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Molecular basis of mitochondrial DNA disease.
Brown MD, Wallace DC. Brown MD, et al. J Bioenerg Biomembr. 1994 Jun;26(3):273-89. doi: 10.1007/BF00763099. J Bioenerg Biomembr. 1994. PMID: 8077181 Review.
Mitochondrial DNA diversity in indigenous populations of the southern extent of Siberia, and the origins of Native American haplogroups.
Starikovskaya EB, Sukernik RI, Derbeneva OA, Volodko NV, Ruiz-Pesini E, Torroni A, Brown MD, Lott MT, Hosseini SH, Huoponen K, Wallace DC. Starikovskaya EB, et al. Ann Hum Genet. 2005 Jan;69(Pt 1):67-89. doi: 10.1046/j.1529-8817.2003.00127.x. Ann Hum Genet. 2005. PMID: 15638829 Free PMC article.
The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.
Brown MD, Starikovskaya E, Derbeneva O, Hosseini S, Allen JC, Mikhailovskaya IE, Sukernik RI, Wallace DC. Brown MD, et al. Hum Genet. 2002 Feb;110(2):130-8. doi: 10.1007/s00439-001-0660-8. Epub 2002 Jan 24. Hum Genet. 2002. PMID: 11935318
Natural selection shaped regional mtDNA variation in humans.
Mishmar D, Ruiz-Pesini E, Golik P, Macaulay V, Clark AG, Hosseini S, Brandon M, Easley K, Chen E, Brown MD, Sukernik RI, Olckers A, Wallace DC. Mishmar D, et al. Proc Natl Acad Sci U S A. 2003 Jan 7;100(1):171-6. doi: 10.1073/pnas.0136972100. Epub 2002 Dec 30. Proc Natl Acad Sci U S A. 2003. PMID: 12509511 Free PMC article.
A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystonia.
Sarzi E, Brown MD, Lebon S, Chretien D, Munnich A, Rotig A, Procaccio V. Sarzi E, et al. Am J Med Genet A. 2007 Jan 1;143A(1):33-41. doi: 10.1002/ajmg.a.31565. Am J Med Genet A. 2007. PMID: 17152068
A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia.
Jun AS, Brown MD, Wallace DC. Jun AS, et al. Proc Natl Acad Sci U S A. 1994 Jun 21;91(13):6206-10. doi: 10.1073/pnas.91.13.6206. Proc Natl Acad Sci U S A. 1994. PMID: 8016139 Free PMC article.
Diseases resulting from mitochondrial DNA point mutations.
Wallace DC, Lott MT, Shoffner JM, Brown MD. Wallace DC, et al. J Inherit Metab Dis. 1992;15(4):472-9. doi: 10.1007/BF01799605. J Inherit Metab Dis. 1992. PMID: 1528007 Review.
A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I.
Brown MD, Yang CC, Trounce I, Torroni A, Lott MT, Wallace DC. Brown MD, et al. Am J Hum Genet. 1992 Aug;51(2):378-85. Am J Hum Genet. 1992. PMID: 1322638 Free PMC article.
Large scale screening of the mitochondrial DNA reveals no pathogenic mutations but a haplotype associated with multiple sclerosis in Caucasians.
Kalman B, Li S, Chatterjee D, O'Connor J, Voehl MR, Brown MD, Alder H. Kalman B, et al. Acta Neurol Scand. 1999 Jan;99(1):16-25. doi: 10.1111/j.1600-0404.1999.tb00653.x. Acta Neurol Scand. 1999. PMID: 9925234
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