PREVALENCE OF MUTATION OF A 657DEL5 GENE OF NBN AMONG CHILDREN WITH ACUTE LEUKEMIA

被引:0
|
作者
Kitsera, N. I. [1 ]
Akopyan, H. [1 ]
Polishchuk, R. [2 ]
Skoropad, L. [2 ]
机构
[1] Inst Hereditary Pathol, Lvov, Ukraine
[2] Reg Specialized Childrens Clin, Lvov, Ukraine
关键词
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
引用
收藏
页码:77 / 77
页数:1
相关论文
共 50 条
  • [1] Elevated frequency of the mutation 657del5 within the NBS1 gene in childhood acute lymphoblastic leukemia.
    Rischewski, JR
    Stanulla, M
    Weber, B
    Bismarck, PV
    Ludwig, WD
    Schrappe, M
    Welte, K
    Schneppenheim, R
    BLOOD, 2000, 96 (11) : 714A - 714A
  • [2] 657DEL5 MUTATION OF THE NBS1 GENE IN MYELODYSPLASTIC SYNDROME
    Bunjevacki, Vera
    Maksimovic, Nela
    Damnjanovic, Tatjana
    Cvjeticanin, Suzana
    Novakovic, Ivana
    Lukovic, Ljiljana
    Ristanovic, Momcilo
    Bogdanovic, Andrija
    Jekic, Biljana
    ARCHIVES OF BIOLOGICAL SCIENCES, 2014, 66 (03) : 1055 - 1059
  • [3] High prevalence of the NBN gene mutation c.657-661del5 in Southeast Germany
    Maurer, M.
    Hoffmann, K.
    Sperling, K.
    Varon, R.
    JOURNAL OF APPLIED GENETICS, 2010, 51 (02) : 211 - 214
  • [4] NBN 657del5 heterozygous mutations and colorectal cancer risk in the Czech Republic
    Pardini, Barbara
    Naccarati, Alessio
    Polakova, Veronika
    Smerhovsky, Zdenek
    Hlavata, Ivona
    Soucek, Pavel
    Novotny, Jan
    Vodickova, Ludmila
    Tomanova, Vera
    Landi, Stefano
    Vodicka, Pavel
    MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2009, 666 (1-2) : 64 - 67
  • [5] Germline 657del5 mutation in the NBS1 gene in breast cancer patients
    Górski, B
    Debniak, T
    Masoic, B
    Mierzejewski, M
    Medrek, K
    Cybulski, C
    Jakubowska, A
    Kurzawski, G
    Chosia, M
    Scott, R
    Lubinski, J
    INTERNATIONAL JOURNAL OF CANCER, 2003, 106 (03) : 379 - 381
  • [6] Identification of the Interactors of Human Nibrin (NBN) and of Its 26 kDa and 70 kDa Fragments Arising from the NBN 657del5 Founder Mutation
    Cilli, Domenica
    Mirasole, Cristiana
    Pennisi, Rosa
    Pallotta, Valeria
    D'Alessandro, Angelo
    Antoccia, Antonio
    Zolla, Lello
    Ascenzi, Paolo
    di Masi, Alessandra
    PLOS ONE, 2014, 9 (12):
  • [7] Increased risk of gastrointestinal lymphoma in carriers of the 657del5 NBS1 gene mutation
    Steffen, Jan
    Maneva, Galina
    Poplawska, Lidia
    Varon, Raymonda
    Mioduszewska, Olga
    Sperling, Karl
    INTERNATIONAL JOURNAL OF CANCER, 2006, 119 (12) : 2970 - 2973
  • [8] 657del5 mutation of the Nijmegen breakage syndrome gene (NBS1) in the Turkish population
    Tekin, M
    Akcayoz, D
    Ucar, C
    Gulen, H
    Akar, N
    HUMAN BIOLOGY, 2005, 77 (03) : 393 - 397
  • [9] Germline 657del5 mutation in the NBS1 gene in patients with malignant melanoma of the skin
    Debniak, T
    Górski, B
    Cybulski, C
    Jakubowska, A
    Kurzawski, G
    Lener, M
    Mierzejewski, M
    Masojc, B
    Medrek, K
    Kladny, J
    Zaluga, E
    Maleszka, R
    Chosia, M
    Lubinski, J
    MELANOMA RESEARCH, 2003, 13 (04) : 365 - 370
  • [10] 657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish family
    Tekin, M
    Dogu, F
    Taçyildiz, N
    Akar, E
    Ikinciogullari, A
    Ogur, G
    Yavuz, G
    Babacan, E
    Akar, N
    CLINICAL GENETICS, 2002, 62 (01) : 84 - 88