263 related articles for article (PubMed ID: 16007594)
1. Mutation analysis of SBDS in pediatric acute myeloblastic leukemia.
Majeed F; Jadko S; Freedman MH; Dror Y
Pediatr Blood Cancer; 2005 Dec; 45(7):920-4. PubMed ID: 16007594
[TBL] [Abstract][Full Text] [Related]
2. The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndrome.
Minelli A; Maserati E; Nicolis E; Zecca M; Sainati L; Longoni D; Lo Curto F; Menna G; Poli F; De Paoli E; Cipolli M; Locatelli F; Pasquali F; Danesino C
Leukemia; 2009 Apr; 23(4):708-11. PubMed ID: 19148133
[TBL] [Abstract][Full Text] [Related]
3. Identification of novel mutations in patients with Shwachman-Diamond syndrome.
Nicolis E; Bonizzato A; Assael BM; Cipolli M
Hum Mutat; 2005 Apr; 25(4):410. PubMed ID: 15776428
[TBL] [Abstract][Full Text] [Related]
4. Severe Shwachman-Diamond syndrome phenotype caused by compound heterozygous missense mutations in the SBDS gene.
Erdos M; Alapi K; Balogh I; Oroszlán G; Rákóczi E; Sümegi J; Maródi L
Exp Hematol; 2006 Nov; 34(11):1517-21. PubMed ID: 17046571
[TBL] [Abstract][Full Text] [Related]
5. SBDS mutations and isochromosome 7q in a patient with Shwachman-Diamond syndrome: no predisposition to malignant transformation?
Mellink CH; Alders M; van der Lelie H; Hennekam RH; Kuijpers TW
Cancer Genet Cytogenet; 2004 Oct; 154(2):144-9. PubMed ID: 15474150
[TBL] [Abstract][Full Text] [Related]
6. Magnetic resonance imaging findings of the pancreas in patients with Shwachman-Diamond syndrome and mutations in the SBDS gene.
Toiviainen-Salo S; Raade M; Durie PR; Ip W; Marttinen E; Savilahti E; Mäkitie O
J Pediatr; 2008 Mar; 152(3):434-6. PubMed ID: 18280855
[TBL] [Abstract][Full Text] [Related]
7. The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies.
Maserati E; Pressato B; Valli R; Minelli A; Sainati L; Patitucci F; Marletta C; Mastronuzzi A; Poli F; Lo Curto F; Locatelli F; Danesino C; Pasquali F
Br J Haematol; 2009 Apr; 145(2):190-7. PubMed ID: 19222471
[TBL] [Abstract][Full Text] [Related]
8. Genetic analysis of Shwachman-Diamond syndrome: phenotypic heterogeneity in patients carrying identical SBDS mutations.
Kawakami T; Mitsui T; Kanai M; Shirahata E; Sendo D; Kanno M; Noro M; Endoh M; Hama A; Tono C; Ito E; Tsuchiya S; Igarashi Y; Abukawa D; Hayasaka K
Tohoku J Exp Med; 2005 Jul; 206(3):253-9. PubMed ID: 15942154
[TBL] [Abstract][Full Text] [Related]
9. Hematologically important mutations: Shwachman-Diamond syndrome.
Costa E; Santos R
Blood Cells Mol Dis; 2008; 40(2):183-4. PubMed ID: 17916435
[TBL] [Abstract][Full Text] [Related]
10. Mechanisms of relapse in acute leukaemia: involvement of p53 mutated subclones in disease progression in acute lymphoblastic leukaemia.
Zhu YM; Foroni L; McQuaker IG; Papaioannou M; Haynes A; Russell HH
Br J Cancer; 1999 Mar; 79(7-8):1151-7. PubMed ID: 10098750
[TBL] [Abstract][Full Text] [Related]
11. Shwachman-Diamond syndrome.
Dror Y
Pediatr Blood Cancer; 2005 Dec; 45(7):892-901. PubMed ID: 16047374
[TBL] [Abstract][Full Text] [Related]
12. RAS, FLT3, and TP53 mutations in therapy-related myeloid malignancies with abnormalities of chromosomes 5 and 7.
Side LE; Curtiss NP; Teel K; Kratz C; Wang PW; Larson RA; Le Beau MM; Shannon KM
Genes Chromosomes Cancer; 2004 Mar; 39(3):217-23. PubMed ID: 14732923
[TBL] [Abstract][Full Text] [Related]
13. Novel SBDS mutations caused by gene conversion in Japanese patients with Shwachman-Diamond syndrome.
Nakashima E; Mabuchi A; Makita Y; Masuno M; Ohashi H; Nishimura G; Ikegawa S
Hum Genet; 2004 Mar; 114(4):345-8. PubMed ID: 14749921
[TBL] [Abstract][Full Text] [Related]
14. Compound heterozygous mutations of the SBDS gene in a patient with Shwachman-Diamond syndrome, type 1 diabetes mellitus and osteoporosis.
Rosendahl J; Teich N; Mossner J; Edelmann J; Koch CA
Pancreatology; 2006; 6(6):549-54. PubMed ID: 17106217
[TBL] [Abstract][Full Text] [Related]
15. Mutations of the SBDS gene are present in most patients with Shwachman-Diamond syndrome.
Woloszynek JR; Rothbaum RJ; Rawls AS; Minx PJ; Wilson RK; Mason PJ; Bessler M; Link DC
Blood; 2004 Dec; 104(12):3588-90. PubMed ID: 15284109
[TBL] [Abstract][Full Text] [Related]
16. Allogeneic stem cell transplantation for patients with acute myeloid leukemia or myelodysplastic syndrome who have chromosome 5 and/or 7 abnormalities.
van der Straaten HM; van Biezen A; Brand R; Schattenberg AV; Egeler RM; Barge RM; Cornelissen JJ; Schouten HC; Ossenkoppele GJ; Verdonck LF;
Haematologica; 2005 Oct; 90(10):1339-45. PubMed ID: 16219570
[TBL] [Abstract][Full Text] [Related]
17. Shwachman-Diamond syndrome.
Shimamura A
Semin Hematol; 2006 Jul; 43(3):178-88. PubMed ID: 16822460
[TBL] [Abstract][Full Text] [Related]
18. AML1/RUNX1 gene point mutations in childhood myeloid malignancies.
Migas A; Savva N; Mishkova O; Aleinikova OV
Pediatr Blood Cancer; 2011 Oct; 57(4):583-7. PubMed ID: 21294243
[TBL] [Abstract][Full Text] [Related]
19. Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies.
Minelli A; Maserati E; Rossi G; Bernardo ME; De Stefano P; Cecchini MP; Valli R; Albano V; Pierani P; Leszl A; Sainati L; Lo Curto F; Danesino C; Locatelli F; Pasquali F
Genes Chromosomes Cancer; 2004 Jul; 40(3):165-71. PubMed ID: 15138996
[TBL] [Abstract][Full Text] [Related]
20. Clinical and genetic analyses of presumed Shwachman-Diamond syndrome in Japan.
Taneichi H; Kanegane H; Futatani T; Otsubo K; Nomura K; Sato Y; Hama A; Kojima S; Kohdera U; Nakano T; Hori H; Kawashima H; Inoh Y; Kamizono J; Adachi N; Osugi Y; Mizuno H; Hotta N; Yoneyama H; Nakashima E; Ikegawa S; Miyawaki T
Int J Hematol; 2006 Jul; 84(1):60-2. PubMed ID: 16867904
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
