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American Journal of Preventive Medicine|May 12, 2000
Developing an evidence-based Guide to Community Preventive Services--methods. The Task Force on Community Preventive ServicesP A Briss, S Zaza, M Pappaioanou, et al.
Human Molecular Genetics|April 24, 2016
A missense mutation in ASRGL1 is involved in causing autosomal recessive retinal degenerationPooja Biswas, Venkata Ramana Murthy Chavali, Giulia Agnello, et al.
Molecular Genetics & Genomic Medicine|January 21, 2016
Hutterite-type cataract maps to chromosome 6p21.32-p21.31, cosegregates with a homozygous mutation in LEMD2, and is associated with sudden cardiac deathPhilip M Boone, Bo Yuan, Shen Gu, et al.
Molecular and Cellular Neurosciences|October 13, 2007
betaA3/A1-crystallin in astroglial cells regulates retinal vascular remodeling during developmentDebasish Sinha, Andrew Klise, Yuri Sergeev, et al.
Angewandte Chemie (International Ed. in English)|April 7, 2021
XFEL Crystal Structures of Peroxidase Compound IIHanna Kwon, Jaswir Basran, Chinar Pathak, et al.
Angewandte Chemie (Weinheim an Der Bergstrasse, Germany)|March 20, 2024
XFEL Crystal Structures of Peroxidase Compound IIHanna Kwon, Jaswir Basran, Chinar Pathak, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|March 7, 2017
Modulation of Antimalarial Activity at a Putative Bisquinoline Receptor In Vivo Using Fluorinated BisquinolinesAlistair J Fielding, Valentina Lukinović, Philip G Evans, et al.
American Journal of Human Genetics|September 21, 2010
A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindnessS Amer Riazuddin, Amber Shahzadi, Christina Zeitz, et al.
Nature Communications|May 25, 2016
FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1Shahid Y Khan, Shivakumar Vasanth, Firoz Kabir, et al.
American Journal of Human Genetics|April 14, 2009
Null mutations in LTBP2 cause primary congenital glaucomaManir Ali, Martin McKibbin, Adam Booth, et al.
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