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GartnerAnton

Gartner, Anton
DNA Damage Response and Genetic Toxicology
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dc.citation.endPage 33 -
dc.citation.number 1-2 -
dc.citation.startPage 17 -
dc.citation.title MOLECULAR AND CELLULAR BIOCHEMISTRY -
dc.citation.volume 329 -
dc.contributor.author Bilitou, Aikaterini -
dc.contributor.author Watson, Julie -
dc.contributor.author Gartner, Anton -
dc.contributor.author Ohnuma, Shin-ichi -
dc.date.accessioned 2023-12-22T07:39:50Z -
dc.date.available 2023-12-22T07:39:50Z -
dc.date.created 2020-01-30 -
dc.date.issued 2009-09 -
dc.description.abstract The NM23 (non-metastatic 23) family is almost universally conserved across all three domains of life: eubacteria, archaea and eucaryotes. Unicellular organisms possess one NM23 ortholog, whilst vertebrates possess several. Gene multiplication through evolution has been accompanied by structural and functional diversification. Many NM23 orthologs are nucleoside diphosphate kinases (NDP kinases), but some more recently evolved members lack NDP kinase activity and/or display other functions, for instance, acting as protein kinases or transcription factors. These members display overlapping but distinct expression patterns during vertebrate development. In this review, we describe the functional differences and similarities among various NM23 family members. Moreover, we establish orthologous relationships through a phylogenetic analysis of NM23 members across vertebrate species, including Xenopus laevis and zebrafish, primitive chordates and several phyla of invertebrates. Finally, we summarize the involvement of NM23 proteins in development, in particular neural development. Carcinogenesis is a process of misregulated development, and NM23 was initially implicated as a metastasis suppressor. A more detailed understanding of the evolution of the family and its role in vertebrate development will facilitate elucidation of the mechanism of NM23 involvement in human cancer. -
dc.identifier.bibliographicCitation MOLECULAR AND CELLULAR BIOCHEMISTRY, v.329, no.1-2, pp.17 - 33 -
dc.identifier.doi 10.1007/s11010-009-0121-6 -
dc.identifier.issn 0300-8177 -
dc.identifier.scopusid 2-s2.0-70449709698 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/31004 -
dc.identifier.url https://link.springer.com/article/10.1007%2Fs11010-009-0121-6 -
dc.identifier.wosid 000268727600002 -
dc.language 영어 -
dc.publisher SPRINGER -
dc.title The NM23 family in development -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Cell Biology -
dc.relation.journalResearchArea Cell Biology -
dc.type.docType Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor NM23 -
dc.subject.keywordAuthor Development -
dc.subject.keywordAuthor Xenopus -
dc.subject.keywordAuthor Neurogenesis -
dc.subject.keywordAuthor NDP kinase -
dc.subject.keywordPlus NUCLEOSIDE-DIPHOSPHATE KINASE -
dc.subject.keywordPlus TUMOR-METASTASIS SUPPRESSOR -
dc.subject.keywordPlus CARCINOMA-CELL-LINE -
dc.subject.keywordPlus NERVE GROWTH-FACTOR -
dc.subject.keywordPlus DICTYOSTELIUM-DISCOIDEUM -
dc.subject.keywordPlus DIFFERENTIAL EXPRESSION -
dc.subject.keywordPlus DROSOPHILA DEVELOPMENT -
dc.subject.keywordPlus MOUSE ORGANOGENESIS -
dc.subject.keywordPlus ENZYMATIC-ACTIVITY -
dc.subject.keywordPlus CANCER METASTASIS -

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