-
1
-
-
0343533273
-
Neurofibromatosis I
-
Levine AJ, Schmidek HH (eds). New York: John Wiley & Sons, Inc.
-
Cawthon R, White R. Neurofibromatosis I. In: Levine AJ, Schmidek HH (eds). Molecular Genetics of Nervous System Tumors. New York: John Wiley & Sons, Inc. 1993:329-40.
-
(1993)
Molecular Genetics of Nervous System Tumors
, pp. 329-340
-
-
Cawthon, R.1
White, R.2
-
2
-
-
0027405720
-
A novel Moesin-, Ezrin-, Radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor
-
Trofatter JA, MacCollin MM, Rutter JL, et al. A novel Moesin-, Ezrin-, Radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor. Cell 1993;72:791-800.
-
(1993)
Cell
, vol.72
, pp. 791-800
-
-
Trofatter, J.A.1
MacCollin, M.M.2
Rutter, J.L.3
-
3
-
-
0027245423
-
Alteration in a new gene encoding a putative membrane-organizing protein causes neurofibromatosis type 2
-
Rouleau GA, Merel P, Lutchman M, et al. Alteration in a new gene encoding a putative membrane-organizing protein causes neurofibromatosis type 2. Nature 1993;363:515-21.
-
(1993)
Nature
, vol.363
, pp. 515-521
-
-
Rouleau, G.A.1
Merel, P.2
Lutchman, M.3
-
4
-
-
0028142499
-
Mutational analysis of patients with neurofibromatosis 2
-
MacCollin M, Ramesh V, Jacoby LB, et al. Mutational analysis of patients with neurofibromatosis 2. Am J Hum Genet 1994;55:314-20.
-
(1994)
Am J Hum Genet
, vol.55
, pp. 314-320
-
-
MacCollin, M.1
Ramesh, V.2
Jacoby, L.B.3
-
5
-
-
0028264119
-
Evidence of the complete inactivation of the NF2 gene in the majority of sporadic meningiomas
-
Ruttledge MH, Sarrazin J, Rangaratnam S, et al. Evidence of the complete inactivation of the NF2 gene in the majority of sporadic meningiomas. Nature Genet 1994;6:180-4.
-
(1994)
Nature Genet
, vol.6
, pp. 180-184
-
-
Ruttledge, M.H.1
Sarrazin, J.2
Rangaratnam, S.3
-
6
-
-
0026480293
-
Cancer risks from germline P53 mutations
-
Frebourg T, Friend SH. Cancer risks from germline P53 mutations. J Clin Invest 1992;90:1637-41.
-
(1992)
J Clin Invest
, vol.90
, pp. 1637-1641
-
-
Frebourg, T.1
Friend, S.H.2
-
7
-
-
0025935859
-
TP53 gene mutations and 17p deletions in human astrocytomas
-
Chung R, Whaley J, Kley N, et al. TP53 gene mutations and 17p deletions in human astrocytomas. Genes Chromosomes Cancer 1991;3:323-31.
-
(1991)
Genes Chromosomes Cancer
, vol.3
, pp. 323-331
-
-
Chung, R.1
Whaley, J.2
Kley, N.3
-
9
-
-
0025938198
-
Infrequent p53 gene mutations in medulloblastomas
-
Saylors RL, Sidransky D, Friedman HS, et al. Infrequent p53 gene mutations in medulloblastomas. Cancer Res 1991;51:4721-3.
-
(1991)
Cancer Res
, vol.51
, pp. 4721-4723
-
-
Saylors, R.L.1
Sidransky, D.2
Friedman, H.S.3
-
10
-
-
0027290895
-
Absence of p53 mutations in childhood central nervous system primitive neuroectodermal tumors
-
Raffel C, Thomas GA, Tishler DM, et al. Absence of p53 mutations in childhood central nervous system primitive neuroectodermal tumors. Neurosurgery 1993;33:301-6.
-
(1993)
Neurosurgery
, vol.33
, pp. 301-306
-
-
Raffel, C.1
Thomas, G.A.2
Tishler, D.M.3
-
11
-
-
0028881850
-
Germline and somatic p53 gene mutations in pediatric brain tumors
-
Felix CA, Slavc I, Dunn M, et al. Germline and somatic p53 gene mutations in pediatric brain tumors. Med Pediatr Oncol 1995; 25:431-6.
