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Marka van Blitterswijk

Showing results (21-30 of 89) with videos related to

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Archives of Neurology|June 13, 2012
Mutations in the TRPV4 gene are not associated with sporadic progressive muscular atrophyLotte Vlam, Helenius J Schelhaas, Marka van Blitterswijk, et al.
Neurobiology of Aging|August 2, 2011
Novel optineurin mutations in sporadic amyotrophic lateral sclerosis patientsMarka van Blitterswijk, Paul W J van Vught, Michael A van Es, et al.
Experimental Neurology|January 10, 2016
C9orf72 promoter hypermethylation is reduced while hydroxymethylation is acquired during reprogramming of ALS patient cellsRustam Esanov, Kinsley C Belle, Marka van Blitterswijk, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|October 26, 2011
Anti-superoxide dismutase antibodies are associated with survival in patients with sporadic amyotrophic lateral sclerosisMarka van Blitterswijk, Sunita Gulati, Elizabeth Smoot, et al.
Neurobiology of Aging|August 11, 2012
VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patientMarka van Blitterswijk, Michael A van Es, Max Koppers, et al.
Neurobiology of Aging|June 9, 2012
UBQLN2 in familial amyotrophic lateral sclerosis in The NetherlandsPerry T C van Doormaal, Wouter van Rheenen, Marka van Blitterswijk, et al.
Molecular Neurodegeneration|December 21, 2024
Targeted long-read sequencing to quantify methylation of the C9orf72 repeat expansionEvan Udine, NiCole A Finch, Mariely DeJesus-Hernandez, et al.
Neurology. Genetics|June 22, 2023
Analysis of Structural Variants Previously Associated With ALS in Europeans Highlights Genomic Architectural Differences in AfricansNomakhosazana R Monnakgotla, Amokelani C Mahungu, Jeannine M Heckmann, et al.
Neurology|December 29, 2017
Unaffected mosaic <i>C9orf72</i> case: RNA foci, dipeptide proteins, but upregulated C9orf72 expressionPhilip McGoldrick, Ming Zhang, Marka van Blitterswijk, et al.
Neurology. Genetics|January 20, 2022
Revealing the Mutational Spectrum in Southern Africans With Amyotrophic Lateral SclerosisMelissa Nel, Amokelani C Mahungu, Nomakhosazana Monnakgotla, et al.
Pageof 9

Showing results (21-30 of 89) with videos related to

Sort By:
Pageof 9
Archives of Neurology|June 13, 2012
Mutations in the TRPV4 gene are not associated with sporadic progressive muscular atrophyLotte Vlam, Helenius J Schelhaas, Marka van Blitterswijk, et al.
Neurobiology of Aging|August 2, 2011
Novel optineurin mutations in sporadic amyotrophic lateral sclerosis patientsMarka van Blitterswijk, Paul W J van Vught, Michael A van Es, et al.
Experimental Neurology|January 10, 2016
C9orf72 promoter hypermethylation is reduced while hydroxymethylation is acquired during reprogramming of ALS patient cellsRustam Esanov, Kinsley C Belle, Marka van Blitterswijk, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|October 26, 2011
Anti-superoxide dismutase antibodies are associated with survival in patients with sporadic amyotrophic lateral sclerosisMarka van Blitterswijk, Sunita Gulati, Elizabeth Smoot, et al.
Neurobiology of Aging|August 11, 2012
VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patientMarka van Blitterswijk, Michael A van Es, Max Koppers, et al.
Neurobiology of Aging|June 9, 2012
UBQLN2 in familial amyotrophic lateral sclerosis in The NetherlandsPerry T C van Doormaal, Wouter van Rheenen, Marka van Blitterswijk, et al.
Molecular Neurodegeneration|December 21, 2024
Targeted long-read sequencing to quantify methylation of the C9orf72 repeat expansionEvan Udine, NiCole A Finch, Mariely DeJesus-Hernandez, et al.
Neurology. Genetics|June 22, 2023
Analysis of Structural Variants Previously Associated With ALS in Europeans Highlights Genomic Architectural Differences in AfricansNomakhosazana R Monnakgotla, Amokelani C Mahungu, Jeannine M Heckmann, et al.
Neurology|December 29, 2017
Unaffected mosaic <i>C9orf72</i> case: RNA foci, dipeptide proteins, but upregulated C9orf72 expressionPhilip McGoldrick, Ming Zhang, Marka van Blitterswijk, et al.
Neurology. Genetics|January 20, 2022
Revealing the Mutational Spectrum in Southern Africans With Amyotrophic Lateral SclerosisMelissa Nel, Amokelani C Mahungu, Nomakhosazana Monnakgotla, et al.
Pageof 9