Go to contentGo to menuGo to searchGo to the news list

MitoVasc : physiopathologie cardiovasculaire et mitochondriale


Main navigation

    Search

    Breadcrumb

    Equipe 1- Mitolab - 2016

    Equipe 1- Mitolab - 2016

    • Share this page on social networks
    • E-mail this page

      Send by mail


      Separated by coma
    • Print this page
    • 1.     Adjeroud N, Besnard J, El Massioui N, Verny C, Prudean A, Scherer C, Gohier B, Bonneau D, and Allain P. Theory of mind and empathy in preclinical and clinical Huntington's disease. Soc Cogn Affect Neurosci 11: 89-99, 2016.
    • 2.     Bereau M, Anheim M, Echaniz-Laguna A, Magot A, Verny C, Goideau-Sevrain M, Barth M, Amati-Bonneau P, Allouche S, Ayrignac X, Bedat-Millet AL, Guyant-Marechal L, Kuntzer T, Ochsner F, Petiot P, Vial C, Omer S, Sole G, Taieb G, Carvalho N, Tio G, Kremer S, Acquaviva-Bourdain C, de Camaret BM, and Tranchant C. The wide POLG-related spectrum: An integrated view. J Neurol Sci 368: 70-76, 2016.
    • 3.     Bonnot O, Bonneau D, Doudard A, and Duverger P. Rationale and protocol for using a smartphone application to study autism spectrum disorders: SMARTAUTISM. BMJ Open 6: e012135, 2016.
    • 4.     Buret L, Rebillard G, Brun E, Angebault C, Pequignot M, Lenoir M, Do-Cruzeiro M, Tournier E, Cornille K, Saleur A, Gueguen N, Reynier P, Amati-Bonneau P, Barakat A, Blanchet C, Chinnery P, Yu-Wai-Man P, Kaplan J, Roux AF, Van Camp G, Wissinger B, Boespflug-Tanguy O, Giraudet F, Puel JL, Lenaers G, Hamel C, Delprat B, and Delettre C. Loss of function of Ywhah in mice induces deafness and cochlear outer hair cells' degeneration. Cell Death Discov 2: 16017, 2016.
    • 5.     Carrouget J, Ammi M, Nedelcu C, Cassereau J, Lebdai S, Azzouzi AR, and Bigot P. Posterior Spinal Cord Syndrome after Flexible Ureteroscopy for Kidney Stones. Urol Int 96: 116-118, 2016.
    • 6.     Cellier L, Tamareille S, Kalakech H, Guillou S, Lenaers G, Prunier F, and Mirebeau-Prunier D. Remote Ischemic Conditioning Influences Mitochondrial Dynamics. Shock 45: 192-197, 2016.
    • 7.     Chao de la Barca JM, Bakhta O, Kalakech H, Simard G, Tamareille S, Catros V, Callebert J, Gadras C, Tessier L, Reynier P, Prunier F, and Mirebeau-Prunier D. Metabolic Signature of Remote Ischemic Preconditioning Involving a Cocktail of Amino Acids and Biogenic Amines. J Am Heart Assoc 5, 2016.
    • 8.     Chao de la Barca JM, Prunier-Mirebeau D, Amati-Bonneau P, Ferre M, Sarzi E, Bris C, Leruez S, Chevrollier A, Desquiret-Dumas V, Gueguen N, Verny C, Hamel C, Milea D, Procaccio V, Bonneau D, Lenaers G, and Reynier P. OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiology. Neurobiol Dis 90: 20-26, 2016.
    • 9.     Chao de la Barca JM, Simard G, Amati-Bonneau P, Safiedeen Z, Prunier-Mirebeau D, Chupin S, Gadras C, Tessier L, Gueguen N, Chevrollier A, Desquiret-Dumas V, Ferre M, Bris C, Kouassi Nzoughet J, Bocca C, Leruez S, Verny C, Milea D, Bonneau D, Lenaers G, Martinez MC, Procaccio V, and Reynier P. The metabolomic signature of Leber's hereditary optic neuropathy reveals endoplasmic reticulum stress. Brain 139: 2864-2876, 2016.
    • 10.     Codron P, Chevrollier A, Kane MS, Echaniz-Laguna A, Latour P, Reynier P, Bonneau D, Verny C, Procaccio V, Lenaers G, and Cassereau J. Increased mitochondrial fusion in a autosomal recessive CMT2A family with mitochondrial GTPase mitofusin 2 mutations. J Peripher Nerv Syst 21: 365-369, 2016.
