Please enable Javascript

Labmeeting uses lots of Javascript - basically you can't use the site without it. So please enable Javascript in your browser. If your browser does not support Javascript, we recommend Firefox.

Papers authored by Reynier P

Collect these papers and discover other ones on Labmeeting. Learn more.

OPA1 functions in mitochondria and dysfunctions in optic nerve.

+ cite this

+ View Abstract

Lenaers G, Reynier P, Elachouri G, Soukkarieh C, Olichon A, Belenguer P, Baricault L, Ducommun B, Hamel C, and Delettre C

The international journal of biochemistry & cell biology 41(10):1866-74, 2009 Oct - Who cited this? | PubMed ID: 19389483 | Fulltext

OPA1-associated disorders: phenotypes and pathophysiology.

+ cite this

+ View Abstract

Amati-Bonneau P, Milea D, Bonneau D, Chevrollier A, Ferré M, Guillet V, Gueguen N, Loiseau D, de Crescenzo MA, Verny C, Procaccio V, Lenaers G, and Reynier P

The international journal of biochemistry & cell biology 41(10):1855-65, 2009 Oct - Who cited this? | PubMed ID: 19389487 | Fulltext

Mitochondrial bioenergetic background confers a survival advantage to HepG2 cells in response to chemotherapy.

+ cite this

+ View Abstract

Loiseau D, Morvan D, Chevrollier A, Demidem A, Douay O, Reynier P, and Stepien G

Molecular carcinogenesis 48(8):733-41, 2009 Aug - Who cited this? | PubMed ID: 19347860 | Fulltext

Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations.

+ cite this

+ View Abstract

Ferré M, Bonneau D, Milea D, Chevrollier A, Verny C, Dollfus H, Ayuso C, Defoort S, Vignal C, Zanlonghi X, Charlin JF, Kaplan J, Odent S, Hamel CP, Procaccio V, Reynier P,

(show remaining authors)

Human mutation 30(7):E692-705, 2009 Jul - Who cited this? | PubMed ID: 19319978 | Fulltext

Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).

+ cite this

+ View Abstract

Cassereau J, Chevrollier A, Gueguen N, Malinge MC, Letournel F, Nicolas G, Richard L, Ferre M, Verny C, Dubas F, Procaccio V, Amati-Bonneau P, Bonneau D, and Reynier P

Neurogenetics 10(2):145-50, 2009 Apr - Who cited this? | PubMed ID: 19089472 | Fulltext

Adrenal necrosis mimicking pheochromocytomas during acute pancreatitis.

+ cite this

+ View Abstract

Gatta B, Reynier P, Gense V, Simonnet G, and Corcuff JB

Annales d'endocrinologie 70(2):133-6, 2009 Apr - Who cited this? | PubMed ID: 19054499 | Fulltext

Acute and late-onset optic atrophy due to a novel OPA1 mutation leading to a mitochondrial coupling defect.

+ cite this

+ View Abstract

Nochez Y, Arsene S, Gueguen N, Chevrollier A, Ferré M, Guillet V, Desquiret V, Toutain A, Bonneau D, Procaccio V, Amati-Bonneau P, Pisella PJ, and Reynier P

Molecular vision 15:598-608, 2009 - Who cited this? | PubMed ID: 19325939 | Fulltext

OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background.

+ cite this

+ View Abstract

Pierron D, Ferré M, Rocher C, Chevrollier A, Murail P, Thoraval D, Amati-Bonneau P, Reynier P, and Letellier T

BMC medical genetics 10:70, 2009 - Who cited this? | PubMed ID: 19619285 | Fulltext

Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitis.

+ cite this

+ View Abstract

Verny C, Amati-Bonneau P, Letournel F, Person B, Dib N, Malinge MC, Slama A, Le Maréchal C, Ferec C, Procaccio V, Reynier P, and Bonneau D

Diabetes & metabolism 34(6):620-6, 2008 Dec - Who cited this? | PubMed ID: 18955007 | Fulltext

Hereditary optic neuropathies share a common mitochondrial coupling defect.

