-
1
-
-
0032517341
-
The p16(INK4a)/CDKN2A tumor suppressor and its relatives
-
Ruas M, Peters G. The p16(INK4a)/CDKN2A tumor suppressor and its relatives. Biochim Biophys Acta. 1998;1378:F115-F177.
-
(1998)
Biochim Biophys Acta
, vol.1378
-
-
Ruas, M.1
Peters, G.2
-
2
-
-
0036180120
-
Molecular aspects of the mammalian cell cycle and cancer
-
Sandal T. Molecular aspects of the mammalian cell cycle and cancer. Oncologist. 2002;7:73-81.
-
(2002)
Oncologist
, vol.7
, pp. 73-81
-
-
Sandal, T.1
-
3
-
-
0031860559
-
Review of alterations of the cyclindependent kinase inhibitor INK4 family genes p15, p16, p18 and p19 in human leukemia-lymphoma cells
-
Drexler HG. Review of alterations of the cyclindependent kinase inhibitor INK4 family genes p15, p16, p18 and p19 in human leukemia-lymphoma cells. Leukemia. 1998;12:845-859.
-
(1998)
Leukemia
, vol.12
, pp. 845-859
-
-
Drexler, H.G.1
-
4
-
-
0037071399
-
Tumor suppressor genes in normal and malignant hematopoiesis
-
Krug U, Ganser A, Koeffler HP. Tumor suppressor genes in normal and malignant hematopoiesis. Oncogene. 2002;21:3475-3495.
-
(2002)
Oncogene
, vol.21
, pp. 3475-3495
-
-
Krug, U.1
Ganser, A.2
Koeffler, H.P.3
-
5
-
-
0030725637
-
Allelic loss in childhood acute lymphoblastic leukemia
-
Baccichet A, Qualman SK, Sinnett D. Allelic loss in childhood acute lymphoblastic leukemia. Leukemia Res. 1997;21:817-823.
-
(1997)
Leukemia Res
, vol.21
, pp. 817-823
-
-
Baccichet, A.1
Qualman, S.K.2
Sinnett, D.3
-
6
-
-
0030670674
-
Homozygous deletions at 9p21 in childhood acute lymphoblastic leukemia detected by microsatellite analysis
-
Takeuchi S, Koike M, Seriu T, et al. Homozygous deletions at 9p21 in childhood acute lymphoblastic leukemia detected by microsatellite analysis. Leukemia. 1997;11:1636-1640.
-
(1997)
Leukemia
, vol.11
, pp. 1636-1640
-
-
Takeuchi, S.1
Koike, M.2
Seriu, T.3
-
7
-
-
0037269170
-
Long-term study of the clinical significance of loss of heterozygosity in childhood acute lymphoblastic leukemia
-
Takeuchi S, Tsukasaki K, Bartram CR, et al. Long-term study of the clinical significance of loss of heterozygosity in childhood acute lymphoblastic leukemia. Leukemia. 2003;17:149-154.
-
(2003)
Leukemia
, vol.17
, pp. 149-154
-
-
Takeuchi, S.1
Tsukasaki, K.2
Bartram, C.R.3
-
8
-
-
17144422895
-
Loss of heterozygosity in childhood acute lymphoblastic leukemia detected by genome-wide microarray single nucleotide polymorphism analysis
-
Irving JA, Bloodworth L, Bown NP, Case MC, Hogarth LA, Hall AG. Loss of heterozygosity in childhood acute lymphoblastic leukemia detected by genome-wide microarray single nucleotide polymorphism analysis. Cancer Res. 2005;65: 3053-3058.
-
(2005)
Cancer Res
, vol.65
, pp. 3053-3058
-
-
Irving, J.A.1
Bloodworth, L.2
Bown, N.P.3
Case, M.C.4
Hogarth, L.A.5
Hall, A.G.6
-
9
-
-
0033170533
-
p27KIP1 deletions in childhood acute lymphoblastic leukemia
-
Komuro H, Valentine MB, Rubnitz JE, et al. p27KIP1 deletions in childhood acute lymphoblastic leukemia. Neoplasia. 1999;1:253-261.
