Reynier P - Search Results

1

Pro-oxidant effect of ALA is implicated in mitochondrial dysfunction of HepG2 cells.

Laafi J, Homedan C, Jacques C, Gueguen N, Schmitt C, Puy H, Reynier P, Carmen Martinez M, Malthièry Y. Laafi J, et al. Among authors: reynier p. Biochimie. 2014 Nov;106:157-66. doi: 10.1016/j.biochi.2014.08.014. Epub 2014 Sep 8. Biochimie. 2014. PMID: 25220386

2

Multiple deletions of the mitochondrial DNA in polymyalgia rheumatica.

Reynier P, Pellissier JF, Harle JR, Malthiéry Y. Reynier P, et al. Biochem Biophys Res Commun. 1994 Nov 30;205(1):375-80. doi: 10.1006/bbrc.1994.2675. Biochem Biophys Res Commun. 1994. PMID: 7999051

3

Association of deletion and homoplasmic point mutation of the mitochondrial DNA in an ocular myopathy.

Reynier P, Figarella-Branger D, Serratrice G, Charvet B, Malthièry Y. Reynier P, et al. Biochem Biophys Res Commun. 1994 Aug 15;202(3):1606-11. doi: 10.1006/bbrc.1994.2116. Biochem Biophys Res Commun. 1994. PMID: 8060346

4

Accumulation of deletions in MtDNA during tissue aging: analysis by long PCR.

Reynier P, Malthiery Y. Reynier P, et al. Biochem Biophys Res Commun. 1995 Dec 5;217(1):59-67. doi: 10.1006/bbrc.1995.2745. Biochem Biophys Res Commun. 1995. PMID: 8526940

5

Male infertility associated with multiple mitochondrial DNA rearrangements.

Reynier P, Chrétien MF, Penisson-Besnier I, Malthièry Y, Rohmer V, Lestienne P. Reynier P, et al. C R Acad Sci III. 1997 Aug;320(8):629-36. doi: 10.1016/s0764-4469(97)85696-x. C R Acad Sci III. 1997. PMID: 9337998

6

Oligoasthenospermia associated with multiple mitochondrial DNA rearrangements.

Lestienne P, Reynier P, Chrétien MF, Penisson-Besnier I, Malthièry Y, Rohmer V. Lestienne P, et al. Among authors: reynier p. Mol Hum Reprod. 1997 Sep;3(9):811-4. doi: 10.1093/molehr/3.9.811. Mol Hum Reprod. 1997. PMID: 9358008

7

Long PCR analysis of human gamete mtDNA suggests defective mitochondrial maintenance in spermatozoa and supports the bottleneck theory for oocytes.

Reynier P, Chrétien MF, Savagner F, Larcher G, Rohmer V, Barrière P, Malthièry Y. Reynier P, et al. Biochem Biophys Res Commun. 1998 Nov 18;252(2):373-7. doi: 10.1006/bbrc.1998.9651. Biochem Biophys Res Commun. 1998. PMID: 9826537

8

mtDNA haplogroup J: a contributing factor of optic neuritis.

Reynier P, Penisson-Besnier I, Moreau C, Savagner F, Vielle B, Emile J, Dubas F, Malthièry Y. Reynier P, et al. Eur J Hum Genet. 1999 Apr;7(3):404-6. doi: 10.1038/sj.ejhg.5200293. Eur J Hum Genet. 1999. PMID: 10234520

9

Recurrent brain hematomas in MELAS associated with an ND5 gene mitochondrial mutation.

Pénisson-Besnier I, Reynier P, Asfar P, Douay O, Sortais A, Dubas F, Emile J, Malthièry Y. Pénisson-Besnier I, et al. Among authors: reynier p. Neurology. 2000 Jul 25;55(2):317-8. doi: 10.1212/wnl.55.2.317. Neurology. 2000. PMID: 10908920 No abstract available.

10

No evidence of thyrotropin receptor and G(s alpha) gene mutation in high iodine uptake thyroid carcinoma.

Bourasseau I, Savagner F, Rodien P, Duquenne M, Reynier P, Guyetant S, Bigorgne JC, Malthièry Y, Rohmer V. Bourasseau I, et al. Among authors: reynier p. Thyroid. 2000 Sep;10(9):761-5. doi: 10.1089/thy.2000.10.761. Thyroid. 2000. PMID: 11041453

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

346 results

Search Page

Filters