-
7
-
-
0026676710
-
Cytogenetic and loss of heterozygosity studies in ependymomas, pilocytic astrocytomas, and oligodendrogliomas
-
(1992)
Genes Chromosomes Cancer
, vol.5
, pp. 348-356
-
-
Ransom, D.T.1
Ritland, S.R.2
Kimmel, D.W.3
Moertel, C.A.4
Dahl, R.J.5
Scheitauer, B.W.6
Kelly, P.J.7
Jenkins, R.B.8
-
8
-
-
0026620656
-
Correlation of cytogenetic analysis and loss of heterozygosity studies in human diffuse astrocytomas and mixed oligoastrocytomas
-
(1992)
Genes Chromosomes Cancer
, vol.5
, pp. 357-374
-
-
Ransom, D.T.1
Ritland, S.R.2
Moertel, C.A.3
Dahl, R.J.4
O'Fallon, J.R.5
Scheitauer, B.W.6
Kimmel, D.W.7
Kelly, P.J.8
Olopade, O.I.9
Diaz, M.O.10
Jenkins, R.B.11
-
9
-
-
0028063055
-
A cytogenetic study of 19 recurrent gliomas
-
(1994)
Cancer Genet Cytogenet
, vol.76
, pp. 85-92
-
-
Pruchon, E.1
Chauveinc, L.2
Sabatier, L.3
Dutrillaux, A.-M.4
Ricoul, M.5
Delattre, J.-Y.6
Vega, F.7
Poisson, M.8
Hor, F.9
Dutrillaux, B.10
-
13
-
-
0028933204
-
Involvement of chromosome 22 in ependymomas
-
(1995)
Cancer Genet Cytogenet
, vol.79
, pp. 173-176
-
-
Wernicke, C.1
Thiel, G.2
Lozanova, T.3
Vogel, S.4
Kintzel, D.5
Jänisch, W.6
Lehmann, K.7
Witkowski, R.8
-
16
-
-
0032756822
-
Cytogenetic study of 33 ependymomas
-
(1999)
Cancer Genet Cytogenet
, vol.115
, pp. 96-99
-
-
Vagner-Capodano, A.M.1
Zarrara-Cannoni, H.2
Gambarelli, D.3
Figarella-Branger, D.4
Lena, G.5
Dufour, H.6
Grisoli, F.7
Choux, M.8
-
17
-
-
0029129297
-
Molecular analysis of genetic changes in ependymomas
-
(1995)
Genes Chromosomes Cancer
, vol.13
, pp. 272-277
-
-
Biljsma, E.K.1
Voesten, A.M.J.2
Bijleveld, E.H.3
Troost, D.4
Westerveld, A.5
Merel, P.6
Thomas, G.7
Hulsebos, T.J.M.8
-
18
-
-
0032931285
-
Chromosome arm 6q loss is the most common recurrent autosomal alteration detected in primary pediatric ependymoma
-
(1999)
Genes Chromosomes Cancer
, vol.24
, pp. 230-237
-
-
Reardon, D.A.1
Entrekin, R.E.2
Sublett, J.3
Ragsdale, S.4
Li, H.5
Boyett, J.6
Kepner, J.L.7
Look, A.T.8
-
19
-
-
0035099106
-
Chromosomal abnormalities subdivide ependymal tumors into clinically relevant groups
-
(2001)
Am J Pathol
, vol.158
, pp. 1137-1143
-
-
Hirose, Y.1
Aldape, K.2
Bollen, A.3
James, C.D.4
Brat, D.5
Lamborn, K.6
Berger, M.7
Feuerstein, B.G.8
-
20
-
-
0026627772
-
Loss of heterozygosity for distal markers on 22q in human gliomas
-
(1992)
Int J Cancer
, vol.51
, pp. 703-706
-
-
Rey, J.A.1
Bello, M.J.2
Jimenez-Lara, A.3
Vaquero, J.4
Kusak, M.E.5
De Campos, J.M.6
Sarasa, J.L.7
Prestaña, A.8
-
21
-
-
0028928886
-
Analysis of the NF2 tumor-suppressor gene and of chromosome 22 deletions in gliomas
-
(1995)
Int J Cancer
, vol.60
, pp. 478-481
-
-
Hoang-Xuan, K.1
Merel, P.2
Vega, F.3
Hugot, J.-P.4
Cornu, P.5
Delattre, J.-Y.6
Poisson, M.7
Thomas, G.8
Delattre, O.9
-
23
-
-
0032734341
-
Evidence for an ependymoma tumour suppressor gene in chromosome region 22pter-22q11.2
-
(1999)
Br J Cancer
, vol.81
, pp. 1150-1154
-
-
Hulsebos, T.J.M.1
Oskam, N.T.2
Bijleveld, E.H.3
Westerveld, A.4
Hermsen, M.A.5
Van den Ouweland, A.M.W.6
Hamel, B.C.7
Tijssen, C.C.8
-
27
-
-
0028144439
-
