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S Verbeek

Showing results (91-100 of 122) with videos related to

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Annals of Neurology|September 26, 2020
CAG Repeat Size Influences the Progression Rate of Spinocerebellar Ataxia Type 3Vanessa B Leotti, Jeroen J de Vries, Camila M Oliveira, et al.
Neurology|December 25, 2003
Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia familyB P C van de Warrenburg, D S Verbeek, S J Piersma, et al.
International Journal of Molecular Sciences|October 26, 2024
Identification and Copy Number Variant Analysis of Enhancer Regions of Genes Causing Spinocerebellar AtaxiaFatemeh Ghorbani, Eddy N de Boer, Michiel R Fokkens, et al.
Diabetologia|December 1, 1993
Chronic overproduction of islet amyloid polypeptide/amylin in transgenic mice: lysosomal localization of human islet amyloid polypeptide and lack of marked hyperglycaemia or hyperinsulinaemiaJ W Höppener, J S Verbeek, E J de Koning, et al.
Blood|June 11, 1999
Human immunoglobulin A receptor (FcalphaRI, CD89) function in transgenic mice requires both FcR gamma chain and CR3 (CD11b/CD18)M van Egmond, A J van Vuuren, H C Morton, et al.
The Journal of Experimental Medicine|April 19, 2000
Markedly different pathogenicity of four immunoglobulin G isotype-switch variants of an antierythrocyte autoantibody is based on their capacity to interact in vivo with the low-affinity Fcgamma receptor IIIL Fossati-Jimack, A Ioan-Facsinay, L Reininger, et al.
Cerebral Cortex (New York, N.Y. : 1991)|October 3, 2017
Neuronal Expression of Opioid Gene is Controlled by Dual Epigenetic and Transcriptional Mechanism in Human BrainIgor Bazov, Daniil Sarkisyan, Olga Kononenko, et al.
Immunity|August 1, 1996
Impaired IgG-dependent anaphylaxis and Arthus reaction in Fc gamma RIII (CD16) deficient miceW L Hazenbos, J E Gessner, F M Hofhuis, et al.
Cellular and Molecular Life Sciences : CMLS|April 10, 2015
Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant mannerAnna Duarri, Meng-Chin A Lin, Michiel R Fokkens, et al.
BMC Medical Genetics|July 21, 2015
First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsyKatrien Smets, Anna Duarri, Tine Deconinck, et al.
Pageof 13

Showing results (91-100 of 122) with videos related to

Sort By:
Pageof 13
Annals of Neurology|September 26, 2020
CAG Repeat Size Influences the Progression Rate of Spinocerebellar Ataxia Type 3Vanessa B Leotti, Jeroen J de Vries, Camila M Oliveira, et al.
Neurology|December 25, 2003
Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia familyB P C van de Warrenburg, D S Verbeek, S J Piersma, et al.
International Journal of Molecular Sciences|October 26, 2024
Identification and Copy Number Variant Analysis of Enhancer Regions of Genes Causing Spinocerebellar AtaxiaFatemeh Ghorbani, Eddy N de Boer, Michiel R Fokkens, et al.
Diabetologia|December 1, 1993
Chronic overproduction of islet amyloid polypeptide/amylin in transgenic mice: lysosomal localization of human islet amyloid polypeptide and lack of marked hyperglycaemia or hyperinsulinaemiaJ W Höppener, J S Verbeek, E J de Koning, et al.
Blood|June 11, 1999
Human immunoglobulin A receptor (FcalphaRI, CD89) function in transgenic mice requires both FcR gamma chain and CR3 (CD11b/CD18)M van Egmond, A J van Vuuren, H C Morton, et al.
The Journal of Experimental Medicine|April 19, 2000
Markedly different pathogenicity of four immunoglobulin G isotype-switch variants of an antierythrocyte autoantibody is based on their capacity to interact in vivo with the low-affinity Fcgamma receptor IIIL Fossati-Jimack, A Ioan-Facsinay, L Reininger, et al.
Cerebral Cortex (New York, N.Y. : 1991)|October 3, 2017
Neuronal Expression of Opioid Gene is Controlled by Dual Epigenetic and Transcriptional Mechanism in Human BrainIgor Bazov, Daniil Sarkisyan, Olga Kononenko, et al.
Immunity|August 1, 1996
Impaired IgG-dependent anaphylaxis and Arthus reaction in Fc gamma RIII (CD16) deficient miceW L Hazenbos, J E Gessner, F M Hofhuis, et al.
Cellular and Molecular Life Sciences : CMLS|April 10, 2015
Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant mannerAnna Duarri, Meng-Chin A Lin, Michiel R Fokkens, et al.
BMC Medical Genetics|July 21, 2015
First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsyKatrien Smets, Anna Duarri, Tine Deconinck, et al.
Pageof 13