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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1992 | 1 |
1993 | 1 |
1998 | 1 |
1999 | 1 |
2005 | 1 |
2024 | 0 |
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Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases.
FASEB J. 1992 Jul;6(10):2791-9. doi: 10.1096/fasebj.6.10.1634041.
FASEB J. 1992.
PMID: 1634041
Review.
Cytochrome c oxidase mutations in Leber hereditary optic neuropathy.
Johns DR, Neufeld MJ.
Johns DR, et al.
Biochem Biophys Res Commun. 1993 Oct 29;196(2):810-5. doi: 10.1006/bbrc.1993.2321.
Biochem Biophys Res Commun. 1993.
PMID: 8240356
Item in Clipboard
Heterogenous point mutations in the mitochondrial tRNA Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from Mongolia.
Pandya A, Xia XJ, Erdenetungalag R, Amendola M, Landa B, Radnaabazar J, Dangaasuren B, Van Tuyle G, Nance WE.
Pandya A, et al.
Am J Hum Genet. 1999 Dec;65(6):1803-6. doi: 10.1086/302658.
Am J Hum Genet. 1999.
PMID: 10577941
Free PMC article.
No abstract available.
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The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression.
Guan MX, Enriquez JA, Fischel-Ghodsian N, Puranam RS, Lin CP, Maw MA, Attardi G.
Guan MX, et al.
Mol Cell Biol. 1998 Oct;18(10):5868-79. doi: 10.1128/MCB.18.10.5868.
Mol Cell Biol. 1998.
PMID: 9742104
Free PMC article.
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Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss.
Yuan H, Qian Y, Xu Y, Cao J, Bai L, Shen W, Ji F, Zhang X, Kang D, Mo JQ, Greinwald JH, Han D, Zhai S, Young WY, Guan MX.
Yuan H, et al.
Am J Med Genet A. 2005 Oct 1;138A(2):133-40. doi: 10.1002/ajmg.a.30952.
Am J Med Genet A. 2005.
PMID: 16152638
Free PMC article.
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