Analysis of the neurofibromatosis 2 gene in human ependymomas and astrocytomas
-
(1994)
Cancer Res
, vol.54
, pp. 45-47
-
-
Rubio, M.-P.1
Correa, K.M.2
Ramesh, V.3
MacCollin, M.M.4
Jacoby, L.B.5
Von Deimling, A.6
Gusella, J.F.7
Louis, D.N.8
-
29
-
-
13344269669
-
Analysis of the neurofibromatosis type 2 gene in different human tumors of neuroectodermal origin
-
(1996)
Hum Genet
, vol.97
, pp. 638-641
-
-
De Vitis, L.R.1
Tedde, A.2
Vitelli, F.3
Ammannati, F.4
Mennonna, P.5
Bono, P.6
Grammatico, B.7
Grammatico, P.8
Radice, P.9
Bigozzi, U.10
Montali, E.11
Papi, L.12
-
30
-
-
0029957733
-
Frequent type 2 neurofibromatosis gene transcript mutations in sporadic intramedullary spinal cord ependymomas
-
(1996)
Neurosurgery
, vol.39
, pp. 135-140
-
-
Birch, B.D.1
Johnson, J.P.2
Parsa, A.3
Desai, R.D.4
Yoon, J.T.5
Lycette, C.A.6
Li, Y.M.7
Bruce, J.N.8
-
34
-
-
0033119495
-
NF2 gene mutations and allelic status of 1p, 14q and 22q in sporadic meningioma
-
(1999)
Oncogene
, vol.18
, pp. 2231-2239
-
-
Leone, P.E.1
Bello, M.J.2
De Campos, J.M.3
Vaquero, J.4
Sarasa, J.L.5
Pestaña, A.6
Rey, J.A.7
-
35
-
-
0027245423
-
Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2
-
(1993)
Nature
, vol.363
, pp. 515-521
-
-
Rouleau, G.A.1
Merel, P.2
Lutchman, M.3
Sanson, M.4
Zumn, J.5
Marineau, C.6
Hoang-Xuan, K.7
Demezuk, S.8
Desmaze, C.9
Plougastel, B.10
Pulst, S.M.11
Lenoir, G.12
Bijlsma, E.13
Fashold, R.14
Dumanski, J.15
De Jong, P.16
Parry, D.17
Eldrige, R.18
Aurias, A.19
Delattre, O.20
Thomas, G.21
more..
-
36
-
-
0028326668
-
Exon scanning for mutation of the NF2 gene in schwannomas
-
(1994)
Hum Mol Genet
, vol.3
, pp. 413-419
-
-
Jacoby, L.B.1
MacCollin, M.2
Louis, D.N.3
Mohney, T.4
Rubio, M.P.5
Pulaski, K.6
Trofatter, J.A.7
Kley, N.8
Seizinger, B.9
Ramesh, V.10
Gusella, J.F.11
-
37
-
-
0032801035
-
Molecular genetic aspects of oligodendrogliomas including analysis by comparative genomic hybridization
-
(1999)
Am J Pathol
, vol.155
, pp. 375-386
-
-
Bigner, S.H.1
Matthews, M.R.2
Rasheed, B.K.A.3
Wiltshire, R.N.4
Friedman, H.S.5
Friedman, A.H.6
Stenzel, T.T.7
Dawes, D.M.8
McLendon, R.E.9
Bigner, D.D.10
-
40
-
-
0029059911
-
Allelic loss at 1p and 19q frequently occurs in association and may represent early oncogeneic events in oligodendroglial tumors
-
(1995)
Int J Cancer
, vol.64
, pp. 207-210
-
-
Bello, M.J.1
Leone, P.E.2
Vaquero, J.3
De Campos, J.M.4
Kusak, M.E.5
Sarasa, J.L.6
Pestaña, A.7
Rey, J.A.8
-
41
-
-
0002161732
-
Shared allelic losses on chromosome 1p and 19q suggest a common origin of oligodenedroglioma and oligoastrocytoma
-
(1995)
J Neuropathol Exp Neurol
, vol.56
, pp. 1098-1104
-
-
Kraus, J.A.1
Koopman, J.2
Kaskel, P.3
Maintz, D.4
Brandner, S.5
Schramm, J.6
Louis, D.N.7
Wiestler, O.D.8
Von Deimling, A.9
-
43
-
-
0035869674
-
Molecular genetic alterations on chromosomes 11 and 22 in ependymomas
-
(2001)
Int J Cancer
, vol.91
, Issue.6
, pp. 803-808
-
-
Lamszus, K.1
Lachenmayer, L.2
Heinemann, U.3
Kluwe, L.4
Finckh, U.5
Hoppner, W.6
Stavrou, D.7
Fillbrandt, R.8
Westphal, M.9
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