1 - 25 of
49
results
for author:"Wallace D.C."
in Literature Citations
| Adenine nucleotide translocator 1 deficiency increases resistance of mouse brain and neurons to excitotoxic insults. Lee J., Schriner S.E., Wallace D.C. Biochim. Biophys. Acta 1787:364-370(2009) · Mapped (2) |
| Mitochondrial variants in schizophrenia, bipolar disorder, and major depressive disorder. Rollins B., Martin M.V., Sequeira P.A., Moon E.A., Morgan L.Z., Watson S.J., Schatzberg A., Akil H., Myers R.M., Jones E.G. et al. PLoS ONE 4:e4913-e4913(2009) · Mapped (4) |
| Heterozygous mutation of Opa1 in Drosophila shortens lifespan mediated through increased reactive oxygen species production. Tang S., Le P.K., Tse S., Wallace D.C., Huang T. PLoS ONE 4:e4492-e4492(2009) · Mapped (2) |
| 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) |
| Mitochondrial genome diversity in arctic Siberians, with particular reference to the evolutionary history of Beringia and Pleistocenic peopling of the Americas. Volodko N.V., Starikovskaya E.B., Mazunin I.O., Eltsov N.P., Naidenko P.V., Wallace D.C., Sukernik R.I. Am. J. Hum. Genet. 82:1084-1100(2008) · UniProtKB (77) |
| Reversible optic neuropathy with OPA1 exon 5b mutation. Cornille K., Milea D., Amati-Bonneau P., Procaccio V., Zazoun L., Guillet V., El Achouri G., Delettre C., Gueguen N., Loiseau D. et al. Ann. Neurol. 63:667-671(2008) · Mapped (2) |
| A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations. Fan W., Waymire K.G., Narula N., Li P., Rocher C., Coskun P.E., Vannan M.A., Narula J., Macgregor G.R., Wallace D.C. Science 319:958-962(2008) · Mapped (10) |
| The molecular mechanisms of OPA1-mediated optic atrophy in Drosophila model and prospects for antioxidant treatment. Yarosh W., Monserrate J., Tong J.J., Tse S., Le P.K., Nguyen K., Brachmann C.B., Wallace D.C., Huang T. PLoS Genet. 4:e6-e6(2008) · Mapped (2) |
| Life extension through neurofibromin mitochondrial regulation and antioxidant therapy for neurofibromatosis-1 in Drosophila melanogaster. Tong J.J., Schriner S.E., McCleary D., Day B.J., Wallace D.C. Nat. Genet. 39:476-485(2007) · Mapped (8) |
| Association of mitochondrial SOD deficiency with salt-sensitive hypertension and accelerated renal senescence. Rodriguez-Iturbe B., Sepassi L., Quiroz Y., Ni Z., Wallace D.C., Vaziri N.D. J. Appl. Physiol. 102:255-260(2007) · Mapped (4) |
| 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) |
| Functional estrogen receptors in the mitochondria of breast cancer cells. Pedram A., Razandi M., Wallace D.C., Levin E.R. Mol. Biol. Cell 17:2125-2137(2006) · Mapped (9) |
| Eliminating the Ant1 isoform produces a mouse with CPEO pathology but normal ocular motility. Yin H., Stahl J.S., Andrade F.H., McMullen C.A., Webb-Wood S., Newman N.J., Biousse V., Wallace D.C., Pardue M.T. Invest. Ophthalmol. Vis. Sci. 46:4555-4562(2005) · Mapped (2) |
| The basal proton conductance of mitochondria depends on adenine nucleotide translocase content. Brand M.D., Pakay J.L., Ocloo A., Kokoszka J., Wallace D.C., Brookes P.S., Cornwall E.J. Biochem. J. 392:353-362(2005) · Mapped (4) |
| Mitochondrial DNA diversity in indigenous populations of the southern extent of Siberia, and the origins of native american haplogroups. Starikovskaya E.B., Sukernik R.I., Derbeneva O.A., Volodko N.V., Ruiz-Pesini E., Torroni A., Brown M.D., Lott M.T., Hosseini S.H., Huoponen K. et al. Ann. Hum. Genet. 69:67-89(2005) · UniProtKB (53) |
| Late-onset Leigh syndrome in a patient with mitochondrial complex I NDUFS8 mutations. Procaccio V., Wallace D.C. Neurology 62:1899-1901(2004) · Mapped (4) |
| The ADP/ATP translocator is not essential for the mitochondrial permeability transition pore. Kokoszka J.E., Waymire K.G., Levy S.E., Sligh J.E., Cai J., Jones D.P., MacGregor G.R., Wallace D.C. Nature 427:461-465(2004) · Mapped (3) |
| Increased adenine nucleotide translocator 1 in reactive astrocytes facilitates glutamate transport. Buck C.R., Jurynec M.J., Gupta D.K., Law A.K., Bilger J., Wallace D.C., McKeon R.J. Exp. Neurol. 181:149-158(2003) · Mapped (1) |
| 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) |
| Mitochondrial DNA variation in Kets and Nganasans and the early peoples of Northern Eurasia. Derbeneva O.A., Starikovskaia E.B., Volod'ko N.V., Wallace D.C., Sukernik R.I. Genetika 38:1554-1560(2002) · UniProtKB (13) |
| Analysis of mitochondrial DNA diversity in the aleuts of the commander islands and its implications for the genetic history of beringia. Derbeneva O.A., Sukernik R.I., Volodko N.V., Hosseini S.H., Lott M.T., Wallace D.C. Am. J. Hum. Genet. 71:415-421(2002) · UniProtKB (19) |
| Animal models for mitochondrial disease. Wallace D.C. Methods Mol. Biol. 197:3-54(2002) · Mapped (1) |
| ARL2 and BART enter mitochondria and bind the adenine nucleotide transporter. Sharer J.D., Shern J.F., Van Valkenburgh H., Wallace D.C., Kahn R.A. Mol. Biol. Cell 13:71-83(2002) · UniProtKB (2) |
| Lifespan extension and rescue of spongiform encephalopathy in superoxide dismutase 2 nullizygous mice treated with superoxide dismutase-catalase mimetics. Melov S., Doctrow S.R., Schneider J.A., Haberson J., Patel M., Coskun P.E., Huffman K., Wallace D.C., Malfroy B. J. Neurosci. 21:8348-8353(2001) · Mapped (4) |
| Ocular pathology in mitochondrial superoxide dismutase (Sod2)-deficient mice. Sandbach J.M., Coscun P.E., Grossniklaus H.E., Kokoszka J.E., Newman N.J., Wallace D.C. Invest. Ophthalmol. Vis. Sci. 42:2173-2178(2001) · Mapped (4) |
