Publications by authors named "Paulette Mezin"

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Biallelic mutation of UNC50, encoding a protein involved in AChR trafficking, is responsible for arthrogryposis.
Emanuela Abiusi, Manuela D'Alessandro, Klaus Dieterich, Loic Quevarec, Sandrina Turczynski, Paulette Mezin

Hum Mol Genet· October 2017

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Anti-Jo-1 antibody-positive patients show a characteristic necrotizing perifascicular myositis.
Lénaig Mescam-Mancini, Yves Allenbach, Baptiste Hervier, Hervé Devilliers, Kuberaka Mariampillay, Paulette Mezin

Brain· September 2015

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Benefits of home-based endurance training in lung transplant recipients.
Isabelle Vivodtzev, Christophe Pison, Karen Guerrero, Paulette Mezin, Elisabeth Maclet

Respir Physiol Neurobiol· July 2011

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Effects of chronic treatment with a low dose of nicorandil on the function of the rat aorta during ageing.
Stéphanie Raveaud, Paulette Mezin, Nicole Lavanchy, Barry Starcher, Robert P Mecham

Clin Exp Pharmacol Physiol· October 2009

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Infection kinetics of human adenovirus serotype 41 in HEK 293 cells.
Joselma Siqueira-Silva, Fernanda Perez Yeda, Anne-Laure Favier, Paulette Mezin, Misael Leonardo Silva

Mem Inst Oswaldo Cruz· August 2009

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Absence of beta-tropomyosin is a new cause of Escobar syndrome associated with nemaline myopathy.
Nicole Monnier, Joel Lunardi, Isabelle Marty, Paulette Mezin, Annick Labarre-Vila

Neuromuscul Disord· February 2009

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Virosome-mediated delivery of tumor antigen to plasmacytoid dendritic cells.
Juliette Angel, Laurence Chaperot, Jean-Paul Molens, Paulette Mezin, Mario Amacker

Vaccine· May 2007

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Correlations between genotype and pharmacological, histological, functional, and clinical phenotypes in malignant hyperthermia susceptibility.
Nicole Monnier, Geneviève Kozak-Ribbens, Renée Krivosic-Horber, Yves Nivoche, Dong Qi, Paulette Mezin

Hum Mutat· November 2005

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Functional coupling of adenine nucleotide translocase and mitochondrial creatine kinase is enhanced after exercise training in lung transplant skeletal muscle.
Karen Guerrero, Bernard Wuyam, Paulette Mezin, Isabelle Vivodtzev, Marko Vendelin

Am J Physiol Regul Integr Comp Physiol· October 2005

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A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegia.
Nicole Monnier, Ana Ferreiro, Isabelle Marty, Annick Labarre-Vila, Paulette Mezin

Hum Mol Genet· May 2003

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