Search research articles
Contact Us
Filters
Showing results (11-20 of 55) with videos related to
Page
of 6
Sort By:
Scientific Reports
|
December 13, 2025
Further characterisation of immortalised human lymphatic endothelial cells to explore their transcriptomic profile and VEGFC response
Kazim 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 mutation
Parastoo 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 Dyskinesia
Patrick 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-parkinsonism
David 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 report
Tom A Yates, Katie Devlin, Abed Arnaout, et al.
Neuroscience Letters
|
October 7, 2004
The tau H2 haplotype is almost exclusively Caucasian in origin
Whitney 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 Volunteers
Ronan M Doyle, Shichina Kannambath, Alan Pittman, et al.
Acta Neuropathologica
|
December 11, 2007
MAPT S305I mutation: implications for argyrophilic grain disease
Gabor 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 Keratinocytes
Ming 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 dystrophy
Edmund S Cauley, Alan Pittman, Swati Mummidivarpu, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 55) with videos related to
Sort By:
Page
of 6
Scientific Reports
|
December 13, 2025
Further characterisation of immortalised human lymphatic endothelial cells to explore their transcriptomic profile and VEGFC response
Kazim 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 mutation
Parastoo 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 Dyskinesia
Patrick 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-parkinsonism
David 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 report
Tom A Yates, Katie Devlin, Abed Arnaout, et al.
Neuroscience Letters
|
October 7, 2004
The tau H2 haplotype is almost exclusively Caucasian in origin
Whitney 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 Volunteers
Ronan M Doyle, Shichina Kannambath, Alan Pittman, et al.
Acta Neuropathologica
|
December 11, 2007
MAPT S305I mutation: implications for argyrophilic grain disease
Gabor 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 Keratinocytes
Ming 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 dystrophy
Edmund S Cauley, Alan Pittman, Swati Mummidivarpu, et al.
Page
of 6