+ cite this

+ View Abstract

Chevrollier A, Guillet V, Loiseau D, Gueguen N, de Crescenzo MA, Verny C, Eng MF, Dollfus H, Odent S, Milea D, Goizet C, Amati-Bonneau P, Procaccio V, Bonneau D, and Reynier P

Annals of neurology 63(6):794-8, 2008 Jun - Who cited this? | PubMed ID: 18496845 | Fulltext

Reversible optic neuropathy with OPA1 exon 5b mutation.

+ cite this

+ View Abstract

Cornille K, Milea D, Amati-Bonneau P, Procaccio V, Zazoun L, Guillet V, El Achouri G, Delettre C, Gueguen N, Loiseau D, Muller A, Ferré M, Chevrollier A, Wallace DC, Bonneau D, Hamel C,

(show remaining authors)

Annals of neurology 63(5):667-71, 2008 May - Who cited this? | PubMed ID: 18360822 | Fulltext

Multiple sclerosis-like disorder in opa1-related autosomal dominant optic atrophy.

+ cite this

Verny C, Loiseau D, Scherer C, Lejeune P, Chevrollier A, Gueguen N, Guillet V, Dubas F, Reynier P, Amati-Bonneau P, and Bonneau D

Neurology 70(13 Pt 2):1152-3, 2008 Mar 25 - Who cited this? | PubMed ID: 18287570 | Fulltext

Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance.

+ cite this

+ View Abstract

Hudson G, Amati-Bonneau P, Blakely EL, Stewart JD, He L, Schaefer AM, Griffiths PG, Ahlqvist K, Suomalainen A, Reynier P, McFarland R, Turnbull DM, Chinnery PF, and Taylor RW

Brain : a journal of neurology 131(Pt 2):329, 2008 Feb - Who cited this? | PubMed ID: 18065439 | Fulltext

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes.

+ cite this

+ View Abstract

Amati-Bonneau P, Valentino ML, Reynier P, Gallardo ME, Bornstein B, Boissière A, Campos Y, Rivera H, de la Aleja JG, Carroccia R, Iommarini L, Labauge P, Figarella-Branger D, Marcorelles P, Furby A, Beauvais K,

(show remaining authors)

Brain : a journal of neurology 131(Pt 2):338, 2008 Feb - Who cited this? | PubMed ID: 18158317 | Fulltext

New evidence of a mitochondrial genetic background paradox: impact of the J haplogroup on the A3243G mutation.

+ cite this

+ View Abstract

Pierron D, Rocher C, Amati-Bonneau P, Reynier P, Martin-Négrier ML, Allouche S, Batandier C, de Camaret BM, Godinot C, Rotig A, Feldmann D, Bellanne-Chantelot C, Arveiler B, Pennarun E, Rossignol R, Crouzet M,

(show remaining authors)

BMC medical genetics 9:41, 2008 - Who cited this? | PubMed ID: 18462486 | Fulltext

Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip.

+ cite this

+ View Abstract

Lévêque M, Marlin S, Jonard L, Procaccio V, Reynier P, Amati-Bonneau P, Baulande S, Pierron D, Lacombe D, Duriez F, Francannet C, Mom T, Journel H, Catros H, Drouin-Garraud V, Obstoy MF,

(show remaining authors)

European journal of human genetics : EJHG 15(11):1145-55, 2007 Nov - Who cited this? | PubMed ID: 17637808 | Fulltext

Effects of OPA1 mutations on mitochondrial morphology and apoptosis: relevance to ADOA pathogenesis.

+ cite this

+ View Abstract

Olichon A, Landes T, Arnauné-Pelloquin L, Emorine LJ, Mils V, Guichet A, Delettre C, Hamel C, Amati-Bonneau P, Bonneau D, Reynier P, Lenaers G, and Belenguer P

Journal of cellular physiology 211(2):423-30, 2007 May - Who cited this? | PubMed ID: 17167772 | Fulltext

Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease.

+ cite this

+ View Abstract

Loiseau D, Chevrollier A, Verny C, Guillet V, Gueguen N, Pou de Crescenzo MA, Ferré M, Malinge MC, Guichet A, Nicolas G, Amati-Bonneau P, Malthièry Y, Bonneau D, and Reynier P

Annals of neurology 61(4):315-23, 2007 Apr - Who cited this? | PubMed ID: 17444508 | Fulltext

Diagnosis of myotubular myopathy in the oldest known manifesting female carrier: a clinical and genetic study.

