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1. A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis.

2. Author Correction: Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease (Nature Communications, (2020), 11, 1, (995), 10.1038/s41467-019-14275-y)

3. DOP07 Ulcerative Colitis associated single nucleotide polymorphisms found in transcription factor binding sites effect key pathogenesis pathways and facilitate patient stratification

4. Evidence for association of OCTN genes and IBD5 with ulcerative colitis

5. P88 The impact of NOD2 deficiency on the gut mycobiota in crohn’s disease patients in remission

8. NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease

9. IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes

10. Gender-stratified analysis of DLG5 R30Q in 4707 patients with Crohn disease and 4973 controls from 12 Caucasian cohorts

11. Association of Genetic Variants in NUDT15 With Thiopurine-Induced Myelosuppression in Patients With Inflammatory Bowel Disease

13. IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes

14. The impact of NOD2 variants on fecal microbiota in Crohn's Disease and controls without gastrointestinal disease

15. OP10 Systems genomics of ulcerative colitis: combining GWAS and signalling networks for patient stratification and individualised drug targeting in ulcerative colitis

16. The impact of NOD2 variants on fecal microbiota in Crohn's disease and controls without gastrointestinal disease

17. IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes

18. Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at $\textit{ADCY7}$

19. Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease

20. HLA-DQA1–HLA-DRB1 variants confer susceptibility to pancreatitis induced by thiopurine immunosuppressants

21. A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis

22. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

23. Inherited determinants of Crohn's disease and ulcerative colitis phenotypes:a genetic association study

24. Ustekinumab as induction and maintenance therapy for Crohn's disease

25. Genome-wide and fine-resolution association analysis of malaria in West Africa

26. Clinical Features and HLA Association of 5-Aminosalicylate (5-ASA)-induced Nephrotoxicity in Inflammatory Bowel Disease

27. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies

28. PWE-082 The Impact Of Nod2 Variants On Gut Microbiota In Crohn’s Disease And Healthy Controls

30. Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.

31. Common variants at five new loci associated with early-onset inflammatory bowel disease.

32. Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.

35. Gender-stratified analysis of DLG5 R30Q in 4707 patients with Crohn disease and 4973 controls from 12 Caucasian cohorts

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38. A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis

39. Severe colitis complicating secukinumab (Cosentyx®) therapy.

40. Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease

41. Genome-wide association study identifies eight loci associated with blood pressure

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