Lacher M - Search Results

1

Inflammatory bowel disease and mutations affecting the interleukin-10 receptor.

Glocker EO, Kotlarz D, Boztug K, Gertz EM, Schäffer AA, Noyan F, Perro M, Diestelhorst J, Allroth A, Murugan D, Hätscher N, Pfeifer D, Sykora KW, Sauer M, Kreipe H, Lacher M, Nustede R, Woellner C, Baumann U, Salzer U, Koletzko S, Shah N, Segal AW, Sauerbrey A, Buderus S, Snapper SB, Grimbacher B, Klein C. Glocker EO, et al. Among authors: lacher m. N Engl J Med. 2009 Nov 19;361(21):2033-45. doi: 10.1056/NEJMoa0907206. Epub 2009 Nov 4. N Engl J Med. 2009. PMID: 19890111 Free PMC article.

2

Nuclear pregnane X receptor single nucleotide polymorphism (-25385C/T) is not associated with inflammatory bowel disease in pediatric patients.

Lacher M, Kappler R, Schroepf S, Berkholz S, Ballauff A, Bufler P, Baurecht H, von Schweinitz D, Koletzko S. Lacher M, et al. J Pediatr Gastroenterol Nutr. 2009 Jul;49(1):147-50. doi: 10.1097/MPG.0b013e31818de1a8. J Pediatr Gastroenterol Nutr. 2009. PMID: 19516190

3

Association of a CXCL9 polymorphism with pediatric Crohn's disease.

Lacher M, Kappler R, Berkholz S, Baurecht H, von Schweinitz D, Koletzko S. Lacher M, et al. Biochem Biophys Res Commun. 2007 Nov 23;363(3):701-7. doi: 10.1016/j.bbrc.2007.09.020. Epub 2007 Sep 18. Biochem Biophys Res Commun. 2007. PMID: 17892861

4

Association of the interleukin-23 receptor gene variant rs11209026 with Crohn's disease in German children.

Lacher M, Schroepf S, Helmbrecht J, Von Schweinitz D, Ballauff A, Koch I, Lohse P, Osterrieder S, Kappler R, Koletzko S. Lacher M, et al. Acta Paediatr. 2010 May;99(5):727-733. doi: 10.1111/j.1651-2227.2009.01680.x. Epub 2010 Feb 26. Acta Paediatr. 2010. PMID: 20192940

5

Strong overexpression of CXCR3 axis components in childhood inflammatory bowel disease.

Schroepf S, Kappler R, Brand S, Prell C, Lohse P, Glas J, Hoster E, Helmbrecht J, Ballauff A, Berger M, von Schweinitz D, Koletzko S, Lacher M. Schroepf S, et al. Among authors: lacher m. Inflamm Bowel Dis. 2010 Nov;16(11):1882-90. doi: 10.1002/ibd.21312. Inflamm Bowel Dis. 2010. PMID: 20848514

6

Autophagy 16-like 1 rs2241880 G allele is associated with Crohn's disease in German children.

Lacher M, Schroepf S, Ballauff A, Lohse P, von Schweinitz D, Kappler R, Koletzko S. Lacher M, et al. Acta Paediatr. 2009 Nov;98(11):1835-40. doi: 10.1111/j.1651-2227.2009.01438.x. Epub 2009 Jul 29. Acta Paediatr. 2009. PMID: 19659808

7

NOD2 mutations predict the risk for surgery in pediatric-onset Crohn's disease.

Lacher M, Helmbrecht J, Schroepf S, Koletzko S, Ballauff A, Classen M, Uhlig H, Hubertus J, Hartl D, Lohse P, von Schweinitz D, Kappler R. Lacher M, et al. J Pediatr Surg. 2010 Aug;45(8):1591-7. doi: 10.1016/j.jpedsurg.2009.10.046. J Pediatr Surg. 2010. PMID: 20713205

8

Novel genetic risk markers for ulcerative colitis in the IL2/IL21 region are in epistasis with IL23R and suggest a common genetic background for ulcerative colitis and celiac disease.

Glas J, Stallhofer J, Ripke S, Wetzke M, Pfennig S, Klein W, Epplen JT, Griga T, Schiemann U, Lacher M, Koletzko S, Folwaczny M, Lohse P, Göke B, Ochsenkühn T, Müller-Myhsok B, Brand S. Glas J, et al. Among authors: lacher m. Am J Gastroenterol. 2009 Jul;104(7):1737-44. doi: 10.1038/ajg.2009.163. Epub 2009 May 19. Am J Gastroenterol. 2009. PMID: 19455118

9

Hirschsprung-associated enterocolitis develops independently of NOD2 variants.

Lacher M, Fitze G, Helmbrecht J, Schroepf S, Berger M, Lohse P, Koletzko S, Ballauff A, Grote V, Goedeke J, von Schweinitz D, Kappler R. Lacher M, et al. J Pediatr Surg. 2010 Sep;45(9):1826-31. doi: 10.1016/j.jpedsurg.2010.02.039. J Pediatr Surg. 2010. PMID: 20850627

10

Functional Toll-Like Receptor (TLR)2 polymorphisms in the susceptibility to inflammatory bowel disease.

Török HP, Bellon V, Konrad A, Lacher M, Tonenchi L, Siebeck M, Brand S, De Toni EN. Török HP, et al. Among authors: lacher m. PLoS One. 2017 Apr 7;12(4):e0175180. doi: 10.1371/journal.pone.0175180. eCollection 2017. PLoS One. 2017. PMID: 28388655 Free PMC article.

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