受强制性开放获取政策约束的文章 - Trevor Carmichael了解详情
无法在其他位置公开访问的文章：1 篇
In vitro pharmaceutical characterization and statistical optimization of a novel topically applied instantly-soluble solid eye drop matrix
RM Moosa, YE Choonara, LC du Toit, P Kumar, LK Tomar, C Tyagi, ...
Pharmaceutical Development and Technology 20 (7), 854-862, 2015
强制性开放获取政策： National Research Foundation, South Africa
可在其他位置公开访问的文章：11 篇
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci
T Aung, M Ozaki, MC Lee, U Schlötzer-Schrehardt, G Thorleifsson, ...
Nature genetics 49 (7), 993-1004, 2017
强制性开放获取政策： US National Institutes of Health, 国家自然科学基金委员会, A*Star, Singapore …
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome
T Aung, M Ozaki, T Mizoguchi, RR Allingham, Z Li, A Haripriya, S Nakano, ...
Nature genetics 47 (4), 387-392, 2015
强制性开放获取政策： US National Institutes of Health, Howard Hughes Medical Institute, National …
Major LOXL1 risk allele is reversed in exfoliation glaucoma in a black South African population
SEI Williams, BT Whigham, Y Liu, TR Carmichael, X Qin, S Schmidt, ...
Molecular vision 16, 705, 2010
强制性开放获取政策： US National Institutes of Health
Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus
MA Hauser, IF Aboobakar, Y Liu, S Miura, BT Whigham, P Challa, ...
Human molecular genetics 24 (22), 6552-6563, 2015
强制性开放获取政策： US National Institutes of Health, German Research Foundation
Association of genetic variants with primary open-angle glaucoma among individuals with African ancestry
Genetics of Glaucoma in People of African Descent (GGLAD) Consortium, ...
Jama 322 (17), 1682-1691, 2019
强制性开放获取政策： US National Institutes of Health, US Department of Education, National …
Myocilin mutations in black South Africans with POAG
BT Whigham, SEI Williams, Y Liu, RM Rautenbach, TR Carmichael, ...
Molecular vision 17, 1064, 2011
强制性开放获取政策： US National Institutes of Health
The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome
D Berner, U Hoja, M Zenkel, JJ Ross, S Uebe, D Paoli, P Frezzotti, ...
Human molecular genetics 28 (15), 2531-2548, 2019
强制性开放获取政策： US National Institutes of Health
Familial congenital cataract, coloboma, and nystagmus phenotype with variable expression caused by mutation in PAX6 in a South African family
S Goolam, N Carstens, M Ross, D Bentley, M Lopes, J Peden, ...
Molecular Vision 24, 407, 2018
强制性开放获取政策： US National Institutes of Health
Association of rare CYP39A1 variants with exfoliation syndrome involving the anterior chamber of the eye
Z Li, Z Wang, MC Lee, M Zenkel, E Peh, M Ozaki, F Topouzis, S Nakano, ...
Jama 325 (8), 753-764, 2021
强制性开放获取政策： US National Institutes of Health, National Medical Research Council …
Novel mutation in the CHST6 gene causes macular corneal dystrophy in a black South African family
N Carstens, S Williams, S Goolam, T Carmichael, MS Cheung, ...
BMC medical genetics 17, 1-9, 2016
强制性开放获取政策： US National Institutes of Health, National Research Foundation, South Africa
The role of lysyl oxidase-like 1 DNA copy number variants in exfoliation glaucoma
Y Liu, BT Whigham, J Wheeler, SEI Williams, RM Rautenbach, A Ziskind, ...
Molecular vision 18, 2976, 2012
强制性开放获取政策： US National Institutes of Health
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