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Showing results (71-80 of 83) with videos related to

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Human Molecular Genetics|November 11, 1999
Unusual 5' transcript complexity of plectin isoforms: novel tissue-specific exons modulate actin binding activityP Fuchs, M Zörer, G A Rezniczek, et al.
Histochemistry and Cell Biology|August 26, 2000
Differences in the distribution of synemin, paranemin, and plectin in skeletal muscles of wild-type and desmin knock-out miceL Carlsson, Z L Li, D Paulin, et al.
Journal of Neuropathology and Experimental Neurology|January 1, 1989
An antigenic profile of Lewy bodies: immunocytochemical indication for protein phosphorylation and ubiquitinationC Bancher, H Lassmann, H Budka, et al.
Neuropathology and Applied Neurobiology|June 3, 2020
Plectin dysfunction in neurons leads to tau accumulation on microtubules affecting neuritogenesis, organelle trafficking, pain sensitivity and memoryR G Valencia, E Mihailovska, L Winter, et al.
Molecular and Cellular Biology|July 13, 2000
Identification of the cytolinker plectin as a major early in vivo substrate for caspase 8 during CD95- and tumor necrosis factor receptor-mediated apoptosisA H Stegh, H Herrmann, S Lampel, et al.
The Journal of Cell Biology|December 21, 2000
MAP1B is required for axon guidance and Is involved in the development of the central and peripheral nervous systemA Meixner, S Haverkamp, H Wässle, et al.
Brain Research|January 16, 1989
Accumulation of abnormally phosphorylated tau precedes the formation of neurofibrillary tangles in Alzheimer's diseaseC Bancher, C Brunner, H Lassmann, et al.
The Journal of Investigative Dermatology|January 29, 2000
Mutation reports: epidermolysis bullosa simplex associated with severe mucous membrane involvement and novel mutations in the plectin geneM Kunz, F Rouan, L Pulkkinen, et al.
Acta Dermato-Venereologica|June 23, 2004
Life-long course and molecular characterization of the original Dutch family with epidermolysis bullosa simplex with muscular dystrophy due to a homozygous novel plectin point mutationD Koss-Harnes, B Høyheim, M F Jonkman, et al.
The American Journal of Pathology|February 13, 2001
A compound heterozygous one amino-acid insertion/nonsense mutation in the plectin gene causes epidermolysis bullosa simplex with plectin deficiencyJ W Bauer, F Rouan, B Kofler, et al.
Pageof 9

Showing results (71-80 of 83) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|November 11, 1999
Unusual 5' transcript complexity of plectin isoforms: novel tissue-specific exons modulate actin binding activityP Fuchs, M Zörer, G A Rezniczek, et al.
Histochemistry and Cell Biology|August 26, 2000
Differences in the distribution of synemin, paranemin, and plectin in skeletal muscles of wild-type and desmin knock-out miceL Carlsson, Z L Li, D Paulin, et al.
Journal of Neuropathology and Experimental Neurology|January 1, 1989
An antigenic profile of Lewy bodies: immunocytochemical indication for protein phosphorylation and ubiquitinationC Bancher, H Lassmann, H Budka, et al.
Neuropathology and Applied Neurobiology|June 3, 2020
Plectin dysfunction in neurons leads to tau accumulation on microtubules affecting neuritogenesis, organelle trafficking, pain sensitivity and memoryR G Valencia, E Mihailovska, L Winter, et al.
Molecular and Cellular Biology|July 13, 2000
Identification of the cytolinker plectin as a major early in vivo substrate for caspase 8 during CD95- and tumor necrosis factor receptor-mediated apoptosisA H Stegh, H Herrmann, S Lampel, et al.
The Journal of Cell Biology|December 21, 2000
MAP1B is required for axon guidance and Is involved in the development of the central and peripheral nervous systemA Meixner, S Haverkamp, H Wässle, et al.
Brain Research|January 16, 1989
Accumulation of abnormally phosphorylated tau precedes the formation of neurofibrillary tangles in Alzheimer's diseaseC Bancher, C Brunner, H Lassmann, et al.
The Journal of Investigative Dermatology|January 29, 2000
Mutation reports: epidermolysis bullosa simplex associated with severe mucous membrane involvement and novel mutations in the plectin geneM Kunz, F Rouan, L Pulkkinen, et al.
Acta Dermato-Venereologica|June 23, 2004
Life-long course and molecular characterization of the original Dutch family with epidermolysis bullosa simplex with muscular dystrophy due to a homozygous novel plectin point mutationD Koss-Harnes, B Høyheim, M F Jonkman, et al.
The American Journal of Pathology|February 13, 2001
A compound heterozygous one amino-acid insertion/nonsense mutation in the plectin gene causes epidermolysis bullosa simplex with plectin deficiencyJ W Bauer, F Rouan, B Kofler, et al.
Pageof 9