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Alexander Gheldof

Showing results (11-20 of 29) with videos related to

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Bioinformatics (Oxford, England)|December 1, 2022
EDIR: exome database of interspersed repeatsLaura D T Vo Ngoc, Randy Osei, Katrin Dohr, et al.
Frontiers in Neurology|October 10, 2022
Case report: Coexistence of myotonia congenita and Brugada syndrome in one familyAnn Cordenier, Anja Flamez, Thomy de Ravel, et al.
Cancer Letters|April 22, 2008
Differential impact of TGF-beta and EGF on fibroblast differentiation and invasion reciprocally promotes colon cancer cell invasionHannelore Denys, Lara Derycke, An Hendrix, et al.
Journal of Assisted Reproduction and Genetics|November 29, 2018
Rare genetic variants potentially involved in ovarian hyperstimulation syndromeKatrien Stouffs, Sari Daelemans, Samuel Santos-Ribeiro, et al.
F&S Reports|July 5, 2021
Novel inactivating follicle-stimulating hormone receptor mutations in a patient with premature ovarian insufficiency identified by next-generation sequencing gene panel analysisAsma Sassi, Julie Désir, Véronique Janssens, et al.
European Journal of Medical Genetics|June 9, 2018
Biallelic mutations in RTTN are associated with microcephaly, short stature and a wide range of brain malformationsKatrien Stouffs, Stéphanie Moortgat, Tim Vanderhasselt, et al.
Molecular Genetics & Genomic Medicine|December 15, 2018
Clinical implementation of gene panel testing for lysosomal storage diseasesAlexander Gheldof, Sara Seneca, Katrien Stouffs, et al.
BMC Cancer|June 13, 2024
Identification of RAD17 as a candidate cancer predisposition gene in families with histories of pancreatic and breast cancersSofie Joris, Philippe Giron, Catharina Olsen, et al.
Endocrinology, Diabetes & Metabolism Case Reports|October 24, 2024
MCM9 compound heterozygosity in an adolescent with premature ovarian insufficiencyElise Nauwynck, Michel De Vos, Alexander Gheldof, et al.
Human Molecular Genetics|November 26, 2020
MSH2 knock-down shows CTG repeat stability and concomitant upstream demethylation at the DMPK locus in myotonic dystrophy type 1 human embryonic stem cellsSilvie Franck, Lise Barbé, Simon Ardui, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Bioinformatics (Oxford, England)|December 1, 2022
EDIR: exome database of interspersed repeatsLaura D T Vo Ngoc, Randy Osei, Katrin Dohr, et al.
Frontiers in Neurology|October 10, 2022
Case report: Coexistence of myotonia congenita and Brugada syndrome in one familyAnn Cordenier, Anja Flamez, Thomy de Ravel, et al.
Cancer Letters|April 22, 2008
Differential impact of TGF-beta and EGF on fibroblast differentiation and invasion reciprocally promotes colon cancer cell invasionHannelore Denys, Lara Derycke, An Hendrix, et al.
Journal of Assisted Reproduction and Genetics|November 29, 2018
Rare genetic variants potentially involved in ovarian hyperstimulation syndromeKatrien Stouffs, Sari Daelemans, Samuel Santos-Ribeiro, et al.
F&S Reports|July 5, 2021
Novel inactivating follicle-stimulating hormone receptor mutations in a patient with premature ovarian insufficiency identified by next-generation sequencing gene panel analysisAsma Sassi, Julie Désir, Véronique Janssens, et al.
European Journal of Medical Genetics|June 9, 2018
Biallelic mutations in RTTN are associated with microcephaly, short stature and a wide range of brain malformationsKatrien Stouffs, Stéphanie Moortgat, Tim Vanderhasselt, et al.
Molecular Genetics & Genomic Medicine|December 15, 2018
Clinical implementation of gene panel testing for lysosomal storage diseasesAlexander Gheldof, Sara Seneca, Katrien Stouffs, et al.
BMC Cancer|June 13, 2024
Identification of RAD17 as a candidate cancer predisposition gene in families with histories of pancreatic and breast cancersSofie Joris, Philippe Giron, Catharina Olsen, et al.
Endocrinology, Diabetes & Metabolism Case Reports|October 24, 2024
MCM9 compound heterozygosity in an adolescent with premature ovarian insufficiencyElise Nauwynck, Michel De Vos, Alexander Gheldof, et al.
Human Molecular Genetics|November 26, 2020
MSH2 knock-down shows CTG repeat stability and concomitant upstream demethylation at the DMPK locus in myotonic dystrophy type 1 human embryonic stem cellsSilvie Franck, Lise Barbé, Simon Ardui, et al.
Pageof 3