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Annals of Neurology
|
September 26, 2020
CAG Repeat Size Influences the Progression Rate of Spinocerebellar Ataxia Type 3
Vanessa 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 family
B 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 Ataxia
Fatemeh 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 hyperinsulinaemia
J 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 III
L 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 Brain
Igor Bazov, Daniil Sarkisyan, Olga Kononenko, et al.
Immunity
|
August 1, 1996
Impaired IgG-dependent anaphylaxis and Arthus reaction in Fc gamma RIII (CD16) deficient mice
W 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 manner
Anna 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 epilepsy
Katrien Smets, Anna Duarri, Tine Deconinck, et al.
Page
of 13
Search research articles
Search
Showing results (91-100 of 122) with videos related to
Sort By:
Page
of 13
Annals of Neurology
|
September 26, 2020
CAG Repeat Size Influences the Progression Rate of Spinocerebellar Ataxia Type 3
Vanessa 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 family
B 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 Ataxia
Fatemeh 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 hyperinsulinaemia
J 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 III
L 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 Brain
Igor Bazov, Daniil Sarkisyan, Olga Kononenko, et al.
Immunity
|
August 1, 1996
Impaired IgG-dependent anaphylaxis and Arthus reaction in Fc gamma RIII (CD16) deficient mice
W 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 manner
Anna 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 epilepsy
Katrien Smets, Anna Duarri, Tine Deconinck, et al.
Page
of 13