Campos Y - Search Results

1

Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA(Lys) gene.

Bornstein B, Mas JA, Patrono C, Fernández-Moreno MA, González-Vioque E, Campos Y, Carrozzo R, Martín MA, del Hoyo P, Santorelli FM, Arenas J, Garesse R. Bornstein B, et al. Among authors: campos y. Biochem J. 2005 May 1;387(Pt 3):773-8. doi: 10.1042/BJ20040949. Biochem J. 2005. PMID: 15554876 Free PMC article.

2

The A8296G mtDNA mutation associated with several mitochondrial diseases does not cause mitochondrial dysfunction in cybrid cell lines.

Bornstein B, Mas JA, Fernández-Moreno MA, Campos Y, Martín MA, del Hoyo P, Rubio JC, Arenas J, Garesse R. Bornstein B, et al. Among authors: campos y. Hum Mutat. 2002 Mar;19(3):234-9. doi: 10.1002/humu.10050. Hum Mutat. 2002. PMID: 11857739

3

A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibers.

Arenas J, Campos Y, Bornstein B, Ribacoba R, Martín MA, Rubio JC, Santorelli FM, Zeviani M, DiMauro S, Garesse R. Arenas J, et al. Among authors: campos y. Neurology. 1999 Jan 15;52(2):377-82. doi: 10.1212/wnl.52.2.377. Neurology. 1999. PMID: 9932960

4

The pathogenic role of point mutations affecting the translational initiation codon of mitochondrial genes.

Fernández-Moreno MA, Bornstein B, Campos Y, Arenas J, Garesse R. Fernández-Moreno MA, et al. Among authors: campos y. Mol Genet Metab. 2000 Jul;70(3):238-40. doi: 10.1006/mgme.2000.3005. Mol Genet Metab. 2000. PMID: 10924280

5

Leigh syndrome associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFS1 gene.

Martín MA, Blázquez A, Gutierrez-Solana LG, Fernández-Moreira D, Briones P, Andreu AL, Garesse R, Campos Y, Arenas J. Martín MA, et al. Among authors: campos y. Arch Neurol. 2005 Apr;62(4):659-61. doi: 10.1001/archneur.62.4.659. Arch Neurol. 2005. PMID: 15824269

6

Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish population.

González-Vioque E, Blázquez A, Fernández-Moreira D, Bornstein B, Bautista J, Arpa J, Navarro C, Campos Y, Fernández-Moreno MA, Garesse R, Arenas J, Martín MA. González-Vioque E, et al. Among authors: campos y. Arch Neurol. 2006 Jan;63(1):107-11. doi: 10.1001/archneur.63.1.107. Arch Neurol. 2006. PMID: 16401742

7

Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNA(Leu(UUR)) mutation of mitochondrial DNA.

Campos Y, Martin MA, Lorenzo G, Aparicio M, Cabello A, Arenas J. Campos Y, et al. Muscle Nerve. 1996 Feb;19(2):187-90. doi: 10.1002/(SICI)1097-4598(199602)19:2<187::AID-MUS10>3.0.CO;2-S. Muscle Nerve. 1996. PMID: 8559168

8

[Molecular genetics of mitochondrial cytopathologies].

Arenas J, Campos Y, Martín MA. Arenas J, et al. Among authors: campos y. Neurologia. 1995 Dec;10 Suppl 1:44-9. Neurologia. 1995. PMID: 8838558 Review. Spanish.

9

Bilateral striatal necrosis and MELAS associated with a new T3308C mutation in the mitochondrial ND1 gene.

Campos Y, Martín MA, Rubio JC, Gutiérrez del Olmo MC, Cabello A, Arenas J. Campos Y, et al. Biochem Biophys Res Commun. 1997 Sep 18;238(2):323-5. doi: 10.1006/bbrc.1997.7166. Biochem Biophys Res Commun. 1997. PMID: 9299504

10

Mitochondrial gene expression and respiratory enzyme activities in cardiac diseases.

Bornstein B, Huertas R, Ochoa P, Campos Y, Guillen F, Garesse R, Arenas J. Bornstein B, et al. Among authors: campos y. Biochim Biophys Acta. 1998 Feb 27;1406(1):85-90. doi: 10.1016/s0925-4439(97)00076-8. Biochim Biophys Acta. 1998. PMID: 9545545 Free article.

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