+ cite this

+ View Abstract

Pénisson-Besnier I, Biancalana V, Reynier P, Cossée M, and Dubas F

Neuromuscular disorders : NMD 17(2):180, 2007 Feb - Who cited this? | PubMed ID: 17251023 | Fulltext

Mitochondrial DNA in the oocyte and the developing embryo.

+ cite this

+ View Abstract

May-Panloup P, Chretien MF, Malthiery Y, and Reynier P

Current topics in developmental biology 77:51-83, 2007 - Who cited this? | PubMed ID: 17222700 | Fulltext

Low serum testosterone assayed by liquid chromatography-tandem mass spectrometry. Comparison with five immunoassay techniques.

+ cite this

+ View Abstract

Moal V, Mathieu E, Reynier P, Malthièry Y, and Gallois Y

Clinica chimica acta; international journal of clinical chemistry 386(1-2):12-9, 2007 - Who cited this? | PubMed ID: 17706625 | Fulltext

[Spermatozoon mitochondrial DNA].

+ cite this

+ View Abstract

May-Panloup P, Chrétien MF, Malthiery Y, and Reynier P

Gynecologie, obstetrique & fertilite 34(9):847-54, 2006 Sep - Who cited this? | PubMed ID: 16962811 | Fulltext

mtDNA controls expression of the Death Associated Protein 3.

+ cite this

+ View Abstract

Jacques C, Chevrollier A, Loiseau D, Lagoutte L, Savagner F, Malthièry Y, and Reynier P

Experimental cell research 312(6):737-45, 2006 Apr 1 - Who cited this? | PubMed ID: 16413536 | Fulltext

The bilateral superficial cervical plexus block with 0.75% ropivacaine administered before or after surgery does not prevent postoperative pain after total thyroidectomy.

+ cite this

+ View Abstract

Herbland A, Cantini O, Reynier P, Valat P, Jougon J, Arimone Y, and Janvier G

Regional anesthesia and pain medicine 31(1):34-9, 2006 - Who cited this? | PubMed ID: 16418022 | Fulltext

Mitochondrial dynamics and disease, OPA1.

+ cite this

+ View Abstract

Olichon A, Guillou E, Delettre C, Landes T, Arnauné-Pelloquin L, Emorine LJ, Mils V, Daloyau M, Hamel C, Amati-Bonneau P, Bonneau D, Reynier P, Lenaers G, and Belenguer P

Biochimica et biophysica acta 1763(5-6):500-9, 2006 - Who cited this? | PubMed ID: 16737747 | Fulltext

[Epidemiology of mitochondrial cytopathies: contribution from the French mitochondrial diseases network].

+ cite this

Reynier P and Réseau "Maladies Mitochondriales"

Annales de biologie clinique 64(6):584-6, 2006 - Who cited this? | PubMed ID: 17256236 | Fulltext

OPA1 R445H mutation in optic atrophy associated with sensorineural deafness.

+ cite this

+ View Abstract

Amati-Bonneau P, Guichet A, Olichon A, Chevrollier A, Viala F, Miot S, Ayuso C, Odent S, Arrouet C, Verny C, Calmels MN, Simard G, Belenguer P, Wang J, Puel JL, Hamel C,

(show remaining authors)

Annals of neurology 58(6):958-63, 2005 Dec - Who cited this? | PubMed ID: 16240368 | Fulltext

Gene profiling reveals specific oncogenic mechanisms and signaling pathways in oncocytic and papillary thyroid carcinoma.

+ cite this

+ View Abstract

Baris O, Mirebeau-Prunier D, Savagner F, Rodien P, Ballester B, Loriod B, Granjeaud S, Guyetant S, Franc B, Houlgatte R, Reynier P, and Malthiery Y

Oncogene 24(25):4155-61, 2005 Jun 9 - Who cited this? | PubMed ID: 15806164 | Fulltext

eOPA1: an online database for OPA1 mutations.

+ cite this

+ View Abstract

Ferré M, Amati-Bonneau P, Tourmen Y, Malthièry Y, and Reynier P

Human mutation 25(5):423-8, 2005 May - Who cited this? | PubMed ID: 15832306 | Fulltext

A novel mutation in the mitochondrial tRNA Asn gene associated with a lethal disease.

