Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Olubunmi Abel

Showing results (1-10 of 8) with videos related to

Pageof 1
Sort By:
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|June 28, 2011
Keeping up with genetic discoveries in amyotrophic lateral sclerosis: the ALSoD and ALSGene databasesChristina M Lill, Olubunmi Abel, Lars Bertram, et al.
Human Mutation|July 4, 2012
ALSoD: A user-friendly online bioinformatics tool for amyotrophic lateral sclerosis geneticsOlubunmi Abel, John F Powell, Peter M Andersen, et al.
Plos One|June 12, 2013
Credibility analysis of putative disease-causing genes using bioinformaticsOlubunmi Abel, John F Powell, Peter M Andersen, et al.
JMIR Mhealth and Uhealth|August 8, 2014
Development of a Smartphone App for a Genetics Website: The Amyotrophic Lateral Sclerosis Online Genetics Database (ALSoD)Olubunmi Abel, Aleksey Shatunov, Ashley R Jones, et al.
Neurobiology of Aging|April 17, 2013
Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeatAshley R Jones, Ione Woollacott, Aleksey Shatunov, et al.
The Lancet. Neurology|August 31, 2010
Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association studyAleksey Shatunov, Kin Mok, Stephen Newhouse, et al.
Nature Communications|July 2, 2024
Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease durationSarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp, et al.
Nature Communications|November 13, 2022
The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease durationSarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|June 28, 2011
Keeping up with genetic discoveries in amyotrophic lateral sclerosis: the ALSoD and ALSGene databasesChristina M Lill, Olubunmi Abel, Lars Bertram, et al.
Human Mutation|July 4, 2012
ALSoD: A user-friendly online bioinformatics tool for amyotrophic lateral sclerosis geneticsOlubunmi Abel, John F Powell, Peter M Andersen, et al.
Plos One|June 12, 2013
Credibility analysis of putative disease-causing genes using bioinformaticsOlubunmi Abel, John F Powell, Peter M Andersen, et al.
JMIR Mhealth and Uhealth|August 8, 2014
Development of a Smartphone App for a Genetics Website: The Amyotrophic Lateral Sclerosis Online Genetics Database (ALSoD)Olubunmi Abel, Aleksey Shatunov, Ashley R Jones, et al.
Neurobiology of Aging|April 17, 2013
Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeatAshley R Jones, Ione Woollacott, Aleksey Shatunov, et al.
The Lancet. Neurology|August 31, 2010
Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association studyAleksey Shatunov, Kin Mok, Stephen Newhouse, et al.
Nature Communications|July 2, 2024
Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease durationSarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp, et al.
Nature Communications|November 13, 2022
The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease durationSarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp, et al.
Pageof 1