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Respiratory Research
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July 16, 2008
The TNFalpha gene relates to clinical phenotype in alpha-1-antitrypsin deficiency
Alice M Wood, Matthew J Simmonds, Darren L Bayley, et al.
Clinical Endocrinology
|
July 15, 2010
Association of Fc receptor-like 5 (FCRL5) with Graves' disease is secondary to the effect of FCRL3
Matthew J Simmonds, Oliver J Brand, Jeffrey C Barrett, et al.
Arthritis and Rheumatism
|
November 13, 2002
A nonsense mutation in exon 2 of the DNase I gene is not present in UK subjects with systemic lupus erythematosus and Graves' disease: Comment on the article by Rood et al
Matthew J Simmonds, Joanne M Heward, M Ann Kelly, et al.
Human Molecular Genetics
|
June 29, 2007
A novel and major association of HLA-C in Graves' disease that eclipses the classical HLA-DRB1 effect
Matthew J Simmonds, Joanna M M Howson, Joanne M Heward, et al.
Clinical Endocrinology
|
February 13, 2010
Association of FcGRIIa with Graves' disease: a potential role for dysregulated autoantibody clearance in disease onset/progression
Kadija Yesmin, Chantal Hargreaves, Paul R Newby, et al.
Transplantation
|
March 19, 2013
Skewing of female X-chromosome inactivation: an epigenetic risk factor for kidney transplantation outcome
Matthew J Simmonds, David Benavente, Oliver J Brand, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 5, 2013
Skewed X chromosome inactivation and female preponderance in autoimmune thyroid disease: an association study and meta-analysis
Matthew J Simmonds, Fotini K Kavvoura, Oliver J Brand, et al.
Plos One
|
December 3, 2010
Thyroid stimulating hormone receptor (TSHR) intron 1 variants are major risk factors for Graves' disease in three European Caucasian cohorts
Rafał Płoski, Oliver J Brand, Beata Jurecka-Lubieniecka, et al.
Plos Genetics
|
August 11, 2011
Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases
Vincent Plagnol, Joanna M M Howson, Deborah J Smyth, et al.
Human Molecular Genetics
|
August 28, 2012
Seven newly identified loci for autoimmune thyroid disease
Jason D Cooper, Matthew J Simmonds, Neil M Walker, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 36) with videos related to
Sort By:
Page
of 4
Respiratory Research
|
July 16, 2008
The TNFalpha gene relates to clinical phenotype in alpha-1-antitrypsin deficiency
Alice M Wood, Matthew J Simmonds, Darren L Bayley, et al.
Clinical Endocrinology
|
July 15, 2010
Association of Fc receptor-like 5 (FCRL5) with Graves' disease is secondary to the effect of FCRL3
Matthew J Simmonds, Oliver J Brand, Jeffrey C Barrett, et al.
Arthritis and Rheumatism
|
November 13, 2002
A nonsense mutation in exon 2 of the DNase I gene is not present in UK subjects with systemic lupus erythematosus and Graves' disease: Comment on the article by Rood et al
Matthew J Simmonds, Joanne M Heward, M Ann Kelly, et al.
Human Molecular Genetics
|
June 29, 2007
A novel and major association of HLA-C in Graves' disease that eclipses the classical HLA-DRB1 effect
Matthew J Simmonds, Joanna M M Howson, Joanne M Heward, et al.
Clinical Endocrinology
|
February 13, 2010
Association of FcGRIIa with Graves' disease: a potential role for dysregulated autoantibody clearance in disease onset/progression
Kadija Yesmin, Chantal Hargreaves, Paul R Newby, et al.
Transplantation
|
March 19, 2013
Skewing of female X-chromosome inactivation: an epigenetic risk factor for kidney transplantation outcome
Matthew J Simmonds, David Benavente, Oliver J Brand, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 5, 2013
Skewed X chromosome inactivation and female preponderance in autoimmune thyroid disease: an association study and meta-analysis
Matthew J Simmonds, Fotini K Kavvoura, Oliver J Brand, et al.
Plos One
|
December 3, 2010
Thyroid stimulating hormone receptor (TSHR) intron 1 variants are major risk factors for Graves' disease in three European Caucasian cohorts
Rafał Płoski, Oliver J Brand, Beata Jurecka-Lubieniecka, et al.
Plos Genetics
|
August 11, 2011
Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases
Vincent Plagnol, Joanna M M Howson, Deborah J Smyth, et al.
Human Molecular Genetics
|
August 28, 2012
Seven newly identified loci for autoimmune thyroid disease
Jason D Cooper, Matthew J Simmonds, Neil M Walker, et al.
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of 4