4
results
for author:"Mishmar D."
in Literature Citations
| A novel NDUFA1 mutation leads to a progressive mitochondrial complex I-specific neurodegenerative disease. Potluri P., Davila A., Ruiz-Pesini E., Mishmar D., O'Hearn S., Hancock S., Simon M., Scheffler I.E., Wallace D.C., Procaccio V. Mol. Genet. Metab. 96:189-195(2009) · Mapped (2) |
| Differences in mtDNA haplogroup distribution among 3 Jewish populations alter susceptibility to T2DM complications. Feder J., Blech I., Ovadia O., Amar S., Wainstein J., Raz I., Dadon S., Arking D.E., Glaser B., Mishmar D. BMC Genomics 9:198-198(2008) · UniProtKB (24) |
| Adaptive selection of mitochondrial complex I subunits during primate radiation. Mishmar D., Ruiz-Pesini E., Mondragon-Palomino M., Procaccio V., Gaut B., Wallace D.C. Gene 378:11-18(2006) · UniProtKB (114) |
| Natural selection shaped regional mtDNA variation in humans. Mishmar D., Ruiz-Pesini E., Golik P., Macaulay V., Clark A.G., Hosseini S., Brandon M., Easley K., Chen E., Brown M.D. et al. Proc. Natl. Acad. Sci. U.S.A. 100:171-176(2003) · UniProtKB (113) |
