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Frank Baas

Showing results (191-200 of 231) with videos related to

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International Journal of Molecular Sciences|August 29, 2024
Loss-of-Function Variants in <i>SUPT5H</i> as Modifying Factors in Beta-ThalassemiaCornelis L Harteveld, Ahlem Achour, Nik Fatma Fairuz Mohd Hasan, et al.
Annals of Neurology|January 27, 2006
Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2Stephan Züchner, Peter De Jonghe, Albena Jordanova, et al.
American Journal of Human Genetics|May 25, 2010
Mechanisms for nonrecurrent genomic rearrangements associated with CMT1A or HNPP: rare CNVs as a cause for missing heritabilityFeng Zhang, Pavel Seeman, Pengfei Liu, et al.
Acta Neuropathologica Communications|May 5, 2018
Systemic inhibition of the membrane attack complex impedes neuroinflammation in chronic relapsing experimental autoimmune encephalomyelitisIliana Michailidou, Aldo Jongejan, Jeroen P Vreijling, et al.
Brain : a Journal of Neurology|February 1, 2013
Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathyMarian A J Weterman, Peter G Barth, Karin Y van Spaendonck-Zwarts, et al.
Nature Genetics|October 1, 2003
Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndromeRaymonda Varon, Rebecca Gooding, Christina Steglich, et al.
Neurobiology of Aging|March 12, 2014
No mutations in hnRNPA1 and hnRNPA2B1 in Dutch patients with amyotrophic lateral sclerosis, frontotemporal dementia, and inclusion body myopathyMeinie Seelen, Anne E Visser, Daniel J Overste, et al.
Brain Communications|December 22, 2025
The role of disease-associated short tandem repeats in amyotrophic lateral sclerosisJoke J F A van Vugt, Ramona A J Zwamborn, Egor Dolzhenko, et al.
Stem Cell Reports|August 4, 2023
CRB1 is required for recycling by RAB11A+ vesicles in human retinal organoidsThilo M Buck, Peter M J Quinn, Lucie P Pellissier, et al.
The Journal of Cell Biology|July 8, 2015
Schwann cell autophagy, myelinophagy, initiates myelin clearance from injured nervesJose A Gomez-Sanchez, Lucy Carty, Marta Iruarrizaga-Lejarreta, et al.
Pageof 24

Showing results (191-200 of 231) with videos related to

Sort By:
Pageof 24
International Journal of Molecular Sciences|August 29, 2024
Loss-of-Function Variants in <i>SUPT5H</i> as Modifying Factors in Beta-ThalassemiaCornelis L Harteveld, Ahlem Achour, Nik Fatma Fairuz Mohd Hasan, et al.
Annals of Neurology|January 27, 2006
Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2Stephan Züchner, Peter De Jonghe, Albena Jordanova, et al.
American Journal of Human Genetics|May 25, 2010
Mechanisms for nonrecurrent genomic rearrangements associated with CMT1A or HNPP: rare CNVs as a cause for missing heritabilityFeng Zhang, Pavel Seeman, Pengfei Liu, et al.
Acta Neuropathologica Communications|May 5, 2018
Systemic inhibition of the membrane attack complex impedes neuroinflammation in chronic relapsing experimental autoimmune encephalomyelitisIliana Michailidou, Aldo Jongejan, Jeroen P Vreijling, et al.
Brain : a Journal of Neurology|February 1, 2013
Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathyMarian A J Weterman, Peter G Barth, Karin Y van Spaendonck-Zwarts, et al.
Nature Genetics|October 1, 2003
Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndromeRaymonda Varon, Rebecca Gooding, Christina Steglich, et al.
Neurobiology of Aging|March 12, 2014
No mutations in hnRNPA1 and hnRNPA2B1 in Dutch patients with amyotrophic lateral sclerosis, frontotemporal dementia, and inclusion body myopathyMeinie Seelen, Anne E Visser, Daniel J Overste, et al.
Brain Communications|December 22, 2025
The role of disease-associated short tandem repeats in amyotrophic lateral sclerosisJoke J F A van Vugt, Ramona A J Zwamborn, Egor Dolzhenko, et al.
Stem Cell Reports|August 4, 2023
CRB1 is required for recycling by RAB11A+ vesicles in human retinal organoidsThilo M Buck, Peter M J Quinn, Lucie P Pellissier, et al.
The Journal of Cell Biology|July 8, 2015
Schwann cell autophagy, myelinophagy, initiates myelin clearance from injured nervesJose A Gomez-Sanchez, Lucy Carty, Marta Iruarrizaga-Lejarreta, et al.
Pageof 24