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Immunogenetics
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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 patients
Justin P Rubio, Melanie Bahlo, Jim Stankovich, et al.
Schizophrenia Research
|
December 13, 2016
Exome array analysis suggests an increased variant burden in families with schizophrenia
Nina 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 sclerosis
Justin 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 cells
Paul 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 disease
Yue 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 studies
Jim Stankovich, Charles J Cox, Rachel B Tan, et al.
Novartis Foundation Symposium
|
July 8, 2005
Multiple sclerosis: a haplotype association study
Simon 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 drive
Sergiy 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 patients
Cathy 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 Europe
Justin P Rubio, Simon Topp, Liling Warren, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 39) with videos related to
Sort By:
Page
of 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 patients
Justin P Rubio, Melanie Bahlo, Jim Stankovich, et al.
Schizophrenia Research
|
December 13, 2016
Exome array analysis suggests an increased variant burden in families with schizophrenia
Nina 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 sclerosis
Justin 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 cells
Paul 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 disease
Yue 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 studies
Jim Stankovich, Charles J Cox, Rachel B Tan, et al.
Novartis Foundation Symposium
|
July 8, 2005
Multiple sclerosis: a haplotype association study
Simon 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 drive
Sergiy 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 patients
Cathy 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 Europe
Justin P Rubio, Simon Topp, Liling Warren, et al.
Page
of 4