-
(1999)
Neoplasia
, vol.1
, pp. 253-261
-
-
Komuro, H.1
Valentine, M.B.2
Rubnitz, J.E.3
-
10
-
-
0035949707
-
Haploinsufficiency of the Pten tumor suppressor gene promotes prostate cancer progression
-
Kwabi-Addo B, Giri D, Schmidt K, et al. Haploinsufficiency of the Pten tumor suppressor gene promotes prostate cancer progression. Proc Natl Acad Sci U S A. 2001;98:11563-11568.
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 11563-11568
-
-
Kwabi-Addo, B.1
Giri, D.2
Schmidt, K.3
-
11
-
-
23844456592
-
Comprehensive analysis of CDKN2A status in microdissected urothelial cell carcinoma reveals potential haploinsufficiency, a high frequency of homozygous co-deletion and associations with clinical phenotype
-
Chapman EJ, Harnden P, Chambers P, Johnston C, Knowles MA. Comprehensive analysis of CDKN2A status in microdissected urothelial cell carcinoma reveals potential haploinsufficiency, a high frequency of homozygous co-deletion and associations with clinical phenotype. Clin Cancer Res. 2005;11:5740-5747.
-
(2005)
Clin Cancer Res
, vol.11
, pp. 5740-5747
-
-
Chapman, E.J.1
Harnden, P.2
Chambers, P.3
Johnston, C.4
Knowles, M.A.5
-
12
-
-
0029121279
-
Homozygous deletions of p16/MTS1 gene are frequent but mutations are infrequent in childhood T-cell acute lymphoblastic leukemia
-
Ohnishi H, Kawamura M, Ida K, et al. Homozygous deletions of p16/MTS1 gene are frequent but mutations are infrequent in childhood T-cell acute lymphoblastic leukemia. Blood. 1995;86: 1269-1275.
-
(1995)
Blood
, vol.86
, pp. 1269-1275
-
-
Ohnishi, H.1
Kawamura, M.2
Ida, K.3
-
13
-
-
0037402496
-
CDKN2A, CDKN2B, and MTAP gene dosage permits precise characterization of mono- and bi-allelic 9p21 deletions in childhood acute lymphoblastic leukemia
-
Bertin R, Acquaviva C, Mirebeau D, Guidal-Giroux C, Vilmer E, Cave H. CDKN2A, CDKN2B, and MTAP gene dosage permits precise characterization of mono- and bi-allelic 9p21 deletions in childhood acute lymphoblastic leukemia. Genes Chromosomes Cancer. 2003;37:44-57.
-
(2003)
Genes Chromosomes Cancer
, vol.37
, pp. 44-57
-
-
Bertin, R.1
Acquaviva, C.2
Mirebeau, D.3
Guidal-Giroux, C.4
Vilmer, E.5
Cave, H.6
-
14
-
-
0030714115
-
Methylation of the multi tumor suppressor gene-2 (MTS2, CDKN1, p15INK4B) in childhood acute lymphoblastic leukemia
-
Iravani M, Dhat R, Price CM. Methylation of the multi tumor suppressor gene-2 (MTS2, CDKN1, p15INK4B) in childhood acute lymphoblastic leukemia. Oncogene. 1997;15:2609-2614.
-
(1997)
Oncogene
, vol.15
, pp. 2609-2614
-
-
Iravani, M.1
Dhat, R.2
Price, C.M.3
-
15
-
-
0034654269
-
Aberrant p15 promoter methylation in adult and childhood acute leukemias of nearly all morphologic subtypes: Potential prognostic implications
-
Wong IH, Ng MH, Huang DP, Lee JC. Aberrant p15 promoter methylation in adult and childhood acute leukemias of nearly all morphologic subtypes: potential prognostic implications. Blood. 2000;95:1942-1949.
-
(2000)
Blood
, vol.95
, pp. 1942-1949
-
-
Wong, I.H.1
Ng, M.H.2
Huang, D.P.3
Lee, J.C.4
-
16
-
-
0141725586
-
Concurrent methylation of multiple genes in childhood ALL: Correlation with phenotype and molecular subgroup
-
Gutierrez MI, Siraj AK, Bhargava M, et al. Concurrent methylation of multiple genes in childhood ALL: correlation with phenotype and molecular subgroup. Leukemia. 2003;17:1845-1850.
