Short somatic alterations at the site of copy number variation in breast cancer

Copy number variation (CNV) is a polymorphism in the human genome involving DNA fragments larger than 1 kb. Copy number variation sites provide hotspots of somatic alterations in cancers. Herein, we examined somatic alterations at sites of CNV in DNA from 20 invasive breast cancers using a Comparati...

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Detalhes bibliográficos
Publicado no:Cancer Sci
Main Authors: Murakami, Fumi, Tsuboi, Yumi, Takahashi, Yuka, Horimoto, Yoshiya, Mogushi, Kaoru, Ito, Takeshi, Emi, Mitsuru, Matsubara, Daisuke, Shibata, Tatsuhiro, Saito, Mitsue, Murakami, Yoshinori
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2020
Assuntos:
Genetics, Genomics, and Proteomics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7780029/
https://ncbi.nlm.nih.gov/pubmed/32860329
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cas.14630
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