Genotype-Phenotype Associations of the CD-Associated Single Nucleotide Polymorphism within the Gene Locus Encoding Protein Tyrosine Phosphatase Non-Receptor Type 22 in Patients of the Swiss IBD Cohort.

Spalinger, Marianne R; Zeitz, Jonas; Biedermann, Luc; Rossel, Jean-Benoit; Sulz, Michael C; Frei, Pascal; Scharl, Sylvie; Vavricka, Stephan R; Fried, Michael; Rogler, Gerhard; Scharl, Michael

Spalinger, Marianne R; Zeitz, Jonas; Biedermann, Luc; Rossel, Jean-Benoit; Sulz, Michael C; Frei, Pascal; Scharl, Sylvie; Vavricka, Stephan R; Fried, Michael; Rogler, Gerhard; Scharl, Michael.

Afiliação

Spalinger MR; Division of Gastroenterology and Hepatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Zeitz J; Division of Gastroenterology and Hepatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Biedermann L; Division of Gastroenterology and Hepatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Rossel JB; Institute of Social and Preventive Medicine, Université de Lausanne, Lausanne, Switzerland.
Sulz MC; Division of Gastroenterology and Hepatology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Frei P; Division of Gastroenterology and Hepatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Scharl S; Division of Gastroenterology and Hepatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Vavricka SR; Division of Gastroenterology and Hepatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Fried M; Zurich Center for Integrative Human Physiology, University of Zurich, Zurich, Switzerland.
Rogler G; Division of Gastroenterology and Hepatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Scharl M; Zurich Center for Integrative Human Physiology, University of Zurich, Zurich, Switzerland.

PLoS One ; 11(7): e0160215, 2016.

Article em En | MEDLINE | ID: mdl-27467733

Assuntos

Doença de Crohn/genética; Genótipo; Doenças Inflamatórias Intestinais/genética; Fenótipo; Proteína Tirosina Fosfatase não Receptora Tipo 22/genética; Adulto; Estudos de Casos e Controles; Estudos de Coortes; Feminino; Predisposição Genética para Doença; Humanos; Masculino; Polimorfismo de Nucleotídeo Único; Suíça; Adulto Jovem

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Doenças Inflamatórias Intestinais / Doença de Crohn / Proteína Tirosina Fosfatase não Receptora Tipo 22 / Genótipo Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Suíça País de publicação: Estados Unidos

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