Moraes CT - Search Results

1

A chemical enucleation method for the transfer of mitochondrial DNA to rho(o) cells.

Bayona-Bafaluy MP, Manfredi G, Moraes CT. Bayona-Bafaluy MP, et al. Among authors: moraes ct. Nucleic Acids Res. 2003 Aug 15;31(16):e98. doi: 10.1093/nar/gng100. Nucleic Acids Res. 2003. PMID: 12907750 Free PMC article.

2

Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA.

Mita S, Rizzuto R, Moraes CT, Shanske S, Arnaudo E, Fabrizi GM, Koga Y, DiMauro S, Schon EA. Mita S, et al. Among authors: moraes ct. Nucleic Acids Res. 1990 Feb 11;18(3):561-7. doi: 10.1093/nar/18.3.561. Nucleic Acids Res. 1990. PMID: 2308845 Free PMC article.

3

A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding gene.

Manfredi G, Schon EA, Moraes CT, Bonilla E, Berry GT, Sladky JT, DiMauro S. Manfredi G, et al. Among authors: moraes ct. Neuromuscul Disord. 1995 Sep;5(5):391-8. doi: 10.1016/0960-8966(94)00079-o. Neuromuscul Disord. 1995. PMID: 7496173 Free article.

4

High levels of mitochondrial DNA with an unstable 260-bp duplication in a patient with a mitochondrial myopathy.

Manfredi G, Servidei S, Bonilla E, Shanske S, Schon EA, DiMauro S, Moraes CT. Manfredi G, et al. Among authors: moraes ct. Neurology. 1995 Apr;45(4):762-8. doi: 10.1212/wnl.45.4.762. Neurology. 1995. PMID: 7723967

5

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.

6

Identification of a mutation in the mitochondrial tRNA(Cys) gene associated with mitochondrial encephalopathy.

Manfredi G, Schon EA, Bonilla E, Moraes CT, Shanske S, DiMauro S. Manfredi G, et al. Among authors: moraes ct. Hum Mutat. 1996;7(2):158-63. doi: 10.1002/(SICI)1098-1004(1996)7:2<158::AID-HUMU12>3.0.CO;2-1. Hum Mutat. 1996. PMID: 8829635 No abstract available.

7

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.

8

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.

9

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.

10

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.

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