Frameshift mutational target gene analysis identifies similarities and differences in constitutional mismatch repair-deficiency and Lynch syndrome.

Maletzki, Claudia; Huehns, Maja; Bauer, Ingrid; Ripperger, Tim; Mork, Maureen M; Vilar, Eduardo; Klöcking, Sabine; Zettl, Heike; Prall, Friedrich; Linnebacher, Michael

Maletzki, Claudia; Huehns, Maja; Bauer, Ingrid; Ripperger, Tim; Mork, Maureen M; Vilar, Eduardo; Klöcking, Sabine; Zettl, Heike; Prall, Friedrich; Linnebacher, Michael.

Afiliação

Maletzki C; Molecular Oncology and Immunotherapy, Rostock University Medical Center, Rostock, Germany.
Huehns M; Institute of Pathology, Rostock University Medical Center, Rostock, Germany.
Bauer I; Institute of Medical Genetics, Rostock University Medical Center, Rostock, Germany.
Ripperger T; Institute of Human Genetics, Hannover Medical School, Hannover, Germany.
Mork MM; Division of Cancer Prevention and Population Sciences, Department of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston,, Texas.
Vilar E; Clinical Cancer Genetics Program, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Klöcking S; Division of Cancer Prevention and Population Sciences, Department of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston,, Texas.
Zettl H; Clinical Cancer Genetics Program, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Prall F; Rostock Cancer Registry, University of Rostock, Rostock, Germany.
Linnebacher M; Rostock Cancer Registry, University of Rostock, Rostock, Germany.

Mol Carcinog ; 56(7): 1753-1764, 2017 07.

Article em En | MEDLINE | ID: mdl-28218421

Assuntos

Biomarcadores Tumorais/genética; Neoplasias Colorretais Hereditárias sem Polipose/genética; Reparo de Erro de Pareamento de DNA/genética; Enzimas Reparadoras do DNA/genética; Mutação da Fase de Leitura/genética; Instabilidade de Microssatélites; Adulto; Criança; Feminino; Seguimentos; Humanos; Masculino; Pessoa de Meia-Idade; Prognóstico

Palavras-chave

coding microsatellite mutations; mononucleotide repeats; tumor associated mutations; tumorigenesis

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais Hereditárias sem Polipose / Biomarcadores Tumorais / Mutação da Fase de Leitura / Enzimas Reparadoras do DNA / Instabilidade de Microssatélites / Reparo de Erro de Pareamento de DNA Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Mol Carcinog Assunto da revista: BIOLOGIA MOLECULAR / NEOPLASIAS Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Alemanha País de publicação: Estados Unidos

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