-
(2003)
Leukemia
, vol.17
, pp. 1845-1850
-
-
Gutierrez, M.I.1
Siraj, A.K.2
Bhargava, M.3
-
17
-
-
0348149013
-
Epigenetic inactivation of INK4/CDK/RB cell cycle pathway in acute leukemias
-
Chim CS, Wong AS, Kwong YL. Epigenetic inactivation of INK4/CDK/RB cell cycle pathway in acute leukemias. Ann Hematol. 2003;82:738-742.
-
(2003)
Ann Hematol
, vol.82
, pp. 738-742
-
-
Chim, C.S.1
Wong, A.S.2
Kwong, Y.L.3
-
18
-
-
4944236206
-
Promoter hypermethylation of cancerrelated genes: A strong independent prognostic factor in acute lymphoblastic leukemia
-
Roman-Gomez J, Jimenez-Velasco A, Castillejo JA, et al. Promoter hypermethylation of cancerrelated genes: a strong independent prognostic factor in acute lymphoblastic leukemia. Blood. 2004;104:2492-2498.
-
(2004)
Blood
, vol.104
, pp. 2492-2498
-
-
Roman-Gomez, J.1
Jimenez-Velasco, A.2
Castillejo, J.A.3
-
19
-
-
14744297076
-
Aberrant methylation in promoter-associated CpG islands of multiple genes in relapsed childhood acute lymphoblastic leukemia
-
Matsushita C, Yang Y, Takeuchi S, et al. Aberrant methylation in promoter-associated CpG islands of multiple genes in relapsed childhood acute lymphoblastic leukemia. Oncol Rep. 2004;12:97-99.
-
(2004)
Oncol Rep
, vol.12
, pp. 97-99
-
-
Matsushita, C.1
Yang, Y.2
Takeuchi, S.3
-
20
-
-
0042888879
-
Analysis of p16 gene mutations and deletions in childhood acute lymphoblastic leukemias
-
Lemos JA, Defavery R, Scrideli CA, Tone LG. Analysis of p16 gene mutations and deletions in childhood acute lymphoblastic leukemias. Sao Paulo Med J. 2003;121:58-62.
-
(2003)
Sao Paulo Med J
, vol.121
, pp. 58-62
-
-
Lemos, J.A.1
Defavery, R.2
Scrideli, C.A.3
Tone, L.G.4
-
21
-
-
0032932735
-
Alterations of the p53, p21, p16, p15 and RAS genes in childhood T-cell acute lymphoblastic leukemia
-
Kawamura M, Ohnishi H, Guo SX, et al. Alterations of the p53, p21, p16, p15 and RAS genes in childhood T-cell acute lymphoblastic leukemia. Leukemia Res. 1999;23:115-126.
-
(1999)
Leukemia Res
, vol.23
, pp. 115-126
-
-
Kawamura, M.1
Ohnishi, H.2
Guo, S.X.3
-
22
-
-
0029008903
-
Analysis of a family of cyclin-dependent kinase inhibitors: P15/MTS2/INK4B, p16/MTS1/INK4A, and p18 genes in acute lymphoblastic leukemia of childhood
-
Takeuchi S, Bartram CR, Seriu T, et al. Analysis of a family of cyclin-dependent kinase inhibitors: p15/MTS2/INK4B, p16/MTS1/INK4A, and p18 genes in acute lymphoblastic leukemia of childhood. Blood. 1995;86:755-760.
-
(1995)
Blood
, vol.86
, pp. 755-760
-
-
Takeuchi, S.1
Bartram, C.R.2
Seriu, T.3
-
23
-
-
0028979454
-
p15ink4B and p16ink4 gene inactivation in acute lymphocytic leukemia
-
Rasool O, Heyman M, Brandter LB, et al. p15ink4B and p16ink4 gene inactivation in acute lymphocytic leukemia. Blood. 1995;85:3431-3436.
-
(1995)
Blood
, vol.85
, pp. 3431-3436
-
-
Rasool, O.1
Heyman, M.2
Brandter, L.B.3
-
24
-
-
0028985436
-
p16 gene homozygous deletions in acute lymphoblastic leukemia
-
Quesnel B, Preudhomme C, Philippe N, et al. p16 gene homozygous deletions in acute lymphoblastic leukemia. Blood. 1995;85:657-663.
