Moraes CT - Search Results

1

ATAD3 controls mitochondrial cristae structure in mouse muscle, influencing mtDNA replication and cholesterol levels.

Peralta S, Goffart S, Williams SL, Diaz F, Garcia S, Nissanka N, Area-Gomez E, Pohjoismäki J, Moraes CT. Peralta S, et al. Among authors: moraes ct. J Cell Sci. 2018 Jul 4;131(13):jcs217075. doi: 10.1242/jcs.217075. J Cell Sci. 2018. PMID: 29898916 Free PMC article.

2

Phenotype-genotype correlations in skeletal muscle of patients with mtDNA deletions.

Moraes CT, Sciacco M, Ricci E, Tengan CH, Hao H, Bonilla E, Schon EA, DiMauro S. Moraes CT, et al. Muscle Nerve Suppl. 1995;3:S150-3. doi: 10.1002/mus.880181429. Muscle Nerve Suppl. 1995. PMID: 7603517

3

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.

4

An out-of-frame cytochrome b gene deletion from a patient with parkinsonism is associated with impaired complex III assembly and an increase in free radical production.

Rana M, de Coo I, Diaz F, Smeets H, Moraes CT. Rana M, et al. Among authors: moraes ct. Ann Neurol. 2000 Nov;48(5):774-81. Ann Neurol. 2000. PMID: 11079541

5

Reactive oxygen species and mitochondrial diseases.

Kirkinezos IG, Moraes CT. Kirkinezos IG, et al. Among authors: moraes ct. Semin Cell Dev Biol. 2001 Dec;12(6):449-57. doi: 10.1006/scdb.2001.0282. Semin Cell Dev Biol. 2001. PMID: 11735379 Review.

6

Human mitochondrial DNA with large deletions repopulates organelles faster than full-length genomes under relaxed copy number control.

Diaz F, Bayona-Bafaluy MP, Rana M, Mora M, Hao H, Moraes CT. Diaz F, et al. Among authors: moraes ct. Nucleic Acids Res. 2002 Nov 1;30(21):4626-33. doi: 10.1093/nar/gkf602. Nucleic Acids Res. 2002. PMID: 12409452 Free PMC article.

7

Mitochondrial DNA structure and function.

Moraes CT, Srivastava S, Kirkinezos I, Oca-Cossio J, van Waveren C, Woischnick M, Diaz F. Moraes CT, et al. Int Rev Neurobiol. 2002;53:3-23. doi: 10.1016/s0074-7742(02)53002-6. Int Rev Neurobiol. 2002. PMID: 12512335 Review. No abstract available.

8

Techniques and pitfalls in the detection of pathogenic mitochondrial DNA mutations.

Moraes CT, Atencio DP, Oca-Cossio J, Diaz F. Moraes CT, et al. J Mol Diagn. 2003 Nov;5(4):197-208. doi: 10.1016/S1525-1578(10)60474-6. J Mol Diagn. 2003. PMID: 14573777 Free PMC article. Review.

9

Double-strand breaks of mouse muscle mtDNA promote large deletions similar to multiple mtDNA deletions in humans.

Srivastava S, Moraes CT. Srivastava S, et al. Among authors: moraes ct. Hum Mol Genet. 2005 Apr 1;14(7):893-902. doi: 10.1093/hmg/ddi082. Epub 2005 Feb 9. Hum Mol Genet. 2005. PMID: 15703189 Free PMC article.

10

Mice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency.

Diaz F, Thomas CK, Garcia S, Hernandez D, Moraes CT. Diaz F, et al. Among authors: moraes ct. Hum Mol Genet. 2005 Sep 15;14(18):2737-48. doi: 10.1093/hmg/ddi307. Epub 2005 Aug 15. Hum Mol Genet. 2005. PMID: 16103131 Free PMC article.

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