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The role of the selenoprotein S (SELS) gene -105G>A promoter polymorphism in inflammatory bowel disease and regulation of SELS gene expression in intestinal inflammation
The role of the selenoprotein S (SELS) gene -105G>A promoter polymorphism in inflammatory bowel disease and regulation of SELS gene expression in intestinal inflammation
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The role of the selenoprotein S (SELS) gene -105G>A promoter polymorphism in inflammatory bowel disease and regulation of SELS gene expression in intestinal inflammation

Seiderer, J ; Dambacher, J ; Kühnlein, B ; Pfennig, S ; Konrad, A ; Haller, D ; Göke, B ; Ochsenkühn, T ; Lohse, P ; Brand, S

Zeitschrift für Gastroenterologie, 2007, Vol.45 (8) [Periódico revisado por pares]

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2
The disease susceptibility risk mediated by gene variants in PHOX2B, NCF4, FAM92B, and in the intergenic region on chromosome 10q21.1 differs between North American and European patients with Crohn's disease
The disease susceptibility risk mediated by gene variants in PHOX2B, NCF4, FAM92B, and in the intergenic region on chromosome 10q21.1 differs between North American and European patients with Crohn's disease
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The disease susceptibility risk mediated by gene variants in PHOX2B, NCF4, FAM92B, and in the intergenic region on chromosome 10q21.1 differs between North American and European patients with Crohn's disease

Diegelmann, J ; Glas, J ; Seiderer, J ; Pasciuto, G ; Tillack, C ; Konrad, A ; Török, HP ; Pfennig, S ; Schiemann, U ; Klein, W ; Epplen, JT ; Griga, T ; Lohse, P ; Göke, B ; Ochsenkühn, T ; Folwaczny, M ; Müller-Myhsok, B ; Brand, S

Zeitschrift für Gastroenterologie, 2008, Vol.46 (9) [Periódico revisado por pares]

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3
The +1059G/C polymorphism in the CRP gene is associated with decreased serum CRP levels and involvement of the terminal ileum in patients with Crohn's disease
The +1059G/C polymorphism in the CRP gene is associated with decreased serum CRP levels and involvement of the terminal ileum in patients with Crohn's disease
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The +1059G/C polymorphism in the CRP gene is associated with decreased serum CRP levels and involvement of the terminal ileum in patients with Crohn's disease

Thalmaier, D ; Dambacher, J ; Seiderer, J ; Konrad, A ; Schachinger, V ; Pfennig, S ; Otte, JM ; Crispin, A ; Göke, B ; Ochsenkühn, T ; Lohse, P ; Brand, S

Zeitschrift für Gastroenterologie, 2006, Vol.44 (10) [Periódico revisado por pares]

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4
The macrophage migration inhibitory factor (MIF) –173G/C promoter polymorphism influences upper gastrointestinal tract involvement and disease activity in patients with Crohn's disease
The macrophage migration inhibitory factor (MIF) –173G/C promoter polymorphism influences upper gastrointestinal tract involvement and disease activity in patients with Crohn's disease
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The macrophage migration inhibitory factor (MIF) –173G/C promoter polymorphism influences upper gastrointestinal tract involvement and disease activity in patients with Crohn's disease

Dambacher, J ; Staudinger, T ; Seiderer, J ; Sisic, Z ; Schnitzler, F ; Pfennig, S ; Hofbauer, K ; Konrad, A ; Tillack, C ; Otte, JM ; Diebold, J ; Göke, B ; Ochsenkühn, T ; Lohse, P ; Brand, S

Zeitschrift für Gastroenterologie, 2006, Vol.44 (10) [Periódico revisado por pares]

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5
IL23R variants are associated with inflammatory bowel disease in the German population
IL23R variants are associated with inflammatory bowel disease in the German population
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IL23R variants are associated with inflammatory bowel disease in the German population

Glas, J ; Seiderer, J ; Wetzke, M ; Konrad, A ; Török, HP ; Schmechel, S ; Tonenchi, L ; Grassl, C ; Dambacher, J ; Pfennig, S ; Maier, K ; Griga, T ; Klein, W ; Epplen, J ; Schiemann, U ; Folwaczny, C ; Lohse, P ; Göke, B ; Ochsenkühn, T ; Müller-Myhsok, B ; Folwaczny, M ; Mussack, T ; Brand, S

Zeitschrift für Gastroenterologie, 2007, Vol.45 (8) [Periódico revisado por pares]

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6
Der TLR4-Asp299Gly-Polymorphismus ist mit Morbus Crohn assoziiert
Der TLR4-Asp299Gly-Polymorphismus ist mit Morbus Crohn assoziiert
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Der TLR4-Asp299Gly-Polymorphismus ist mit Morbus Crohn assoziiert

Brand, S ; Staudinger, T ; Hofbauer, K ; Schnitzler, F ; Seiderer, J ; Tillack, C ; Konrad, A ; Göke, B ; Ochsenkühn, T ; Lohse, P

Zeitschrift für Gastroenterologie, 2004, Vol.42 (8) [Periódico revisado por pares]

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7
The NOD2 variants rs2066843 and rs2076756 are novel independent Crohn's disease susceptibility gene variants associated with severe penetrating disease phenotype resulting in frequent need for surgery
The NOD2 variants rs2066843 and rs2076756 are novel independent Crohn's disease susceptibility gene variants associated with severe penetrating disease phenotype resulting in frequent need for surgery
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The NOD2 variants rs2066843 and rs2076756 are novel independent Crohn's disease susceptibility gene variants associated with severe penetrating disease phenotype resulting in frequent need for surgery

Seiderer, J ; Glas, J ; Diegelmann, J ; Pasciuto, G ; Tillack, C ; Pfennig, S ; Jürgens, M ; Konrad, A ; Török, HP ; Schiemann, U ; Griga, T ; Klein, W ; Epplen, JT ; Mussack, T ; Lohse, P ; Göke, B ; Ochsenkühn, T ; Folwaczny, M ; Müller-Myhsok, B ; Brand, S

Zeitschrift für Gastroenterologie, 2008 [Periódico revisado por pares]

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