-
(1995)
Blood
, vol.85
, pp. 657-663
-
-
Quesnel, B.1
Preudhomme, C.2
Philippe, N.3
-
25
-
-
0035003350
-
The Leukaemia Research Fund/United Kingdom Cancer Cytogenetics Group karyotype database in acute lymphoblastic leukaemia: A valuable resource for patient management
-
Harrison CJ, Martineau M, Secker-Walker LM. The Leukaemia Research Fund/United Kingdom Cancer Cytogenetics Group karyotype database in acute lymphoblastic leukaemia: a valuable resource for patient management. Br J Haematol. 2001;113:3-10.
-
(2001)
Br J Haematol
, vol.113
, pp. 3-10
-
-
Harrison, C.J.1
Martineau, M.2
Secker-Walker, L.M.3
-
26
-
-
0028121279
-
A cell cycle regulator potentially involved in genesis of many tumor types
-
Kamb A, Gruis NA, Weaver-Feldhaus J, et al. A cell cycle regulator potentially involved in genesis of many tumor types. Science. 1994;264:436-440.
-
(1994)
Science
, vol.264
, pp. 436-440
-
-
Kamb, A.1
Gruis, N.A.2
Weaver-Feldhaus, J.3
-
27
-
-
0029843950
-
Methylation-specific PCR: A novel PCR assay for methylation status of CpG islands
-
Herman JG, Graff JR, Myohanen S, Nelkin BD, Baylin SB. Methylation-specific PCR: a novel PCR assay for methylation status of CpG islands. Proc Natl Acad Sci U S A. 1996;93:9821-9826.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 9821-9826
-
-
Herman, J.G.1
Graff, J.R.2
Myohanen, S.3
Nelkin, B.D.4
Baylin, S.B.5
-
28
-
-
22244453416
-
A robust algorithm for copy number detection using highdensity oligonucleotide single nucleotide polymorphism genotyping arrays
-
Nannya Y, Sanada M, Nakazaki K, et al. A robust algorithm for copy number detection using highdensity oligonucleotide single nucleotide polymorphism genotyping arrays. Cancer Res. 2005; 65:6071-6079.
-
(2005)
Cancer Res
, vol.65
, pp. 6071-6079
-
-
Nannya, Y.1
Sanada, M.2
Nakazaki, K.3
-
29
-
-
33744474290
-
Complex genomic alterations and gene expression in acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21
-
Strefford JC, van Delft FW, Robinson HM, et al. Complex genomic alterations and gene expression in acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21. Proc Natl Acad Sci U S A. 2006;103:8167-8172.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, pp. 8167-8172
-
-
Strefford, J.C.1
van Delft, F.W.2
Robinson, H.M.3
-
30
-
-
19944418773
-
Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNA
-
Barrett MT, Scheffer A, Ben-Dor A, et al. Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNA. Proc Natl Acad Sci U S A. 2004;101:17765-17770.
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, pp. 17765-17770
-
-
Barrett, M.T.1
Scheffer, A.2
Ben-Dor, A.3
-
31
-
-
34249668665
-
Genome complexity in acute lymphoblastic leukemia is revealed by array-based comparative genomic hybridization
-
Strefford JC, Worley H, Barber K, et al. Genome complexity in acute lymphoblastic leukemia is revealed by array-based comparative genomic hybridization. Oncogene. 2007;26:4306-4318.
-
(2007)
Oncogene
, vol.26
, pp. 4306-4318
-
-
Strefford, J.C.1
Worley, H.2
Barber, K.3
-
32
-
-
38349056439
-
Disruption of ETV6 in intron 2 results in upregulatory and insertional events in childhood acute lymphoblastic leukaemia
-
Jalali GR, An Q, Konn ZJ, et al. Disruption of ETV6 in intron 2 results in upregulatory and insertional events in childhood acute lymphoblastic leukaemia. Leukemia. 2007;22:114-123.
