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Disease Models & Mechanisms|October 31, 2023
Genetic background determines severity of Loxl1-mediated systemic and ocular elastosis in miceMaria F Suarez, Heather M Schmitt, Megan S Kuhn, et al.Human Genetics|April 14, 2005
Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson diseaseMaher A Noureddine, Xue-Jun Qin, Sofia A Oliveira, et al.Molecular Vision|December 20, 2008
Optineurin coding variants in Ghanaian patients with primary open-angle glaucomaYutao Liu, Stephen Akafo, Cecile Santiago-Turla, et al.Journal of Neurogenetics|November 8, 2002
A novel mutation in the gene encoding noggin is not causative in human neural tube defectsKim A Bauer, Timothy M George, David S Enterline, et al.Molecular Therapy. Nucleic Acids|May 1, 2014
RNAi-mediated Gene Silencing of Mutant Myotilin Improves Myopathy in LGMD1A MiceJian Liu, Lindsay M Wallace, Sara E Garwick-Coppens, et al.Investigative Ophthalmology & Visual Science|August 29, 2007
Haplotypes spanning the complement factor H gene are protective against age-related macular degenerationKylee L Spencer, Michael A Hauser, Lana M Olson, et al.Ophthalmology|January 24, 2007
Independent effects of complement factor H Y402H polymorphism and cigarette smoking on risk of age-related macular degenerationWilliam K Scott, Silke Schmidt, Michael A Hauser, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 18, 2006
Family-based case-control study of MAOA and MAOB polymorphisms in Parkinson diseaseSun J Kang, William K Scott, Yi-Ju Li, et al.Nature Medicine|March 5, 2002
Modular flexibility of dystrophin: implications for gene therapy of Duchenne muscular dystrophyScott Q Harper, Michael A Hauser, Christiana DelloRusso, et al.Molecular Vision|May 10, 2011
Myocilin mutations in black South Africans with POAGBenjamin T Whigham, Susan E I Williams, Yutao Liu, et al.Pageof 17