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Alexander Gheldof

Showing results (21-30 of 29) with videos related to

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Biology Open|January 12, 2022
Myotonic dystrophy type 1 embryonic stem cells show decreased myogenic potential, increased CpG methylation at the DMPK locus and RNA mis-splicingSilvie Franck, Edouard Couvreu De Deckersberg, Jodi L Bubenik, et al.
Journal of Assisted Reproduction and Genetics|January 27, 2025
Oocyte/zygote/embryo maturation arrest: a clinical study expanding the phenotype of NOBOX variantsAnnelore Van Der Kelen, Sophie Uyttebroeck, Stefanie Van de Voorde, et al.
Journal of Medical Genetics|March 5, 2017
Bi-allelic variants in <i>COL3A1</i> encoding the ligand to GPR56 are associated with cobblestone-like cortical malformation, white matter changes and cerebellar cystsLaura Vandervore, Katrien Stouffs, Ibrahim Tanyalçin, et al.
Human Reproduction Update|December 26, 2022
A systematic review and evidence assessment of monogenic gene-disease relationships in human female infertility and differences in sex developmentAnnelore Van Der Kelen, Özlem Okutman, Elodie Javey, et al.
Cell Death and Differentiation|May 9, 2025
Development and validation of a high-throughput screening pipeline of compound libraries to target EMTSven Jonckheere, Joachim Taminau, Jamie Adams, et al.
Pediatric Neurology|July 4, 2024
Congenital Myasthenic Syndromes in Belgium: Genetic and Clinical Characterization of Pediatric and Adult PatientsNathalie Smeets, Alexander Gheldof, Bart Dequeker, et al.
American Journal of Human Genetics|January 19, 2022
Impaired catabolism of free oligosaccharides due to MAN2C1 variants causes a neurodevelopmental disorderNuno Maia, Sven Potelle, Hamide Yildirim, et al.
Endocrine Connections|October 13, 2022
The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centresLuca Persani, Martine Cools, Stamatina Ioakim, et al.
Brain : a Journal of Neurology|March 18, 2019
Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamicsLaura V Vandervore, Rachel Schot, Esmee Kasteleijn, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Biology Open|January 12, 2022
Myotonic dystrophy type 1 embryonic stem cells show decreased myogenic potential, increased CpG methylation at the DMPK locus and RNA mis-splicingSilvie Franck, Edouard Couvreu De Deckersberg, Jodi L Bubenik, et al.
Journal of Assisted Reproduction and Genetics|January 27, 2025
Oocyte/zygote/embryo maturation arrest: a clinical study expanding the phenotype of NOBOX variantsAnnelore Van Der Kelen, Sophie Uyttebroeck, Stefanie Van de Voorde, et al.
Journal of Medical Genetics|March 5, 2017
Bi-allelic variants in <i>COL3A1</i> encoding the ligand to GPR56 are associated with cobblestone-like cortical malformation, white matter changes and cerebellar cystsLaura Vandervore, Katrien Stouffs, Ibrahim Tanyalçin, et al.
Human Reproduction Update|December 26, 2022
A systematic review and evidence assessment of monogenic gene-disease relationships in human female infertility and differences in sex developmentAnnelore Van Der Kelen, Özlem Okutman, Elodie Javey, et al.
Cell Death and Differentiation|May 9, 2025
Development and validation of a high-throughput screening pipeline of compound libraries to target EMTSven Jonckheere, Joachim Taminau, Jamie Adams, et al.
Pediatric Neurology|July 4, 2024
Congenital Myasthenic Syndromes in Belgium: Genetic and Clinical Characterization of Pediatric and Adult PatientsNathalie Smeets, Alexander Gheldof, Bart Dequeker, et al.
American Journal of Human Genetics|January 19, 2022
Impaired catabolism of free oligosaccharides due to MAN2C1 variants causes a neurodevelopmental disorderNuno Maia, Sven Potelle, Hamide Yildirim, et al.
Endocrine Connections|October 13, 2022
The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centresLuca Persani, Martine Cools, Stamatina Ioakim, et al.
Brain : a Journal of Neurology|March 18, 2019
Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamicsLaura V Vandervore, Rachel Schot, Esmee Kasteleijn, et al.
Pageof 3