-
(2007)
Leukemia
, vol.22
, pp. 114-123
-
-
Jalali, G.R.1
An, Q.2
Konn, Z.J.3
-
33
-
-
34147161800
-
Five members of the CEBP transcription factor family are targeted by recurrent IGH translocations in B-cell precursor acute lymphoblastic leukemia (BCP-ALL)
-
Akasaka T, Balasas T, Russell LJ, et al. Five members of the CEBP transcription factor family are targeted by recurrent IGH translocations in B-cell precursor acute lymphoblastic leukemia (BCP-ALL). Blood. 2007;109:3451-3461.
-
(2007)
Blood
, vol.109
, pp. 3451-3461
-
-
Akasaka, T.1
Balasas, T.2
Russell, L.J.3
-
35
-
-
0033568342
-
Biologic and biochemical analyses of p16(INK4a) mutations from primary tumors
-
Yarbrough WG, Buckmire RA, Bessho M, Liu ET. Biologic and biochemical analyses of p16(INK4a) mutations from primary tumors. J Natl Cancer Inst. 1999;91:1569-1574.
-
(1999)
J Natl Cancer Inst
, vol.91
, pp. 1569-1574
-
-
Yarbrough, W.G.1
Buckmire, R.A.2
Bessho, M.3
Liu, E.T.4
-
36
-
-
0037430195
-
Clinical course of bladder neoplasms and single nucleotide polymorphisms in the CDKN2A gene
-
Sakano S, Berggren P, Kumar R, et al. Clinical course of bladder neoplasms and single nucleotide polymorphisms in the CDKN2A gene. Int J Cancer. 2003;104:98-103.
-
(2003)
Int J Cancer
, vol.104
, pp. 98-103
-
-
Sakano, S.1
Berggren, P.2
Kumar, R.3
-
37
-
-
0038135029
-
High prognostic value of p16INK4 alterations in gastrointestinal stromal tumors
-
Schneider-Stock R, Boltze C, Lasota J, et al. High prognostic value of p16INK4 alterations in gastrointestinal stromal tumors. J Clin Oncol. 2003;21: 1688-1697.
-
(2003)
J Clin Oncol
, vol.21
, pp. 1688-1697
-
-
Schneider-Stock, R.1
Boltze, C.2
Lasota, J.3
-
38
-
-
30644466740
-
Methylation of the INK4A/ARF locus in blood mononuclear cells
-
Deligezer U, Erten N, Akisik EE, Dalay N. Methylation of the INK4A/ARF locus in blood mononuclear cells. Ann Hematol. 2006;85:102-107.
-
(2006)
Ann Hematol
, vol.85
, pp. 102-107
-
-
Deligezer, U.1
Erten, N.2
Akisik, E.E.3
Dalay, N.4
-
39
-
-
34147224008
-
Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia
-
Mullighan CG, Goorha S, Radtke I, et al. Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia. Nature. 2007; 446:758-764.
-
(2007)
Nature
, vol.446
, pp. 758-764
-
-
Mullighan, C.G.1
Goorha, S.2
Radtke, I.3
-
40
-
-
43049161332
-
CDKN2A deletions in acute lymphoblastic leukemia of adolescents and young adults: An array CGH study
-
Usvasalo A, Savola S, Raty R, et al. CDKN2A deletions in acute lymphoblastic leukemia of adolescents and young adults: an array CGH study. Leukemia Res. 2008;32:1228-1235.
-
(2008)
Leukemia Res
, vol.32
, pp. 1228-1235
-
-
Usvasalo, A.1
Savola, S.2
Raty, R.3
-
41
-
-
38349177862
-
Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray
-
Kawamata N, Ogawa S, Zimmermann M, et al. Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray. Blood. 2008;111:776-784.
-
(2008)
Blood
, vol.111
, pp. 776-784
-
-
Kawamata, N.1
Ogawa, S.2
Zimmermann, M.3
-
42
-
-
33745781461
-
The prognostic significance of CDKN2A, CDKN2B and MTAP inactivation in B-lineage acute lymphoblastic leukemia of childhood: Results of the EORTC studies 58881 and 58951
-
Mirebeau D, Acquaviva C, Suciu S, et al. The prognostic significance of CDKN2A, CDKN2B and MTAP inactivation in B-lineage acute lymphoblastic leukemia of childhood: results of the EORTC studies 58881 and 58951. Haematologica. 2006;91:881-885.
