PROGNOSTIC IMPACT OF MUTATIONS OF THE GENES OF THE COHESIN COMPLEX IN PATIENTS WITH SMD

被引:0
|
作者
Martin-Izquierdo, M. [1 ]
Lopez-Cadenas, F. [2 ]
Sanchez del Real, J. [3 ]
Hernandez-Sanchez, A. [4 ]
Hernandez-Sanchez, J. M. [1 ]
Janusz, K. [2 ]
Diez-Campelo, M. [1 ]
Tormo, M. [2 ]
Megido, M. [1 ]
Olivier, C.
Madinaveitia-Ochoa, A. [3 ]
Martin-Nunez, G. [5 ]
Davila, J. [6 ]
Aguilar, C. [7 ]
Rodriguez, J. N. [8 ]
Alonso, J. M. [9 ]
Sierra, M. [10 ]
Vargas, M. [11 ]
Santos-Minguez, S. [12 ]
Miguel-Garcia, C. [13 ]
Diaz-Martin, A. B. [14 ]
Hernandez-Rivas, J. M. [15 ]
Ramos, F. [1 ]
Abaigar, M. [2 ]
机构
[1] Univ Salamanca, Unidad Diagnost Mol & Celular Canc, Ctr Invest Canc, IBMCC,USAL,CSIC, Salamanca, Spain
[2] Inst Invest Biomed Salamanca IBSAL, Genet Mol Oncohematol, Salamanca, Spain
[3] Hosp Univ Salamanca, Hematol, Salamanca, Spain
[4] Hosp Univ Leon, Hematol, Leon, Spain
[5] Hosp Clin Valencia, Hematol, Valencia, Spain
[6] Hosp Bierzo, Hematol, Ponferrada, Spain
[7] Hosp Gen Segovia, Hematol, Segovia, Spain
[8] Hosp Univ Miguel Servet, Hematol, Zaragoza, Spain
[9] Hosp Virgen del Puerto, Hematol, Plasencia, Spain
[10] Hosp Nuestra Senora Sonsoles, Hematol, Avila, Spain
[11] Hosp Santa Barbara, Hematol, Soria, Spain
[12] Hosp Juan Ramon Jimenez, Hematol, Huelva, Spain
[13] Hosp Rio Carr, Hematol, Palencia, Spain
[14] Hosp Virgen de la Concha, Hematol, Zamora, Spain
[15] Hosp Jarrio, Hematol, Asturias, Spain
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
CO-103
引用
收藏
页码:75 / 76
页数:2
相关论文
共 50 条
  • [21] Recurrent Mutations of Multiple Components of Cohesin Complex in Myeloid Neoplasms
    Kon, Ayana
    Shih, Lee-Yung
    Minamino, Masashi
    Sanada, Masashi
    Shiraishi, Yuichi
    Nagata, Yasunobu
    Yoshida, Kenichi
    Okuno, Yusuke
    Bando, Masashige
    Ishikawa, Shumpei
    Sato-Otsubo, Aiko
    Nagae, Genta
    Haferlach, Claudia
    Nowak, Daniel
    Sato, Yusuke
    Alpermann, Tamara
    Nagasaki, Masao
    Shimamura, Teppei
    Tanaka, Hiroko
    Chiba, Kenichi
    Yamamoto, Ryo
    Yamaguchi, Tomoyuki
    Otsu, Makoto
    Obara, Naoshi
    Sakata-Yanagimoto, Mamiko
    Nakamaki, Tsuyoshi
    Ishiyama, Ken
    Nolte, Florian
    Hofmann, Wolf-Karsten
    Miyawaki, Shuichi
    Chiba, Shigeru
    Mori, Hiraku
    Nakauchi, Hiromitsu
    Koeffler, H. Phillip
    Aburatani, Hiroyuki
    Haferlach, Torsten
    Shirahige, Katsuhiko
    Miyano, Satoru
    Ogawa, Seishi
    BLOOD, 2012, 120 (21)
  • [22] Prognostic impact of mismatch repair genes germline defects in colorectal cancer patients: are all mutations equal?
    Maccaroni, Elena
    Bracci, Raffaella
    Giampieri, Riccardo
    Bianchi, Francesca
    Belvederesi, Laura
    Brugiati, Cristiana
    Pagliaretta, Silvia
    Del Prete, Michela
    Scartozzi, Mario
    Cascinu, Stefano
    ONCOTARGET, 2015, 6 (36) : 38737 - 38748
  • [23] Prognostic Impact of Mutations in a Large Series of Patients with Myelofibrosis
    Guglielmelli, Paola
    Biamonte, Flavia
    Pereira, Arturo
    Score, Johannah
    Mannarelli, Carmela
    Rotunno, Giada
    Susini, Maria Chiara
    Spolverini, Ambra
    Pancrazzi, Alessandro
    Bosi, Alberto
    Jones, Amy
    Zoi, Katerina
    Reiter, Andreas
    Duncombe, Andrew
    Pietra, Daniela
    Rumi, Elisa
    Cervantes, Francisco
    Barosi, Gianni
    Cazzola, Mario
    Cross, Nick C. P.