-
(1995)
Med Pediatr Oncol
, vol.25
, pp. 431-436
-
-
Felix, C.A.1
Slavc, I.2
Dunn, M.3
-
12
-
-
0028970197
-
The molecular basis of Turcot's syndrome
-
Hamilton SR, Liu B, Parsons RE, et al. The molecular basis of Turcot's syndrome. N Engl J Med 1995;332:839-47.
-
(1995)
N Engl J Med
, vol.332
, pp. 839-847
-
-
Hamilton, S.R.1
Liu, B.2
Parsons, R.E.3
-
13
-
-
0023158819
-
Evidence that the gene tor tuberous sclerosis is on chromosome 9
-
Fryer AE, Chalmers A, Connor JM, et al. Evidence that the gene tor tuberous sclerosis is on chromosome 9. Lancet 1987;1:659-61.
-
(1987)
Lancet
, vol.1
, pp. 659-661
-
-
Fryer, A.E.1
Chalmers, A.2
Connor, J.M.3
-
14
-
-
0026922021
-
Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease
-
Kandt RS, Haines JL, Smith M. Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease. Nature Genet 1992;2:37-41.
-
(1992)
Nature Genet
, vol.2
, pp. 37-41
-
-
Kandt, R.S.1
Haines, J.L.2
Smith, M.3
-
15
-
-
0029826812
-
Loss of heterozygosity in tuberous sclerosis hamartomas
-
Sepp T, Yates JRW, Green AJ. Loss of heterozygosity in tuberous sclerosis hamartomas. J Med Genet 1996;33:962-4.
-
(1996)
J Med Genet
, vol.33
, pp. 962-964
-
-
Sepp, T.1
Yates, J.R.W.2
Green, A.J.3
-
16
-
-
0344994937
-
Identification of the tuberous sclerosis gene on chromosome 16
-
The European Chromosome 16 Tuberous Sclerosis Consortium: Identification of the tuberous sclerosis gene on chromosome 16. Cell 1993;5:1305-15.
-
(1993)
Cell
, vol.5
, pp. 1305-1315
-
-
-
17
-
-
0030972969
-
The tuberous sclerosis-2 gene-product, tuberin, functions as a RAB5 GTPase-activating-protein (GAP) in modulating endocytosis
-
Xiao GH, Shoarinejad F, Jin F, et al. The tuberous sclerosis-2 gene-product, tuberin, functions as a RAB5 GTPase-activating-protein (GAP) in modulating endocytosis. J Biol Chem 1997;272:6097-6100.
-
(1997)
J Biol Chem
, vol.272
, pp. 6097-6100
-
-
Xiao, G.H.1
Shoarinejad, F.2
Jin, F.3
-
18
-
-
0030921443
-
Primitive neuroectodermal tumors of the central nervous system
-
Rorke LB, Trojanowski JQ, Lee VM-Y, et al. Primitive neuroectodermal tumors of the central nervous system. Brain Pathol 1997;7:765-87.
-
(1997)
Brain Pathol
, vol.7
, pp. 765-787
-
-
Rorke, L.B.1
Trojanowski, J.Q.2
Lee, V.M.-Y.3
-
19
-
-
0024926048
-
Isochromosome 17q in primitive neuroectodermal tumors of the central nervous system
-
Biegel JA, Rorke LB, Packer RJ, et al. Isochromosome 17q in primitive neuroectodermal tumors of the central nervous system. Genes Chromosomes Cancer 1989;1:139-47.
-
(1989)
Genes Chromosomes Cancer
, vol.1
, pp. 139-147
-
-
Biegel, J.A.1
Rorke, L.B.2
Packer, R.J.3
-
20
-
-
0028856578
-
No preferential loss of one parental allele of chromosome 17p13.3 in childhood medulloblastoma
-
Scheurlen WG, Krauss J, Kuhl J, et al. No preferential loss of one parental allele of chromosome 17p13.3 in childhood medulloblastoma. Int J Cancer 1995;63:373-4.