    • 11.     Colin E, Barth M, Boussion F, Latour P, Piguet-Lacroix G, Guichet A, Ziegler A, Triau S, Loisel D, Sentilhes L, and Bonneau D. In Utero Diagnosis of Niemann-Pick Type C in the Absence of Family History. JIMD Rep 28: 105-110, 2016.
    • 12.     Colin E, Daniel J, Ziegler A, Wakim J, Scrivo A, Haack TB, Khiati S, Denomme AS, Amati-Bonneau P, Charif M, Procaccio V, Reynier P, Aleck KA, Botto LD, Herper CL, Kaiser CS, Nabbout R, N'Guyen S, Mora-Lorca JA, Assmann B, Christ S, Meitinger T, Strom TM, Prokisch H, Consortium F, Miranda-Vizuete A, Hoffmann GF, Lenaers G, Bomont P, Liebau E, and Bonneau D. Biallelic Variants in UBA5 Reveal that Disruption of the UFM1 Cascade Can Result in Early-Onset Encephalopathy. Am J Hum Genet 99: 695-703, 2016.
    • 13.     de Diego-Balaguer R, Schramm C, Rebeix I, Dupoux E, Durr A, Brice A, Charles P, Cleret de Langavant L, Youssov K, Verny C, Damotte V, Azulay JP, Goizet C, Simonin C, Tranchant C, Maison P, Rialland A, Schmitz D, Jacquemot C, Fontaine B, Bachoud-Levi AC, and French Speaking Huntington G. COMT Val158Met Polymorphism Modulates Huntington's Disease Progression. PLoS One 11: e0161106, 2016.
    • 14.     Desamericq G, Youssov K, Charles P, Saleh N, Olivier A, Sherer-Gagou C, Verny C, multidisciplinary working g, and Bachoud-Levi AC. Guidelines for clinical pharmacological practices in Huntington's disease. Rev Neurol (Paris) 172: 423-432, 2016.
    • 15.     El Haj M, Caillaud M, Verny C, Fasotti L, and Allain P. Destination and source memory in Huntington's disease. J Neuropsychol 10: 77-89, 2016.
    • 16.     Fradin M, Colin E, Hannouche-Bared D, Audo I, Sahel JA, Biskup S, Carre W, Ziegler A, Wilhelm C, Guichet A, Odent S, and Bonneau D. Run of homozygosity analysis reveals a novel nonsense variant of the CNGB1 gene involved in retinitis pigmentosa 45. Ophthalmic Genet 37: 357-359, 2016.
    • 17.     Girard JM, Drevin G, Brasme JF, Pissard S, Reynier P, Simard G, and Denis MC. Clinical and biological specificity of beta-thalassemia intermedia: a case report. Ann Biol Clin (Paris) 74: 688-692, 2016.
    • 18.     Grenier J, Meunier I, Daien V, Baudoin C, Halloy F, Bocquet B, Blanchet C, Delettre C, Esmenjaud E, Roubertie A, Lenaers G, and Hamel CP. WFS1 in Optic Neuropathies: Mutation Findings in Nonsyndromic Optic Atrophy and Assessment of Clinical Severity. Ophthalmology 123: 1989-1998, 2016.
    • 19.     Isidor B, Kury S, Rosenfeld JA, Besnard T, Schmitt S, Joss S, Davies SJ, Lebel RR, Henderson A, Schaaf CP, Streff HE, Yang Y, Jain V, Chida N, Latypova X, Le Caignec C, Cogne B, Mercier S, Vincent M, Colin E, Bonneau D, Denomme AS, Parent P, Gilbert-Dussardier B, Odent S, Toutain A, Piton A, Dina C, Donnart A, Lindenbaum P, Charpentier E, Redon R, Iemura K, Ikeda M, Tanaka K, and Bezieau S. De Novo Truncating Mutations in the Kinetochore-Microtubules Attachment Gene CHAMP1 Cause Syndromic Intellectual Disability. Hum Mutat 37: 354-358, 2016.
    • 20.     Jean-Charles A, Merle H, Audo I, Desoudin C, Bocquet B, Baudoin C, Sidibe M, Mauget-Faysse M, Wolff B, Fichard A, Lenaers G, Sahel JA, Gaudric A, Cohen SY, Hamel CP, and Meunier I. Martinique Crinkled Retinal Pigment Epitheliopathy: Clinical Stages and Pathophysiologic Insights. Ophthalmology 123: 2196-2204, 2016.
    • 21.     Kauffenstein G, Tamareille S, Prunier F, Roy C, Ayer A, Toutain B, Billaud M, Isakson BE, Grimaud L, Loufrani L, Rousseau P, Abraham P, Procaccio V, Monyer H, de Wit C, Boeynaems JM, Robaye B, Kwak BR, and Henrion D. Central Role of P2Y6 UDP Receptor in Arteriolar Myogenic Tone. Arterioscler Thromb Vasc Biol 36: 1598-1606, 2016.
