Moraes CT - Search Results

1

A metabolic shift induced by a PPAR panagonist markedly reduces the effects of pathogenic mitochondrial tRNA mutations.

Wenz T, Wang X, Marini M, Moraes CT. Wenz T, et al. Among authors: moraes ct. J Cell Mol Med. 2011 Nov;15(11):2317-25. doi: 10.1111/j.1582-4934.2010.01223.x. J Cell Mol Med. 2011. PMID: 21129152 Free PMC article.

2

Segregation patterns of a novel mutation in the mitochondrial tRNA glutamic acid gene associated with myopathy and diabetes mellitus.

Hao H, Bonilla E, Manfredi G, DiMauro S, Moraes CT. Hao H, et al. Among authors: moraes ct. Am J Hum Genet. 1995 May;56(5):1017-25. Am J Hum Genet. 1995. PMID: 7726154 Free PMC article.

3

Functional and molecular mitochondrial abnormalities associated with a C --> T transition at position 3256 of the human mitochondrial genome. The effects of a pathogenic mitochondrial tRNA point mutation in organelle translation and RNA processing.

Hao H, Moraes CT. Hao H, et al. Among authors: moraes ct. J Biol Chem. 1996 Jan 26;271(4):2347-52. doi: 10.1074/jbc.271.4.2347. J Biol Chem. 1996. PMID: 8567699 Free article.

4

Mitochondrial disorders.

Moraes CT. Moraes CT. Curr Opin Neurol. 1996 Oct;9(5):369-74. doi: 10.1097/00019052-199610000-00010. Curr Opin Neurol. 1996. PMID: 8894413 Review.

5

Functional and structural features of a tandem duplication of the human mtDNA promoter region.

Hao H, Manfredi G, Moraes CT. Hao H, et al. Among authors: moraes ct. Am J Hum Genet. 1997 Jun;60(6):1363-72. doi: 10.1086/515474. Am J Hum Genet. 1997. PMID: 9199557 Free PMC article.

6

Expanding the functional human mitochondrial DNA database by the establishment of primate xenomitochondrial cybrids.

Kenyon L, Moraes CT. Kenyon L, et al. Among authors: moraes ct. Proc Natl Acad Sci U S A. 1997 Aug 19;94(17):9131-5. doi: 10.1073/pnas.94.17.9131. Proc Natl Acad Sci U S A. 1997. PMID: 9256447 Free PMC article.

7

A disease-associated G5703A mutation in human mitochondrial DNA causes a conformational change and a marked decrease in steady-state levels of mitochondrial tRNA(Asn).

Hao H, Moraes CT. Hao H, et al. Among authors: moraes ct. Mol Cell Biol. 1997 Dec;17(12):6831-7. doi: 10.1128/MCB.17.12.6831. Mol Cell Biol. 1997. PMID: 9372914 Free PMC article.

8

Suppression of a mitochondrial tRNA gene mutation phenotype associated with changes in the nuclear background.

Hao H, Morrison LE, Moraes CT. Hao H, et al. Among authors: moraes ct. Hum Mol Genet. 1999 Jun;8(6):1117-24. doi: 10.1093/hmg/8.6.1117. Hum Mol Genet. 1999. PMID: 10332045

9

Mechanisms of human mitochondrial DNA maintenance: the determining role of primary sequence and length over function.

Moraes CT, Kenyon L, Hao H. Moraes CT, et al. Mol Biol Cell. 1999 Oct;10(10):3345-56. doi: 10.1091/mbc.10.10.3345. Mol Biol Cell. 1999. PMID: 10512871 Free PMC article.

10

A novel myopathy-associated mitochondrial DNA mutation altering the conserved size of the tRNA(Gln) anticodon loop.

Dey R, Tengan CH, Morita MP, Kiyomoto BH, Moraes CT. Dey R, et al. Among authors: moraes ct. Neuromuscul Disord. 2000 Oct;10(7):488-92. doi: 10.1016/s0960-8966(00)00125-5. Neuromuscul Disord. 2000. PMID: 10996779 Free article.

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