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Showing results (1031-1040 of 1,055) with videos related to

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Nature Genetics|August 15, 2006
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disabilityCharles Shaw-Smith, Alan M Pittman, Lionel Willatt, et al.
Journal of Neurochemistry|June 30, 2006
Altered cleavage and localization of PINK1 to aggresomes in the presence of proteasomal stressMiratul M K Muqit, Patrick M Abou-Sleiman, Adrian T Saurin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2006
The alpha-synuclein gene in multiple system atrophyT Ozawa, D G Healy, P M Abou-Sleiman, et al.
Journal of Occupational and Environmental Medicine|March 28, 2023
Association of Occupational Exposures and Chronic Obstructive Pulmonary Disease MorbidityJennifer S Rous, Peter S J Lees, Kirsten Koehler, et al.
JCI Insight|October 4, 2019
Donor and host B7-H4 expression negatively regulates acute graft-versus-host disease lethalityAsim Saha, Patricia A Taylor, Christopher J Lees, et al.
Brain : a Journal of Neurology|December 10, 2003
The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's diseaseRina Bandopadhyay, Ann E Kingsbury, Mark R Cookson, et al.
Annals of Neurology|August 2, 2018
Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotypeEdwin Jabbari, John Woodside, Manuela M X Tan, et al.
Brain : a Journal of Neurology|July 15, 2011
A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathiesTammaryn Lashley, Jonathan D Rohrer, Rina Bandopadhyay, et al.
Neurology|June 27, 2001
Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotypeH Houlden, M Baker, H R Morris, et al.
Neuropathology and Applied Neurobiology|July 30, 2022
Pathological substrate of memory impairment in multiple system atrophyYasuo Miki, Kunikazu Tanji, Kana Shinnai, et al.
Pageof 106

Showing results (1031-1040 of 1,055) with videos related to

Sort By:
Pageof 106
Nature Genetics|August 15, 2006
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disabilityCharles Shaw-Smith, Alan M Pittman, Lionel Willatt, et al.
Journal of Neurochemistry|June 30, 2006
Altered cleavage and localization of PINK1 to aggresomes in the presence of proteasomal stressMiratul M K Muqit, Patrick M Abou-Sleiman, Adrian T Saurin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2006
The alpha-synuclein gene in multiple system atrophyT Ozawa, D G Healy, P M Abou-Sleiman, et al.
Journal of Occupational and Environmental Medicine|March 28, 2023
Association of Occupational Exposures and Chronic Obstructive Pulmonary Disease MorbidityJennifer S Rous, Peter S J Lees, Kirsten Koehler, et al.
JCI Insight|October 4, 2019
Donor and host B7-H4 expression negatively regulates acute graft-versus-host disease lethalityAsim Saha, Patricia A Taylor, Christopher J Lees, et al.
Brain : a Journal of Neurology|December 10, 2003
The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's diseaseRina Bandopadhyay, Ann E Kingsbury, Mark R Cookson, et al.
Annals of Neurology|August 2, 2018
Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotypeEdwin Jabbari, John Woodside, Manuela M X Tan, et al.
Brain : a Journal of Neurology|July 15, 2011
A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathiesTammaryn Lashley, Jonathan D Rohrer, Rina Bandopadhyay, et al.
Neurology|June 27, 2001
Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotypeH Houlden, M Baker, H R Morris, et al.
Neuropathology and Applied Neurobiology|July 30, 2022
Pathological substrate of memory impairment in multiple system atrophyYasuo Miki, Kunikazu Tanji, Kana Shinnai, et al.
Pageof 106