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Rob Willemsen

Showing results (131-140 of 157) with videos related to

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Human Molecular Genetics|March 5, 2002
Knockout mouse model for Fxr2: a model for mental retardationCarola J M Bontekoe, Kellie L McIlwain, Ingeborg M Nieuwenhuizen, et al.
Annals of Neurology|November 5, 2003
Variable phenotypic expression and extensive tau pathology in two families with the novel tau mutation L315REsther van Herpen, Sonia M Rosso, Lies-Anne Serverijnen, et al.
The Journal of Clinical Investigation|April 8, 2009
Cd1d-dependent regulation of bacterial colonization in the intestine of miceEdward E S Nieuwenhuis, Tetsuya Matsumoto, Dicky Lindenbergh, et al.
Acta Neuropathologica|July 26, 2011
Widespread non-central nervous system organ pathology in fragile X premutation carriers with fragile X-associated tremor/ataxia syndrome and CGG knock-in miceMichael R Hunsaker, Claudia M Greco, Marian A Spath, et al.
Human Molecular Genetics|October 30, 2009
Fibroblast phenotype in male carriers of FMR1 premutation allelesDolores Garcia-Arocena, Jane E Yang, Judith R Brouwer, et al.
Human Molecular Genetics|June 11, 2015
Reversibility of neuropathology and motor deficits in an inducible mouse model for FXTASRenate K Hukema, Ronald A M Buijsen, Martijn Schonewille, et al.
Stem Cell Reports|November 1, 2014
Epigenetic characterization of the FMR1 promoter in induced pluripotent stem cells from human fibroblasts carrying an unmethylated full mutationCeline E F de Esch, Mehrnaz Ghazvini, Friedemann Loos, et al.
Communications Biology|June 4, 2021
Loss of Gap Junction Delta-2 (GJD2) gene orthologs leads to refractive error in zebrafishWim H Quint, Kirke C D Tadema, Erik de Vrieze, et al.
American Journal of Human Genetics|February 21, 2012
Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver diseaseMarialuisa Quadri, Antonio Federico, Tianna Zhao, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Biochemical methods to assess CFTR expression and membrane localizationCarlos M Farinha, Deborah Penque, Mónica Roxo-Rosa, et al.
Pageof 16

Showing results (131-140 of 157) with videos related to

Sort By:
Pageof 16
Human Molecular Genetics|March 5, 2002
Knockout mouse model for Fxr2: a model for mental retardationCarola J M Bontekoe, Kellie L McIlwain, Ingeborg M Nieuwenhuizen, et al.
Annals of Neurology|November 5, 2003
Variable phenotypic expression and extensive tau pathology in two families with the novel tau mutation L315REsther van Herpen, Sonia M Rosso, Lies-Anne Serverijnen, et al.
The Journal of Clinical Investigation|April 8, 2009
Cd1d-dependent regulation of bacterial colonization in the intestine of miceEdward E S Nieuwenhuis, Tetsuya Matsumoto, Dicky Lindenbergh, et al.
Acta Neuropathologica|July 26, 2011
Widespread non-central nervous system organ pathology in fragile X premutation carriers with fragile X-associated tremor/ataxia syndrome and CGG knock-in miceMichael R Hunsaker, Claudia M Greco, Marian A Spath, et al.
Human Molecular Genetics|October 30, 2009
Fibroblast phenotype in male carriers of FMR1 premutation allelesDolores Garcia-Arocena, Jane E Yang, Judith R Brouwer, et al.
Human Molecular Genetics|June 11, 2015
Reversibility of neuropathology and motor deficits in an inducible mouse model for FXTASRenate K Hukema, Ronald A M Buijsen, Martijn Schonewille, et al.
Stem Cell Reports|November 1, 2014
Epigenetic characterization of the FMR1 promoter in induced pluripotent stem cells from human fibroblasts carrying an unmethylated full mutationCeline E F de Esch, Mehrnaz Ghazvini, Friedemann Loos, et al.
Communications Biology|June 4, 2021
Loss of Gap Junction Delta-2 (GJD2) gene orthologs leads to refractive error in zebrafishWim H Quint, Kirke C D Tadema, Erik de Vrieze, et al.
American Journal of Human Genetics|February 21, 2012
Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver diseaseMarialuisa Quadri, Antonio Federico, Tianna Zhao, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Biochemical methods to assess CFTR expression and membrane localizationCarlos M Farinha, Deborah Penque, Mónica Roxo-Rosa, et al.
Pageof 16