+ cite this

+ View Abstract

Coulbault L, Herlicoviez D, Chapon F, Read MH, Penniello MJ, Reynier P, Fayet G, Lombès A, Jauzac P, and Allouche S

Biochemical and biophysical research communications 329(3):1152-4, 2005 Apr 15 - Who cited this? | PubMed ID: 15752774 | Fulltext

Two-step differential expression analysis reveals a new set of genes involved in thyroid oncocytic tumors.

+ cite this

+ View Abstract

Jacques C, Baris O, Prunier-Mirebeau D, Savagner F, Rodien P, Rohmer V, Franc B, Guyetant S, Malthiery Y, and Reynier P

The Journal of clinical endocrinology and metabolism 90(4):2314-20, 2005 Apr - Who cited this? | PubMed ID: 15623817 | Fulltext

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

+ cite this

+ View Abstract

Verny C, Amati-Bonneau P, Dubas F, Malthiéry Y, Reynier P, and Bonneau D

Revue neurologique 161(4):451-4, 2005 Apr - Who cited this? | PubMed ID: 15924081 | Fulltext

Low oocyte mitochondrial DNA content in ovarian insufficiency.

+ cite this

+ View Abstract

May-Panloup P, Chrétien MF, Jacques C, Vasseur C, Malthièry Y, and Reynier P

Human reproduction (Oxford, England) 20(3):593-7, 2005 Mar - Who cited this? | PubMed ID: 15608038 | Fulltext

Maternal smoking is associated with mitochondrial DNA depletion and respiratory chain complex III deficiency in placenta.

+ cite this

+ View Abstract

Bouhours-Nouet N, May-Panloup P, Coutant R, de Casson FB, Descamps P, Douay O, Reynier P, Ritz P, Malthièry Y, and Simard G

American journal of physiology. Endocrinology and metabolism 288(1):E171-7, 2005 Jan - Who cited this? | PubMed ID: 15585597 | Fulltext

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

+ cite this

Amati-Bonneau P, Pasquier L, Lainey E, Ferré M, Odent S, Malthièry Y, Bonneau D, and Reynier P

Clinical genetics 67(1):102-3, 2005 Jan - Who cited this? | PubMed ID: 15617556 | Fulltext

Increase of mitochondrial DNA content and transcripts in early bovine embryogenesis associated with upregulation of mtTFA and NRF1 transcription factors.

+ cite this

+ View Abstract

May-Panloup P, Vignon X, Chrétien MF, Heyman Y, Tamassia M, Malthièry Y, and Reynier P

Reproductive biology and endocrinology : RB&E 3:65, 2005 - Who cited this? | PubMed ID: 16285882 | Fulltext

Mitochondrial diseases preferentially involve proteins with prokaryote homologues.

+ cite this

+ View Abstract

Tourmen Y, Ferré M, Malthièry Y, Dessen P, and Reynier P

Comptes rendus biologies 327(12):1095-101, 2004 Dec - Who cited this? | PubMed ID: 15656352 | Fulltext

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

+ cite this

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, and Bonneau D

Journal of medical genetics 41(9):e110, 2004 Sep - Who cited this? | PubMed ID: 15342707 | Fulltext

In vitro embryo production efficiency in cattle and its association with oocyte adenosine triphosphate content, quantity of mitochondrial DNA, and mitochondrial DNA haplogroup.

+ cite this

+ View Abstract

Tamassia M, Nuttinck F, May-Panloup P, Reynier P, Heyman Y, Charpigny G, Stojkovic M, Hiendleder S, Renard JP, and Chastant-Maillard S

Biology of reproduction 71(2):697-704, 2004 Aug - Who cited this? | PubMed ID: 15084486 | Fulltext

A hydroxyethylated cholesterol-based cationic lipid for DNA delivery: effect of conditioning.

+ cite this

+ View Abstract

Percot A, Briane D, Coudert R, Reynier P, Bouchemal N, Lièvre N, Hantz E, Salzmann JL, and Cao A

International journal of pharmaceutics 278(1):143, 2004 Jun 18 - Who cited this? | PubMed ID: 15158957 | Fulltext

Decreased expression of thyrotropin receptor gene suggests a high-risk subgroup for oncocytic adenoma.

