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Alan Pittman

Showing results (21-30 of 55) with videos related to

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Neurobiology of Aging|January 16, 2015
Investigation of next-generation sequencing technologies as a diagnostic tool for amyotrophic lateral sclerosisSarah Morgan, Maryam Shoai, Pietro Fratta, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 2, 2018
Younger age of onset in familial amyotrophic lateral sclerosis is a result of pathogenic gene variants, rather than ascertainment biasPuja R Mehta, Ashley R Jones, Sarah Opie-Martin, et al.
Neurobiology of Aging|October 14, 2014
Analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonismLucia V Schottlaender, James M Polke, Helen Ling, et al.
European Journal of Human Genetics : EJHG|March 20, 2019
De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genesNirmal Vadgama, Alan Pittman, Michael Simpson, et al.
Plos One|October 13, 2022
Investigation of clinical characteristics and genome associations in the 'UK Lipoedema' cohortDionysios Grigoriadis, Ege Sackey, Katie Riches, et al.
Open Forum Infectious Diseases|December 3, 2020
Genome-Wide Association Study Identifies Novel Colony Stimulating Factor 1 Locus Conferring Susceptibility to Cryptococcosis in Human Immunodeficiency Virus-Infected South AfricansShichina Kannambath, Joseph N Jarvis, Rachel M Wake, et al.
Brain : a Journal of Neurology|April 22, 2017
A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UKSarah Morgan, Aleksey Shatunov, William Sproviero, et al.
The Journal of Investigative Dermatology|June 19, 2024
RNA Therapy for Oncogenic NRAS-Driven Nevi Induces ApoptosisDale Bryant, Sara Barberan-Martin, Ruhina Maeshima, et al.
The Journal of Investigative Dermatology|September 16, 2023
Mosaic BRAF Fusions Are a Recurrent Cause of Congenital Melanocytic Nevi Targetable by MAPK Pathway InhibitionSara Barberan Martin, Satyamaanasa Polubothu, Alicia Lopez Bruzos, et al.
Neurology|July 11, 2014
Extended phenotypic spectrum of KIF5A mutations: From spastic paraplegia to axonal neuropathyYo-Tsen Liu, Matilde Laurá, Joshua Hersheson, et al.
Pageof 6

Showing results (21-30 of 55) with videos related to

Sort By:
Pageof 6
Neurobiology of Aging|January 16, 2015
Investigation of next-generation sequencing technologies as a diagnostic tool for amyotrophic lateral sclerosisSarah Morgan, Maryam Shoai, Pietro Fratta, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 2, 2018
Younger age of onset in familial amyotrophic lateral sclerosis is a result of pathogenic gene variants, rather than ascertainment biasPuja R Mehta, Ashley R Jones, Sarah Opie-Martin, et al.
Neurobiology of Aging|October 14, 2014
Analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonismLucia V Schottlaender, James M Polke, Helen Ling, et al.
European Journal of Human Genetics : EJHG|March 20, 2019
De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genesNirmal Vadgama, Alan Pittman, Michael Simpson, et al.
Plos One|October 13, 2022
Investigation of clinical characteristics and genome associations in the 'UK Lipoedema' cohortDionysios Grigoriadis, Ege Sackey, Katie Riches, et al.
Open Forum Infectious Diseases|December 3, 2020
Genome-Wide Association Study Identifies Novel Colony Stimulating Factor 1 Locus Conferring Susceptibility to Cryptococcosis in Human Immunodeficiency Virus-Infected South AfricansShichina Kannambath, Joseph N Jarvis, Rachel M Wake, et al.
Brain : a Journal of Neurology|April 22, 2017
A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UKSarah Morgan, Aleksey Shatunov, William Sproviero, et al.
The Journal of Investigative Dermatology|June 19, 2024
RNA Therapy for Oncogenic NRAS-Driven Nevi Induces ApoptosisDale Bryant, Sara Barberan-Martin, Ruhina Maeshima, et al.
The Journal of Investigative Dermatology|September 16, 2023
Mosaic BRAF Fusions Are a Recurrent Cause of Congenital Melanocytic Nevi Targetable by MAPK Pathway InhibitionSara Barberan Martin, Satyamaanasa Polubothu, Alicia Lopez Bruzos, et al.
Neurology|July 11, 2014
Extended phenotypic spectrum of KIF5A mutations: From spastic paraplegia to axonal neuropathyYo-Tsen Liu, Matilde Laurá, Joshua Hersheson, et al.
Pageof 6