Wallace DC - Search Results

1

Y chromosome polymorphisms in native American and Siberian populations: identification of native American Y chromosome haplotypes.

Lell JT, Brown MD, Schurr TG, Sukernik RI, Starikovskaya YB, Torroni A, Moore LG, Troup GM, Wallace DC. Lell JT, et al. Among authors: wallace dc. Hum Genet. 1997 Oct;100(5-6):536-43. doi: 10.1007/s004390050548. Hum Genet. 1997. PMID: 9341867

2

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. Among authors: wallace dc. Am J Hum Genet. 1992 Aug;51(2):378-85. Am J Hum Genet. 1992. PMID: 1322638 Free PMC article.

3

Southeast Asian mitochondrial DNA analysis reveals genetic continuity of ancient mongoloid migrations.

Ballinger SW, Schurr TG, Torroni A, Gan YY, Hodge JA, Hassan K, Chen KH, Wallace DC. Ballinger SW, et al. Among authors: wallace dc. Genetics. 1992 Jan;130(1):139-52. doi: 10.1093/genetics/130.1.139. Genetics. 1992. PMID: 1346259 Free PMC article.

4

American Indian prehistory as written in the mitochondrial DNA: a review.

Wallace DC, Torroni A. Wallace DC, et al. Hum Biol. 1992 Jun;64(3):403-16. Hum Biol. 1992. PMID: 1351474

5

Differential expression of adenine nucleotide translocator isoforms in mammalian tissues and during muscle cell differentiation.

Stepien G, Torroni A, Chung AB, Hodge JA, Wallace DC. Stepien G, et al. Among authors: wallace dc. J Biol Chem. 1992 Jul 25;267(21):14592-7. J Biol Chem. 1992. PMID: 1378836 Free article.

6

Mitochondrial tRNA(Thr) mutations and lethal infantile mitochondrial myopathy.

Brown MD, Torroni A, Shoffner JM, Wallace DC. Brown MD, et al. Among authors: wallace dc. Am J Hum Genet. 1992 Aug;51(2):446-7. Am J Hum Genet. 1992. PMID: 1379415 Free PMC article. No abstract available.

7

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.

8

Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases.

Brown MD, Voljavec AS, Lott MT, MacDonald I, Wallace DC. Brown MD, et al. Among authors: wallace dc. FASEB J. 1992 Jul;6(10):2791-9. doi: 10.1096/fasebj.6.10.1634041. FASEB J. 1992. PMID: 1634041 Review.

9

The structure of human mitochondrial DNA variation.

Merriwether DA, Clark AG, Ballinger SW, Schurr TG, Soodyall H, Jenkins T, Sherry ST, Wallace DC. Merriwether DA, et al. Among authors: wallace dc. J Mol Evol. 1991 Dec;33(6):543-55. doi: 10.1007/BF02102807. J Mol Evol. 1991. PMID: 1685753

10

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. doi: 10.1093/genetics/130.1.163. Genetics. 1992. PMID: 1732158 Free PMC article.

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