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British Journal of Haematology
|
June 22, 2010
Evidence for a common genetic aetiology in high-risk families with multiple haematological malignancy subtypes
Elizabeth M Tegg, Russell J Thomson, Jim Stankovich, et al.
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.
Arthritis Research & Therapy
|
October 22, 2014
An Immunochip-based interrogation of scleroderma susceptibility variants identifies a novel association at DNASE1L3
Jane Zochling, Felicity Newell, Jac C Charlesworth, et al.
European Journal of Neurology
|
September 11, 2020
Speech metrics, general disability, brain imaging and quality of life in multiple sclerosis
G Noffs, F M C Boonstra, T Perera, et al.
BMC Infectious Diseases
|
October 9, 2012
Investigating a cluster of vulvar cancer in young women: a cross-sectional study of genital human papillomavirus prevalence
Alice R Rumbold, Sarah E Tan, John R Condon, et al.
Biochemistry
|
January 10, 1998
Iron-sulfur cluster cysteine-to-serine mutants of Anabaena -2Fe-2S- ferredoxin exhibit unexpected redox properties and are competent in electron transfer to ferredoxin:NADP+ reductase
J K Hurley, A M Weber-Main, A E Hodges, et al.
European Journal of Human Genetics : EJHG
|
October 3, 2008
Identification of a prostate cancer susceptibility gene on chromosome 5p13q12 associated with risk of both familial and sporadic disease
Liesel M FitzGerald, Briony Patterson, Russell Thomson, 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.
The Journal of Steroid Biochemistry and Molecular Biology
|
February 12, 2013
Vitamin D status: multifactorial contribution of environment, genes and other factors in healthy Australian adults across a latitude gradient
Robyn M Lucas, Anne-Louise Ponsonby, Keith Dear, et al.
Human Genetics
|
April 22, 2010
Genome-wide linkage scan and association study of PARL to the expression of LHON families in Thailand
Nopasak Phasukkijwatana, Bussaraporn Kunhapan, Jim Stankovich, et al.
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of 21
Search research articles
Search
Showing results (161-170 of 203) with videos related to
Sort By:
Page
of 21
British Journal of Haematology
|
June 22, 2010
Evidence for a common genetic aetiology in high-risk families with multiple haematological malignancy subtypes
Elizabeth M Tegg, Russell J Thomson, Jim Stankovich, et al.
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.
Arthritis Research & Therapy
|
October 22, 2014
An Immunochip-based interrogation of scleroderma susceptibility variants identifies a novel association at DNASE1L3
Jane Zochling, Felicity Newell, Jac C Charlesworth, et al.
European Journal of Neurology
|
September 11, 2020
Speech metrics, general disability, brain imaging and quality of life in multiple sclerosis
G Noffs, F M C Boonstra, T Perera, et al.
BMC Infectious Diseases
|
October 9, 2012
Investigating a cluster of vulvar cancer in young women: a cross-sectional study of genital human papillomavirus prevalence
Alice R Rumbold, Sarah E Tan, John R Condon, et al.
Biochemistry
|
January 10, 1998
Iron-sulfur cluster cysteine-to-serine mutants of Anabaena -2Fe-2S- ferredoxin exhibit unexpected redox properties and are competent in electron transfer to ferredoxin:NADP+ reductase
J K Hurley, A M Weber-Main, A E Hodges, et al.
European Journal of Human Genetics : EJHG
|
October 3, 2008
Identification of a prostate cancer susceptibility gene on chromosome 5p13q12 associated with risk of both familial and sporadic disease
Liesel M FitzGerald, Briony Patterson, Russell Thomson, 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.
The Journal of Steroid Biochemistry and Molecular Biology
|
February 12, 2013
Vitamin D status: multifactorial contribution of environment, genes and other factors in healthy Australian adults across a latitude gradient
Robyn M Lucas, Anne-Louise Ponsonby, Keith Dear, et al.
Human Genetics
|
April 22, 2010
Genome-wide linkage scan and association study of PARL to the expression of LHON families in Thailand
Nopasak Phasukkijwatana, Bussaraporn Kunhapan, Jim Stankovich, et al.
Page
of 21