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Anne Gregor

Showing results (11-20 of 35) with videos related to

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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 12, 2003
A Phase I study of gemcitabine with concurrent radiotherapy in stage III, locally advanced non-small cell lung cancerJohn W G van Putten, Allen Price, Annya H D van der Leest, et al.
Scientific Reports|February 5, 2024
NDUFS7 variant in dogs with Leigh syndrome and its functional validation in a Drosophila melanogaster modelMatthias Christen, Anne Gregor, Rodrigo Gutierrez-Quintana, et al.
European Journal of Human Genetics : EJHG|October 28, 2025
Heterozygous loss of SRRM1 may be associated with neurodevelopmental phenotypes and anomalies in cell growth and neurite morphologyMelek Firat Altay, Anne Gregor, Dominique Braun, et al.
American Journal of Human Genetics|June 11, 2013
De novo mutations in the genome organizer CTCF cause intellectual disabilityAnne Gregor, Martin Oti, Evelyn N Kouwenhoven, et al.
American Journal of Medical Genetics. Part A|August 19, 2023
Novel association of Dandy-Walker malformation with CAPN15 variants expands the phenotype of oculogastrointestinal neurodevelopmental syndromeM Makenzie Beaman, Lucia Guidugli, Monia Hammer, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 7, 2021
Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritanceFranck Rapaport, Bertrand Boisson, Anne Gregor, et al.
Human Mutation|June 1, 2010
Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expressionMarkus Zweier, Anne Gregor, Christiane Zweier, et al.
American Journal of Human Genetics|August 22, 2017
Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar HypoplasiaIsaac Marin-Valencia, Andreas Gerondopoulos, Maha S Zaki, et al.
BMC Medical Genetics|August 11, 2011
Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1Anne Gregor, Beate Albrecht, Ingrid Bader, et al.
Neuron|February 5, 2019
Zika Virus Protease Cleavage of Host Protein Septin-2 Mediates Mitotic Defects in Neural ProgenitorsHongda Li, Laura Saucedo-Cuevas, Ling Yuan, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 12, 2003
A Phase I study of gemcitabine with concurrent radiotherapy in stage III, locally advanced non-small cell lung cancerJohn W G van Putten, Allen Price, Annya H D van der Leest, et al.
Scientific Reports|February 5, 2024
NDUFS7 variant in dogs with Leigh syndrome and its functional validation in a Drosophila melanogaster modelMatthias Christen, Anne Gregor, Rodrigo Gutierrez-Quintana, et al.
European Journal of Human Genetics : EJHG|October 28, 2025
Heterozygous loss of SRRM1 may be associated with neurodevelopmental phenotypes and anomalies in cell growth and neurite morphologyMelek Firat Altay, Anne Gregor, Dominique Braun, et al.
American Journal of Human Genetics|June 11, 2013
De novo mutations in the genome organizer CTCF cause intellectual disabilityAnne Gregor, Martin Oti, Evelyn N Kouwenhoven, et al.
American Journal of Medical Genetics. Part A|August 19, 2023
Novel association of Dandy-Walker malformation with CAPN15 variants expands the phenotype of oculogastrointestinal neurodevelopmental syndromeM Makenzie Beaman, Lucia Guidugli, Monia Hammer, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 7, 2021
Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritanceFranck Rapaport, Bertrand Boisson, Anne Gregor, et al.
Human Mutation|June 1, 2010
Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expressionMarkus Zweier, Anne Gregor, Christiane Zweier, et al.
American Journal of Human Genetics|August 22, 2017
Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar HypoplasiaIsaac Marin-Valencia, Andreas Gerondopoulos, Maha S Zaki, et al.
BMC Medical Genetics|August 11, 2011
Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1Anne Gregor, Beate Albrecht, Ingrid Bader, et al.
Neuron|February 5, 2019
Zika Virus Protease Cleavage of Host Protein Septin-2 Mediates Mitotic Defects in Neural ProgenitorsHongda Li, Laura Saucedo-Cuevas, Ling Yuan, et al.
Pageof 4