Bibliografia

Buslov KG, Iyevleva AG, Chekmariova EV, Suspitsin EN, Togo AV, Kuligina ES, Sokolenko AP, Matsko DE, Turkevich EA, Lazareva YR, Chagunava OL, Bit-Sava EM, Semiglazov VF, Devilee P, Cornelisse C, Hanson KP, Imyanitov EN.
NBS1 657del5 mutation may contribute only to a limited fraction of breast cancer cases in Russia.
Int J Cancer. 2004 Dec 1; [Epub ahead of print]

Carlomagno F, Chang-Claude J, Dunning AM, Ponder BA.
Determination of the frequency of the common 657Del5 Nijmegen breakage syndrome mutation in the German population: no association with risk of breast cancer.
Genes Chromosomes Cancer. 1999;25:393-5.

Cerosaletti KM, Morrison VA, Sabath DE, Willerford DM, Concannon P.
Mutations and molecular variants of the NBS1 gene in non-Hodgkin lymphoma.
Genes Chromosomes Cancer. 2002;35:282-6.

Chrzanowska KH, Piekutowska-Abramczuk D, Popowska E, Gladkowska-Dura M, Maldyk J, Syczewska M, Krajewska-Walasek M, Goryluk-Kozakiewicz B, Bubala H, Gadomski A, Gaworczyk A, Kazanowska B, Koltan A, Kuzmicz M, Luszawska-Kutrzeba T, Maciejka-Kapuscinska L, Stolarska M, Stefanska K, Sznurkowska K, Wakulinska A, Wieczorek M, Szczepanski T, Kowalczyk J.
Carrier frequency of mutation 657del5 in the NBS1 gene in a population of Polish pediatric patients with sporadic lymphoid malignancies.
Int J Cancer. 2006 Mar 1;118(5):1269-74.

Cybulski C, Gorski B, Debniak T, Gliniewicz B, Mierzejewski M, Masojc B, Jakubowska A, Matyjasik J, Zlowocka E, Sikorski A, Narod SA, Lubinski J.
NBS1 is a prostate cancer susceptibility gene.
Cancer Res. 2004;64:1215-9.

Debniak T, Gorski 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.
Germline 657del5 mutation in the NBS1 gene in patients with malignant melanoma of the skin.
Melanoma Res. 2003;13:365-70.

Gorski B, Debniak T, Masojc B, Mierzejewski M, Medrek K, Cybulski C, Jakubowska A, Kurzawski G, Chosia M, Scott R, Lubinski J.
Germline 657del5 mutation in the NBS1 gene in breast cancer patients.
Int J Cancer. 2003;106:379-81. Erratum in: Int J Cancer. 2003;106:984.

Heikkinen K, Karppinen SM, Soini Y, Makinen M, Winqvist R.
Mutation screening of Mre11 complex genes: indication of RAD50 involvement in breast and ovarian cancer susceptibility.
J Med Genet. 2003;40:e131.

Plisiecka-Halasa J, Dansonka-Mieszkowska A, Rembiszewska A, Bidzinski M, Steffen J, Kupryjanczyk J.
Nijmegen breakage syndrome gene (NBS1) alterations and its protein (nibrin) expression in human ovarian tumours.
Ann Hum Genet. 2002;66:353-9.

Resnick IB, Kondratenko I, Pashanov E, Maschan AA, Karachunsky A, Togoev O, Timakov A, Polyakov A, Tverskaya S, Evgrafov O, Roumiantsev AG.
657del5 mutation in the gene for Nijmegen breakage syndrome (NBS1) in a cohort of Russian children with lymphoid tissue malignancies and controls.
Am J Med Genet. 2003;120A:174-9.

Seemanova E, Sperling K, Neitzel H, Varon R, Hadac J, Butova O, Schrock E, Seeman P, Digweed M.
Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instability.
J Med Genet. 2006 Mar;43(3):218-24. Epub 2005 Jul 20.

Soucek P, Gut I, Trneny M, Skovlund E, Grenaker Alnaes G, Kristensen T, Borresen-Dale AL, Kristensen VN.
Multiplex single-tube screening for mutations in the Nijmegen Breakage Syndrome (NBS1) gene in Hodgkin's and non-Hodgkin's lymphoma patients of Slavic origin.
Eur J Hum Genet. 2003;11:416-9.

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, Bidzinski M, Gawrychowski K, Sperling K.
Increased cancer risk of heterozygotes with NBS1 germline mutations in Poland.
Int J Cancer. 2004;111:67-71.

Taylor GM, O'Brien HP, Greaves MF, Ravetto PF, Eden OB.
Correspondence re: R. Varon et al., Mutations in the Nijmegen breakage syndrome gene (NBS1) in childhood acute lymphoblastic leukemia. Cancer Res., 61: 3570-3572, 2001.
Cancer Res. 2003;63:6563-4; author reply 6565.

Varon R, Reis A, Henze G, von Einsiedel HG, Sperling K, Seeger K.
Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL).
Cancer Res. 2001;61:3570-2.


Database citati:
http://www.ncbi.nlm.nih.gov/SNP (03-01-2005)