173 related articles for article (PubMed ID: 34608183)
1. NBS1 I171V variant underlies individual differences in chromosomal radiosensitivity within human populations.
Tomioka K; Miyamoto T; Akutsu SN; Yanagihara H; Fujita K; Royba E; Tauchi H; Yamamoto T; Koh I; Hirata E; Kudo Y; Kobayashi M; Okada S; Matsuura S
Sci Rep; 2021 Oct; 11(1):19661. PubMed ID: 34608183
[TBL] [Abstract][Full Text] [Related]
2. A rare polymorphic variant of NBS1 reduces DNA repair activity and elevates chromosomal instability.
Yamamoto Y; Miyamoto M; Tatsuda D; Kubo M; Nakagama H; Nakamura Y; Satoh H; Matsuda K; Watanabe T; Ohta T
Cancer Res; 2014 Jul; 74(14):3707-15. PubMed ID: 24830725
[TBL] [Abstract][Full Text] [Related]
3. Association of ionizing radiation-induced foci of NBS1 with chromosomal instability and breast cancer susceptibility.
Someya M; Sakata K; Tauchi H; Matsumoto Y; Nakamura A; Komatsu K; Hareyama M
Radiat Res; 2006 Oct; 166(4):575-82. PubMed ID: 17007554
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Impact of heterozygous c.657-661del, p.I171V and p.R215W mutations in NBN on nibrin functions.
Dzikiewicz-Krawczyk A; Mosor M; Januszkiewicz D; Nowak J
Mutagenesis; 2012 May; 27(3):337-43. PubMed ID: 22131123
[TBL] [Abstract][Full Text] [Related]
6. Evaluation of ATM heterozygous mutations underlying individual differences in radiosensitivity using genome editing in human cultured cells.
Royba E; Miyamoto T; Natsuko Akutsu S; Hosoba K; Tauchi H; Kudo Y; Tashiro S; Yamamoto T; Matsuura S
Sci Rep; 2017 Jul; 7(1):5996. PubMed ID: 28729543
[TBL] [Abstract][Full Text] [Related]
7. Heterozygous germline mutations in NBS1 among Korean patients with high-risk breast cancer negative for BRCA1/2 mutation.
Kim H; Cho DY; Choi DH; Jung GH; Shin I; Park W; Huh SJ; Kim SW; Park SK; Lee JW; Nam SJ; Lee JE; Gil WH; Kim SW
Fam Cancer; 2015 Sep; 14(3):365-71. PubMed ID: 25712764
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Telomere instability in a human tumor cell line expressing NBS1 with mutations at sites phosphorylated by ATM.
Bai Y; Murnane JP
Mol Cancer Res; 2003 Dec; 1(14):1058-69. PubMed ID: 14707289
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Increased risk of larynx cancer in heterozygous carriers of the I171V mutation of the NBS1 gene.
Ziólkowska I; Mosor M; Wierzbicka M; Rydzanicz M; Pernak-Schwarz M; Nowak J
Cancer Sci; 2007 Nov; 98(11):1701-5. PubMed ID: 17894553
[TBL] [Abstract][Full Text] [Related]
12. Screening of homologous recombination gene polymorphisms in lung cancer patients reveals an association of the NBS1-185Gln variant and p53 gene mutations.
Medina PP; Ahrendt SA; Pollan M; Fernandez P; Sidransky D; Sanchez-Cespedes M
Cancer Epidemiol Biomarkers Prev; 2003 Aug; 12(8):699-704. PubMed ID: 12917199
[TBL] [Abstract][Full Text] [Related]
13. New mutations and protein variants of NBS1 are identified in cancer cell lines.
Tessitore A; Biordi L; Flati V; Toniato E; Marchetti P; Ricevuto E; Ficorella C; Scotto L; Giannini G; Frati L; Masciocchi C; Tombolini V; Gulino A; Martinotti S
Genes Chromosomes Cancer; 2003 Feb; 36(2):198-204. PubMed ID: 12508248
[TBL] [Abstract][Full Text] [Related]
14. A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling "Nijmegen breakage syndrome" phenotype.
Berardinelli F; di Masi A; Salvatore M; Banerjee S; Myung K; De Villartay JP; Revy P; Plebani A; Soresina A; Taruscio D; Tanzarella C; Antoccia A
Eur J Med Genet; 2007; 50(3):176-87. PubMed ID: 17395558
[TBL] [Abstract][Full Text] [Related]
15. Importin KPNA2 is required for proper nuclear localization and multiple functions of NBS1.
Tseng SF; Chang CY; Wu KJ; Teng SC
J Biol Chem; 2005 Nov; 280(47):39594-600. PubMed ID: 16188882
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Association of DNA-PK activity and radiation-induced NBS1 foci formation in lymphocytes with clinical malignancy in breast cancer patients.
Someya M; Sakata K; Matsumoto Y; Tauchi H; Narimatsu H; Hareyama M
Oncol Rep; 2007 Oct; 18(4):873-8. PubMed ID: 17786349
[TBL] [Abstract][Full Text] [Related]
18. c-Myc directly regulates the transcription of the NBS1 gene involved in DNA double-strand break repair.
Chiang YC; Teng SC; Su YN; Hsieh FJ; Wu KJ
J Biol Chem; 2003 May; 278(21):19286-91. PubMed ID: 12637527
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Associations of DNA-repair gene polymorphisms with a genetic susceptibility to ionizing radiation in residents of areas with high radon (222Rn) concentration.
Sinitsky MY; Larionov AV; Asanov MA; Druzhinin VG
Int J Radiat Biol; 2015 Jun; 91(6):486-94. PubMed ID: 25651041
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
