shi Yu Derek, Lim, Etienne C E, Wang, Yik Weng, Yew, John E A, Common, Hazel H, Oon, Hao, Li
Publikováno v:
JID innovations : skin science from molecules to population health. 2(4)
Atopic dermatitis (AD) is a skin inflammatory disease in which the opportunistic pathogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::eb88e023e5c09ba04aeabbe32ef1509d
https://pubmed.ncbi.nlm.nih.gov/35860448
https://pubmed.ncbi.nlm.nih.gov/35860448
Autor:
Hong Liu, Yi Li, Ken Kwok Hon Hung, Na Wang, Chuan Wang, Xuechao Chen, Donglai Sheng, Xi'an Fu, Kelvin See, Jia Nee Foo, Huiqi Low, Herty Liany, Ishak Darryl Irwan, Jian Liu, Baoqi Yang, Mingfei Chen, Yongxiang Yu, Gongqi Yu, Guiye Niu, Jiabao You, Yan Zhou, Shanshan Ma, Ting Wang, Xiaoxiao Yan, Boon Kee Goh, John E A Common, Birgitte E Lane, Yonghu Sun, Guizhi Zhou, Xianmei Lu, Zhenhua Wang, Hongqing Tian, Yuanhua Cao, Shumin Chen, Qiji Liu, Jianjun Liu, Furen Zhang
Publikováno v:
PLoS ONE, Vol 9, Iss 2, p e87250 (2014)
As a genetic disorder of abnormal pigmentation, the molecular basis of dyschromatosis universalis hereditaria (DUH) had remained unclear until recently when ABCB6 was reported as a causative gene of DUH.We performed genome-wide linkage scan using Ill
Externí odkaz:
https://doaj.org/article/12befc761e4c478db72d4c3c7b4edf87
Autor:
Tong San, Tan, Yi Zhen, Ng, Cedric, Badowski, Tram, Dang, John E A, Common, Lukas, Lacina, Ildikó, Szeverényi, E Birgitte, Lane
Publikováno v:
Methods in enzymology. 568
The discovery of the causative link between keratin mutations and a growing number of human diseases opened the way for a better understanding of the function of the whole intermediate filament families of cytoskeleton proteins. This chapter describe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4235ef05fc70be757b7c88b568438372
https://pubmed.ncbi.nlm.nih.gov/26795473
https://pubmed.ncbi.nlm.nih.gov/26795473