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Justin P Rubio

Showing results (21-30 of 39) with videos related to

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Immunogenetics|January 27, 2007
Analysis of extended HLA haplotypes in multiple sclerosis and narcolepsy families confirms a predisposing effect for the class I region in Tasmanian MS patientsJustin P Rubio, Melanie Bahlo, Jim Stankovich, et al.
Schizophrenia Research|December 13, 2016
Exome array analysis suggests an increased variant burden in families with schizophreniaNina S McCarthy, Phillip E Melton, Sarah V Ward, et al.
Human Genetics|March 12, 2004
Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosisJustin P Rubio, Melanie Bahlo, Niall Tubridy, et al.
Plos One|October 21, 2021
Transcriptomic effects of rs4845604, an IBD and allergy-associated RORC variant, in stimulated ex vivo CD4+ T cellsPaul A Wilson, Sara Santos Franco, Liu He, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 13, 2007
Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's diseaseYue Huang, Glenda M Halliday, Himesha Vandebona, et al.
Human Genetics|January 13, 2006
On the utility of data from the International HapMap Project for Australian association studiesJim Stankovich, Charles J Cox, Rachel B Tan, et al.
Novartis Foundation Symposium|July 8, 2005
Multiple sclerosis: a haplotype association studySimon J Foote, Justin P Rubio, Melanie Bahlo, et al.
Cell|December 16, 2011
SIRT1 activates MAO-A in the brain to mediate anxiety and exploratory driveSergiy Libert, Kelli Pointer, Eric L Bell, et al.
Plos One|April 7, 2010
Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patientsCathy J Jensen, Jim Stankovich, Anneke Van der Walt, et al.
Human Mutation|March 15, 2012
Deep sequencing of the LRRK2 gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in EuropeJustin P Rubio, Simon Topp, Liling Warren, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Immunogenetics|January 27, 2007
Analysis of extended HLA haplotypes in multiple sclerosis and narcolepsy families confirms a predisposing effect for the class I region in Tasmanian MS patientsJustin P Rubio, Melanie Bahlo, Jim Stankovich, et al.
Schizophrenia Research|December 13, 2016
Exome array analysis suggests an increased variant burden in families with schizophreniaNina S McCarthy, Phillip E Melton, Sarah V Ward, et al.
Human Genetics|March 12, 2004
Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosisJustin P Rubio, Melanie Bahlo, Niall Tubridy, et al.
Plos One|October 21, 2021
Transcriptomic effects of rs4845604, an IBD and allergy-associated RORC variant, in stimulated ex vivo CD4+ T cellsPaul A Wilson, Sara Santos Franco, Liu He, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 13, 2007
Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's diseaseYue Huang, Glenda M Halliday, Himesha Vandebona, et al.
Human Genetics|January 13, 2006
On the utility of data from the International HapMap Project for Australian association studiesJim Stankovich, Charles J Cox, Rachel B Tan, et al.
Novartis Foundation Symposium|July 8, 2005
Multiple sclerosis: a haplotype association studySimon J Foote, Justin P Rubio, Melanie Bahlo, et al.
Cell|December 16, 2011
SIRT1 activates MAO-A in the brain to mediate anxiety and exploratory driveSergiy Libert, Kelli Pointer, Eric L Bell, et al.
Plos One|April 7, 2010
Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patientsCathy J Jensen, Jim Stankovich, Anneke Van der Walt, et al.
Human Mutation|March 15, 2012
Deep sequencing of the LRRK2 gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in EuropeJustin P Rubio, Simon Topp, Liling Warren, et al.
Pageof 4