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Genes and Immunity
|
June 20, 2008
Detailed assessment of NOD2/CARD15 exonic variation in inflammatory bowel disease in Scotland: implications for disease pathogenesis
R K Russell, H E Drummond, D C Wilson, et al.
Nature Communications
|
November 26, 2016
Integrative epigenome-wide analysis demonstrates that DNA methylation may mediate genetic risk in inflammatory bowel disease
N T Ventham, N A Kennedy, A T Adams, et al.
Genes and Immunity
|
June 11, 2004
NOD2/CARD15, TLR4 and CD14 mutations in Scottish and Irish Crohn's disease patients: evidence for genetic heterogeneity within Europe?
I D R Arnott, E R Nimmo, H E Drummond, et al.
The Journal of Pediatrics
|
February 20, 2007
The contribution of the DLG5 113A variant in early-onset inflammatory bowel disease
R K Russell, H E Drummond, E R Nimmo, et al.
Gut
|
February 14, 2006
Analysis of the influence of OCTN1/2 variants within the IBD5 locus on disease susceptibility and growth indices in early onset inflammatory bowel disease
R K Russell, H E Drummond, E R Nimmo, et al.
Gut
|
March 6, 2007
IL23R Arg381Gln is associated with childhood onset inflammatory bowel disease in Scotland
J Van Limbergen, R K Russell, E R Nimmo, et al.
Inflammatory Bowel Diseases
|
May 2, 2009
Filaggrin loss-of-function variants are associated with atopic comorbidity in pediatric inflammatory bowel disease
J Van Limbergen, R K Russell, E R Nimmo, et al.
Inflammatory Bowel Diseases
|
December 20, 2007
Autophagy gene ATG16L1 influences susceptibility and disease location but not childhood-onset in Crohn's disease in Northern Europe
J Van Limbergen, R K Russell, E R Nimmo, et al.
Inflammatory Bowel Diseases
|
February 8, 2007
Contribution of the NOD1/CARD4 insertion/deletion polymorphism +32656 to inflammatory bowel disease in Northern Europe
J Van Limbergen, R K Russell, E R Nimmo, et al.
Journal of Medical Genetics
|
August 19, 2007
Gender-stratified analysis of DLG5 R30Q in 4707 patients with Crohn disease and 4973 controls from 12 Caucasian cohorts
B L Browning, V Annese, M L Barclay, et al.
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of 3
Search research articles
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Showing results (21-30 of 30) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 30 results.
Genes and Immunity
|
June 20, 2008
Detailed assessment of NOD2/CARD15 exonic variation in inflammatory bowel disease in Scotland: implications for disease pathogenesis
R K Russell, H E Drummond, D C Wilson, et al.
Nature Communications
|
November 26, 2016
Integrative epigenome-wide analysis demonstrates that DNA methylation may mediate genetic risk in inflammatory bowel disease
N T Ventham, N A Kennedy, A T Adams, et al.
Genes and Immunity
|
June 11, 2004
NOD2/CARD15, TLR4 and CD14 mutations in Scottish and Irish Crohn's disease patients: evidence for genetic heterogeneity within Europe?
I D R Arnott, E R Nimmo, H E Drummond, et al.
The Journal of Pediatrics
|
February 20, 2007
The contribution of the DLG5 113A variant in early-onset inflammatory bowel disease
R K Russell, H E Drummond, E R Nimmo, et al.
Gut
|
February 14, 2006
Analysis of the influence of OCTN1/2 variants within the IBD5 locus on disease susceptibility and growth indices in early onset inflammatory bowel disease
R K Russell, H E Drummond, E R Nimmo, et al.
Gut
|
March 6, 2007
IL23R Arg381Gln is associated with childhood onset inflammatory bowel disease in Scotland
J Van Limbergen, R K Russell, E R Nimmo, et al.
Inflammatory Bowel Diseases
|
May 2, 2009
Filaggrin loss-of-function variants are associated with atopic comorbidity in pediatric inflammatory bowel disease
J Van Limbergen, R K Russell, E R Nimmo, et al.
Inflammatory Bowel Diseases
|
December 20, 2007
Autophagy gene ATG16L1 influences susceptibility and disease location but not childhood-onset in Crohn's disease in Northern Europe
J Van Limbergen, R K Russell, E R Nimmo, et al.
Inflammatory Bowel Diseases
|
February 8, 2007
Contribution of the NOD1/CARD4 insertion/deletion polymorphism +32656 to inflammatory bowel disease in Northern Europe
J Van Limbergen, R K Russell, E R Nimmo, et al.
Journal of Medical Genetics
|
August 19, 2007
Gender-stratified analysis of DLG5 R30Q in 4707 patients with Crohn disease and 4973 controls from 12 Caucasian cohorts
B L Browning, V Annese, M L Barclay, et al.
Page
of 3