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The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.
Newman NJ, Lott MT, Wallace DC. Newman NJ, et al. Among authors: wallace dc. Am J Ophthalmol. 1991 Jun 15;111(6):750-62. doi: 10.1016/s0002-9394(14)76784-4. Am J Ophthalmol. 1991. PMID: 2039048
Insulin resistance associated with maternally inherited diabetes and deafness.
Gebhart SS, Shoffner JM, Koontz D, Kaufman A, Wallace D. Gebhart SS, et al. Among authors: wallace d. Metabolism. 1996 Apr;45(4):526-31. doi: 10.1016/s0026-0495(96)90231-0. Metabolism. 1996. PMID: 8609843
Clinical, genetic, and biochemical characterization of a Leber hereditary optic neuropathy family containing both the 11778 and 14484 primary mutations.
Brown MD, Allen JC, Van Stavern GP, Newman NJ, Wallace DC. Brown MD, et al. Among authors: wallace dc. Am J Med Genet. 2001 Dec 15;104(4):331-8. Am J Med Genet. 2001. PMID: 11754070
Maternal germ-line transmission of mutant mtDNAs from embryonic stem cell-derived chimeric mice.
Sligh JE, Levy SE, Waymire KG, Allard P, Dillehay DL, Nusinowitz S, Heckenlively JR, MacGregor GR, Wallace DC. Sligh JE, et al. Among authors: wallace dc. Proc Natl Acad Sci U S A. 2000 Dec 19;97(26):14461-6. doi: 10.1073/pnas.250491597. Proc Natl Acad Sci U S A. 2000. PMID: 11106380 Free PMC article.
Production of transmitochondrial mouse cell lines by cybrid rescue of rhodamine-6G pre-treated L-cells.
Trounce I, Wallace DC. Trounce I, et al. Among authors: wallace dc. Somat Cell Mol Genet. 1996 Jan;22(1):81-5. doi: 10.1007/BF02374379. Somat Cell Mol Genet. 1996. PMID: 8643997
Mitochondrial DNA "clock" for the Amerinds and its implications for timing their entry into North America.
Torroni A, Neel JV, Barrantes R, Schurr TG, Wallace DC. Torroni A, et al. Among authors: wallace dc. Proc Natl Acad Sci U S A. 1994 Feb 1;91(3):1158-62. doi: 10.1073/pnas.91.3.1158. Proc Natl Acad Sci U S A. 1994. PMID: 8302846 Free PMC article.
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. Among authors: wallace dc. 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.
Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease.
Wallace DC, Zheng XX, Lott MT, Shoffner JM, Hodge JA, Kelley RI, Epstein CM, Hopkins LC. Wallace DC, et al. Cell. 1988 Nov 18;55(4):601-10. doi: 10.1016/0092-8674(88)90218-8. Cell. 1988. PMID: 3180221
Classification of European mtDNAs from an analysis of three European populations.
Torroni A, Huoponen K, Francalacci P, Petrozzi M, Morelli L, Scozzari R, Obinu D, Savontaus ML, Wallace DC. Torroni A, et al. Among authors: wallace dc. Genetics. 1996 Dec;144(4):1835-50. Genetics. 1996. PMID: 8978068 Free PMC article.
Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.
Brown MD, Voljavec AS, Lott MT, Torroni A, Yang CC, Wallace DC. Brown MD, et al. Among authors: wallace dc. Genetics. 1992 Jan;130(1):163-73. Genetics. 1992. PMID: 1732158 Free PMC article.
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