    Vannucchi, Alessandro M.
    BLOOD, 2012, 120 (21)
  • [24] Prognostic impact of RAS mutations in patients with myelodysplastic syndrome
    Al-Kali, Aref
    Quintas-Cardama, Alfonso
    Luthra, Raja
    Bueso-Ramos, Carlos
    Pierce, Sherry
    Kadia, Tapan
    Borthakur, Gautam
    Estrov, Zeev
    Jabbour, Elias
    Faderl, Stefan
    Ravandi, Farhad
    Cortes, Jorges
    Tefferi, Ayalew
    Kantarjian, Hagop
    Garcia-Manero, Guillermo
    AMERICAN JOURNAL OF HEMATOLOGY, 2013, 88 (05) : 365 - 369
  • [25] Cohesin Complex Mutations in Myeloid Neoplasms Reveal Frequent Co-Mutations in Spliceosome Genes, NRAS, and RUNX1 with a Normal Karyotype
    Hirt, C.
    Michaels, P.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2022, 24 (10): : S41 - S41
  • [26] Cohesin Complex Interacting with Promoters of MMP Genes for in Pterygium Occurrence
    Han, Shichao
    Zhu, Wei
    Guo, Qianqian
    CURRENT EYE RESEARCH, 2025,
  • [27] PROGNOSTIC IMPACT OF THE STUDY THROUGH MASS SEQUENCING OF THE MUTATIONS OF THE GENES INVOLVED IN MYELOFIBROSIS
    Ana A, Martin Lopez
    Monica, Del Rey
    Cristina, Robledo
    Alicia, Arenas
    Rocio, Benito
    Inmaculada, Rayado
    Rosa, Ayala
    Jesus M, Hernandez-Sanchez
    Natalia, De las Heras
    Marta, Castellanos
    Felix, Lopez-Cadenas
    Guillermo, Martin
    Erik, De Cabo
    Jorge, Labrador
    Alejandro, Corrales
    Carmen, Olivier
    Jose M, Alonso
    Carlos, Aguilar
    Joaquin, Martinez
    Jose R, Gonzalez-Porras
    Jesus M, Hernandez-Rivas
    HAEMATOLOGICA, 2016, 101 : 83 - 84
  • [28] Recurrent pathway mutations of multiple components of cohesin complex in myeloid neoplasms
    Kon, Ayana
    Shih, Lee Yung
    Minamino, Masashi
    Sanada, Masashi
    Shiraishi, Yuichi
    Nagata, Yasunobu
    Yoshida, Kenichi
    Okuno, Yusuke
    Bando, Masashige
    Ishikawa, Shunpei
    Sato-Otsubo, Aiko
    Nagae, Genta
    Nishimoto, Aiko
    Haferiach, Claudia
    Nowak, Daniel
    Sato, Yusuke
    Alpermann, Tamara
    Shimamura, Teppei
    Tanaka, Hiroko
    Chiba, Kenichi
    Yamamoto, Ryo
    Yamaguchi, Tomoyuki
    Otsu, Makoto
    Obara, Naoshi
    Sakata-Yanagimoto, Mamiko
    Nakamaki, Tsuyoshi
    Ishiyama, Ken
    Nolte, Florian
    Hofmann, Wolf-Karsten
    Miyawaki, Shuichi
    Chiba, Shigeru
    Mori, Hiraku
    Nakauchi, Hiromitso
    Koeffler, H. Phillip
    Aburatani, Hiroyuki
    Haferlach, Torsten
    Shirahige, Katsuhiko
    Miyano, Satoru
    Ogawa, Seishi
    CANCER RESEARCH, 2013, 73 (08)
  • [29] Mutations in Genes Coding for Synaptonemal Complex Proteins and Their Impact on Human Fertility
    Geisinger, Adriana
    Benavente, Ricardo
    CYTOGENETIC AND GENOME RESEARCH, 2016, 150 (02) : 77 - 85
  • [30] A cohesive look at leukemogenesis: The cohesin complex and other driving mutations in AML
    Heimbruch, Katelyn E.
    Meyer, Alison E.
    Agrawal, Puja
    Viny, Aaron D.
    Rao, Sridhar
    NEOPLASIA, 2021, 23 (03): : 337 - 347