+ cite this

+ View Abstract

Mirebeau-Prunier D, Guyétant S, Rodien P, Franc B, Baris O, Rohmer V, Reynier P, Tourmen Y, Malthièry Y, and Savagner F

European journal of endocrinology / European Federation of Endocrine Societies 150(3):269-76, 2004 Mar - Who cited this? | PubMed ID: 15012610 | Fulltext

Transcriptional profiling reveals coordinated up-regulation of oxidative metabolism genes in thyroid oncocytic tumors.

+ cite this

+ View Abstract

Baris O, Savagner F, Nasser V, Loriod B, Granjeaud S, Guyetant S, Franc B, Rodien P, Rohmer V, Bertucci F, Birnbaum D, Malthièry Y, Reynier P, and Houlgatte R

The Journal of clinical endocrinology and metabolism 89(2):994-1005, 2004 Feb - Who cited this? | PubMed ID: 14764826 | Fulltext

Modifications in the head group and in the spacer of cholesterol-based cationic lipids promote transfection in melanoma B16-F10 cells and tumours.

+ cite this

+ View Abstract

Reynier P, Briane D, Coudert R, Fadda G, Bouchemal N, Bissieres P, Taillandier E, and Cao A

Journal of drug targeting 12(1):25-38, 2004 Jan - Who cited this? | PubMed ID: 15203909 | Fulltext

[Mitochondria and reproduction].

+ cite this

+ View Abstract

May-Panloup P, Chrétien MF, Malthièry Y, and Reynier P

Medecine sciences : M/S 20(8-9):779-83, 2004 - Who cited this? | PubMed ID: 15361344 | Fulltext

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

+ cite this

+ View Abstract

Amati-Bonneau P, Odent S, Derrien C, Pasquier L, Malthiéry Y, Reynier P, and Bonneau D

American journal of ophthalmology 136(6):1170-1, 2003 Dec - Who cited this? | PubMed ID: 14644237 | Fulltext

PGC-1-related coactivator and targets are upregulated in thyroid oncocytoma.

+ cite this

+ View Abstract

Savagner F, Mirebeau D, Jacques C, Guyetant S, Morgan C, Franc B, Reynier P, and Malthièry Y

Biochemical and biophysical research communications 310(3):779-84, 2003 Oct 24 - Who cited this? | PubMed ID: 14550271 | Fulltext

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

+ cite this

+ View Abstract

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,

(show remaining authors)

Human mutation 21(6):656, 2003 Jun - Who cited this? | PubMed ID: 14961560 | Fulltext

Transfer into a mesothelioma cell line of tumor suppressor gene p16 by cholesterol-based cationic lipids.

+ cite this

+ View Abstract

Piperno-Neumann S, Oudar O, Reynier P, Briane D, Cao A, Jaurand MC, Naejus R, Kraemer M, Breau JL, and Taillandier E

Biochimica et biophysica acta 1611(1-2):131-9, 2003 Apr 1 - Who cited this? | PubMed ID: 12659954 | Fulltext

Increased sperm mitochondrial DNA content in male infertility.

+ cite this

+ View Abstract

May-Panloup P, Chrétien MF, Savagner F, Vasseur C, Jean M, Malthièry Y, and Reynier P

Human reproduction (Oxford, England) 18(3):550-6, 2003 Mar - Who cited this? | PubMed ID: 12615823 | Fulltext

In vitro and in vivo transfection of melanoma cells B16-F10 mediated by cholesterol-based cationic liposomes.

+ cite this

+ View Abstract

Reynier P, Briane D, Cao A, Lievre N, Naejus R, Bissieres P, Salzmann JL, and Taillandier E

Journal of drug targeting 10(7):557-66, 2002 Nov - Who cited this? | PubMed ID: 12683723 | Fulltext

Search Google Scholar for Reynier P

Join Labmeeting

Organize and search your PDF collection
Collect papers
Search millions of papers
Keep up to date with paper alerts
Read your papers from anywhere
Recommend papers to colleagues
Manage your lab

Labmeeting is a web service for researchers. Sign up with your academic email address.

Individuals or corporations not affiliated with an academic institution can request a trial subscription.

Got a question?
The Labmeeting Network
has the answer.
Ask scientists at top universities like Harvard, Stanford, and MIT for their expert opinion!