BRCC3 mutations in myeloid neoplasms

Next generation sequencing technologies have provided insights into the molecular heterogeneity of various myeloid neoplasms, revealing previously unknown somatic genetic events. In our cohort of 1444 cases analyzed by next generation sequencing, somatic mutations in the gene BRCA1-BRCA2-containing...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:Haematologica
Κύριοι συγγραφείς: Huang, Dayong, Nagata, Yasunobu, Grossmann, Vera, Radivoyevitch, Tomas, Okuno, Yusuke, Nagae, Genta, Hosono, Naoko, Schnittger, Susanne, Sanada, Masashi, Przychodzen, Bartlomiej, Kon, Ayana, Polprasert, Chantana, Shen, Wenyi, Clemente, Michael J., Phillips, James G., Alpermann, Tamara, Yoshida, Kenichi, Nadarajah, Niroshan, Sekeres, Mikkael A., Oakley, Kevin, Nguyen, Nhu, Shiraishi, Yuichi, Shiozawa, Yusuke, Chiba, Kenichi, Tanaka, Hiroko, Koeffler, H. Phillip, Klein, Hans-Ulrich, Dugas, Martin, Aburatani, Hiroyuki, Miyano, Satoru, Haferlach, Claudia, Kern, Wolfgang, Haferlach, Torsten, Du, Yang, Ogawa, Seishi, Makishima, Hideki
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Ferrata Storti Foundation 2015
Θέματα:
Articles
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5004421/
https://ncbi.nlm.nih.gov/pubmed/26001790
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2014.111989
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