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Susan Marschall

Showing results (21-30 of 52) with videos related to

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Reproduction (Cambridge, England)|April 29, 2025
Towards a kingdom of reproductive life - the core sperm proteomeTaylor Pini, Brett Nixon, Timothy L Karr, et al.
Brain Communications|November 12, 2025
New treatment for pyridoxine-dependent epilepsy due to ALDH7A1 deficiency: first proof-of-principle of upstream enzyme inhibition in the mouseClara D M van Karnebeek, Valérie Gailus-Durner, Udo F Engelke, et al.
Science Advances|May 27, 2021
Disruption of paternal circadian rhythm affects metabolic health in male offspring via nongerm cell factorsMaximilian Lassi, Archana Tomar, Gemma Comas-Armangué, et al.
Immunity|December 17, 2017
Roquin Suppresses the PI3K-mTOR Signaling Pathway to Inhibit T Helper Cell Differentiation and Conversion of Treg to Tfr CellsKatharina Essig, Desheng Hu, Joao C Guimaraes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 9, 2022
Biallelic loss-of-function variants in RABGAP1 cause a novel neurodevelopmental syndromeRachel Youjin Oh, Ashish R Deshwar, Ashish Marwaha, et al.
Disease Models & Mechanisms|December 29, 2021
Post-synaptic scaffold protein TANC2 in psychiatric and somatic disease riskLillian Garrett, Patricia Da Silva-Buttkus, Birgit Rathkolb, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 9, 2023
Knockout mouse models as a resource for the study of rare diseasesPatricia da Silva-Buttkus, Nadine Spielmann, Tanja Klein-Rodewald, et al.
Nucleic Acids Research|September 29, 2009
EMMA--mouse mutant resources for the international scientific communityPhil Wilkinson, Jitka Sengerova, Raffaele Matteoni, et al.
Arthritis and Rheumatism|February 10, 2011
A novel N-ethyl-N-nitrosourea-induced mutation in phospholipase Cγ2 causes inflammatory arthritis, metabolic defects, and male infertility in vitro in a murine modelKoichiro Abe, Helmut Fuchs, Auke Boersma, et al.
Science Advances|April 11, 2025
Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenitaAdrián Sanz-Moreno, Lore Becker, Kan Xie, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

Sort By:
Pageof 6
Reproduction (Cambridge, England)|April 29, 2025
Towards a kingdom of reproductive life - the core sperm proteomeTaylor Pini, Brett Nixon, Timothy L Karr, et al.
Brain Communications|November 12, 2025
New treatment for pyridoxine-dependent epilepsy due to ALDH7A1 deficiency: first proof-of-principle of upstream enzyme inhibition in the mouseClara D M van Karnebeek, Valérie Gailus-Durner, Udo F Engelke, et al.
Science Advances|May 27, 2021
Disruption of paternal circadian rhythm affects metabolic health in male offspring via nongerm cell factorsMaximilian Lassi, Archana Tomar, Gemma Comas-Armangué, et al.
Immunity|December 17, 2017
Roquin Suppresses the PI3K-mTOR Signaling Pathway to Inhibit T Helper Cell Differentiation and Conversion of Treg to Tfr CellsKatharina Essig, Desheng Hu, Joao C Guimaraes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 9, 2022
Biallelic loss-of-function variants in RABGAP1 cause a novel neurodevelopmental syndromeRachel Youjin Oh, Ashish R Deshwar, Ashish Marwaha, et al.
Disease Models & Mechanisms|December 29, 2021
Post-synaptic scaffold protein TANC2 in psychiatric and somatic disease riskLillian Garrett, Patricia Da Silva-Buttkus, Birgit Rathkolb, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 9, 2023
Knockout mouse models as a resource for the study of rare diseasesPatricia da Silva-Buttkus, Nadine Spielmann, Tanja Klein-Rodewald, et al.
Nucleic Acids Research|September 29, 2009
EMMA--mouse mutant resources for the international scientific communityPhil Wilkinson, Jitka Sengerova, Raffaele Matteoni, et al.
Arthritis and Rheumatism|February 10, 2011
A novel N-ethyl-N-nitrosourea-induced mutation in phospholipase Cγ2 causes inflammatory arthritis, metabolic defects, and male infertility in vitro in a murine modelKoichiro Abe, Helmut Fuchs, Auke Boersma, et al.
Science Advances|April 11, 2025
Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenitaAdrián Sanz-Moreno, Lore Becker, Kan Xie, et al.
Pageof 6