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Book Chapter: Nasopharyngeal Carcinoma: Genetics and Genomics

TitleNasopharyngeal Carcinoma: Genetics and Genomics
Authors
KeywordsCell signaling pathways
DNA repair gene
Genetic predisposition
GWAS
HLA
Methylation
MST1R
Nasopharyngeal carcinoma
Telomere
Whole-exome sequencing
Issue Date2019
PublisherAcademic Press.
Citation
Nasopharyngeal Carcinoma: Genetics and Genomics. In Lee, AWM, Lung, ML and Ng, WT (Eds.), Nasopharyngeal Carcinoma: From Etiology to Clinical Practice, p. 17-44. London: Academic Press, 2019 How to Cite?
AbstractThis chapter introduces the genetics and genomics of nasopharyngeal carcinoma (NPC). We introduce, in brief, findings leading to the current state of knowledge of what we know about the molecular genetic basis of NPC prior to new molecular advances in next-generation sequencing, which have allowed a more global view of the impact of genetic variations, epigenetic regulation, and cell signaling pathways that contribute to NPC development. Discussions on germline genetic predisposition for NPC include MST1R, HLA, telomere, and DNA repair studies, the subjects of which appear to play important roles in inherited NPC. Landscape methylome, genome, and transcriptome sequencing studies have identified important genes and cell signaling aberrations, providing new insights into the genomics of NPC. These studies all indicate the complex multifactorial nature of NPC development.
Persistent Identifierhttp://hdl.handle.net/10722/261043
ISBN

 

DC FieldValueLanguage
dc.contributor.authorLung, ML-
dc.contributor.authorDai, W-
dc.contributor.authorKo, JMY-
dc.date.accessioned2018-09-14T08:51:29Z-
dc.date.available2018-09-14T08:51:29Z-
dc.date.issued2019-
dc.identifier.citationNasopharyngeal Carcinoma: Genetics and Genomics. In Lee, AWM, Lung, ML and Ng, WT (Eds.), Nasopharyngeal Carcinoma: From Etiology to Clinical Practice, p. 17-44. London: Academic Press, 2019-
dc.identifier.isbn9780128149362-
dc.identifier.urihttp://hdl.handle.net/10722/261043-
dc.description.abstractThis chapter introduces the genetics and genomics of nasopharyngeal carcinoma (NPC). We introduce, in brief, findings leading to the current state of knowledge of what we know about the molecular genetic basis of NPC prior to new molecular advances in next-generation sequencing, which have allowed a more global view of the impact of genetic variations, epigenetic regulation, and cell signaling pathways that contribute to NPC development. Discussions on germline genetic predisposition for NPC include MST1R, HLA, telomere, and DNA repair studies, the subjects of which appear to play important roles in inherited NPC. Landscape methylome, genome, and transcriptome sequencing studies have identified important genes and cell signaling aberrations, providing new insights into the genomics of NPC. These studies all indicate the complex multifactorial nature of NPC development.-
dc.languageeng-
dc.publisherAcademic Press.-
dc.relation.ispartofNasopharyngeal Carcinoma: From Etiology to Clinical Practice-
dc.subjectCell signaling pathways-
dc.subjectDNA repair gene-
dc.subjectGenetic predisposition-
dc.subjectGWAS-
dc.subjectHLA-
dc.subjectMethylation-
dc.subjectMST1R-
dc.subjectNasopharyngeal carcinoma-
dc.subjectTelomere-
dc.subjectWhole-exome sequencing-
dc.titleNasopharyngeal Carcinoma: Genetics and Genomics-
dc.typeBook_Chapter-
dc.identifier.emailLung, ML: mlilung@hku.hk-
dc.identifier.emailDai, W: weidai2@hku.hk-
dc.identifier.emailKo, JMY: joko@hku.hk-
dc.identifier.authorityLung, ML=rp00300-
dc.identifier.authorityDai, W=rp02146-
dc.identifier.authorityKo, JMY=rp02011-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/B978-0-12-814936-2.00002-X-
dc.identifier.scopuseid_2-s2.0-85082446771-
dc.identifier.hkuros290091-
dc.identifier.hkuros298984-
dc.identifier.hkuros302893-
dc.identifier.spage17-
dc.identifier.epage44-
dc.publisher.placeLondon-

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