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Elife
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May 1, 2018
Reduced expression of C/EBPβ-LIP extends health and lifespan in mice
Christine 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 23
Cleo 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 Phenotype
Marlous 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 cooperation
Julia 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 Significance
Fatemeh 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 23
Georgy 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 complement
A 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 ataxia
Fatemeh 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 19
Anna Duarri, Justyna Jezierska, Michiel Fokkens, et al.
Page
of 13
Search research articles
Search
Showing results (111-120 of 122) with videos related to
Sort By:
Page
of 13
Elife
|
May 1, 2018
Reduced expression of C/EBPβ-LIP extends health and lifespan in mice
Christine 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 23
Cleo 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 Phenotype
Marlous 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 cooperation
Julia 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 Significance
Fatemeh 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 23
Georgy 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 complement
A 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 ataxia
Fatemeh 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 19
Anna Duarri, Justyna Jezierska, Michiel Fokkens, et al.
Page
of 13