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P Blair

Showing results (271-280 of 396) with videos related to

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Ophthalmic Surgery, Lasers & Imaging Retina|February 11, 2022
Exudative Retinal Detachment Following Chimeric Antigen Receptor T-Cell Therapy in Relapsed B-Cell Acute Lymphoblastic LeukemiaSaira Khanna, Anna G Mackin, David T Dao, et al.
Nature Genetics|May 1, 1996
The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3G A Nicholson, J L Dawkins, I P Blair, et al.
Applied Optics|December 15, 2010
Components for the implementation of free-space optical crossbarsC P Barrett, P Blair, G S Buller, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|November 9, 2019
Theme 3 In vitro experimental modelsShu Yang, Sharlynn Wu, Jennifer Fifita, et al.
Genomics|September 20, 1995
The mouse homolog of the Wiskott-Aldrich syndrome protein (WASP) gene is highly conserved and maps near the scurfy (sf) mutation on the X chromosomeJ M Derry, P Wiedemann, P Blair, et al.
Scientific Reports|August 22, 2015
Distinct partitioning of ALS associated TDP-43, FUS and SOD1 mutants into cellular inclusionsNatalie E Farrawell, Isabella A Lambert-Smith, Sadaf T Warraich, et al.
Neurobiology of Aging|June 22, 2012
UBQLN2/ubiquilin 2 mutation and pathology in familial amyotrophic lateral sclerosisKelly L Williams, Sadaf T Warraich, Shu Yang, et al.
Journal of Neuromuscular Diseases|August 28, 2023
Characterising the Genetic Landscape of Amyotrophic Lateral Sclerosis: A Catalogue and Assessment of Over 1,000 Published Genetic VariantsEmily P McCann, Natalie Grima, Jennifer A Fifita, et al.
Journal of Psychiatric Research|October 22, 2022
Ventral striatal subregional dysfunction in late-life grief: Relationships with yearning and depressive symptomsNutta-On P Blair, Alexander D Cohen, B Douglas Ward, et al.
Neurology|May 5, 1998
Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophyP A Silburn, G A Nicholson, B T Teh, et al.
Pageof 40

Showing results (271-280 of 396) with videos related to

Sort By:
Pageof 40
Ophthalmic Surgery, Lasers & Imaging Retina|February 11, 2022
Exudative Retinal Detachment Following Chimeric Antigen Receptor T-Cell Therapy in Relapsed B-Cell Acute Lymphoblastic LeukemiaSaira Khanna, Anna G Mackin, David T Dao, et al.
Nature Genetics|May 1, 1996
The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3G A Nicholson, J L Dawkins, I P Blair, et al.
Applied Optics|December 15, 2010
Components for the implementation of free-space optical crossbarsC P Barrett, P Blair, G S Buller, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|November 9, 2019
Theme 3 In vitro experimental modelsShu Yang, Sharlynn Wu, Jennifer Fifita, et al.
Genomics|September 20, 1995
The mouse homolog of the Wiskott-Aldrich syndrome protein (WASP) gene is highly conserved and maps near the scurfy (sf) mutation on the X chromosomeJ M Derry, P Wiedemann, P Blair, et al.
Scientific Reports|August 22, 2015
Distinct partitioning of ALS associated TDP-43, FUS and SOD1 mutants into cellular inclusionsNatalie E Farrawell, Isabella A Lambert-Smith, Sadaf T Warraich, et al.
Neurobiology of Aging|June 22, 2012
UBQLN2/ubiquilin 2 mutation and pathology in familial amyotrophic lateral sclerosisKelly L Williams, Sadaf T Warraich, Shu Yang, et al.
Journal of Neuromuscular Diseases|August 28, 2023
Characterising the Genetic Landscape of Amyotrophic Lateral Sclerosis: A Catalogue and Assessment of Over 1,000 Published Genetic VariantsEmily P McCann, Natalie Grima, Jennifer A Fifita, et al.
Journal of Psychiatric Research|October 22, 2022
Ventral striatal subregional dysfunction in late-life grief: Relationships with yearning and depressive symptomsNutta-On P Blair, Alexander D Cohen, B Douglas Ward, et al.
Neurology|May 5, 1998
Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophyP A Silburn, G A Nicholson, B T Teh, et al.
Pageof 40