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Jean Muller

Showing results (21-30 of 103) with videos related to

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Nucleic Acids Research|May 22, 2023
The AnnotSV webserver in 2023: updated visualization and rankingVéronique Geoffroy, Jean-Baptiste Lamouche, Thomas Guignard, et al.
Clinical Genetics|February 18, 2022
In Vitro Fertilization assisted by IntraCytoplasmic Sperm Injection in a male patient with Bardet-Biedl syndromeCécile Grèze, Jean Muller, Larissa Schindler, et al.
Nucleic Acids Research|December 31, 2005
ICDS database: interrupted CoDing sequences in prokaryotic genomesEmmanuel Perrodou, Caroline Deshayes, Jean Muller, et al.
Journal of Neurology|May 28, 2016
Expanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxiaMathilde Renaud, Claire Guissart, Martial Mallaret, et al.
Frontiers in Genetics|February 15, 2019
Identification and Characterization of Known Biallelic Mutations in the <i>IFT27</i> (<i>BBS19</i>) Gene in a Novel Family With Bardet-Biedl SyndromeElise Schaefer, Clarisse Delvallée, Laura Mary, et al.
ACS Applied Materials & Interfaces|November 19, 2022
Spray-Deposited Anisotropic Assemblies of Plasmonic Nanowires for Direction-Sensitive Strain MeasurementJean Muller, Charchit Kumar, Anik Kumar Ghosh, et al.
The Journal of Clinical Endocrinology and Metabolism|August 25, 2020
Reproduction Function in Male Patients With Bardet Biedl SyndromeIsabelle Koscinski, Manuel Mark, Nadia Messaddeq, et al.
Clinical Genetics|June 21, 2025
PIK3C2A-Related Clinical Phenotype and Cellular Charaterization Linked to Functional SHH Primary Cilia DefectAdella Karam, Clarisse Delvallée, Bénédicte Gérard, et al.
Frontiers in Genetics|September 25, 2020
Atypical Retinal Phenotype in a Patient With Alström Syndrome and Biallelic Novel Pathogenic Variants in <i>ALMS1</i>, Including a <i>de novo</i> VariationLaura Mauring, Louise Frances Porter, Valerie Pelletier, et al.
Nucleic Acids Research|May 23, 2021
AnnotSV and knotAnnotSV: a web server for human structural variations annotations, ranking and analysisVéronique Geoffroy, Thomas Guignard, Arnaud Kress, et al.
Pageof 11

Showing results (21-30 of 103) with videos related to

Sort By:
Pageof 11
Nucleic Acids Research|May 22, 2023
The AnnotSV webserver in 2023: updated visualization and rankingVéronique Geoffroy, Jean-Baptiste Lamouche, Thomas Guignard, et al.
Clinical Genetics|February 18, 2022
In Vitro Fertilization assisted by IntraCytoplasmic Sperm Injection in a male patient with Bardet-Biedl syndromeCécile Grèze, Jean Muller, Larissa Schindler, et al.
Nucleic Acids Research|December 31, 2005
ICDS database: interrupted CoDing sequences in prokaryotic genomesEmmanuel Perrodou, Caroline Deshayes, Jean Muller, et al.
Journal of Neurology|May 28, 2016
Expanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxiaMathilde Renaud, Claire Guissart, Martial Mallaret, et al.
Frontiers in Genetics|February 15, 2019
Identification and Characterization of Known Biallelic Mutations in the <i>IFT27</i> (<i>BBS19</i>) Gene in a Novel Family With Bardet-Biedl SyndromeElise Schaefer, Clarisse Delvallée, Laura Mary, et al.
ACS Applied Materials & Interfaces|November 19, 2022
Spray-Deposited Anisotropic Assemblies of Plasmonic Nanowires for Direction-Sensitive Strain MeasurementJean Muller, Charchit Kumar, Anik Kumar Ghosh, et al.
The Journal of Clinical Endocrinology and Metabolism|August 25, 2020
Reproduction Function in Male Patients With Bardet Biedl SyndromeIsabelle Koscinski, Manuel Mark, Nadia Messaddeq, et al.
Clinical Genetics|June 21, 2025
PIK3C2A-Related Clinical Phenotype and Cellular Charaterization Linked to Functional SHH Primary Cilia DefectAdella Karam, Clarisse Delvallée, Bénédicte Gérard, et al.
Frontiers in Genetics|September 25, 2020
Atypical Retinal Phenotype in a Patient With Alström Syndrome and Biallelic Novel Pathogenic Variants in <i>ALMS1</i>, Including a <i>de novo</i> VariationLaura Mauring, Louise Frances Porter, Valerie Pelletier, et al.
Nucleic Acids Research|May 23, 2021
AnnotSV and knotAnnotSV: a web server for human structural variations annotations, ranking and analysisVéronique Geoffroy, Thomas Guignard, Arnaud Kress, et al.
Pageof 11