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Alan Pittman

Showing results (11-20 of 55) with videos related to

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Scientific Reports|December 13, 2025
Further characterisation of immortalised human lymphatic endothelial cells to explore their transcriptomic profile and VEGFC responseKazim Ogmen, Ruby Moy, Sara E Dobbins, et al.
Neurobiology of Aging|August 29, 2007
Clinical and pathological features of an Alzheimer's disease patient with the MAPT Delta K280 mutationParastoo Momeni, Alan Pittman, Tammaryn Lashley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 15, 2021
Impaired Pre-Motor Circuit Activity and Movement in a Drosophila Model of KCNMA1-Linked DyskinesiaPatrick Kratschmer, Simon A Lowe, Edgar Buhl, et al.
Brain : a Journal of Neurology|March 25, 2005
Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonismDavid R Williams, Rohan de Silva, Dominic C Paviour, et al.
Journal of Medical Case Reports|April 6, 2023
Presacral malakoplakia presenting as foot drop: a case reportTom A Yates, Katie Devlin, Abed Arnaout, et al.
Neuroscience Letters|October 7, 2004
The tau H2 haplotype is almost exclusively Caucasian in originWhitney Evans, Hon Chung Fung, John Steele, et al.
The Journal of Infectious Diseases|August 19, 2024
Ex Vivo Host Transcriptomics During Cryptococcus neoformans, Cryptococcus gattii, and Candida albicans Infection of Peripheral Blood Mononuclear Cells From South African VolunteersRonan M Doyle, Shichina Kannambath, Alan Pittman, et al.
Acta Neuropathologica|December 11, 2007
MAPT S305I mutation: implications for argyrophilic grain diseaseGabor G Kovacs, Alan Pittman, Tamas Revesz, et al.
The Journal of Investigative Dermatology|November 10, 2019
Allele-Specific Small Interfering RNA Corrects Aberrant Cellular Phenotype in Keratitis-Ichthyosis-Deafness Syndrome KeratinocytesMing Yang Lee, Hong-Zhan Wang, Thomas W White, et al.
Molecular Genetics & Genomic Medicine|September 16, 2020
Novel mutation identification and copy number variant detection via exome sequencing in congenital muscular dystrophyEdmund S Cauley, Alan Pittman, Swati Mummidivarpu, et al.
Pageof 6

Showing results (11-20 of 55) with videos related to

Sort By:
Pageof 6
Scientific Reports|December 13, 2025
Further characterisation of immortalised human lymphatic endothelial cells to explore their transcriptomic profile and VEGFC responseKazim Ogmen, Ruby Moy, Sara E Dobbins, et al.
Neurobiology of Aging|August 29, 2007
Clinical and pathological features of an Alzheimer's disease patient with the MAPT Delta K280 mutationParastoo Momeni, Alan Pittman, Tammaryn Lashley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 15, 2021
Impaired Pre-Motor Circuit Activity and Movement in a Drosophila Model of KCNMA1-Linked DyskinesiaPatrick Kratschmer, Simon A Lowe, Edgar Buhl, et al.
Brain : a Journal of Neurology|March 25, 2005
Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonismDavid R Williams, Rohan de Silva, Dominic C Paviour, et al.
Journal of Medical Case Reports|April 6, 2023
Presacral malakoplakia presenting as foot drop: a case reportTom A Yates, Katie Devlin, Abed Arnaout, et al.
Neuroscience Letters|October 7, 2004
The tau H2 haplotype is almost exclusively Caucasian in originWhitney Evans, Hon Chung Fung, John Steele, et al.
The Journal of Infectious Diseases|August 19, 2024
Ex Vivo Host Transcriptomics During Cryptococcus neoformans, Cryptococcus gattii, and Candida albicans Infection of Peripheral Blood Mononuclear Cells From South African VolunteersRonan M Doyle, Shichina Kannambath, Alan Pittman, et al.
Acta Neuropathologica|December 11, 2007
MAPT S305I mutation: implications for argyrophilic grain diseaseGabor G Kovacs, Alan Pittman, Tamas Revesz, et al.
The Journal of Investigative Dermatology|November 10, 2019
Allele-Specific Small Interfering RNA Corrects Aberrant Cellular Phenotype in Keratitis-Ichthyosis-Deafness Syndrome KeratinocytesMing Yang Lee, Hong-Zhan Wang, Thomas W White, et al.
Molecular Genetics & Genomic Medicine|September 16, 2020
Novel mutation identification and copy number variant detection via exome sequencing in congenital muscular dystrophyEdmund S Cauley, Alan Pittman, Swati Mummidivarpu, et al.
Pageof 6