-
(1995)
Int J Cancer
, vol.63
, pp. 373-374
-
-
Scheurlen, W.G.1
Krauss, J.2
Kuhl, J.3
-
21
-
-
0031023313
-
No preferential parent of origin for the isochromosome 17q in childhood primitive neuroectodermal tumor-medulloblastoma
-
Biegel JA, Wentz E. No preferential parent of origin for the isochromosome 17q in childhood primitive neuroectodermal tumor-medulloblastoma. Genes Chromosomes Cancer 1997;18:143-6.
-
(1997)
Genes Chromosomes Cancer
, vol.18
, pp. 143-146
-
-
Biegel, J.A.1
Wentz, E.2
-
22
-
-
0029031125
-
Prognostic implications of chromosome 17p deletions in human medulloblastomas
-
Batra SK, McLendon RE, Koo JK, et al. Prognostic implications of chromosome 17p deletions in human medulloblastomas. J Neurooncol 1995;24:39-45.
-
(1995)
J Neurooncol
, vol.24
, pp. 39-45
-
-
Batra, S.K.1
McLendon, R.E.2
Koo, J.K.3
-
23
-
-
0029944362
-
Tumor suppressor genes and medulloblastoma
-
Coaen PH, McDonald JD. Tumor suppressor genes and medulloblastoma. J Neurooncol 1996;29:103-12.
-
(1996)
J Neurooncol
, vol.29
, pp. 103-112
-
-
Coaen, P.H.1
McDonald, J.D.2
-
24
-
-
0030988932
-
Prognostic significance of chromosome 17p deletions in childhood primitive neuroectodermal tumors (medulloblastomas) of the central nervous system
-
Biegel JA, Janss AJ, Raffel C et al. Prognostic significance of chromosome 17p deletions in childhood primitive neuroectodermal tumors (medulloblastomas) of the central nervous system. Clinical Cancer Research 1997;3:473-8.
-
(1997)
Clinical Cancer Research
, vol.3
, pp. 473-478
-
-
Biegel, J.A.1
Janss, A.J.2
Raffel, C.3
-
25
-
-
0026634161
-
Evidence for a 17p tumor related locus distinct from p53 in pediatric central nervous system primitive neuroectodermal tumors
-
Biegel JA, Burk CD, Barr FG, et al. Evidence for a 17p tumor related locus distinct from p53 in pediatric central nervous system primitive neuroectodermal tumors. Cancer Res 1992;52:3391-5.
-
(1992)
Cancer Res
, vol.52
, pp. 3391-3395
-
-
Biegel, J.A.1
Burk, C.D.2
Barr, F.G.3
-
26
-
-
0026087925
-
Loss of heterozygosity on 6q, 16q and 17p in human central nervous system primitive neuroectodermal tumors
-
Thomas GA, Raffel C. Loss of heterozygosity on 6q, 16q and 17p in human central nervous system primitive neuroectodermal tumors. Cancer Res 1991;51:639-43.
-
(1991)
Cancer Res
, vol.51
, pp. 639-643
-
-
Thomas, G.A.1
Raffel, C.2
-
27
-
-
0029153985
-
Isochromosome 17q demonstrated by interphase FISH in primitive neuroectodermal tumors of the central nervous system
-
Biegel JA, Rorke LB, Janss AJ, et al. Isochromosome 17q demonstrated by interphase FISH in primitive neuroectodermal tumors of the central nervous system. Genes Chromosomes Cancer 1995;14:85-96.
-
(1995)
Genes Chromosomes Cancer
, vol.14
, pp. 85-96
-
-
Biegel, J.A.1
Rorke, L.B.2
Janss, A.J.3
-
28
-
-
0031570322
-
Molecular characterization of a genetically unstable region containing the SMS critical area and a breakpoint cluster for human PNETs
-
Wilgenbus KK, Seranski P, Brown A, et al. Molecular characterization of a genetically unstable region containing the SMS critical area and a breakpoint cluster for human PNETs. Genomics 1997;42:1-10.
-
(1997)
Genomics
, vol.42
, pp. 1-10
-
-
Wilgenbus, K.K.1
Seranski, P.2
Brown, A.3
-
29
-
-
0344563829
-
LOH detected by single strand conformation polymorphism analysis of PEDF in CNS primitive neuroectodermal tumors
-
Slave I, Rodriguez IR, Mazuruk K, et al. LOH detected by single strand conformation polymorphism analysis of PEDF in CNS primitive neuroectodermal tumors. Med Pediatr Oncol 1995;25:P174.
