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Alain Calender

Showing results (11-20 of 71) with videos related to

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Blood Cells, Molecules & Diseases|September 25, 2010
Nonsense-mediated mRNA decay (NMD) blockage promotes nonsense mRNA stabilization in protein 4.1R deficient cells carrying the 4.1R Coimbra variant of hereditary elliptocytosisMadeleine Morinière, François Delhommeau, Alain Calender, et al.
Rheumatology (Oxford, England)|July 21, 2023
Whole exome sequencing of a German sarcoidosis family with four affected and one spontaneous remission casePeter Kvacskay, Thomas El Jammal, Hanns-Martin Lorenz, et al.
Genes|November 27, 2021
Identification and Characterization of New <i>Alu</i> Element Insertion in the <i>BRCA1</i> Exon 14 Associated with Hereditary Breast and Ovarian CancerAhmed Bouras, Melanie Leone, Valerie Bonadona, et al.
Psychiatric Genetics|February 28, 2003
Clinical, cytogenetic, and molecular description of a FRAXE French familyGaëtan Lesca, Valérie Biancalana, Marie-Jo Brunel, et al.
Trends in Immunology|March 4, 2020
Sarcoidosis and the mTOR, Rac1, and Autophagy TriadYves Pacheco, Clarice X Lim, Thomas Weichhart, et al.
European Journal of Medical Genetics|March 27, 2007
Mutation screening of the MECP2 gene in a large cohort of 613 fragile-X negative patients with mental retardationGaëtan Lesca, Virginie Bernard, Muriel Bozon, et al.
Electrophoresis|March 26, 2003
Efficient mutation detection in MEN1 gene using a combination of single-strand conformation polymorphism (MDGA) and heteroduplex analysisMichel Crépin, Fabienne Escande, Pascal Pigny, et al.
Gastroenterologie Clinique Et Biologique|January 20, 2005
Prevalence, characteristics and prognosis of MEN 1-associated glucagonomas, VIPomas, and somatostatinomas: study from the GTE (Groupe des Tumeurs Endocrines) registryNathalie Lévy-Bohbot, Corinne Merle, Pierre Goudet, et al.
Sarcoidosis, Vasculitis, and Diffuse Lung Diseases : Official Journal of WASOG|August 1, 2014
Lack of correlation of BTNL2 polymorphism and cancer risk in sarcoidosis. BTNL2 and cancer risk in sarcoidosisMaud Gaillot-Drevon, Alain Calender, Jean Yves Blay, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 4, 2012
BRCA2 deep intronic mutation causing activation of a cryptic exon: opening toward a new preventive therapeutic strategyOlga Anczuków, Monique Buisson, Mélanie Léoné, et al.
Pageof 8

Showing results (11-20 of 71) with videos related to

Sort By:
Pageof 8
Blood Cells, Molecules & Diseases|September 25, 2010
Nonsense-mediated mRNA decay (NMD) blockage promotes nonsense mRNA stabilization in protein 4.1R deficient cells carrying the 4.1R Coimbra variant of hereditary elliptocytosisMadeleine Morinière, François Delhommeau, Alain Calender, et al.
Rheumatology (Oxford, England)|July 21, 2023
Whole exome sequencing of a German sarcoidosis family with four affected and one spontaneous remission casePeter Kvacskay, Thomas El Jammal, Hanns-Martin Lorenz, et al.
Genes|November 27, 2021
Identification and Characterization of New <i>Alu</i> Element Insertion in the <i>BRCA1</i> Exon 14 Associated with Hereditary Breast and Ovarian CancerAhmed Bouras, Melanie Leone, Valerie Bonadona, et al.
Psychiatric Genetics|February 28, 2003
Clinical, cytogenetic, and molecular description of a FRAXE French familyGaëtan Lesca, Valérie Biancalana, Marie-Jo Brunel, et al.
Trends in Immunology|March 4, 2020
Sarcoidosis and the mTOR, Rac1, and Autophagy TriadYves Pacheco, Clarice X Lim, Thomas Weichhart, et al.
European Journal of Medical Genetics|March 27, 2007
Mutation screening of the MECP2 gene in a large cohort of 613 fragile-X negative patients with mental retardationGaëtan Lesca, Virginie Bernard, Muriel Bozon, et al.
Electrophoresis|March 26, 2003
Efficient mutation detection in MEN1 gene using a combination of single-strand conformation polymorphism (MDGA) and heteroduplex analysisMichel Crépin, Fabienne Escande, Pascal Pigny, et al.
Gastroenterologie Clinique Et Biologique|January 20, 2005
Prevalence, characteristics and prognosis of MEN 1-associated glucagonomas, VIPomas, and somatostatinomas: study from the GTE (Groupe des Tumeurs Endocrines) registryNathalie Lévy-Bohbot, Corinne Merle, Pierre Goudet, et al.
Sarcoidosis, Vasculitis, and Diffuse Lung Diseases : Official Journal of WASOG|August 1, 2014
Lack of correlation of BTNL2 polymorphism and cancer risk in sarcoidosis. BTNL2 and cancer risk in sarcoidosisMaud Gaillot-Drevon, Alain Calender, Jean Yves Blay, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 4, 2012
BRCA2 deep intronic mutation causing activation of a cryptic exon: opening toward a new preventive therapeutic strategyOlga Anczuków, Monique Buisson, Mélanie Léoné, et al.
Pageof 8