-
1
-
-
0028172248
-
p53 Gene mutation and mdm2 gene amplification are uncommon in medulloblastoma
-
Adesina AM, Nalbantoglu J, Cavenee WK. p53 Gene mutation and mdm2 gene amplification are uncommon in medulloblastoma. Cancer Res 1994; 54: 5649
-
(1994)
Cancer Res
, vol.54
, pp. 5649
-
-
Adesina, A.M.1
Nalbantoglu, J.2
Cavenee, W.K.3
-
2
-
-
0025869612
-
Interphase cytogenetics reveals somatic pairing of chromosome 17 centromeres in normal human brain tissue, but no trisomy 8 or sex-chromosome loss
-
Arnoldus EPJ, Noordermeer IA, Peters ACB, Raap AK, van der Ploeg M. Interphase cytogenetics reveals somatic pairing of chromosome 17 centromeres in normal human brain tissue, but no trisomy 8 or sex-chromosome loss. Cytoyenet Cell Genet 1991; 56: 214-6
-
(1991)
Cytoyenet Cell Genet
, vol.56
, pp. 214-216
-
-
Arnoldus, E.P.J.1
Noordermeer, I.A.2
Peters, A.C.B.3
Raap, A.K.4
Van Der Ploeg, M.5
-
3
-
-
0024926048
-
Isochrome 17q in primitive neuroectodermal tumors of the central nervous system
-
Biegel JA, Rorke LB, Packer RJ et al. Isochrome 17q in primitive neuroectodermal tumors of the central nervous system. Genes Chromosom Cancer 1989; 1: 139-47
-
(1989)
Genes Chromosom Cancer
, vol.1
, pp. 139-147
-
-
Biegel, J.A.1
Rorke, L.B.2
Packer, R.J.3
-
4
-
-
0026634161
-
Evidence for a 17p tumor related locus distinct from p53 in pediatric primitive neuroectodermal tumors
-
Biegel JA, Burk CD, Barr FG, Emanuel BS. Evidence for a 17p tumor related locus distinct from p53 in pediatric primitive neuroectodermal tumors. Cancer Res 1992; 52: 3391
-
(1992)
Cancer Res
, vol.52
, pp. 3391
-
-
Biegel, J.A.1
Burk, C.D.2
Barr, F.G.3
Emanuel, B.S.4
-
5
-
-
0029153985
-
Isochrome 17q demonstrated by interphase fluorescence in situ hybridization in primitive neuroectodermal tumors of the central nervous system
-
Biegel JA, Rorke LB, Janss AJ, Sutton LN, Parmiter AH. Isochrome 17q demonstrated by interphase fluorescence in situ hybridization in primitive neuroectodermal tumors of the central nervous system. Genes Chromosom Cancer 1995; 14: 85-96
-
(1995)
Genes Chromosom Cancer
, vol.14
, pp. 85-96
-
-
Biegel, J.A.1
Rorke, L.B.2
Janss, A.J.3
Sutton, L.N.4
Parmiter, A.H.5
-
6
-
-
7344246543
-
Structural chromosomal abnormalities in pediatric brain tumors
-
Bigner SH, Mark J, Friedman HS, Biegel JA, Bigner DD. Structural chromosomal abnormalities in pediatric brain tumors. Cancer Res 1988; 48: 91-101
-
(1988)
Cancer Res
, vol.48
, pp. 91-101
-
-
Bigner, S.H.1
Mark, J.2
Friedman, H.S.3
Biegel, J.A.4
Bigner, D.D.5
-
7
-
-
0029944362
-
Tumor suppressor genes and medulloblastoma
-
Cogen PH, Mc Donald JD. Tumor suppressor genes and medulloblastoma. J Neuro-Oncol 1996; 29: 103-12
-
(1996)
J Neuro-Oncol
, vol.29
, pp. 103-112
-
-
Cogen, P.H.1
Mc Donald, J.D.2
-
9
-
-
0029620728
-
Prognostic factors in adult medulloblastoma. A clinico-pathologic study
-
Giordana MT, Cavalla P, Chio A et al. Prognostic factors in adult medulloblastoma. A clinico-pathologic study. Tumori 1995; 81: 338-46
-
(1995)
Tumori
, vol.81
, pp. 338-346
-
-
Giordana, M.T.1
Cavalla, P.2
Chio, A.3
-
10
-
-
0030752227
-
Is medulloblastoma the same tumor in children and adults?
