Lenaers G - Search Results

1

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy.

Delettre C, Lenaers G, Griffoin JM, Gigarel N, Lorenzo C, Belenguer P, Pelloquin L, Grosgeorge J, Turc-Carel C, Perret E, Astarie-Dequeker C, Lasquellec L, Arnaud B, Ducommun B, Kaplan J, Hamel CP. Delettre C, et al. Among authors: lenaers g. Nat Genet. 2000 Oct;26(2):207-10. doi: 10.1038/79936. Nat Genet. 2000. PMID: 11017079

2

Identification and transcription control of fission yeast genes repressed by an ammonium starvation growth arrest.

Bonnet C, Perret E, Dumont X, Picard A, Caput D, Lenaers G. Bonnet C, et al. Among authors: lenaers g. Yeast. 2000 Jan 15;16(1):23-33. doi: 10.1002/(SICI)1097-0061(20000115)16:1<23::AID-YEA503>3.0.CO;2-A. Yeast. 2000. PMID: 10620772

3

Identification of rpaP1-5 and rpaP2-6 genes encoding two additional variants of the 60S acidic ribosomal proteins of Schizosaccharomyces pombe.

Bonnet C, Perret E, Bonnin O, Picard A, Caput D, Lenaers G. Bonnet C, et al. Among authors: lenaers g. Genome. 2000 Feb;43(1):205-7. doi: 10.1139/g99-102. Genome. 2000. PMID: 10701132

4

Mutation spectrum and splicing variants in the OPA1 gene.

Delettre C, Griffoin JM, Kaplan J, Dollfus H, Lorenz B, Faivre L, Lenaers G, Belenguer P, Hamel CP. Delettre C, et al. Among authors: lenaers g. Hum Genet. 2001 Dec;109(6):584-91. doi: 10.1007/s00439-001-0633-y. Epub 2001 Oct 30. Hum Genet. 2001. PMID: 11810270

5

OPA1 (Kjer type) dominant optic atrophy: a novel mitochondrial disease.

Delettre C, Lenaers G, Pelloquin L, Belenguer P, Hamel CP. Delettre C, et al. Among authors: lenaers g. Mol Genet Metab. 2002 Feb;75(2):97-107. doi: 10.1006/mgme.2001.3278. Mol Genet Metab. 2002. PMID: 11855928 Review.

6

The human dynamin-related protein OPA1 is anchored to the mitochondrial inner membrane facing the inter-membrane space.

Olichon A, Emorine LJ, Descoins E, Pelloquin L, Brichese L, Gas N, Guillou E, Delettre C, Valette A, Hamel CP, Ducommun B, Lenaers G, Belenguer P. Olichon A, et al. Among authors: lenaers g. FEBS Lett. 2002 Jul 17;523(1-3):171-6. doi: 10.1016/s0014-5793(02)02985-x. FEBS Lett. 2002. PMID: 12123827 Free article.

7

What similarity between human and fission yeast proteins is required for orthology?

Lenaers G, Pelloquin L, Olichon A, Emorine LJ, Guillou E, Delettre C, Hamel CP, Ducommun B, Belenguer P. Lenaers G, et al. Yeast. 2002 Sep 30;19(13):1125-6. doi: 10.1002/yea.901. Yeast. 2002. PMID: 12237853 No abstract available.

8

Loss of OPA1 perturbates the mitochondrial inner membrane structure and integrity, leading to cytochrome c release and apoptosis.

Olichon A, Baricault L, Gas N, Guillou E, Valette A, Belenguer P, Lenaers G. Olichon A, et al. Among authors: lenaers g. J Biol Chem. 2003 Mar 7;278(10):7743-6. doi: 10.1074/jbc.C200677200. Epub 2002 Dec 31. J Biol Chem. 2003. PMID: 12509422 Free article.

9

Gene structure and chromosomal localization of mouse Opa1 : its exclusion from the Bst locus.

Delettre C, Lenaers G, Belenguer P, Hamel CP. Delettre C, et al. Among authors: lenaers g. BMC Genet. 2003 May 7;4:8. doi: 10.1186/1471-2156-4-8. BMC Genet. 2003. PMID: 12735796 Free PMC article.

10

OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract.

Reynier P, Amati-Bonneau P, Verny C, Olichon A, Simard G, Guichet A, Bonnemains C, Malecaze F, Malinge MC, Pelletier JB, Calvas P, Dollfus H, Belenguer P, Malthièry Y, Lenaers G, Bonneau D. Reynier P, et al. Among authors: lenaers g. J Med Genet. 2004 Sep;41(9):e110. doi: 10.1136/jmg.2003.016576. J Med Genet. 2004. PMID: 15342707 Free PMC article. No abstract available.

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