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Showing results (111-120 of 122) with videos related to

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Elife|May 1, 2018
Reduced expression of C/EBPβ-LIP extends health and lifespan in miceChristine Müller, Laura M Zidek, Tobias Ackermann, et al.
Molecular Brain|January 22, 2021
Rare functional missense variants in CACNA1H: What can we learn from Writer's cramp?Miaozhen Huang, Esther A R Nibbeling, Tjerk J Lagrand, et al.
Brain : a Journal of Neurology|July 15, 2015
Elevated mutant dynorphin A causes Purkinje cell loss and motor dysfunction in spinocerebellar ataxia type 23Cleo J L M Smeets, Justyna Jezierska, Hiroyuki Watanabe, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 17, 2020
A Gain-of-Function Variant in Dopamine D2 Receptor and Progressive Chorea and Dystonia PhenotypeMarlous C M van der Weijden, Dayana Rodriguez-Contreras, Cathérine C S Delnooz, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 25, 2005
Macrophages induce the inflammatory response in the pulmonary Arthus reaction through G alpha i2 activation that controls C5aR and Fc receptor cooperationJulia Skokowa, Syed R Ali, Olga Felda, et al.
Frontiers in Genetics|April 11, 2022
Feasibility of Follow-Up Studies and Reclassification in Spinocerebellar Ataxia Gene Variants of Unknown SignificanceFatemeh Ghorbani, Mohamed Z Alimohamed, Juliana F Vilacha, et al.
American Journal of Human Genetics|November 2, 2010
Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23Georgy Bakalkin, Hiroyuki Watanabe, Justyna Jezierska, et al.
International Journal of Obesity (2005)|August 31, 2017
IgG is elevated in obese white adipose tissue but does not induce glucose intolerance via Fcγ-receptor or complementA D van Dam, L van Beek, A C M Pronk, et al.
Journal of Neurology|July 21, 2022
Prevalence of intronic repeat expansions in RFC1 in Dutch patients with CANVAS and adult-onset ataxiaFatemeh Ghorbani, Jelkje de Boer-Bergsma, Corien C Verschuuren-Bemelmans, et al.
Annals of Neurology|January 3, 2013
Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19Anna Duarri, Justyna Jezierska, Michiel Fokkens, et al.
Pageof 13

Showing results (111-120 of 122) with videos related to

Sort By:
Pageof 13
Elife|May 1, 2018
Reduced expression of C/EBPβ-LIP extends health and lifespan in miceChristine Müller, Laura M Zidek, Tobias Ackermann, et al.
Molecular Brain|January 22, 2021
Rare functional missense variants in CACNA1H: What can we learn from Writer's cramp?Miaozhen Huang, Esther A R Nibbeling, Tjerk J Lagrand, et al.
Brain : a Journal of Neurology|July 15, 2015
Elevated mutant dynorphin A causes Purkinje cell loss and motor dysfunction in spinocerebellar ataxia type 23Cleo J L M Smeets, Justyna Jezierska, Hiroyuki Watanabe, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 17, 2020
A Gain-of-Function Variant in Dopamine D2 Receptor and Progressive Chorea and Dystonia PhenotypeMarlous C M van der Weijden, Dayana Rodriguez-Contreras, Cathérine C S Delnooz, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 25, 2005
Macrophages induce the inflammatory response in the pulmonary Arthus reaction through G alpha i2 activation that controls C5aR and Fc receptor cooperationJulia Skokowa, Syed R Ali, Olga Felda, et al.
Frontiers in Genetics|April 11, 2022
Feasibility of Follow-Up Studies and Reclassification in Spinocerebellar Ataxia Gene Variants of Unknown SignificanceFatemeh Ghorbani, Mohamed Z Alimohamed, Juliana F Vilacha, et al.
American Journal of Human Genetics|November 2, 2010
Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23Georgy Bakalkin, Hiroyuki Watanabe, Justyna Jezierska, et al.
International Journal of Obesity (2005)|August 31, 2017
IgG is elevated in obese white adipose tissue but does not induce glucose intolerance via Fcγ-receptor or complementA D van Dam, L van Beek, A C M Pronk, et al.
Journal of Neurology|July 21, 2022
Prevalence of intronic repeat expansions in RFC1 in Dutch patients with CANVAS and adult-onset ataxiaFatemeh Ghorbani, Jelkje de Boer-Bergsma, Corien C Verschuuren-Bemelmans, et al.
Annals of Neurology|January 3, 2013
Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19Anna Duarri, Justyna Jezierska, Michiel Fokkens, et al.
Pageof 13