-
(1995)
Med Pediatr Oncol
, vol.25
-
-
Slave, I.1
Rodriguez, I.R.2
Mazuruk, K.3
-
30
-
-
0028918623
-
Prognostic significance of the c-erbB-2 oncogene product in childhood medulloblastoma
-
Gilbertson RJ, Pearson ADJ, Perry RH, et al. Prognostic significance of the c-erbB-2 oncogene product in childhood medulloblastoma. Br J Cancer 1995;73:473-7.
-
(1995)
Br J Cancer
, vol.73
, pp. 473-477
-
-
Gilbertson, R.J.1
Pearson, A.D.J.2
Perry, R.H.3
-
31
-
-
0023831581
-
Chromosome abnormalities in pediatric brain tumors
-
Griffin CA, Hawkins AL, Packer RJ, et al. Chromosome 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
-
32
-
-
0027739843
-
Cytogenetic analysis of 109 pediatric central nervous system tumors
-
Neumann E, Kalousek DK, Norman MG, et al. Cytogenetic analysis of 109 pediatric central 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
-
34
-
-
0025143557
-
Loss of genetic information in central nervous system tumors common to children and young adults
-
James CD, He J, Carlbom E, et al. Loss of genetic information in central nervous system tumors common to children and young adults. Genes Chromosomes Cancer 1990;2:94-102.
-
(1990)
Genes Chromosomes Cancer
, vol.2
, pp. 94-102
-
-
James, C.D.1
He, J.2
Carlbom, E.3
-
36
-
-
0025184893
-
Monosomy 22 in rhabdoid or atypical teratoid tumors of the brain
-
Biegel JA, Rorke LB, Packer RJ, et al. Monosomy 22 in rhabdoid or atypical teratoid tumors of the brain. J Neurosurg 1990;73:710-4.
-
(1990)
J Neurosurg
, vol.73
, pp. 710-714
-
-
Biegel, J.A.1
Rorke, L.B.2
Packer, R.J.3
-
37
-
-
0029934329
-
Central nervous system atypical teratoid/rhabdoid tumors of infancy and childhood: Definition of an entity
-
Rorke LB, Packer RJ, Biegel JA. Central nervous system atypical teratoid/rhabdoid tumors of infancy and childhood: definition of an entity. J Neurosurg 1996;85:56-65.
-
(1996)
J Neurosurg
, vol.85
, pp. 56-65
-
-
Rorke, L.B.1
Packer, R.J.2
Biegel, J.A.3
-
38
-
-
0029900741
-
Mapping of chromosomal gains and losses in primitive neuroectodermal tumors by comparative genomic hybridization
-
Schutz BR, Scheurlen W, Krauss J, et al. Mapping of chromosomal gains and losses in primitive neuroectodermal tumors by comparative genomic hybridization. Genes Chromosomes Cancer 1996;16:196-203.
-
(1996)
Genes Chromosomes Cancer
, vol.16
, pp. 196-203
-
-
Schutz, B.R.1
Scheurlen, W.2
Krauss, J.3
-
39
-
-
0345426005
-
Characterization of the molecular abnormalities of childhood medulloblastoma using comparative genomic hybridization
-
Abstract #8
-
Reardon DA, Michalkiewicz E, Sublett, et al. Characterization of the molecular abnormalities of childhood medulloblastoma using comparative genomic hybridization. Seventh International Symposium Pediatric Neuro-Oncology 1996 Abstract #8.
-
(1996)
Seventh International Symposium Pediatric Neuro-Oncology
-
-
Reardon, D.A.1
Michalkiewicz, E.2
Sublett3
-
40
-
-
0031002840
-
Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome
-
Kimonis VE, Goldstein AM, Pastakia B, et al. Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome. Am J Med Genet 1997;69:299-308.
