These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

100 related articles for article (PubMed ID: 16634478)

  • 1. [Mutations in tumor suppressor gene NBS1 in adult patients with malignancies].
    Seemanová E; Hoch J; Herzogová J; Kawaciuk I; Janda J; Kohoutová M; Seeman P; Varon R; Sperling K
    Cas Lek Cesk; 2006; 145(3):201-3. PubMed ID: 16634478
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Increased risk of malignancies in heterozygotes in families of patients with Nijmegen breakage syndrome].
    Seemanová E; Jarolím P; Seeman P; Varon R; Sperling K
    Cas Lek Cesk; 2006; 145(2):138-43. PubMed ID: 16521404
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [Nijmegen breakage syndrome in Slovakia].
    Seemanová E; Pohanka V; Seeman P; Misovicová N; Behunová J; Kvasnicová M; Dlholucký S; Valachová A; Cisarik F; Veghová E; Varon R; Sperling K
    Cas Lek Cesk; 2004; 143(8):538-41; discussion 542. PubMed ID: 15446459
    [TBL] [Abstract][Full Text] [Related]  

  • 5. I171V germline mutation in the NBS1 gene significantly increases risk of breast cancer.
    Roznowski K; Januszkiewicz-Lewandowska D; Mosor M; Pernak M; Litwiniuk M; Nowak J
    Breast Cancer Res Treat; 2008 Jul; 110(2):343-8. PubMed ID: 17899368
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Heterozygous carriers of the I171V mutation of the NBS1 gene have a significantly increased risk of solid malignant tumours.
    Nowak J; Mosor M; Ziółkowska I; Wierzbicka M; Pernak-Schwarz M; Przyborska M; Roznowski K; Pławski A; Słomski R; Januszkiewicz D
    Eur J Cancer; 2008 Mar; 44(4):627-30. PubMed ID: 18280732
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL).
    Varon R; Reis A; Henze G; von Einsiedel HG; Sperling K; Seeger K
    Cancer Res; 2001 May; 61(9):3570-2. PubMed ID: 11325820
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Carrier frequency of mutation 657del5 in the NBS1 gene in a population of Polish pediatric patients with sporadic lymphoid malignancies.
    Chrzanowska KH; Piekutowska-Abramczuk D; Popowska E; Gładkowska-Dura M; Małdyk J; Syczewska M; Krajewska-Walasek M; Goryluk-Kozakiewicz B; Bubała H; Gadomski A; Gaworczyk A; Kazanowska B; Kołtan A; Kuźmicz M; Luszawska-Kutrzeba T; Maciejka-Kapuścińska L; Stolarska M; Stefańska K; Sznurkowska K; Wakulińska A; Wieczorek M; Szczepański T; Kowalczyk J
    Int J Cancer; 2006 Mar; 118(5):1269-74. PubMed ID: 16152606
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Increased cancer risk of heterozygotes with NBS1 germline mutations in Poland.
    Steffen J; Varon R; Mosor M; Maneva G; Maurer M; Stumm M; Nowakowska D; Rubach M; Kosakowska E; Ruka W; Nowecki Z; Rutkowski P; Demkow T; Sadowska M; Bidziński M; Gawrychowski K; Sperling K
    Int J Cancer; 2004 Aug; 111(1):67-71. PubMed ID: 15185344
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. 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]  

  • 14. Unique morphological spectrum of lymphomas in Nijmegen breakage syndrome (NBS) patients with high frequency of consecutive lymphoma formation.
    Gładkowska-Dura M; Dzierzanowska-Fangrat K; Dura WT; van Krieken JH; Chrzanowska KH; van Dongen JJ; Langerak AW
    J Pathol; 2008 Nov; 216(3):337-44. PubMed ID: 18788073
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical ascertainment of Nijmegen breakage syndrome (NBS) and prevalence of the major mutation, 657del5, in three Slav populations.
    Varon R; Seemanova E; Chrzanowska K; Hnateyko O; Piekutowska-Abramczuk D; Krajewska-Walasek M; Sykut-Cegielska J; Sperling K; Reis A
    Eur J Hum Genet; 2000 Nov; 8(11):900-2. PubMed ID: 11093281
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Nijmegen breakage syndrome gene (NBS1) is not the tumor suppressor gene at 8q21.3 involved in colorectal carcinoma.
    Varon R; Gosse-Brun S; Bignon YJ; Sperling K; Uhrhammer N
    Oncol Rep; 2002; 9(4):709-11. PubMed ID: 12066197
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fertility defects revealing germline biallelic nonsense NBN mutations.
    Warcoin M; Lespinasse J; Despouy G; Dubois d'Enghien C; Laugé A; Portnoï MF; Christin-Maitre S; Stoppa-Lyonnet D; Stern MH
    Hum Mutat; 2009 Mar; 30(3):424-30. PubMed ID: 19105185
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Heterozygous germ-line mutations in the NBN gene predispose to medulloblastoma in pediatric patients.
    Ciara E; Piekutowska-Abramczuk D; Popowska E; Grajkowska W; Barszcz S; Perek D; Dembowska-Bagińska B; Perek-Polnik M; Kowalewska E; Czajńska A; Syczewska M; Czornak K; Krajewska-Walasek M; Roszkowski M; Chrzanowska KH
    Acta Neuropathol; 2010 Mar; 119(3):325-34. PubMed ID: 19908051
    [TBL] [Abstract][Full Text] [Related]  

  • 20. NBN 657del5 heterozygous mutations and colorectal cancer risk in the Czech Republic.
    Pardini B; Naccarati A; Polakova V; Smerhovsky Z; Hlavata I; Soucek P; Novotny J; Vodickova L; Tomanova V; Landi S; Vodicka P
    Mutat Res; 2009 Jun; 666(1-2):64-7. PubMed ID: 19393249
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.