Török HP, Bellon V, Konrad A, Lacher M, Tonenchi L, Siebeck M, Brand S, De
Toni EN. Functional Toll-Like Receptor (TLR)2 polymorphisms in the susceptibility
to inflammatory bowel disease. PLoS One. 2017 Apr 7;12(4):e0175180
Ginzel M, Yu Y, Klemann C, Feng X, von Wasielewski R, Park JK, Hornef MW, Torow N, Vieten G, Ure BM, Kuebler JF, Lacher M. The viral dsRNA analogue poly (I:C) induces necrotizing enterocolitis in neonatal mice. Pediatr Res. 2016 Apr;79(4):596-602.
Yu Y, Klemann C, Feng X, Ginzel M, Vieten G, Lacher M, Ure B, Kuebler JF.
Increased inflammatory reaction to intestinal ischemia-reperfusion in neonatal
versus adult mice. Eur J Pediatr Surg. 2015 Feb;25(1):46-50
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. Strong overexpression of CXCR3 axis components in childhood inflammatory bowel disease. Inflamm Bowel Dis. 2010 Nov;16(11):1882-90
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. NOD2 mutations predict the risk for surgery in pediatric-onset Crohn's disease. J Pediatr Surg. 2010 Aug;45(8):1591-7
Marcos V, Latzin P, Hector A, Sonanini S, Hoffmann F, Lacher M, Koller B, Bufler P, Nicolai T, Hartl D, Griese M. Expression, regulation and clinical significance of soluble and membrane CD14 receptors in pediatric inflammatory lung diseases. Respir Res. 2010 Mar 19;11:32
Lacher M, Schroepf S, Helmbrecht J, von Schweinitz D, Ballauff A, Koch I, Lohse P, Osterrieder S, Kappler R, Koletzko S. Association of the interleukin-23 receptor gene variant rs11209026 with Crohn's disease in German children. ActaPaediatr. 2010 May;99(5):727-33
Glocker EO, Kotlarz D, Boztug K, GertzEM, 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. Inflammatory bowel disease and mutations affecting the interleukin-10 receptor.
N Engl J Med. 2009 Nov 19;361(21):2033-45
Lacher M, Schroepf S, Ballauff A, Lohse P, von Schweinitz D, Kappler R, Koletzko S. Autophagy 16-like 1 rs2241880 G allele is associated with Crohn's disease in German children. ActaPaediatr. 2009 Nov;98(11):1835-40
Lacher M, Kappler R, Schroepf S, Berkholz S, Ballauff A, Bufler P, Baurecht H, von Schweinitz D, Koletzko S. Nuclear pregnane X receptor single nucleotide polymorphism (-25385C/T) is not associated with inflammatory bowel disease in pediatric patients. J PediatrGastroenterolNutr. 2009 Jul;49(1):147-50
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. 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. Am J Gastroenterol. 2009 Jul;104(7):1737-44
Lacher M, Kappler R, Berkholz S, Baurecht H, von Schweinitz D, Koletzko S. Association of a CXCL9 polymorphism with pediatric Crohn's disease. BiochemBiophys Res Commun. 2007 Nov 23;363(3):701-7
Schröder W, Stippel D, Lacher M, Gutschow CA, BeckurtsKT, Hölscher AH. Does continuous mucosal partial carbon dioxide pressure measurement predict leakage ofintrathoracic esophagogastrostomy? Ann Thorac Surg. 2002 Dec;74(6):1917-22
Schröder W, Stippel D, BeckurtsKT, Lacher M, Gutschow C, Hölscher AH. Intraoperative changes of mucosal pCO2 during gastric tube formation. Langenbecks Arch Surg. 2001 Aug;386(5):324-7