BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 16392640)

  • 1. 657del5 mutation of the Nijmegen breakage syndrome gene (NBS1) in the Turkish population.
    Tekin M; Akcayoz D; Ucar C; Gulen H; Akar N
    Hum Biol; 2005 Jun; 77(3):393-7. PubMed ID: 16392640
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instability.
    Seemanová E; Sperling K; Neitzel H; Varon R; Hadac J; Butova O; Schröck E; Seeman P; Digweed M
    J Med Genet; 2006 Mar; 43(3):218-24. PubMed ID: 16033915
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Regional distribution of heterozygous 657del5 mutation carriers of the NBS1 gene in Wielkopolska province (Poland).
    Ziółkowska I; Mosor M; Nowak J
    J Appl Genet; 2006; 47(3):269-72. PubMed ID: 16877808
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Role of the Nijmegen breakage syndrome 1 gene in familial and sporadic prostate cancer.
    Hebbring SJ; Fredriksson H; White KA; Maier C; Ewing C; McDonnell SK; Jacobsen SJ; Cerhan J; Schaid DJ; Ikonen T; Autio V; Tammela TL; Herkommer K; Paiss T; Vogel W; Gielzak M; Sauvageot J; Schleutker J; Cooney KA; Isaacs W; Thibodeau SN
    Cancer Epidemiol Biomarkers Prev; 2006 May; 15(5):935-8. PubMed ID: 16702373
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The R215W mutation in NBS1 impairs gamma-H2AX binding and affects DNA repair: molecular bases for the severe phenotype of 657del5/R215W Nijmegen breakage syndrome patients.
    di Masi A; Viganotti M; Polticelli F; Ascenzi P; Tanzarella C; Antoccia A
    Biochem Biophys Res Commun; 2008 May; 369(3):835-40. PubMed ID: 18328813
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Nijmegen breakage syndrome.
    Kondratenko I; Paschenko O; Polyakov A; Bologov A
    Adv Exp Med Biol; 2007; 601():61-7. PubMed ID: 17712992
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish family.
    Tekin M; Doğu F; Taçyíldiz N; Akar E; Ikincioğullari A; Oğur G; Yavuz G; Babacan E; Akar N
    Clin Genet; 2002 Jul; 62(1):84-8. PubMed ID: 12123493
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Nijmegen Breakage Syndrome mutations and risk of breast cancer.
    Bogdanova N; Feshchenko S; Schürmann P; Waltes R; Wieland B; Hillemanns P; Rogov YI; Dammann O; Bremer M; Karstens JH; Sohn C; Varon R; Dörk T
    Int J Cancer; 2008 Feb; 122(4):802-6. PubMed ID: 17957789
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Screening of Nijmegen breakage syndrome 1 mutations in four unrelated families by polymerase chain reaction using sequence-specific primers.
    Di Masi A; Antoccia A; Spadoni E; Varon-Mateeva R; Maraschio P; Tanzarella C
    Genet Test; 2006; 10(1):24-30. PubMed ID: 16544999
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cancer risk of heterozygotes with the NBN founder mutation.
    Seemanová E; Jarolim P; Seeman P; Varon R; Digweed M; Swift M; Sperling K
    J Natl Cancer Inst; 2007 Dec; 99(24):1875-80. PubMed ID: 18073374
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Slavic NBN Founder Mutation: A Role for Reproductive Fitness?
    Seemanova E; Varon R; Vejvalka J; Jarolim P; Seeman P; Chrzanowska KH; Digweed M; Resnick I; Kremensky I; Saar K; Hoffmann K; Dutrannoy V; Karbasiyan M; Ghani M; Barić I; Tekin M; Kovacs P; Krawczak M; Reis A; Sperling K; Nothnagel M
    PLoS One; 2016; 11(12):e0167984. PubMed ID: 27936167
    [TBL] [Abstract][Full Text] [Related]  

  • 12. NBS1, the Nijmegen breakage syndrome gene product, regulates neuronal proliferation and differentiation.
    Lee WT; Chang WH; Huang CH; Wu KJ
    J Neurochem; 2007 Jul; 102(1):141-52. PubMed ID: 17442057
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nijmegen breakage syndrome and functions of the responsible protein, NBS1.
    Antoccia A; Kobayashi J; Tauchi H; Matsuura S; Komatsu K
    Genome Dyn; 2006; 1():191-205. PubMed ID: 18724061
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Heterozygous carriers of Slavic mutation 657del5 of NBN gene in patients with colorectal cancer].
    Seemanová E; Hoch J; Seeman P
    Cas Lek Cesk; 2011; 150(2):97-9. PubMed ID: 21560448
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical variability and expression of the NBN c.657del5 allele in Nijmegen Breakage Syndrome.
    Lins S; Kim R; Krüger L; Chrzanowska KH; Seemanova E; Digweed M
    Gene; 2009 Nov; 447(1):12-7. PubMed ID: 19635536
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Significant association between Nijmegen breakage syndrome 1 657del5 polymorphism and breast cancer risk.
    Zhang G; Zeng Y; Liu Z; Wei W
    Tumour Biol; 2013 Oct; 34(5):2753-7. PubMed ID: 23765759
    [TBL] [Abstract][Full Text] [Related]  

  • 17. NBS1 interacts with HP1 to ensure genome integrity.
    Bosso G; Cipressa F; Moroni ML; Pennisi R; Albanesi J; Brandi V; Cugusi S; Renda F; Ciapponi L; Polticelli F; Antoccia A; di Masi A; Cenci G
    Cell Death Dis; 2019 Dec; 10(12):951. PubMed ID: 31836699
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations in the Nijmegen breakage syndrome gene in medulloblastomas.
    Huang J; Grotzer MA; Watanabe T; Hewer E; Pietsch T; Rutkowski S; Ohgaki H
    Clin Cancer Res; 2008 Jul; 14(13):4053-8. PubMed ID: 18593981
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Increased risk of gastrointestinal lymphoma in carriers of the 657del5 NBS1 gene mutation.
    Steffen J; Maneva G; Popławska L; Varon R; Mioduszewska O; Sperling K
    Int J Cancer; 2006 Dec; 119(12):2970-3. PubMed ID: 16998789
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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 D; Mirasole C; Pennisi R; Pallotta V; D'Alessandro A; Antoccia A; Zolla L; Ascenzi P; di Masi A
    PLoS One; 2014; 9(12):e114651. PubMed ID: 25485873
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.