Showing results (1-10 of 8) with videos related to
Sort By:
Pageof 1
The Journal of Cell Biology|August 22, 2007
OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1LZhiyin Song, Hsiuchen Chen, Maja Fiket, et al.Journal of Neurochemistry|April 19, 2008
Characterization of OPA1 isoforms isolated from mouse tissuesVasudheva Reddy Akepati, Eva-Christina Müller, Albrecht Otto, et al.Investigative Ophthalmology & Visual Science|October 27, 2004
OPA1, the disease gene for autosomal dominant optic atrophy, is specifically expressed in ganglion cells and intrinsic neurons of the retinaUlrike E A Pesch, Julia E Fries, Stefanie Bette, et al.Probiotics and Antimicrobial Proteins|November 26, 2013
Lactobacillus paracasei DSMZ16671 Reduces Mutans Streptococci: A Short-Term Pilot StudyCaterina Holz, Christiane Alexander, Christina Balcke, et al.Molecular Neurodegeneration|June 16, 2010
Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophyNico Fuhrmann, Simone Schimpf, York Kamenisch, et al.Investigative Ophthalmology & Visual Science|May 31, 2002
A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophyDawn L Thiselton, Christiane Alexander, Jan-Willem Taanman, et al.Human Genetics|January 26, 2002
A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 geneTin Aung, Louise Ocaka, Neil D Ebenezer, et al.The EMBO Journal|April 11, 2009
SLP-2 is required for stress-induced mitochondrial hyperfusionDaniel Tondera, Stéphanie Grandemange, Alexis Jourdain, et al.Pageof 1