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Peter Heutink

Showing results (101-110 of 240) with videos related to

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Plos One|September 16, 2016
Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia PatientsGamze Guven, Ebba Lohmann, Jose Bras, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 19, 2007
Family-based and case-control studies reveal no association of lipocalin-type prostaglandin D2 synthase with schizophreniaDina Ruano, António Macedo, Maria João Soares, et al.
Science (New York, N.Y.)|May 21, 2005
Mutations in Col4a1 cause perinatal cerebral hemorrhage and porencephalyDouglas B Gould, F Campbell Phalan, Guido J Breedveld, et al.
Journal of Alzheimer'S Disease : JAD|February 26, 2010
Translational research in genomics of Alzheimer's disease: a review of current practice and future perspectivesRaluca Mihaescu, Symone B Detmar, Martina C Cornel, et al.
Current Alzheimer Research|March 15, 2016
Serum Levels of Progranulin Do Not Reflect Cerebrospinal Fluid Levels in Neurodegenerative DiseaseCarlo Wilke, Frank Gillardon, Christian Deuschle, et al.
Plos Pathogens|October 27, 2021
Novel regulators of PrPC biosynthesis revealed by genome-wide RNA interferenceDaniel Heinzer, Merve Avar, Daniel Patrick Pease, et al.
The New England Journal of Medicine|April 7, 2006
Role of COL4A1 in small-vessel disease and hemorrhagic strokeDouglas B Gould, F Campbell Phalan, Saskia E van Mil, et al.
Annals of Neurology|February 9, 2002
Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (PARK7) in an independent datasetVincenzo Bonifati, Guido J Breedveld, Ferdinando Squitieri, et al.
Annals of Neurology|March 14, 2002
A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's diseaseSonia M Rosso, Esther van Herpen, Wout Deelen, et al.
Neurology. Genetics|April 12, 2016
Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson diseaseSuzanne Lesage, Jose Bras, Florence Cormier-Dequaire, et al.
Pageof 24

Showing results (101-110 of 240) with videos related to

Sort By:
Pageof 24
Plos One|September 16, 2016
Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia PatientsGamze Guven, Ebba Lohmann, Jose Bras, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 19, 2007
Family-based and case-control studies reveal no association of lipocalin-type prostaglandin D2 synthase with schizophreniaDina Ruano, António Macedo, Maria João Soares, et al.
Science (New York, N.Y.)|May 21, 2005
Mutations in Col4a1 cause perinatal cerebral hemorrhage and porencephalyDouglas B Gould, F Campbell Phalan, Guido J Breedveld, et al.
Journal of Alzheimer'S Disease : JAD|February 26, 2010
Translational research in genomics of Alzheimer's disease: a review of current practice and future perspectivesRaluca Mihaescu, Symone B Detmar, Martina C Cornel, et al.
Current Alzheimer Research|March 15, 2016
Serum Levels of Progranulin Do Not Reflect Cerebrospinal Fluid Levels in Neurodegenerative DiseaseCarlo Wilke, Frank Gillardon, Christian Deuschle, et al.
Plos Pathogens|October 27, 2021
Novel regulators of PrPC biosynthesis revealed by genome-wide RNA interferenceDaniel Heinzer, Merve Avar, Daniel Patrick Pease, et al.
The New England Journal of Medicine|April 7, 2006
Role of COL4A1 in small-vessel disease and hemorrhagic strokeDouglas B Gould, F Campbell Phalan, Saskia E van Mil, et al.
Annals of Neurology|February 9, 2002
Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (PARK7) in an independent datasetVincenzo Bonifati, Guido J Breedveld, Ferdinando Squitieri, et al.
Annals of Neurology|March 14, 2002
A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's diseaseSonia M Rosso, Esther van Herpen, Wout Deelen, et al.
Neurology. Genetics|April 12, 2016
Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson diseaseSuzanne Lesage, Jose Bras, Florence Cormier-Dequaire, et al.
Pageof 24