    • 22.     Le Page S, Niro M, Fauconnier J, Cellier L, Tamareille S, Gharib A, Chevrollier A, Loufrani L, Grenier C, Kamel R, Sarzi E, Lacampagne A, Ovize M, Henrion D, Reynier P, Lenaers G, Mirebeau-Prunier D, and Prunier F. Increase in Cardiac Ischemia-Reperfusion Injuries in Opa1+/- Mouse Model. PLoS One 11: e0164066, 2016.
    • 23.     May-Panloup P, Boucret L, Chao de la Barca JM, Desquiret-Dumas V, Ferre-L'Hotellier V, Moriniere C, Descamps P, Procaccio V, and Reynier P. Ovarian ageing: the role of mitochondria in oocytes and follicles. Hum Reprod Update 22: 725-743, 2016.
    • 24.     Meunier I, Lenaers G, Bocquet B, Baudoin C, Piro-Megy C, Cubizolle A, Quiles M, Jean-Charles A, Cohen SY, Merle H, Gaudric A, Labesse G, Manes G, Pequignot M, Cazevieille C, Dhaenens CM, Fichard A, Ronkina N, Arthur SJ, Gaestel M, and Hamel CP. A dominant mutation in MAPKAPK3, an actor of p38 signaling pathway, causes a new retinal dystrophy involving Bruch's membrane and retinal pigment epithelium. Hum Mol Genet 25: 916-926, 2016.
    • 25.     Millet AM, Bertholet AM, Daloyau M, Reynier P, Galinier A, Devin A, Wissinguer B, Belenguer P, and Davezac N. Loss of functional OPA1 unbalances redox state: implications in dominant optic atrophy pathogenesis. Ann Clin Transl Neurol 3: 408-421, 2016.
    • 26.     Morimoto M, Myung C, Beirnes K, Choi K, Asakura Y, Bokenkamp A, Bonneau D, Brugnara M, Charrow J, Colin E, Davis A, Deschenes G, Gentile M, Giordano M, Gormley AK, Govender R, Joseph M, Keller K, Lerut E, Levtchenko E, Massella L, Mayfield C, Najafian B, Parham D, Spranger J, Stenzel P, Yis U, Yu Z, Zonana J, Hendson G, and Boerkoel CF. Increased Wnt and Notch signaling: a clue to the renal disease in Schimke immuno-osseous dysplasia? Orphanet J Rare Dis 11: 149, 2016.
    • 27.     Petit M, Guihot AL, Grimaud L, Vessieres E, Toutain B, Menet MC, Nivet-Antoine V, Arnal JF, Loufrani L, Procaccio V, and Henrion D. Resveratrol Improved Flow-Mediated Outward Arterial Remodeling in Ovariectomized Rats with Hypertrophic Effect at High Dose. PLoS One 11: e0146148, 2016.
    • 28.     Potluri P, Procaccio V, Scheffler IE, and Wallace DC. High throughput gene complementation screening permits identification of a mammalian mitochondrial protein synthesis (rho(-)) mutant. Biochim Biophys Acta 1857: 1336-1343, 2016.
    • 29.     Salem L, Saleh N, Desamericq G, Youssov K, Dolbeau G, Cleret L, Bourhis ML, Azulay JP, Krystkowiak P, Verny C, Morin F, Moutereau S, French Huntington Study G, Bachoud-Levi AC, and Maison P. Insulin-Like Growth Factor-1 but Not Insulin Predicts Cognitive Decline in Huntington's Disease. PLoS One 11: e0162890, 2016.
    • 30.     Sarzi E, Seveno M, Angebault C, Milea D, Ronnback C, Quiles M, Adrian M, Grenier J, Caignard A, Lacroux A, Lavergne C, Reynier P, Larsen M, Hamel CP, Lenaers G, and Muller A. Increased steroidogenesis promotes early-onset and severe vision loss in females with OPA1 dominant optic atrophy. Hum Mol Genet 25: 2539-2551, 2016.
    • 31.     Signolet I, Chenouard R, Oca F, Barth M, Reynier P, Denis MC, and Simard G. Recurrent Isolated Neonatal Hemolytic Anemia: Think About Glutathione Synthetase Deficiency. Pediatrics 138, 2016.
    • 32.     Tarhouni K, Guihot AL, Vessieres E, Procaccio V, Grimaud L, Abraham P, Lenfant F, Arnal JF, Favre J, Loufrani L, and Henrion D. Estrogens are needed for the improvement in endothelium-mediated dilation induced by a chronic increase in blood flow in rat mesenteric arteries. Vascul Pharmacol 80: 35-42, 2016.