Petit N - Search Results

1

Mutation analysis in 16 patients with mtDNA depletion.

Carrozzo R, Bornstein B, Lucioli S, Campos Y, de la Pena P, Petit N, Dionisi-Vici C, Vilarinho L, Rizza T, Bertini E, Garesse R, Santorelli FM, Arenas J. Carrozzo R, et al. Among authors: petit n. Hum Mutat. 2003 Apr;21(4):453-4. doi: 10.1002/humu.9135. Hum Mutat. 2003. PMID: 12655576

2

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. Among authors: petit n. Mol Genet Metab. 2000 Nov;71(3):481-95. doi: 10.1006/mgme.2000.3083. Mol Genet Metab. 2000. PMID: 11073716 Review.

3

Technical knockout, a Drosophila model of mitochondrial deafness.

Toivonen JM, O'Dell KM, Petit N, Irvine SC, Knight GK, Lehtonen M, Longmuir M, Luoto K, Touraille S, Wang Z, Alziari S, Shah ZH, Jacobs HT. Toivonen JM, et al. Among authors: petit n. Genetics. 2001 Sep;159(1):241-54. doi: 10.1093/genetics/159.1.241. Genetics. 2001. PMID: 11560901 Free PMC article.

4

Developmental changes in heteroplasmy level and mitochondrial gene expression in a Drosophila subobscura mitochondrial deletion mutant.

Petit N, Touraille S, Debise R, Morel F, Renoux M, Lécher P, Alziari S. Petit N, et al. Curr Genet. 1998 May;33(5):330-9. doi: 10.1007/s002940050344. Curr Genet. 1998. PMID: 9618583

5

Biochemical and molecular consequences of massive mitochondrial gene loss in different tissues of a mutant strain of Drosophila subobscura.

Béziat F, Touraille S, Debise R, Morel F, Petit N, Lécher P, Alziari S. Béziat F, et al. Among authors: petit n. J Biol Chem. 1997 Sep 5;272(36):22583-90. doi: 10.1074/jbc.272.36.22583. J Biol Chem. 1997. PMID: 9278413 Free article.

6

The nuclear genome is involved in heteroplasmy control in a mitochondrial mutant strain of Drosophila subobscura.

Farge G, Touraille S, Le Goff S, Petit N, Renoux M, Morel F, Alziari S. Farge G, et al. Among authors: petit n. Eur J Biochem. 2002 Feb;269(3):998-1005. doi: 10.1046/j.0014-2956.2001.02737.x. Eur J Biochem. 2002. PMID: 11846802 Free article.

7

Localization by ultrastructural in situ hybridization of mitochondrial transcripts in epithelial cells of a Drosophila subobscura deletion mutant.

Lécher P, Petit N, Beziat F, Alziari S. Lécher P, et al. Among authors: petit n. Eur J Cell Biol. 1996 Dec;71(4):423-7. Eur J Cell Biol. 1996. PMID: 8980915 No abstract available.

8

Quantitative analysis, by ultrastructural in situ hybridization, of mitochondrial genomes and their expression in mid-gut and ovarian cells of a mutant strain of Drosophila subobscura.

Lécher P, Petit N, Le Goff S, Alziari S. Lécher P, et al. Among authors: petit n. Biol Cell. 2000 Aug;92(5):341-50. doi: 10.1016/s0248-4900(00)01075-3. Biol Cell. 2000. PMID: 11071043

9

Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome.

Moghadaszadeh B, Petit N, Jaillard C, Brockington M, Quijano Roy S, Merlini L, Romero N, Estournet B, Desguerre I, Chaigne D, Muntoni F, Topaloglu H, Guicheney P. Moghadaszadeh B, et al. Among authors: petit n. Nat Genet. 2001 Sep;29(1):17-8. doi: 10.1038/ng713. Nat Genet. 2001. PMID: 11528383

10

Selenoprotein N: an endoplasmic reticulum glycoprotein with an early developmental expression pattern.

Petit N, Lescure A, Rederstorff M, Krol A, Moghadaszadeh B, Wewer UM, Guicheney P. Petit N, et al. Hum Mol Genet. 2003 May 1;12(9):1045-53. doi: 10.1093/hmg/ddg115. Hum Mol Genet. 2003. PMID: 12700173

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