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Thomas Gasser

Showing results (181-190 of 476) with videos related to

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Oncogene|May 4, 2004
E2F3 amplification and overexpression is associated with invasive tumor growth and rapid tumor cell proliferation in urinary bladder cancerMartin Oeggerli, Sanja Tomovska, Peter Schraml, et al.
Parkinsonism & Related Disorders|December 12, 2025
Assessment of SLC25A46 variants in idiopathic Parkinson's diseaseZachary Schneider, Hui Liu, Mohammad Dehestani, et al.
Dementia and Geriatric Cognitive Disorders|November 30, 2011
Association of clusterin gene polymorphisms with late-onset Alzheimer's diseaseHuiying Gu, Xing Wei, Shirley Chen, et al.
Neurosurgical Review|August 11, 2010
Spontaneous cerebellar hemorrhage--experience with 57 surgically treated patients and review of the literaturePhilipp Dammann, Siamak Asgari, Hischam Bassiouni, et al.
Frontiers in Molecular Neuroscience|October 30, 2016
Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS CohortStefanie Krüger, Florian Battke, Andrea Sprecher, et al.
Annals of Neurology|October 22, 2005
Myoclonus-dystonia due to genomic deletions in the epsilon-sarcoglycan geneFriedrich Asmus, Farid Salih, Lena Elisabeth Hjermind, et al.
Journal of Alzheimer'S Disease : JAD|February 17, 2010
The CST3 BB genotype and low cystatin C cerebrospinal fluid levels are associated with dementia in Lewy body diseaseWalter Maetzler, Benjamin Schmid, Matthis Synofzik, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 29, 2007
Genetic variability in the SNCA gene influences alpha-synuclein levels in the blood and brainJulia Fuchs, Ales Tichopad, Yulia Golub, et al.
Neurobiology of Disease|June 2, 2009
No differences of butyrylcholinesterase protein activity and allele frequency in Lewy body diseasesWalter Maetzler, Stefanie Keller, Joan Michelis, et al.
Journal of Medical Genetics|March 8, 2024
Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insightsBurcu Atasu, Javier Simón-Sánchez, Hasmet Hanagasi, et al.
Pageof 48

Showing results (181-190 of 476) with videos related to

Sort By:
Pageof 48
Oncogene|May 4, 2004
E2F3 amplification and overexpression is associated with invasive tumor growth and rapid tumor cell proliferation in urinary bladder cancerMartin Oeggerli, Sanja Tomovska, Peter Schraml, et al.
Parkinsonism & Related Disorders|December 12, 2025
Assessment of SLC25A46 variants in idiopathic Parkinson's diseaseZachary Schneider, Hui Liu, Mohammad Dehestani, et al.
Dementia and Geriatric Cognitive Disorders|November 30, 2011
Association of clusterin gene polymorphisms with late-onset Alzheimer's diseaseHuiying Gu, Xing Wei, Shirley Chen, et al.
Neurosurgical Review|August 11, 2010
Spontaneous cerebellar hemorrhage--experience with 57 surgically treated patients and review of the literaturePhilipp Dammann, Siamak Asgari, Hischam Bassiouni, et al.
Frontiers in Molecular Neuroscience|October 30, 2016
Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS CohortStefanie Krüger, Florian Battke, Andrea Sprecher, et al.
Annals of Neurology|October 22, 2005
Myoclonus-dystonia due to genomic deletions in the epsilon-sarcoglycan geneFriedrich Asmus, Farid Salih, Lena Elisabeth Hjermind, et al.
Journal of Alzheimer'S Disease : JAD|February 17, 2010
The CST3 BB genotype and low cystatin C cerebrospinal fluid levels are associated with dementia in Lewy body diseaseWalter Maetzler, Benjamin Schmid, Matthis Synofzik, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 29, 2007
Genetic variability in the SNCA gene influences alpha-synuclein levels in the blood and brainJulia Fuchs, Ales Tichopad, Yulia Golub, et al.
Neurobiology of Disease|June 2, 2009
No differences of butyrylcholinesterase protein activity and allele frequency in Lewy body diseasesWalter Maetzler, Stefanie Keller, Joan Michelis, et al.
Journal of Medical Genetics|March 8, 2024
Dissecting genetic architecture of rare dystonia: genetic, molecular and clinical insightsBurcu Atasu, Javier Simón-Sánchez, Hasmet Hanagasi, et al.
Pageof 48