-
(2006)
Haematologica
, vol.91
, pp. 881-885
-
-
Mirebeau, D.1
Acquaviva, C.2
Suciu, S.3
-
43
-
-
38049126095
-
t(6;14)(p22; q32): A new recurrent IGH@ translocation involving ID4 in B-cell precursor acute lymphoblastic leukemia (BCP-ALL)
-
Russell LJ, Akasaka T, Majid A, et al. t(6;14)(p22; q32): a new recurrent IGH@ translocation involving ID4 in B-cell precursor acute lymphoblastic leukemia (BCP-ALL). Blood. 2008;111:387-391.
-
(2008)
Blood
, vol.111
, pp. 387-391
-
-
Russell, L.J.1
Akasaka, T.2
Majid, A.3
-
44
-
-
25444510786
-
Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event
-
Teh MT, Blaydon D, Chaplin T, et al. Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event. Cancer Res. 2005;65:8597-8603.
-
(2005)
Cancer Res
, vol.65
, pp. 8597-8603
-
-
Teh, M.T.1
Blaydon, D.2
Chaplin, T.3
-
45
-
-
20144388722
-
Genome-wide association study in esophageal cancer using Gene-Chip mapping 10K array
-
Hu N, Wang C, Hu Y, et al. Genome-wide association study in esophageal cancer using Gene-Chip mapping 10K array. Cancer Res. 2005;65: 2542-2546.
-
(2005)
Cancer Res
, vol.65
, pp. 2542-2546
-
-
Hu, N.1
Wang, C.2
Hu, Y.3
-
46
-
-
12544257171
-
Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias
-
Raghavan M, Lillington DM, Skoulakis S, et al. Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias. Cancer Res. 2005;65:375-378.
-
(2005)
Cancer Res
, vol.65
, pp. 375-378
-
-
Raghavan, M.1
Lillington, D.M.2
Skoulakis, S.3
-
47
-
-
20144363192
-
Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
-
Baxter EJ, Scott LM, Campbell PJ, et al. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders. Lancet. 2005;365: 1054-1061.
-
(2005)
Lancet
, vol.365
, pp. 1054-1061
-
-
Baxter, E.J.1
Scott, L.M.2
Campbell, P.J.3
-
48
-
-
27144478643
-
Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias
-
Fitzgibbon J, Smith LL, Raghavan M, et al. Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias. Cancer Res. 2005;65:9152-9154.
-
(2005)
Cancer Res
, vol.65
, pp. 9152-9154
-
-
Fitzgibbon, J.1
Smith, L.L.2
Raghavan, M.3
-
49
-
-
0141923915
-
Outcome heterogeneity in childhood high-hyperdiploid acute lymphoblastic leukemia
-
Moorman AV, Richards SM, Martineau M, et al. Outcome heterogeneity in childhood high-hyperdiploid acute lymphoblastic leukemia. Blood. 2003;102:2756-2762.
-
(2003)
Blood
, vol.102
, pp. 2756-2762
-
-
Moorman, A.V.1
Richards, S.M.2
Martineau, M.3
-
50
-
-
0035863837
-
Hemizygous p16(INK4A) deletion in pediatric acute lymphoblastic leukemia predicts independent risk of relapse
-
Carter TL, Watt PM, Kumar R, et al. Hemizygous p16(INK4A) deletion in pediatric acute lymphoblastic leukemia predicts independent risk of relapse. Blood. 2001;97:572-574.
-
(2001)
Blood
, vol.97
, pp. 572-574
-
-
Carter, T.L.1
Watt, P.M.2
Kumar, R.3
-
51
-
-
0035100030
-
In vitro drug resistance and prognostic impact of p16INK4A/P15INK4B deletions in childhood T-cell acute lymphoblastic leukaemia
-
Ramakers-van Woerden NL, Pieters R, Slater RM, et al. In vitro drug resistance and prognostic impact of p16INK4A/P15INK4B deletions in childhood T-cell acute lymphoblastic leukaemia. Br J Haematol. 2001;112:680-690.
