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Richard Crook

Showing results (21-30 of 36) with videos related to

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Human Mutation|March 17, 2010
De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosisMariely DeJesus-Hernandez, Jannet Kocerha, NiCole Finch, et al.
Perfusion|January 10, 2023
Rapid desensitization through immunoadsorption during cardiopulmonary bypass. A novel method to facilitate human leukocyte antigen incompatible heart transplantationRichard W Issitt, Eamonn Cudworth, Mario Cortina-Borja, et al.
Annals of Neurology|September 1, 2005
Phosphodiesterase 4D and 5-lipoxygenase activating protein in ischemic strokeJames F Meschia, Thomas G Brott, Robert D Brown, et al.
Neurobiology of Disease|March 16, 2002
A presenilin 1 mutation associated with familial frontotemporal dementia inhibits gamma-secretase cleavage of APP and notchZareen Amtul, Patrick A Lewis, Sian Piper, et al.
Archives of Neurology|December 15, 2004
Genome-wide analysis of the parkinsonism-dementia complex of GuamHuw R Morris, John C Steele, Richard Crook, et al.
Brain : a Journal of Neurology|January 23, 2009
Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family membersNiCole Finch, Matt Baker, Richard Crook, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 22, 2010
Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS familyAdam L Boxer, Ian R Mackenzie, Bradley F Boeve, et al.
Acta Neuropathologica|April 19, 2024
Abundant transcriptomic alterations in the human cerebellum of patients with a C9orf72 repeat expansionEvan Udine, Mariely DeJesus-Hernandez, Shulan Tian, et al.
Nature|July 25, 2006
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17Matt Baker, Ian R Mackenzie, Stuart M Pickering-Brown, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 25, 2005
Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's diseasePeter Holmans, Marian Hamshere, Paul Hollingworth, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Human Mutation|March 17, 2010
De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosisMariely DeJesus-Hernandez, Jannet Kocerha, NiCole Finch, et al.
Perfusion|January 10, 2023
Rapid desensitization through immunoadsorption during cardiopulmonary bypass. A novel method to facilitate human leukocyte antigen incompatible heart transplantationRichard W Issitt, Eamonn Cudworth, Mario Cortina-Borja, et al.
Annals of Neurology|September 1, 2005
Phosphodiesterase 4D and 5-lipoxygenase activating protein in ischemic strokeJames F Meschia, Thomas G Brott, Robert D Brown, et al.
Neurobiology of Disease|March 16, 2002
A presenilin 1 mutation associated with familial frontotemporal dementia inhibits gamma-secretase cleavage of APP and notchZareen Amtul, Patrick A Lewis, Sian Piper, et al.
Archives of Neurology|December 15, 2004
Genome-wide analysis of the parkinsonism-dementia complex of GuamHuw R Morris, John C Steele, Richard Crook, et al.
Brain : a Journal of Neurology|January 23, 2009
Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family membersNiCole Finch, Matt Baker, Richard Crook, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 22, 2010
Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS familyAdam L Boxer, Ian R Mackenzie, Bradley F Boeve, et al.
Acta Neuropathologica|April 19, 2024
Abundant transcriptomic alterations in the human cerebellum of patients with a C9orf72 repeat expansionEvan Udine, Mariely DeJesus-Hernandez, Shulan Tian, et al.
Nature|July 25, 2006
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17Matt Baker, Ian R Mackenzie, Stuart M Pickering-Brown, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 25, 2005
Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's diseasePeter Holmans, Marian Hamshere, Paul Hollingworth, et al.
Pageof 4