111 related articles for article (PubMed ID: 9233578)
21. 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]
22. Homozygous deletions of cyclin-dependent kinase inhibitor genes, p16(INK4A) and p18, in childhood T cell lineage acute lymphoblastic leukemias.
Iolascon A; Faienza MF; Coppola B; della Ragione F; Schettini F; Biondi A
Leukemia; 1996 Feb; 10(2):255-60. PubMed ID: 8637234
[TBL] [Abstract][Full Text] [Related]
23. Inverse correlation between Ink4-locus deletions and ICM-DNA hyperdiploidy in childhood acute lymphoblastic leukaemia, relation to clinical characteristics and outcome.
Moreno TC; Widell S; Czader M; Grandér D; Söderhäll S; Gustafsson G; Einhorn S; Porwit A; Heyman M
Eur J Haematol; 2000 Dec; 65(6):390-8. PubMed ID: 11168496
[TBL] [Abstract][Full Text] [Related]
24. The prognostic significance of p16INK4a/p14ARF and p15INK4b deletions in adult acute lymphoblastic leukemia.
Faderl S; Kantarjian HM; Manshouri T; Chan CY; Pierce S; Hays KJ; Cortes J; Thomas D; Estrov Z; Albitar M
Clin Cancer Res; 1999 Jul; 5(7):1855-61. PubMed ID: 10430092
[TBL] [Abstract][Full Text] [Related]
25. p16ink4a gene and hematological malignancies.
Quesnel B; Preudhomme C; Fenaux P
Leuk Lymphoma; 1996 Jun; 22(1-2):11-24. PubMed ID: 8724524
[TBL] [Abstract][Full Text] [Related]
26. Association of rat p15INK4B/p16INK4 deletions with monosomy 5 in kidney epithelial cell lines but not primary renal tumors.
Knapek DF; Serrano M; Beach D; Trono D; Walker CL
Cancer Res; 1995 Apr; 55(8):1607-12. PubMed ID: 7712460
[TBL] [Abstract][Full Text] [Related]
27. Exclusive p15INK4B gene deletions in acute lymphocytic leukemia include the E1 beta exon of the p16INK4 gene.
Heyman M; Rasool O; Brandter LB; Liu Y; Grandér D; Einhorn S; Söderhäll S
Blood; 1996 Feb; 87(4):1657-8. PubMed ID: 8608263
[No Abstract] [Full Text] [Related]
28. Frequent loss of heterozygosity on chromosome 9, and low incidence of mutations of cyclin-dependent kinase inhibitors p15 (MTS2) and p16 (MTS1) genes in gliomas.
Li YJ; Hoang-Xuan K; Delattre JY; Poisson M; Thomas G; Hamelin R
Oncogene; 1995 Aug; 11(3):597-600. PubMed ID: 7630644
[TBL] [Abstract][Full Text] [Related]
29. Aberrant methylation of p16INK4a and deletion of p15INK4b are frequent events in human esophageal cancer in Linxian, China.
Xing EP; Nie Y; Wang LD; Yang GY; Yang CS
Carcinogenesis; 1999 Jan; 20(1):77-84. PubMed ID: 9934853
[TBL] [Abstract][Full Text] [Related]
30. Molecular analysis of P16(Ink4)/CDKN2 and P15(INK4B)/MTS2 genes in primary human testicular germ cell tumors.
Heidenreich A; Gaddipati JP; Moul JW; Srivastava S
J Urol; 1998 May; 159(5):1725-30. PubMed ID: 9554401
[TBL] [Abstract][Full Text] [Related]
31. Deletion mapping indicates that MTS1 is the target of frequent deletions at chromosome 9p21 in paediatric acute lymphoblastic leukaemias.
Guidal-Giroux C; Gérard B; Cavé H; Duval M; Rohrlich P; Elion J; Vilmer E; Grandchamp B
Br J Haematol; 1996 Feb; 92(2):410-9. PubMed ID: 8603008
[TBL] [Abstract][Full Text] [Related]
32. Analysis of the Rb gene and cyclin-dependent kinase 4 inhibitor genes (p16INK4 and p15INK4B) in human ovarian carcinoma cell lines.
