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Peter Heutink

Showing results (121-130 of 240) with videos related to

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American Journal of Human Genetics|January 12, 2010
Functional gene group analysis reveals a role of synaptic heterotrimeric G proteins in cognitive abilityDina Ruano, Gonçalo R Abecasis, Beate Glaser, et al.
Blood Cells, Molecules & Diseases|January 28, 2003
Dominant hemochromatosis due to N144H mutation of SLC11A3: clinical and biological characteristicsOmer T Njajou, Gerard de Jong, Bianca Berghuis, et al.
Plos One|June 1, 2012
A fine-mapping study of 7 top scoring genes from a GWAS for major depressive disorderEva C Verbeek, Ingrid M C Bakker, Marianna R Bevova, et al.
Journal of Psychiatric Research|December 5, 2006
Association of the gene encoding neurogranin with schizophrenia in malesDina Ruano, Yurii S Aulchenko, António Macedo, et al.
Journal of Psychiatric Research|May 24, 2006
Transthyretin: no association between serum levels or gene variants and schizophreniaDina Ruano, António Macedo, Maria J Soares, et al.
American Journal of Human Genetics|June 15, 2007
A genomewide screen for late-onset Alzheimer disease in a genetically isolated Dutch populationFan Liu, Alejandro Arias-Vásquez, Kristel Sleegers, et al.
Cerebellum (London, England)|January 17, 2015
Clinical and Neuropathological Features of Spastic Ataxia in a Spanish Family with Novel Compound Heterozygous Mutations in STUB1Conceição Bettencourt, Justo García de Yébenes, José Luis López-Sendón, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 20, 2026
The Global Parkinson's Disease Genetics (GP2) Genome BrowserZih-Hua Fang, Riley H Grant, Dan Vitale, et al.
Annals of Neurology|August 2, 2003
Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutationStephen Hague, Ekaterina Rogaeva, Dena Hernandez, et al.
Neuro-Oncology Advances|November 2, 2020
Experimental glioma with high bHLH expression harbor increased replicative stress and are sensitive toward ATR inhibitionMarilin Sophia Koch, Stefan Czemmel, Felix Lennartz, et al.
Pageof 24

Showing results (121-130 of 240) with videos related to

Sort By:
Pageof 24
American Journal of Human Genetics|January 12, 2010
Functional gene group analysis reveals a role of synaptic heterotrimeric G proteins in cognitive abilityDina Ruano, Gonçalo R Abecasis, Beate Glaser, et al.
Blood Cells, Molecules & Diseases|January 28, 2003
Dominant hemochromatosis due to N144H mutation of SLC11A3: clinical and biological characteristicsOmer T Njajou, Gerard de Jong, Bianca Berghuis, et al.
Plos One|June 1, 2012
A fine-mapping study of 7 top scoring genes from a GWAS for major depressive disorderEva C Verbeek, Ingrid M C Bakker, Marianna R Bevova, et al.
Journal of Psychiatric Research|December 5, 2006
Association of the gene encoding neurogranin with schizophrenia in malesDina Ruano, Yurii S Aulchenko, António Macedo, et al.
Journal of Psychiatric Research|May 24, 2006
Transthyretin: no association between serum levels or gene variants and schizophreniaDina Ruano, António Macedo, Maria J Soares, et al.
American Journal of Human Genetics|June 15, 2007
A genomewide screen for late-onset Alzheimer disease in a genetically isolated Dutch populationFan Liu, Alejandro Arias-Vásquez, Kristel Sleegers, et al.
Cerebellum (London, England)|January 17, 2015
Clinical and Neuropathological Features of Spastic Ataxia in a Spanish Family with Novel Compound Heterozygous Mutations in STUB1Conceição Bettencourt, Justo García de Yébenes, José Luis López-Sendón, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 20, 2026
The Global Parkinson's Disease Genetics (GP2) Genome BrowserZih-Hua Fang, Riley H Grant, Dan Vitale, et al.
Annals of Neurology|August 2, 2003
Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutationStephen Hague, Ekaterina Rogaeva, Dena Hernandez, et al.
Neuro-Oncology Advances|November 2, 2020
Experimental glioma with high bHLH expression harbor increased replicative stress and are sensitive toward ATR inhibitionMarilin Sophia Koch, Stefan Czemmel, Felix Lennartz, et al.
Pageof 24