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European Journal of Gastroenterology & Hepatology|August 20, 2015
A randomized-controlled study to compare the efficacy of sequential therapy with standard triple therapy for Helicobacter pylori eradication in an Irish populationRana B Haider, Denise E Brennan, Joseph Omorogbe, et al.
Scientific Reports|April 8, 2017
Multimodal Regulation Orchestrates Normal and Complex Disease States in the RetinaA M Olivares, A S Jelcick, J Reinecke, et al.
Gene Therapy|January 25, 2024
Preclinical dose response study shows NR2E3 can attenuate retinal degeneration in the retinitis pigmentosa mouse model RhoP23H+/Shannon M McNamee, Natalie P Chan, Monica Akula, et al.
Genomics|July 20, 1999
The cloning and developmental expression of unconventional myosin IXA (MYO9A) a gene in the Bardet-Biedl syndrome (BBS4) region at chromosome 15q22-q23S W Gorman, N B Haider, U Grieshammer, et al.
Gene Therapy|March 4, 2020
Nr2e3 is a genetic modifier that rescues retinal degeneration and promotes homeostasis in multiple models of retinitis pigmentosaSujun Li, Shyamtanu Datta, Emily Brabbit, et al.
Plos One|July 23, 2011
Genetic variations strongly influence phenotypic outcome in the mouse retinaAustin S Jelcick, Yang Yuan, Barrett D Leehy, et al.
Human Molecular Genetics|August 14, 2003
CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retinaAdrienne K Mehalow, Shuhei Kameya, Richard S Smith, et al.
Plos One|September 5, 2014
Characterization of a spontaneous retinal neovascular mouse modelEiichi Hasegawa, Harry Sweigard, Deeba Husain, et al.
Gene Therapy|May 16, 2024
Retinoic acid related orphan receptor α is a genetic modifier that rescues retinal degeneration in a mouse model of Stargardt disease and Dry AMDM Akula, S M McNamee, Z Love, et al.
Nature Genetics|February 2, 2000
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fateN B Haider, S G Jacobson, A V Cideciyan, et al.
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