Nunes V - Search Results

1

Respiratory chain activity and mitochondrial DNA content of nonpurified and purified pancreatic islet cells.

Conget I, Barrientos A, Manzanares JM, Casademont J, Viñas O, Barceló J, Nunes V, Gomis R, Cardellach F. Conget I, et al. Among authors: nunes v. Metabolism. 1997 Sep;46(9):984-7. doi: 10.1016/s0026-0495(97)90265-1. Metabolism. 1997. PMID: 9284883

2

Sporadic heteroplasmic single 5.5 kb mitochondrial DNA deletion associated with cerebellar ataxia, hypogonadotropic hypogonadism, choroidal dystrophy, and mitochondrial respiratory chain complex I deficiency.

Barrientos A, Casademont J, Genís D, Cardellach F, Fernández-Real JM, Grau JM, Urbano-Márquez A, Estivill X, Nunes V. Barrientos A, et al. Among authors: nunes v. Hum Mutat. 1997;10(3):212-6. doi: 10.1002/(SICI)1098-1004(1997)10:3<212::AID-HUMU6>3.0.CO;2-K. Hum Mutat. 1997. PMID: 9298821

3

[Progressive external ophthalmoplegia and the Kearns-Sayre syndrome: a clinical and molecular study of 6 cases].

Barrientos A, Casademont J, Grau JM, Cardellach F, Montoya J, Estivill X, Urbano-Márquez A, Nunes V. Barrientos A, et al. Among authors: nunes v. Med Clin (Barc). 1995 Jul 1;105(5):180-4. Med Clin (Barc). 1995. PMID: 7630231 Spanish.

4

The 9-bp deletion in region V of mitochondrial DNA: evidence of mutation recurrence.

Barrientos A, Casademont J, Solans A, Moral P, Cardellach F, Urbano-Márquez A, Estivill X, Nunes V. Barrientos A, et al. Among authors: nunes v. Hum Genet. 1995 Aug;96(2):225-8. doi: 10.1007/BF00207385. Hum Genet. 1995. PMID: 7635476

5

A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome.

Barrientos A, Volpini V, Casademont J, Genís D, Manzanares JM, Ferrer I, Corral J, Cardellach F, Urbano-Márquez A, Estivill X, Nunes V. Barrientos A, et al. Among authors: nunes v. J Clin Invest. 1996 Apr 1;97(7):1570-6. doi: 10.1172/JCI118581. J Clin Invest. 1996. PMID: 8601620 Free PMC article.

6

Autosomal recessive Wolfram syndrome associated with an 8.5-kb mtDNA single deletion.

Barrientos A, Casademont J, Saiz A, Cardellach F, Volpini V, Solans A, Tolosa E, Urbano-Marquez A, Estivill X, Nunes V. Barrientos A, et al. Among authors: nunes v. Am J Hum Genet. 1996 May;58(5):963-70. Am J Hum Genet. 1996. PMID: 8651280 Free PMC article.

7

[Rearrangement of the mitochondrial DNA in Kearns-Sayre syndrome: is it necessary to differentiate deletions from duplications or polymerization?].

Barrientos A, Casademont J, Nunes V. Barrientos A, et al. Among authors: nunes v. Neurologia. 1996 Aug-Sep;11(7):257-60. Neurologia. 1996. PMID: 8974426 Review. Spanish. No abstract available.

8

Qualitative and quantitative changes in skeletal muscle mtDNA and expression of mitochondrial-encoded genes in the human aging process.

Barrientos A, Casademont J, Cardellach F, Ardite E, Estivill X, Urbano-Márquez A, Fernández-Checa JC, Nunes V. Barrientos A, et al. Among authors: nunes v. Biochem Mol Med. 1997 Dec;62(2):165-71. doi: 10.1006/bmme.1997.2647. Biochem Mol Med. 1997. PMID: 9441868

9

Reduced steady-state levels of mitochondrial RNA and increased mitochondrial DNA amount in human brain with aging.

Barrientos A, Casademont J, Cardellach F, Estivill X, Urbano-Marquez A, Nunes V. Barrientos A, et al. Among authors: nunes v. Brain Res Mol Brain Res. 1997 Dec 15;52(2):284-9. doi: 10.1016/s0169-328x(97)00278-7. Brain Res Mol Brain Res. 1997. PMID: 9495550

10

Biochemical and molecular effects of chronic haloperidol administration on brain and muscle mitochondria of rats.

Barrientos A, Marín C, Miró O, Casademont J, Gómez M, Nunes V, Tolosa E, Urbano-Márquez A, Cardellach F. Barrientos A, et al. Among authors: nunes v. J Neurosci Res. 1998 Aug 15;53(4):475-81. doi: 10.1002/(SICI)1097-4547(19980815)53:4<475::AID-JNR9>3.0.CO;2-3. J Neurosci Res. 1998. PMID: 9710267

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