Whole-exome sequencing reveals genetic variants in low-risk and high-risk neuroblastoma.

Altun, Zekiye; Yuan, Hongling; Baran, Burçin; Aktas, Safiye; Sönmez, Esra Esmeray; Küçük, Can; Olgun, Nur

Altun, Zekiye; Yuan, Hongling; Baran, Burçin; Aktas, Safiye; Sönmez, Esra Esmeray; Küçük, Can; Olgun, Nur.

Afiliação

Altun Z; Department of Basic Oncology, Institute of Oncology, Dokuz Eylül University, Izmir, Turkey. Electronic address: zekiye.altun@deu.edu.tr.
Yuan H; Department of Basic Oncology, Institute of Oncology, Dokuz Eylül University, Izmir, Turkey.
Baran B; Department of Basic Oncology, Institute of Oncology, Dokuz Eylül University, Izmir, Turkey.
Aktas S; Department of Basic Oncology, Institute of Oncology, Dokuz Eylül University, Izmir, Turkey.
Sönmez EE; Izmir Biomedicine and Genome Center, Izmir, Turkey; Izmir Biomedicine and Genome Institute, Dokuz Eylül University, Izmir, Turkey.
Küçük C; Izmir Biomedicine and Genome Center, Izmir, Turkey; Izmir Biomedicine and Genome Institute, Dokuz Eylül University, Izmir, Turkey; Department of Medical Biology, Faculty of Medicine, Dokuz Eylül University, Izmir, Turkey.
Olgun N; Department of Pediatric Oncology, Institute of Oncology, Dokuz Eylül University, Izmir, Turkey.

Gene ; 860: 147233, 2023 Apr 15.

Article em En | MEDLINE | ID: mdl-36736507

Assuntos

Neuroblastoma; Oncogenes; Humanos; Sequenciamento do Exoma; Genômica; Fatores de Risco; Neuroblastoma/genética; Neuroblastoma/patologia

Palavras-chave

COSMIC; Gene variations; Neuroblastoma; Whole-exome sequencing; cBioportal

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oncogenes / Neuroblastoma Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Gene Ano de publicação: 2023 Tipo de documento: Article

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