Yaginuma Y; Hayashi H; Kawai K; Kurakane T; Saitoh Y; Kitamura S; Sengoku K; Ishikawa M
Exp Cell Res; 1997 Jun; 233(2):233-9. PubMed ID: 9194486
[TBL] [Abstract][Full Text] [Related]
33. A T cell lymphoblastic lymphoma patient with two malignant cell populations carrying different 9p deletions including the p16INK4 and p15INK4B genes: Clinical response to interferon-alpha therapy in one of the subclones.
Heyman M; Nordgren A; Jeddi-Tehrani M; Rasool O; Liu Y; Grander D; Ost A; Wallberg B; Johansson B
Leukemia; 1996 May; 10(5):909-17. PubMed ID: 8656689
[No Abstract] [Full Text] [Related]
34. Deletion of the Ink4-locus (the p16ink4a, p14ARF and p15ink4b genes) predicts relapse in children with ALL treated according to the Nordic protocols NOPHO-86 and NOPHO-92.
Calero Moreno TM; Gustafsson G; Garwicz S; Grandér D; Jonmundsson GK; Frost BM; Mäkipernaa A; Rasool O; Savolainen ER; Schmiegelow K; Söderhäll S; Vettenranta K; Wesenberg F; Einhorn S; Heyman M
Leukemia; 2002 Oct; 16(10):2037-45. PubMed ID: 12357355
[TBL] [Abstract][Full Text] [Related]
35. Frequent loss of heterozygosity on the long arm of chromosome 6: identification of two distinct regions of deletion in childhood acute lymphoblastic leukemia.
Takeuchi S; Koike M; Seriu T; Bartram CR; Schrappe M; Reiter A; Park S; Taub HE; Kubonishi I; Miyoshi I; Koeffler HP
Cancer Res; 1998 Jun; 58(12):2618-23. PubMed ID: 9635588
[TBL] [Abstract][Full Text] [Related]
36. Homozygous deletion of the MTS1/p16 and MTS2/p15 genes and amplification of the CDK4 gene in glioma.
Sonoda Y; Yoshimoto T; Sekiya T
Oncogene; 1995 Nov; 11(10):2145-9. PubMed ID: 7478535
[TBL] [Abstract][Full Text] [Related]
37. Alterations of the tumor suppressor genes CDKN2A (p16(INK4a)), p14(ARF), CDKN2B (p15(INK4b)), and CDKN2C (p18(INK4c)) in atypical and anaplastic meningiomas.
Boström J; Meyer-Puttlitz B; Wolter M; Blaschke B; Weber RG; Lichter P; Ichimura K; Collins VP; Reifenberger G
Am J Pathol; 2001 Aug; 159(2):661-9. PubMed ID: 11485924
[TBL] [Abstract][Full Text] [Related]
38. Microsatellite instability and other molecular abnormalities in childhood acute lymphoblastic leukaemia.
Takeuchi S; Seriu T; Tasaka T; Koike M; Cho SK; Park S; Slater J; Mufti I; Hatta Y; Miyoshi I; Bartram CR; Koeffler HP
Br J Haematol; 1997 Jul; 98(1):134-9. PubMed ID: 9233576
[TBL] [Abstract][Full Text] [Related]
39. Loss of heterozygosity in the chromosomal region 12p12-13 is very common in childhood acute lymphoblastic leukemia and permits the precise localization of a tumor-suppressor gene distinct from p27KIP1.
Cavé H; Gérard B; Martin E; Guidal C; Devaux I; Weissenbach J; Elion J; Vilmer E; Grandchamp B
Blood; 1995 Nov; 86(10):3869-75. PubMed ID: 7579355
[TBL] [Abstract][Full Text] [Related]
40. Mutational analysis of the Hel-N1 gene in childhood acute lymphoblastic leukemia with LOH at 9p21.
Takeuchi C; Takeuchi S; Ikezoe T; Bartram CR; Koeffler HP; Taguchi H
Leukemia; 1999 Apr; 13(4):650-1. PubMed ID: 10214879
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]