119 related articles for article (PubMed ID: 16810201)
1. Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukemia.
Mosor M; Ziółkowska I; Pernak-Schwarz M; Januszkiewicz-Lewandowska D; Nowak J
Leukemia; 2006 Aug; 20(8):1454-6. PubMed ID: 16810201
[No Abstract] [Full Text] [Related]
2. 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]
3. Germline mutation of the p27/Kip1 gene in childhood acute lymphoblastic leukemia.
Takeuchi C; Takeuchi S; Ikezoe T; Bartram CR; Taguchi H; Koeffler HP
Leukemia; 2002 May; 16(5):956-8. PubMed ID: 11986963
[No Abstract] [Full Text] [Related]
4. 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.
Taylor GM; O'Brien HP; Greaves MF; Ravetto PF; Eden OB
Cancer Res; 2003 Oct; 63(19):6563-4; author reply 6565. PubMed ID: 14559852
[No 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. Germline configuration of the p27(Kip1) gene in childhood acute lymphoblastic leukemia (ALL).
Seriu T; Erz D; Bartram CR
Leukemia; 1996 Feb; 10(2):345. PubMed ID: 8637245
[No Abstract] [Full Text] [Related]
7. No evidence of significant silencing of Fanconi genes FANCF and FANCB or Nijmegen breakage syndrome gene NBS1 by DNA hyper-methylation in sporadic childhood leukaemia.
Meyer S; White DJ; Will AM; Eden T; Sim A; Brown R; Strathdee G
Br J Haematol; 2006 Jul; 134(1):61-3. PubMed ID: 16803569
[TBL] [Abstract][Full Text] [Related]
8. Is the NBN gene mutation I171V a potential risk factor for malignant solid tumors in children?
Nowak J; Mosor M; Nowicka K; Rembowska J; Januszkiewicz D
J Pediatr Hematol Oncol; 2011 Aug; 33(6):e248-9. PubMed ID: 21436738
[TBL] [Abstract][Full Text] [Related]
9. Polymorphisms and haplotypes of the NBS1 gene in childhood acute leukaemia.
Mosor M; Ziółkowska I; Januszkiewicz-Lewandowska D; Nowak J
Eur J Cancer; 2008 Oct; 44(15):2226-32. PubMed ID: 18691878
[TBL] [Abstract][Full Text] [Related]
10. Role of 657del5 NBN mutation and 7p12.2 (IKZF1), 9p21 (CDKN2A), 10q21.2 (ARID5B) and 14q11.2 (CEBPE) variation and risk of childhood ALL in the Polish population.
Pastorczak A; Górniak P; Sherborne A; Hosking F; Trelińska J; Lejman M; Szczepański T; Borowiec M; Fendler W; Kowalczyk J; Houlston RS; Młynarski W
Leuk Res; 2011 Nov; 35(11):1534-6. PubMed ID: 21889209
[TBL] [Abstract][Full Text] [Related]
11. Heterozygous carriers of germline c.657_661del5 founder mutation in
Tomasik B; Pastorczak A; Fendler W; Bartłomiejczyk M; Braun M; Mycko M; Madzio J; Polakowska E; Ulińska E; Matysiak M; Derwich K; Lejman M; Kowalczyk J; Badowska W; Kazanowska B; Szczepański T; Styczyński J; Irga-Jaworska N; Młynarski W;
Haematologica; 2018 May; 103(5):e200-e203. PubMed ID: 29419426
[No Abstract] [Full Text] [Related]
12. Clonality analysis suggests that early-onset acute lymphoblastic leukaemia is of single-cell origin and implies no major role for germ cell mutations in parents.
Rinaldi F; Mairs RJ; Wheldon TE; Katz F; Chessells JM; Gibson BE
Br J Cancer; 1999 May; 80(5-6):909-13. PubMed ID: 10360674
[TBL] [Abstract][Full Text] [Related]
13. First case of aplastic anemia in a Japanese child with a homozygous missense mutation in the NBS1 gene (I171V) associated with genomic instability.
Shimada H; Shimizu K; Mimaki S; Sakiyama T; Mori T; Shimasaki N; Yokota J; Nakachi K; Ohta T; Ohki M
Hum Genet; 2004 Oct; 115(5):372-6. PubMed ID: 15338273
[TBL] [Abstract][Full Text] [Related]
14. Mutation analysis of the HOX paralogous 4-13 genes in children with acute lymphoid malignancies: identification of a novel germline mutation of HOXD4 leading to a partial loss-of-function.
van Scherpenzeel Thim V; Remacle S; Picard J; Cornu G; Gofflot F; Rezsohazy R; Verellen-Dumoulin C
Hum Mutat; 2005 Apr; 25(4):384-95. PubMed ID: 15776434
[TBL] [Abstract][Full Text] [Related]
15. Germline NBS1 mutations in families with aggregation of Breast and/or ovarian cancer from north-east Poland.
Kanka C; Brozek I; Skalska B; Siemiatkowska A; Limon J
Anticancer Res; 2007; 27(4C):3015-8. PubMed ID: 17695489
[TBL] [Abstract][Full Text] [Related]
16. Homozygous deletions of p16/MTS1 and p15/MTS2 genes are frequent in t(1;19)-negative but not in t(1;19)-positive B precursor acute lymphoblastic leukemia in childhood.
Ohnishi H; Hanada R; Horibe K; Hongo T; Kawamura M; Naritaka S; Bessho F; Yanagisawa M; Nobori T; Yamamori S; Hayashi Y
Leukemia; 1996 Jul; 10(7):1104-10. PubMed ID: 8683987
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Clonal duplication of a germline PTPN11 mutation due to acquired uniparental disomy in acute lymphoblastic leukemia blasts from a patient with Noonan syndrome.
Karow A; Steinemann D; Göhring G; Hasle H; Greiner J; Harila-Saari A; Flotho C; Zenker M; Schlegelberger B; Niemeyer CM; Kratz CP
Leukemia; 2007 Jun; 21(6):1303-5. PubMed ID: 17361219
[No Abstract] [Full Text] [Related]
19. NBS1 variant I171V and breast cancer risk.
Bogdanova N; Schürmann P; Waltes R; Feshchenko S; Zalutsky IV; Bremer M; Dörk T
Breast Cancer Res Treat; 2008 Nov; 112(1):75-9. PubMed ID: 18049891
[TBL] [Abstract][Full Text] [Related]
20. Familial risks for childhood acute lymphocytic leukaemia in Sweden and Finland: far exceeding the effects of known germline variants.
Kharazmi E; da Silva Filho MI; Pukkala E; Sundquist K; Thomsen H; Hemminki K
Br J Haematol; 2012 Dec; 159(5):585-8. PubMed ID: 23025517
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]