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Jill M Weimer

Showing results (21-30 of 84) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|July 2, 2013
Mutations in VLDLR associated with ataxia with secondary vitamin E deficiencyMichael C Kruer, Tyler N Jepperson, Jill M Weimer, et al.
Neuroscience Letters|August 10, 2005
Novel CLN3 mutation predicted to cause complete loss of protein function does not modify the classical JNCL phenotypeJennifer M Kwon, Paul G Rothberg, Adam R Leman, et al.
Genes & Development|December 15, 2007
Reinduction of ErbB2 in astrocytes promotes radial glial progenitor identity in adult cerebral cortexH T Ghashghaei, Jill M Weimer, Ralf S Schmid, et al.
Traffic (Copenhagen, Denmark)|November 11, 2021
Collagen has a unique SEC24 preference for efficient export from the endoplasmic reticulumChung-Ling Lu, Steven Ortmeier, Jon Brudvig, et al.
Neuronal Signaling|April 10, 2020
Modulation of CRMP2 via (<i>S</i>)-Lacosamide shows therapeutic promise but is ultimately ineffective in a mouse model of CLN6-Batten diseaseKatherine A White, Jacob T Cain, Helen Magee, et al.
Stem Cells Translational Medicine|February 11, 2017
Concise Review: Fat and Furious: Harnessing the Full Potential of Adipose-Derived Stromal Vascular FractionJordan A Dykstra, Tiffany Facile, Ryan J Patrick, et al.
Orphanet Journal of Rare Diseases|November 11, 2022
Sex-split analysis of pathology and motor-behavioral outcomes in a mouse model of CLN8-Batten disease reveals an increased disease burden and trajectory in female Cln8<sup>mnd</sup> miceAndrew D Holmes, Katherine A White, Melissa A Pratt, et al.
Molecular Neurobiology|March 28, 2019
Dysregulation of CRMP2 Post-Translational Modifications Drive Its Pathological FunctionsAubin Moutal, Katherine A White, Aude Chefdeville, et al.
Brain Research|February 24, 2009
Cerebellar defects in a mouse model of juvenile neuronal ceroid lipofuscinosisJill M Weimer, Jared W Benedict, Amanda L Getty, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|July 27, 2017
Genetic ataxia telangiectasia porcine model phenocopies the multisystemic features of the human diseaseRosanna Beraldi, David K Meyerholz, Alexei Savinov, et al.
Pageof 9

Showing results (21-30 of 84) with videos related to

Sort By:
Pageof 9
Movement Disorders : Official Journal of the Movement Disorder Society|July 2, 2013
Mutations in VLDLR associated with ataxia with secondary vitamin E deficiencyMichael C Kruer, Tyler N Jepperson, Jill M Weimer, et al.
Neuroscience Letters|August 10, 2005
Novel CLN3 mutation predicted to cause complete loss of protein function does not modify the classical JNCL phenotypeJennifer M Kwon, Paul G Rothberg, Adam R Leman, et al.
Genes & Development|December 15, 2007
Reinduction of ErbB2 in astrocytes promotes radial glial progenitor identity in adult cerebral cortexH T Ghashghaei, Jill M Weimer, Ralf S Schmid, et al.
Traffic (Copenhagen, Denmark)|November 11, 2021
Collagen has a unique SEC24 preference for efficient export from the endoplasmic reticulumChung-Ling Lu, Steven Ortmeier, Jon Brudvig, et al.
Neuronal Signaling|April 10, 2020
Modulation of CRMP2 via (<i>S</i>)-Lacosamide shows therapeutic promise but is ultimately ineffective in a mouse model of CLN6-Batten diseaseKatherine A White, Jacob T Cain, Helen Magee, et al.
Stem Cells Translational Medicine|February 11, 2017
Concise Review: Fat and Furious: Harnessing the Full Potential of Adipose-Derived Stromal Vascular FractionJordan A Dykstra, Tiffany Facile, Ryan J Patrick, et al.
Orphanet Journal of Rare Diseases|November 11, 2022
Sex-split analysis of pathology and motor-behavioral outcomes in a mouse model of CLN8-Batten disease reveals an increased disease burden and trajectory in female Cln8<sup>mnd</sup> miceAndrew D Holmes, Katherine A White, Melissa A Pratt, et al.
Molecular Neurobiology|March 28, 2019
Dysregulation of CRMP2 Post-Translational Modifications Drive Its Pathological FunctionsAubin Moutal, Katherine A White, Aude Chefdeville, et al.
Brain Research|February 24, 2009
Cerebellar defects in a mouse model of juvenile neuronal ceroid lipofuscinosisJill M Weimer, Jared W Benedict, Amanda L Getty, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|July 27, 2017
Genetic ataxia telangiectasia porcine model phenocopies the multisystemic features of the human diseaseRosanna Beraldi, David K Meyerholz, Alexei Savinov, et al.
Pageof 9