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Jean Muller

Showing results (11-20 of 103) with videos related to

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Bioinformatics (Oxford, England)|April 19, 2018
AnnotSV: an integrated tool for structural variations annotationVéronique Geoffroy, Yvan Herenger, Arnaud Kress, et al.
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|August 20, 2011
Orthology prediction methods: a quality assessment using curated protein familiesKalliopi Trachana, Tomas A Larsson, Sean Powell, et al.
Nucleic Acids Research|October 19, 2007
eggNOG: automated construction and annotation of orthologous groups of genesLars Juhl Jensen, Philippe Julien, Michael Kuhn, et al.
Medecine Sciences : M/S|November 15, 2006
[Bardet-Biedl syndrome: a unique family for a major gene (BBS10)]Hélène Dollfus, Jean Muller, Corinne Stoetzel, et al.
Stem Cell Research|April 26, 2026
Generation of an induced pluripotent stem cell line from an Alström syndrome patient with biallelic ALMS1 pathogenic variantsSamira Secula, Nejla Erkilic, Cathy Obringer, et al.
Obesity (Silver Spring, Md.)|September 2, 2025
Real-World Efficacy and Safety of Setmelanotide in Adults With Monogenic or Syndromic Obesity: A Prospective Cohort StudyFrancois Mifsud, Sarah Chalopin, Emilie Guillon, et al.
NAR Genomics and Bioinformatics|November 21, 2025
Genome region aware CADD thresholds for noncoding variant prioritizationJude-Félix Tenywa, Jean-Baptiste Lamouche, Sarah Baer, et al.
Genes|April 5, 2020
Homozygous Splice Site Mutation in <i>ZP1</i> Causes Familial Oocyte Maturation DefectÖzlem Okutman, Cem Demirel, Firat Tülek, et al.
BMC Genomics|August 31, 2007
Design and evaluation of Actichip, a thematic microarray for the study of the actin cytoskeletonJean Muller, André Mehlen, Guillaume Vetter, et al.
Peerj|March 18, 2015
VaRank: a simple and powerful tool for ranking genetic variantsVéronique Geoffroy, Cécile Pizot, Claire Redin, et al.
Pageof 11

Showing results (11-20 of 103) with videos related to

Sort By:
Pageof 11
Bioinformatics (Oxford, England)|April 19, 2018
AnnotSV: an integrated tool for structural variations annotationVéronique Geoffroy, Yvan Herenger, Arnaud Kress, et al.
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|August 20, 2011
Orthology prediction methods: a quality assessment using curated protein familiesKalliopi Trachana, Tomas A Larsson, Sean Powell, et al.
Nucleic Acids Research|October 19, 2007
eggNOG: automated construction and annotation of orthologous groups of genesLars Juhl Jensen, Philippe Julien, Michael Kuhn, et al.
Medecine Sciences : M/S|November 15, 2006
[Bardet-Biedl syndrome: a unique family for a major gene (BBS10)]Hélène Dollfus, Jean Muller, Corinne Stoetzel, et al.
Stem Cell Research|April 26, 2026
Generation of an induced pluripotent stem cell line from an Alström syndrome patient with biallelic ALMS1 pathogenic variantsSamira Secula, Nejla Erkilic, Cathy Obringer, et al.
Obesity (Silver Spring, Md.)|September 2, 2025
Real-World Efficacy and Safety of Setmelanotide in Adults With Monogenic or Syndromic Obesity: A Prospective Cohort StudyFrancois Mifsud, Sarah Chalopin, Emilie Guillon, et al.
NAR Genomics and Bioinformatics|November 21, 2025
Genome region aware CADD thresholds for noncoding variant prioritizationJude-Félix Tenywa, Jean-Baptiste Lamouche, Sarah Baer, et al.
Genes|April 5, 2020
Homozygous Splice Site Mutation in <i>ZP1</i> Causes Familial Oocyte Maturation DefectÖzlem Okutman, Cem Demirel, Firat Tülek, et al.
BMC Genomics|August 31, 2007
Design and evaluation of Actichip, a thematic microarray for the study of the actin cytoskeletonJean Muller, André Mehlen, Guillaume Vetter, et al.
Peerj|March 18, 2015
VaRank: a simple and powerful tool for ranking genetic variantsVéronique Geoffroy, Cécile Pizot, Claire Redin, et al.
Pageof 11