Fernández-Moreno MA - Search Results

1

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. Hum Mutat. 2002 Mar;19(3):234-9. doi: 10.1002/humu.10050. Hum Mutat. 2002. PMID: 11857739

2

The highly compact structure of the mitochondrial DNA polymerase genomic region of Drosophila melanogaster: functional and evolutionary implications.

Lefai E, Fernández-Moreno MA, Kaguni LS, Garesse R. Lefai E, et al. Insect Mol Biol. 2000 Jun;9(3):315-22. doi: 10.1046/j.1365-2583.2000.00191.x. Insect Mol Biol. 2000. PMID: 10886416

3

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. Mol Genet Metab. 2000 Jul;70(3):238-40. doi: 10.1006/mgme.2000.3005. Mol Genet Metab. 2000. PMID: 10924280

4

Differential regulation of the catalytic and accessory subunit genes of Drosophila mitochondrial DNA polymerase.

Lefai E, Fernandez-Moreno MA, Alahari A, Kaguni LS, Garesse R. Lefai E, et al. J Biol Chem. 2000 Oct 20;275(42):33123-33. doi: 10.1074/jbc.M003024200. J Biol Chem. 2000. PMID: 10930405

5

The pathophysiology of mitochondrial biogenesis: towards four decades of mitochondrial DNA research.

Fernández-Moreno MA, Bornstein B, Petit N, Garesse R. Fernández-Moreno MA, et al. Mol Genet Metab. 2000 Nov;71(3):481-95. doi: 10.1006/mgme.2000.3083. Mol Genet Metab. 2000. PMID: 11073716 Review.

6

Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome C oxidase II gene.

Campos Y, García-Redondo A, Fernández-Moreno MA, Martínez-Pardo M, Goda G, Rubio JC, Martín MA, del Hoyo P, Cabello A, Bornstein B, Garesse R, Arenas J. Campos Y, et al. Ann Neurol. 2001 Sep;50(3):409-13. doi: 10.1002/ana.1141. Ann Neurol. 2001. PMID: 11558799

7

Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family.

de la Peña P, Bornstein B, del Hoyo P, Fernández-Moreno MA, Martín MA, Campos Y, Gómez-Escalonilla C, Molina JA, Cabello A, Arenas J, Garesse R. de la Peña P, et al. Neurology. 2001 Oct 9;57(7):1235-8. doi: 10.1212/wnl.57.7.1235. Neurology. 2001. PMID: 11591842

8

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. Biochem J. 2005 May 1;387(Pt 3):773-8. doi: 10.1042/BJ20040949. Biochem J. 2005. PMID: 15554876 Free PMC article.

9

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. Arch Neurol. 2006 Jan;63(1):107-11. doi: 10.1001/archneur.63.1.107. Arch Neurol. 2006. PMID: 16401742

10

Modeling human mitochondrial diseases in flies.

Sánchez-Martínez A, Luo N, Clemente P, Adán C, Hernández-Sierra R, Ochoa P, Fernández-Moreno MA, Kaguni LS, Garesse R. Sánchez-Martínez A, et al. Biochim Biophys Acta. 2006 Sep-Oct;1757(9-10):1190-8. doi: 10.1016/j.bbabio.2006.05.008. Epub 2006 May 13. Biochim Biophys Acta. 2006. PMID: 16806050 Free PMC article. Review.

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