Bonilla E - Search Results

1

Mitochondrial involvement in Alzheimer's disease.

Bonilla E, Tanji K, Hirano M, Vu TH, DiMauro S, Schon EA. Bonilla E, et al. Biochim Biophys Acta. 1999 Feb 9;1410(2):171-82. doi: 10.1016/s0005-2728(98)00165-0. Biochim Biophys Acta. 1999. PMID: 10076025 Free article. Review.

2

A key role for MAM in mediating mitochondrial dysfunction in Alzheimer disease.

Area-Gomez E, de Groof A, Bonilla E, Montesinos J, Tanji K, Boldogh I, Pon L, Schon EA. Area-Gomez E, et al. Among authors: bonilla e. Cell Death Dis. 2018 Feb 28;9(3):335. doi: 10.1038/s41419-017-0215-0. Cell Death Dis. 2018. PMID: 29491396 Free PMC article. Review.

3

Mitochondrial abnormalities in muscle and other aging cells: classification, causes, and effects.

DiMauro S, Tanji K, Bonilla E, Pallotti F, Schon EA. DiMauro S, et al. Among authors: bonilla e. Muscle Nerve. 2002 Nov;26(5):597-607. doi: 10.1002/mus.10194. Muscle Nerve. 2002. PMID: 12402281 Review.

4

Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene.

Mancuso M, Filosto M, Bonilla E, Hirano M, Shanske S, Vu TH, DiMauro S. Mancuso M, et al. Among authors: bonilla e. Arch Neurol. 2003 Jul;60(7):1007-9. doi: 10.1001/archneur.60.7.1007. Arch Neurol. 2003. PMID: 12873860

5

Mitochondrial DNA dysfunction in oncocytic hepatocytes.

Tanji K, Bhagat G, Vu TH, Monzon L, Bonilla E, Lefkowitch JH. Tanji K, et al. Among authors: bonilla e. Liver Int. 2003 Oct;23(5):397-403. doi: 10.1034/j.1478-3231.2003.00864.x. Liver Int. 2003. PMID: 14708902

6

The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle.

Moraes CT, Ricci E, Bonilla E, DiMauro S, Schon EA. Moraes CT, et al. Among authors: bonilla e. Am J Hum Genet. 1992 May;50(5):934-49. Am J Hum Genet. 1992. PMID: 1315123 Free PMC article.

7

Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: a new approach to the study of mitochondrial myopathies.

Andreetta F, Tritschler HJ, Schon EA, DiMauro S, Bonilla E. Andreetta F, et al. Among authors: bonilla e. J Neurol Sci. 1991 Sep;105(1):88-92. doi: 10.1016/0022-510x(91)90123-o. J Neurol Sci. 1991. PMID: 1665507 Free article.

8

Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome.

Mita S, Schmidt B, Schon EA, DiMauro S, Bonilla E. Mita S, et al. Among authors: bonilla e. Proc Natl Acad Sci U S A. 1989 Dec;86(23):9509-13. doi: 10.1073/pnas.86.23.9509. Proc Natl Acad Sci U S A. 1989. PMID: 2556715 Free PMC article.

9

Paucity of deleted mitochondrial DNAs in brain regions of Huntington's disease patients.

Chen X, Bonilla E, Sciacco M, Schon EA. Chen X, et al. Among authors: bonilla e. Biochim Biophys Acta. 1995 May 24;1271(1):229-33. doi: 10.1016/0925-4439(95)00032-y. Biochim Biophys Acta. 1995. PMID: 7599213 Free article.

10

A mitochondrial tRNA anticodon swap associated with a muscle disease.

Moraes CT, Ciacci F, Bonilla E, Ionasescu V, Schon EA, DiMauro S. Moraes CT, et al. Among authors: bonilla e. Nat Genet. 1993 Jul;4(3):284-8. doi: 10.1038/ng0793-284. Nat Genet. 1993. PMID: 7689388

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