-
(2001)
Br J Haematol
, vol.112
, pp. 680-690
-
-
Ramakers-van Woerden, N.L.1
Pieters, R.2
Slater, R.M.3
-
52
-
-
0036529831
-
p16INK4a immunocytochemical analysis is an independent prognostic factor in childhood acute lymphoblastic leukemia
-
Dalle JH, Fournier M, Nelken B, et al. p16INK4a immunocytochemical analysis is an independent prognostic factor in childhood acute lymphoblastic leukemia. Blood. 2002;99:2620-2623.
-
(2002)
Blood
, vol.99
, pp. 2620-2623
-
-
Dalle, J.H.1
Fournier, M.2
Nelken, B.3
-
53
-
-
0030941174
-
Incidence and clinical significance of CDKN2/MTS1/ P16ink4A and MTS2/P15ink4B gene deletions in childhood acute lymphoblastic leukemia
-
Zhou M, Gu L, Yeager AM, Findley HW. Incidence and clinical significance of CDKN2/MTS1/ P16ink4A and MTS2/P15ink4B gene deletions in childhood acute lymphoblastic leukemia. Pediatr Hematol Oncol. 1997;14:141-150.
-
(1997)
Pediatr Hematol Oncol
, vol.14
, pp. 141-150
-
-
Zhou, M.1
Gu, L.2
Yeager, A.M.3
Findley, H.W.4
-
54
-
-
0029029358
-
Detection of homozygous deletions of the cyclin-dependent kinase 4 inhibitor (p16) gene in acute lymphoblastic leukemia and association with adverse prognostic features
-
Fizzotti M, Cimino G, Pisegna S, et al. Detection of homozygous deletions of the cyclin-dependent kinase 4 inhibitor (p16) gene in acute lymphoblastic leukemia and association with adverse prognostic features. Blood. 1995;85:2685-2690.
-
(1995)
Blood
, vol.85
, pp. 2685-2690
-
-
Fizzotti, M.1
Cimino, G.2
Pisegna, S.3
-
55
-
-
21744454690
-
CDKN2 deletions have no prognostic value in childhood precursor-B acute lymphoblastic leukaemia
-
van Zutven LJ, van Drunen E, de Bont JM, et al. CDKN2 deletions have no prognostic value in childhood precursor-B acute lymphoblastic leukaemia. Leukemia. 2005;19:1281-1284.
-
(2005)
Leukemia
, vol.19
, pp. 1281-1284
-
-
van Zutven, L.J.1
van Drunen, E.2
de Bont, J.M.3
-
56
-
-
0037097584
-
Deletion analysis of p16INKa and p15INKb in relapsed childhood acute lymphoblastic leukemia
-
Graf Einsiedel H, Taube T, Hartmann R, et al. Deletion analysis of p16INKa and p15INKb in relapsed childhood acute lymphoblastic leukemia. Blood. 2002;99:4629-4631.
-
(2002)
Blood
, vol.99
, pp. 4629-4631
-
-
Graf Einsiedel, H.1
Taube, T.2
Hartmann, R.3
-
57
-
-
13044266372
-
Association of chromosome arm 9p abnormalities with adverse risk in childhood acute lymphoblastic leukemia: A report from the Children's Cancer Group
-
Heerema NA, Sather HN, Sensel MG, et al. Association of chromosome arm 9p abnormalities with adverse risk in childhood acute lymphoblastic leukemia: a report from the Children's Cancer Group. Blood. 1999;94:1537-1544.
-
(1999)
Blood
, vol.94
, pp. 1537-1544
-
-
Heerema, N.A.1
Sather, H.N.2
Sensel, M.G.3
-
58
-
-
0035021732
-
Determinants of outcome after intensified therapy of childhood lymphoblastic leukaemia: Results from Medical Research Council United Kingdom acute lymphoblastic leukaemia XI protocol
-
Hann I, Vora A, Harrison G, et al. Determinants of outcome after intensified therapy of childhood lymphoblastic leukaemia: results from Medical Research Council United Kingdom acute lymphoblastic leukaemia XI protocol. Br J Haematol. 2001;113:103-114.
-
(2001)
Br J Haematol
, vol.113
, pp. 103-114
-
-
Hann, I.1
Vora, A.2
Harrison, G.3
|