-
Giordana MT, Cavalla P, Dutto A, Borsotti L, Chiò A, Schiffer D. Is medulloblastoma the same tumor in children and adults? J Neuro-Oncol 1997; 35: 169-76
-
(1997)
J Neuro-Oncol
, vol.35
, pp. 169-176
-
-
Giordana, M.T.1
Cavalla, P.2
Dutto, A.3
Borsotti, L.4
Chiò, A.5
Schiffer, D.6
-
11
-
-
0023831581
-
Chromosomal abnormalities in pediatric brain tumors
-
Griffin CA, Hawkins AL, Packer RJ, Rorke LB, Emanuel BS. Chromosomal abnormalities in pediatric brain tumors. Cancer Res 1988; 48: 175-80
-
(1988)
Cancer Res
, vol.48
, pp. 175-180
-
-
Griffin, C.A.1
Hawkins, A.L.2
Packer, R.J.3
Rorke, L.B.4
Emanuel, B.S.5
-
12
-
-
0026196872
-
Detection of numerical chromosome aberrations using in situ hybridization in paraffin sections of routinely processed bladder cancers
-
Hopman AHN, van Mooren E, de Kaa CA, Vooijs PGP, Ramaekers FCS. Detection of numerical chromosome aberrations using in situ hybridization in paraffin sections of routinely processed bladder cancers. Modern Pathol 1991; 4: 503-13
-
(1991)
Modern Pathol
, vol.4
, pp. 503-513
-
-
Hopman, A.H.N.1
Van Mooren, E.2
De Kaa, C.A.3
Vooijs, P.G.P.4
Ramaekers, F.C.S.5
-
14
-
-
0027235886
-
The cytogenetic scenario of chronic myeloid leukemia
-
Mitelmann F. The cytogenetic scenario of chronic myeloid leukemia. Lenk Lymph 1993; 11 (Suppl. 1): 11-5
-
(1993)
Lenk Lymph
, vol.11
, Issue.1 SUPPL.
, pp. 11-15
-
-
Mitelmann, F.1
-
15
-
-
0026483865
-
Detection of an i[17q] chromosome by fluorescent in situ hybridization with a chromosome alpha satellite DNA probe
-
Nakagawa H, Inazawa J, Misawa S et al. Detection of an i[17q] chromosome by fluorescent in situ hybridization with a chromosome alpha satellite DNA probe. Cancer Genet Cytogenet 1992; 62: 140-3
-
(1992)
Cancer Genet Cytogenet
, vol.62
, pp. 140-143
-
-
Nakagawa, H.1
Inazawa, J.2
Misawa, S.3
-
16
-
-
0027739843
-
Cytogenetic analysis of 109 pediatric nervous system tumors
-
Neumann E, Kalousek DK, Norman MG, Steinbok P, Cochrane DD, Goddard K. Cytogenetic analysis of 109 pediatric nervous system tumors. Cancer Genet Cytogenet 1993; 71: 40-9
-
(1993)
Cancer Genet Cytogenet
, vol.71
, pp. 40-49
-
-
Neumann, E.1
Kalousek, D.K.2
Norman, M.G.3
Steinbok, P.4
Cochrane, D.D.5
Goddard, K.6
-
17
-
-
0026347639
-
p53 mutations in nonastrocytic human brain tumors
-
Ohgaki M, Eibl RH, Wiestler OD, Yasargil MC, Newcomb EW, Kleihues P. p53 mutations in nonastrocytic human brain tumors. Cancer Res 1991; 51: 6202-5
-
(1991)
Cancer Res
, vol.51
, pp. 6202-6205
-
-
Ohgaki, M.1
Eibl, R.H.2
Wiestler, O.D.3
Yasargil, M.C.4
Newcomb, E.W.5
Kleihues, P.6
-
18
-
-
0028787405
-
Chromosome 17 abnormalities and lack of TP53 mutations in pediatric central nervous system tumours
-
Phelan CM, Liu L, Ruttledge MH, Muntzning K, Ridderheim P, Collins VP. Chromosome 17 abnormalities and lack of TP53 mutations in pediatric central nervous system tumours. Hum Genet 1995; 96: 684-90
-
(1995)
Hum Genet
, vol.96
, pp. 684-690
-
-
Phelan, C.M.1
Liu, L.2
Ruttledge, M.H.3
Muntzning, K.4
Ridderheim, P.5
Collins, V.P.6
-
19
-
-
0026720795
-
Isochromosomes in childhood acute lymphoblastic leukemia: A collaborative study of 83 cases
-
Pui C-H, Carrol AJ, Raimondi SC et al. Isochromosomes in childhood acute lymphoblastic leukemia: a collaborative study of 83 cases. Blood 1992; 79: 2384-91
-
(1992)
Blood
, vol.79
, pp. 2384-2391
-
-
Pui, C.-H.1
Carrol, A.J.2
Raimondi, S.C.3
-
20
-
-
0031014667
-
High-resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in chromosome band 17p11
-
Scheurlen WG, Seranski P, Mincheva A et al. High-resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in chromosome band 17p11. Genes Chrom Cancer 1997; 18: 50-8
-
(1997)
Genes Chrom Cancer
, vol.18
, pp. 50-58
-
-
Scheurlen, W.G.1
Seranski, P.2
Mincheva, A.3
-
21
-
-
0027960780
-
Detection of i[17q] chromosome by fluorescent in situ hybridization (FISH) with interphase nuclei in medulloblastoma
-
Vagner-Capodano AM, Zattara-Cannoni H, Gambarelli D et al. Detection of i[17q] chromosome by fluorescent in situ hybridization (FISH) with interphase nuclei in medulloblastoma. Cancer Genet Cytogenet 1994; 78: 1-6
-
(1994)
Cancer Genet Cytogenet
, vol.78
, pp. 1-6
-
-
Vagner-Capodano, A.M.1
Zattara-Cannoni, H.2
Gambarelli, D.3
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