Ballinger SW - Search Results

1

Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion.

Ballinger SW, Shoffner JM, Hedaya EV, Trounce I, Polak MA, Koontz DA, Wallace DC. Ballinger SW, et al. Nat Genet. 1992 Apr;1(1):11-5. doi: 10.1038/ng0492-11. Nat Genet. 1992. PMID: 1301992

2

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. Genetics. 1992 Jan;130(1):139-52. doi: 10.1093/genetics/130.1.139. Genetics. 1992. PMID: 1346259 Free PMC article.

3

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: ballinger sw. J Mol Evol. 1991 Dec;33(6):543-55. doi: 10.1007/BF02102807. J Mol Evol. 1991. PMID: 1685753

4

Amerindian mitochondrial DNAs have rare Asian mutations at high frequencies, suggesting they derived from four primary maternal lineages.

Schurr TG, Ballinger SW, Gan YY, Hodge JA, Merriwether DA, Lawrence DN, Knowler WC, Weiss KM, Wallace DC. Schurr TG, et al. Among authors: ballinger sw. Am J Hum Genet. 1990 Mar;46(3):613-23. Am J Hum Genet. 1990. PMID: 1968708 Free PMC article.

5

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.

Shoffner JM, Lott MT, Lezza AM, Seibel P, Ballinger SW, Wallace DC. Shoffner JM, et al. Among authors: ballinger sw. Cell. 1990 Jun 15;61(6):931-7. doi: 10.1016/0092-8674(90)90059-n. Cell. 1990. PMID: 2112427

6

Mitochondrial DNA mutations in human degenerative diseases and aging.

Wallace DC, Shoffner JM, Trounce I, Brown MD, Ballinger SW, Corral-Debrinski M, Horton T, Jun AS, Lott MT. Wallace DC, et al. Among authors: ballinger sw. Biochim Biophys Acta. 1995 May 24;1271(1):141-51. doi: 10.1016/0925-4439(95)00021-u. Biochim Biophys Acta. 1995. PMID: 7599200 Free article. Review.

7

Mitochondrial diabetes revisited.

Ballinger SW, Shoffner JM, Gebhart S, Koontz DA, Wallace DC. Ballinger SW, et al. Nat Genet. 1994 Aug;7(4):458-9. doi: 10.1038/ng0894-458. Nat Genet. 1994. PMID: 7951312 No abstract available.

8

Mitochondrial myopathy with anemia, cardiomyopathy, and lactic acidosis: a distinct late onset mitochondrial disorder.

Van Hove JL, Shanske S, Ciacci F, Ballinger S, Shoffner JS, Wallace DC, Hanioka T, Folkers K, Bossen EH, Kussin PS, et al. Van Hove JL, et al. Am J Med Genet. 1994 Jun 1;51(2):114-20. doi: 10.1002/ajmg.1320510207. Am J Med Genet. 1994. PMID: 8092186

9

Mitochondrial DNA mutations in epilepsy and neurological disease.

Wallace DC, Lott MT, Shoffner JM, Ballinger S. Wallace DC, et al. Epilepsia. 1994;35 Suppl 1:S43-50. doi: 10.1111/j.1528-1157.1994.tb05928.x. Epilepsia. 1994. PMID: 8293723

10

Mitochondrial genetic background modulates bioenergetics and susceptibility to acute cardiac volume overload.

Fetterman JL, Zelickson BR, Johnson LW, Moellering DR, Westbrook DG, Pompilius M, Sammy MJ, Johnson M, Dunham-Snary KJ, Cao X, Bradley WE, Zhang J, Wei CC, Chacko B, Schurr TG, Kesterson RA, Dell'italia LJ, Darley-Usmar VM, Welch DR, Ballinger SW. Fetterman JL, et al. Among authors: ballinger sw. Biochem J. 2013 Oct 15;455(2):157-67. doi: 10.1042/BJ20130029. Biochem J. 2013. PMID: 23924350 Free PMC article.

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