Ngā hua rapu - C. Labasse
- E whakaatu ana i te 1 - 4 hua o te 4
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1
Caveolae and Bin1 form ring-shaped platforms for T-tubule initiation mā Eline Lemerle, Jeanne Lainé, Marion Benoist, Gilles Moulay, Anne Bigot, C. Labasse, A. Madelaine, Alexis Canette, Perrine Aubin, Jean‐Michel Vallat, Norma B. Romero, Marc Bitoun, Vincent Mouly, Isabelle Marty, Bruno Cadot, Laura Picas, Stéphane Vassilopoulos
I whakaputaina 2023Artigo -
2
‘Dusty core disease’ (DuCD): expanding morphological spectrum of RYR1 recessive myopathies mā Matteo Garibaldi, John Rendu, Julie Brocard, Emmanuelle Lacène, Julien Fauré, Guy Brochier, Maud Beuvin, C. Labasse, A. Madelaine, Edoardo Malfatti, Jorge A. Bevilacqua, Fabiana Lubieniecki, Soledad Monges, Ana Lía Taratuto, Jocelyn Laporte, Isabelle Marty, Giovanni Antonini, Norma B. Romero
I whakaputaina 2019Artigo -
3
ACTN2 mutations cause “Multiple structured Core Disease” (MsCD) mā Xavière Lornage, Norma B. Romero, Claire A Grosgogeat, E. Malfatti, Sandra Donkervoort, Michael Mario Marchetti, Sarah Neuhaus, A. Reghan Foley, C. Labasse, Raphaël Schneider, Robert Carlier, Katherine R. Chao, Līvija Medne, Jean‐François Deleuze, David Orlikowski, Carsten G. Bönnemann, Vandana Gupta, Michel Fardeau, Johann Böhm, Jocelyn Laporte
I whakaputaina 2019Artigo -
4
QIL1 mutation causes MICOS disassembly and early onset fatal mitochondrial encephalopathy with liver disease mā Virgínia Guarani, Claude Jardel, Dominique Chrétien, Anne Lombès, Paule Bénit, C. Labasse, Emmanuelle Lacène, Agnès Bourillon, Apolline Imbard, Jean‐François Benoist, Imen Dorboz, Martine Gilleron, Eric S. Goetzman, Pauline Gaignard, Abdelhamid Slama, Monique Elmaleh, Norma B. Romero, Pierre Rustin, Hélène Ogier de Baulny, João A. Paulo, J. Wade Harper, Manuel Schiff
I whakaputaina 2016Artigo
Ngā utauta rapu:
Ngā marau whai pānga
Biology
Gene
Medicine
Pathology
Biopsy
Cell biology
Genetics
Internal medicine
Muscle biopsy
Mutation
Myopathy
Actinin
Anatomy
Biochemistry
Biogenesis
Calcium
Caveolae
Cell
Central core disease
Chemistry
Cirrhosis
Congenital myopathy
Cytoskeleton
Disease
Encephalopathy
Endocrinology
Endoplasmic reticulum
Exome sequencing
Hepatic encephalopathy
Immunohistochemistry