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D Bird

Showing results (571-580 of 780) with videos related to

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Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|November 18, 2008
Comparing test-specific distress of susceptibility versus deterministic genetic testing for Alzheimer's diseaseMichael R Cassidy, J Scott Roberts, Thomas D Bird, et al.
Neuron|May 20, 2016
TREM2 Haplodeficiency in Mice and Humans Impairs the Microglia Barrier Function Leading to Decreased Amyloid Compaction and Severe Axonal DystrophyPeng Yuan, Carlo Condello, C Dirk Keene, et al.
Archives of Neurology|August 1, 1991
Factors associated with slow progression in Huntington's diseaseR H Myers, D S Sax, W J Koroshetz, et al.
Neuron|October 7, 2016
TREM2 Haplodeficiency in Mice and Humans Impairs the Microglia Barrier Function Leading to Decreased Amyloid Compaction and Severe Axonal DystrophyPeng Yuan, Carlo Condello, C Dirk Keene, et al.
Neuroscience Letters|February 6, 2014
Clinical and molecular studies reveal a PSEN1 mutation (L153V) in a Peruvian family with early-onset Alzheimer's diseaseMario R Cornejo-Olivas, Chang-En Yu, Pilar Mazzetti, et al.
Journal of Burn Care & Research : Official Publication of the American Burn Association|October 15, 2009
Proteasomes in human bronchoalveolar lavage fluid after burn and inhalation injuryJoslyn M Albright, Jacqueline Romero, Vikas Saini, et al.
Human Mutation|April 1, 1998
Missense mutations in the chromosome 14 familial Alzheimer's disease presenilin 1 geneP Poorkaj, V Sharma, L Anderson, et al.
Cardiovascular Research|May 22, 2003
The human adult cardiomyocyte phenotypeS D Bird, P A Doevendans, M A van Rooijen, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|January 1, 1983
Lack of cholinergic deficit in the neocortex in Pick's diseaseP L Wood, N P Nair, P Etienne, et al.
Molecular Neurodegeneration|February 8, 2018
Pathological phosphorylation of tau and TDP-43 by TTBK1 and TTBK2 drives neurodegenerationLaura M Taylor, Pamela J McMillan, Nicole F Liachko, et al.
Pageof 78

Showing results (571-580 of 780) with videos related to

Sort By:
Pageof 78
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|November 18, 2008
Comparing test-specific distress of susceptibility versus deterministic genetic testing for Alzheimer's diseaseMichael R Cassidy, J Scott Roberts, Thomas D Bird, et al.
Neuron|May 20, 2016
TREM2 Haplodeficiency in Mice and Humans Impairs the Microglia Barrier Function Leading to Decreased Amyloid Compaction and Severe Axonal DystrophyPeng Yuan, Carlo Condello, C Dirk Keene, et al.
Archives of Neurology|August 1, 1991
Factors associated with slow progression in Huntington's diseaseR H Myers, D S Sax, W J Koroshetz, et al.
Neuron|October 7, 2016
TREM2 Haplodeficiency in Mice and Humans Impairs the Microglia Barrier Function Leading to Decreased Amyloid Compaction and Severe Axonal DystrophyPeng Yuan, Carlo Condello, C Dirk Keene, et al.
Neuroscience Letters|February 6, 2014
Clinical and molecular studies reveal a PSEN1 mutation (L153V) in a Peruvian family with early-onset Alzheimer's diseaseMario R Cornejo-Olivas, Chang-En Yu, Pilar Mazzetti, et al.
Journal of Burn Care & Research : Official Publication of the American Burn Association|October 15, 2009
Proteasomes in human bronchoalveolar lavage fluid after burn and inhalation injuryJoslyn M Albright, Jacqueline Romero, Vikas Saini, et al.
Human Mutation|April 1, 1998
Missense mutations in the chromosome 14 familial Alzheimer's disease presenilin 1 geneP Poorkaj, V Sharma, L Anderson, et al.
Cardiovascular Research|May 22, 2003
The human adult cardiomyocyte phenotypeS D Bird, P A Doevendans, M A van Rooijen, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|January 1, 1983
Lack of cholinergic deficit in the neocortex in Pick's diseaseP L Wood, N P Nair, P Etienne, et al.
Molecular Neurodegeneration|February 8, 2018
Pathological phosphorylation of tau and TDP-43 by TTBK1 and TTBK2 drives neurodegenerationLaura M Taylor, Pamela J McMillan, Nicole F Liachko, et al.
Pageof 78