Association of the rs1346044 Polymorphism of the Werner Syndrome Gene RECQL2 with Increased Risk and Premature Onset of Breast Cancer.

Zins, Karin; Frech, Barbara; Taubenschuss, Eva; Schneeberger, Christian; Abraham, Dietmar; Schreiber, Martin

Zins, Karin; Frech, Barbara; Taubenschuss, Eva; Schneeberger, Christian; Abraham, Dietmar; Schreiber, Martin.

Afiliación

Zins K; Laboratory for Molecular Cellular Biology, Center for Anatomy and Cell Biology, Medical University of Vienna, A-1090 Vienna, Austria. karin.zins@meduniwien.ac.at.
Frech B; Department of Obstetrics and Gynecology, Medical University of Vienna, Waehringer Guertel 18-20, A-1090 Vienna, Austria. barbara.frech@gmx.net.
Taubenschuss E; Department of Obstetrics and Gynecology, Medical University of Vienna, Waehringer Guertel 18-20, A-1090 Vienna, Austria. eva.taubenschuss@gmx.at.
Schneeberger C; Department of Obstetrics and Gynecology, Medical University of Vienna, Waehringer Guertel 18-20, A-1090 Vienna, Austria. christian.schneeberger@meduniwien.ac.at.
Abraham D; Laboratory for Molecular Cellular Biology, Center for Anatomy and Cell Biology, Medical University of Vienna, A-1090 Vienna, Austria. dietmar.abraham@meduniwien.ac.at.
Schreiber M; Comprehensive Cancer Center (CCC), Medical University of Vienna, A-1090 Vienna, Austria. dietmar.abraham@meduniwien.ac.at.

Int J Mol Sci ; 16(12): 29643-53, 2015 Dec 10.

Article en En | MEDLINE | ID: mdl-26690424

Asunto(s)

Neoplasias de la Mama/genética; Exodesoxirribonucleasas/genética; RecQ Helicasas/genética; Edad de Inicio; Estudios de Casos y Controles; Femenino; Frecuencia de los Genes; Estudios de Asociación Genética; Predisposición Genética a la Enfermedad; Humanos; Persona de Mediana Edad; Polimorfismo de Nucleótido Simple; Riesgo; Síndrome de Werner/genética; Helicasa del Síndrome de Werner

Palabras clave

RECQL2; WRN; Werner syndrome; breast cancer; rs1346044; rs3087425; single nucleotide polymorphism (SNP)

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Exodesoxirribonucleasas / RecQ Helicasas Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Middle aged Idioma: En Revista: Int J Mol Sci Año: 2015 Tipo del documento: Article País de afiliación: Austria

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