134 related articles for article (PubMed ID: 9477137)
1. Two Japanese siblings with Bloom syndrome gene mutation and B-cell lymphoma.
Kaneko H; Inoue R; Fukao T; Kasahara K; Tashita H; Teramoto T; Kondo N
Leuk Lymphoma; 1997 Nov; 27(5-6):539-42. PubMed ID: 9477137
[TBL] [Abstract][Full Text] [Related]
2. Relatively common mutations of the Bloom syndrome gene in the Japanese population.
Kaneko H; Isogai K; Fukao T; Matsui E; Kasahara K; Yachie A; Seki H; Koizumi S; Arai M; Utunomiya J; Miki Y; Kondo N
Int J Mol Med; 2004 Sep; 14(3):439-42. PubMed ID: 15289897
[TBL] [Abstract][Full Text] [Related]
3. Expression of the BLM gene in human haematopoietic cells.
Kaneko H; Matsui E; Fukao T; Kasahara K; Morimoto W; Kondo N
Clin Exp Immunol; 1999 Nov; 118(2):285-9. PubMed ID: 10540192
[TBL] [Abstract][Full Text] [Related]
4. Microsatellite instability in B-cell lymphoma originating from Bloom syndrome.
Kaneko H; Inoue R; Yamada Y; Sukegawa K; Fukao T; Tashita H; Teramoto T; Kasahara K; Takami T; Kondo N
Int J Cancer; 1996 Dec; 69(6):480-3. PubMed ID: 8980251
[TBL] [Abstract][Full Text] [Related]
5. The DNA helicase activity of BLM is necessary for the correction of the genomic instability of bloom syndrome cells.
Neff NF; Ellis NA; Ye TZ; Noonan J; Huang K; Sanz M; Proytcheva M
Mol Biol Cell; 1999 Mar; 10(3):665-76. PubMed ID: 10069810
[TBL] [Abstract][Full Text] [Related]
6. The function of RecQ helicase gene family (especially BLM) in DNA recombination and joining.
Kaneko H; Fukao T; Kondo N
Adv Biophys; 2004; 38():45-64. PubMed ID: 15493327
[TBL] [Abstract][Full Text] [Related]
7. Augmented cell death with Bloom syndrome helicase deficiency.
Kaneko H; Fukao T; Kasahara K; Yamada T; Kondo N
Mol Med Rep; 2011; 4(4):607-9. PubMed ID: 21567087
[TBL] [Abstract][Full Text] [Related]
8. Expression of BLM (the causative gene for Bloom syndrome) and screening of Bloom syndrome.
Morimoto W; Kaneko H; Isogai K; Kasahara K; Kondo N
Int J Mol Med; 2002 Jul; 10(1):95-9. PubMed ID: 12060858
[TBL] [Abstract][Full Text] [Related]
9. Clinical features of Bloom syndrome and function of the causative gene, BLM helicase.
Kaneko H; Kondo N
Expert Rev Mol Diagn; 2004 May; 4(3):393-401. PubMed ID: 15137905
[TBL] [Abstract][Full Text] [Related]
10. High frequency of a common Bloom syndrome Ashkenazi mutation among Jews of Polish origin.
Shahrabani-Gargir L; Shomrat R; Yaron Y; Orr-Urtreger A; Groden J; Legum C
Genet Test; 1998; 2(4):293-6. PubMed ID: 10464606
[TBL] [Abstract][Full Text] [Related]
11. Bloom helicase is involved in DNA surveillance in early S phase in vertebrate cells.
Imamura O; Fujita K; Shimamoto A; Tanabe H; Takeda S; Furuichi Y; Matsumoto T
Oncogene; 2001 Mar; 20(10):1143-51. PubMed ID: 11313858
[TBL] [Abstract][Full Text] [Related]
12. [Bloom syndrome].
Kondo N
Nihon Rinsho; 2000 Jul; 58(7):1460-6. PubMed ID: 10921324
[TBL] [Abstract][Full Text] [Related]
13. Ashkenazi Jewish population frequency of the Bloom syndrome gene 2281 delta 6ins7 mutation.
Roa BB; Savino CV; Richards CS
Genet Test; 1999; 3(2):219-21. PubMed ID: 10464671
[TBL] [Abstract][Full Text] [Related]
14. Transfection of BLM into cultured bloom syndrome cells reduces the sister-chromatid exchange rate toward normal.
Ellis NA; Proytcheva M; Sanz MM; Ye TZ; German J
Am J Hum Genet; 1999 Nov; 65(5):1368-74. PubMed ID: 10521302
[TBL] [Abstract][Full Text] [Related]
15. Telomerase activity in cell lines and lymphoma originating from Bloom syndrome.
Kaneko H; Morimoto W; Fukao T; Kasahara K; Kondo N
Leuk Lymphoma; 2001 Aug; 42(4):757-60. PubMed ID: 11697506
[TBL] [Abstract][Full Text] [Related]
16. A novel frameshift mutation in BLM gene associated with high sister chromatid exchanges (SCE) in heterozygous family members.
Ben Salah G; Hadj Salem I; Masmoudi A; Kallabi F; Turki H; Fakhfakh F; Ayadi H; Kamoun H
Mol Biol Rep; 2014 Nov; 41(11):7373-80. PubMed ID: 25129257
[TBL] [Abstract][Full Text] [Related]
17. Structural basis of Bloom syndrome (BS) causing mutations in the BLM helicase domain.
Rong SB; Väliaho J; Vihinen M
Mol Med; 2000 Mar; 6(3):155-64. PubMed ID: 10965492
[TBL] [Abstract][Full Text] [Related]
18. Chromosomal instability associated with a novel BLM frameshift mutation (c.1980-1982delAA) in two unrelated Tunisian families with Bloom syndrome.
Ben Salah G; Salem IH; Masmoudi A; Ben Rhouma B; Turki H; Fakhfakh F; Ayadi H; Kamoun H
J Eur Acad Dermatol Venereol; 2014 Oct; 28(10):1318-23. PubMed ID: 24118499
[TBL] [Abstract][Full Text] [Related]
19. Characterization of a new BLM mutation associated with a topoisomerase II alpha defect in a patient with Bloom's syndrome.
Foucault F; Vaury C; Barakat A; Thibout D; Planchon P; Jaulin C; Praz F; Amor-Guéret M
Hum Mol Genet; 1997 Sep; 6(9):1427-34. PubMed ID: 9285778
[TBL] [Abstract][Full Text] [Related]
20. Three new BLM gene mutations associated with Bloom syndrome.
Amor-Guéret M; Dubois-d'Enghien C; Laugé A; Onclercq-Delic R; Barakat A; Chadli E; Bousfiha AA; Benjelloun M; Flori E; Doray B; Laugel V; Lourenço MT; Gonçalves R; Sousa S; Couturier J; Stoppa-Lyonnet D
Genet Test; 2008 Jun; 12(2):257-61. PubMed ID: 18471088
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
