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Stephan Züchner

Showing results (81-90 of 198) with videos related to

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Human Mutation|February 26, 2009
Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10Xueying Liang, Michael Slifer, Eden R Martin, et al.
Behavior Genetics|December 21, 2020
Correction to: Effects of Environmental Stress and Gender on Associations among Symptoms of Depression and the Serotonin Transporter Gene Linked Polymorphic Region (5-HTTLPR)Beverly H Brummett, Stephen H Boyle, Ilene C Siegler, et al.
Human Molecular Genetics|May 17, 2014
Haplotype-specific modulation of a SOX10/CREB response element at the Charcot-Marie-Tooth disease type 4C locus SH3TC2Megan Hwa Brewer, Ki Hwan Ma, Gary W Beecham, et al.
Brain : a Journal of Neurology|August 8, 2018
GDAP2 mutations implicate susceptibility to cellular stress in a new form of cerebellar ataxiaIlse Eidhof, Jonathan Baets, Erik-Jan Kamsteeg, et al.
Neurology|February 15, 2013
Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson diseaseKaren Nuytemans, Guney Bademci, Vanessa Inchausti, et al.
Psychosomatic Medicine|September 4, 2007
Sleep quality varies as a function of 5-HTTLPR genotype and stressBeverly H Brummett, Andrew D Krystal, Allison Ashley-Koch, et al.
Neuron|May 19, 2019
Glutathione S-Transferase Regulates Mitochondrial Populations in Axons through Increased Glutathione OxidationGaynor A Smith, Tzu-Huai Lin, Amy E Sheehan, et al.
Brain : a Journal of Neurology|May 11, 2023
GAA-FGF14 ataxia (SCA27B): phenotypic profile, natural history progression and 4-aminopyridine treatment responseCarlo Wilke, David Pellerin, David Mengel, et al.
Annals of Clinical and Translational Neurology|March 20, 2024
Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autismMaike F Dohrn, Guney Bademci, Adriana P Rebelo, et al.
Brain Communications|September 14, 2023
Spinocerebellar ataxia 27B: episodic symptoms and acetazolamide response in 34 patientsCatherine Ashton, Elisabetta Indelicato, David Pellerin, et al.
Pageof 20

Showing results (81-90 of 198) with videos related to

Sort By:
Pageof 20
Human Mutation|February 26, 2009
Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10Xueying Liang, Michael Slifer, Eden R Martin, et al.
Behavior Genetics|December 21, 2020
Correction to: Effects of Environmental Stress and Gender on Associations among Symptoms of Depression and the Serotonin Transporter Gene Linked Polymorphic Region (5-HTTLPR)Beverly H Brummett, Stephen H Boyle, Ilene C Siegler, et al.
Human Molecular Genetics|May 17, 2014
Haplotype-specific modulation of a SOX10/CREB response element at the Charcot-Marie-Tooth disease type 4C locus SH3TC2Megan Hwa Brewer, Ki Hwan Ma, Gary W Beecham, et al.
Brain : a Journal of Neurology|August 8, 2018
GDAP2 mutations implicate susceptibility to cellular stress in a new form of cerebellar ataxiaIlse Eidhof, Jonathan Baets, Erik-Jan Kamsteeg, et al.
Neurology|February 15, 2013
Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson diseaseKaren Nuytemans, Guney Bademci, Vanessa Inchausti, et al.
Psychosomatic Medicine|September 4, 2007
Sleep quality varies as a function of 5-HTTLPR genotype and stressBeverly H Brummett, Andrew D Krystal, Allison Ashley-Koch, et al.
Neuron|May 19, 2019
Glutathione S-Transferase Regulates Mitochondrial Populations in Axons through Increased Glutathione OxidationGaynor A Smith, Tzu-Huai Lin, Amy E Sheehan, et al.
Brain : a Journal of Neurology|May 11, 2023
GAA-FGF14 ataxia (SCA27B): phenotypic profile, natural history progression and 4-aminopyridine treatment responseCarlo Wilke, David Pellerin, David Mengel, et al.
Annals of Clinical and Translational Neurology|March 20, 2024
Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autismMaike F Dohrn, Guney Bademci, Adriana P Rebelo, et al.
Brain Communications|September 14, 2023
Spinocerebellar ataxia 27B: episodic symptoms and acetazolamide response in 34 patientsCatherine Ashton, Elisabetta Indelicato, David Pellerin, et al.
Pageof 20