Reynier P - Search Results

1

Autophagy controls the pathogenicity of OPA1 mutations in dominant optic atrophy.

Kane MS, Alban J, Desquiret-Dumas V, Gueguen N, Ishak L, Ferre M, Amati-Bonneau P, Procaccio V, Bonneau D, Lenaers G, Reynier P, Chevrollier A. Kane MS, et al. Among authors: reynier p. J Cell Mol Med. 2017 Oct;21(10):2284-2297. doi: 10.1111/jcmm.13149. Epub 2017 Apr 4. J Cell Mol Med. 2017. PMID: 28378518 Free PMC article.

2

Mitochondrial activity in XTC.UC1 cells derived from thyroid oncocytoma.

Savagner F, Chevrollier A, Loiseau D, Morgan C, Reynier P, Clark O, Stepien G, Malthiery Y. Savagner F, et al. Among authors: reynier p. Thyroid. 2001 Apr;11(4):327-33. doi: 10.1089/10507250152039055. Thyroid. 2001. PMID: 11349830

3

Oxygen consumption and expression of the adenine nucleotide translocator in cells lacking mitochondrial DNA.

Loiseau D, Chevrollier A, Douay O, Vavasseur F, Renier G, Reynier P, Malthièry Y, Stepien G. Loiseau D, et al. Among authors: reynier p. Exp Cell Res. 2002 Aug 1;278(1):12-8. doi: 10.1006/excr.2002.5553. Exp Cell Res. 2002. PMID: 12126953

4

The association of autosomal dominant optic atrophy and moderate deafness may be due to the R445H mutation in the OPA1 gene.

Amati-Bonneau P, Odent S, Derrien C, Pasquier L, Malthiéry Y, Reynier P, Bonneau D. Amati-Bonneau P, et al. Among authors: reynier p. Am J Ophthalmol. 2003 Dec;136(6):1170-1. doi: 10.1016/s0002-9394(03)00665-2. Am J Ophthalmol. 2003. PMID: 14644237

5

Fourteen novel OPA1 mutations in autosomal dominant optic atrophy including two de novo mutations in sporadic optic atrophy.

Baris O, Delettre C, Amati-Bonneau P, Surget MO, Charlin JF, Catier A, Derieux L, Guyomard JL, Dollfus H, Jonveaux P, Ayuso C, Maumenee I, Lorenz B, Mohammed S, Tourmen Y, Bonneau D, Malthièry Y, Hamel C, Reynier P. Baris O, et al. Among authors: reynier p. Hum Mutat. 2003 Jun;21(6):656. doi: 10.1002/humu.9152. Hum Mutat. 2003. PMID: 14961560

6

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. 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.

7

Sporadic optic atrophy due to synonymous codon change altering mRNA splicing of OPA1.

Amati-Bonneau P, Pasquier L, Lainey E, Ferré M, Odent S, Malthièry Y, Bonneau D, Reynier P. Amati-Bonneau P, et al. Among authors: reynier p. Clin Genet. 2005 Jan;67(1):102-3. doi: 10.1111/j.1399-0004.2004.00358.x. Clin Genet. 2005. PMID: 15617556 No abstract available.

8

Mitochondrial diseases preferentially involve proteins with prokaryote homologues.

Tourmen Y, Ferré M, Malthièry Y, Dessen P, Reynier P. Tourmen Y, et al. Among authors: reynier p. C R Biol. 2004 Dec;327(12):1095-101. doi: 10.1016/j.crvi.2004.09.005. C R Biol. 2004. PMID: 15656352 Free article.

9

eOPA1: an online database for OPA1 mutations.

Ferré M, Amati-Bonneau P, Tourmen Y, Malthièry Y, Reynier P. Ferré M, et al. Among authors: reynier p. Hum Mutat. 2005 May;25(5):423-8. doi: 10.1002/humu.20161. Hum Mutat. 2005. PMID: 15832306

10

[An OPA3 gene mutation is responsible for the disease associating optic atrophy and cataract with extrapyramidal signs].

Verny C, Amati-Bonneau P, Dubas F, Malthiéry Y, Reynier P, Bonneau D. Verny C, et al. Among authors: reynier p. Rev Neurol (Paris). 2005 Apr;161(4):451-4. doi: 10.1016/s0035-3787(05)85075-1. Rev Neurol (Paris). 2005. PMID: 15924081 French.

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