-
(1997)
Am J Med Genet
, vol.69
, pp. 299-308
-
-
Kimonis, V.E.1
Goldstein, A.M.2
Pastakia, B.3
-
41
-
-
0026043909
-
The incidence of Gorlin syndrome in 173 consecutive cases of medulloblastoma
-
Evans DGR, Farndon PA, Burnell LD, et al. The incidence of Gorlin syndrome in 173 consecutive cases of medulloblastoma. Br J Cancer 1991;64:959-61.
-
(1991)
Br J Cancer
, vol.64
, pp. 959-961
-
-
Evans, D.G.R.1
Farndon, P.A.2
Burnell, L.D.3
-
42
-
-
15844386165
-
Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome
-
Hahn H, Wicking C, Zuphiropoulos PG, et al. Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome. Cell 1996;85:841-51.
-
(1996)
Cell
, vol.85
, pp. 841-851
-
-
Hahn, H.1
Wicking, C.2
Zuphiropoulos, P.G.3
-
43
-
-
15844381336
-
Human homolog of patched, a candidate gene for basal cell nevus syndrome
-
Johnson RL, Rothman AL, Xie J, et al. Human homolog of patched, a candidate gene for basal cell nevus syndrome. Science 1996;272:1668-71.
-
(1996)
Science
, vol.272
, pp. 1668-1671
-
-
Johnson, R.L.1
Rothman, A.L.2
Xie, J.3
-
44
-
-
0030933277
-
Oncoprotein networks
-
Hunter T. Oncoprotein networks. Cell 1997;88:333-46.
-
(1997)
Cell
, vol.88
, pp. 333-346
-
-
Hunter, T.1
-
45
-
-
0030955557
-
Basal cell carcinomas in mice overexpressing sonic hedgehog
-
Oro AE, Higgis KM, Hu Z, et al. Basal cell carcinomas in mice overexpressing sonic hedgehog. Science 1997;276:817-21
-
(1997)
Science
, vol.276
, pp. 817-821
-
-
Oro, A.E.1
Higgis, K.M.2
Hu, Z.3
-
46
-
-
0031036694
-
Sporadic medulloblastomas contain PTCH mutations
-
Raffel C, Jenkins RB, Frederick L, et al. Sporadic medulloblastomas contain PTCH mutations. Cancer Res 1996;57:842-5.
-
(1996)
Cancer Res
, vol.57
, pp. 842-845
-
-
Raffel, C.1
Jenkins, R.B.2
Frederick, L.3
-
47
-
-
0028350888
-
Germ-line and somatic mutations of the APC gene in patients with Turcot-syndrome and analysis of APC mutations in brain tumors
-
Mori T, Nagase H, Horii A, et al. Germ-line and somatic mutations of the APC gene in patients with Turcot-syndrome and analysis of APC mutations in brain tumors. Genes Chromosomes Cancer 1994;9:168-72.
-
(1994)
Genes Chromosomes Cancer
, vol.9
, pp. 168-172
-
-
Mori, T.1
Nagase, H.2
Horii, A.3
-
48
-
-
0030944065
-
b-catenin as oncogene: The smoking gun
-
Peifer M. b-catenin as oncogene: the smoking gun. Science 1997;275:1752-4.
-
(1997)
Science
, vol.275
, pp. 1752-1754
-
-
Peifer, M.1
-
49
-
-
0028568009
-
Expression of the neurotrophin receptor trkC linked to a favorable outcome in medulloblastoma
-
Segal RA, Goumnerova LC, Kwon YK, et al. Expression of the neurotrophin receptor trkC linked to a favorable outcome in medulloblastoma. Proc Natl Acad Sci USA 1994;91:2867-71.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 2867-2871
-
-
Segal, R.A.1
Goumnerova, L.C.2
Kwon, Y.K.3
-
51
-
-
0018149630
-
Histopathology and prognosis of Wilms tumors: Results from the First National Wilms' Tumor Study
-
Beckwith JB, Palmer NF. Histopathology and prognosis of Wilms tumors: results from the First National Wilms' Tumor Study. Cancer 1978;41:1937-48.
-
(1978)
Cancer
, vol.41
, pp. 1937-1948
-
-
Beckwith, J.B.1
Palmer, N.F.2
-
52
-
-
0021749530
-
The association of embryonal tumors originating in the kidney and in the brain
-
Bonnin JM, Rubinstein LJ, Palmer NF, et al. The association of embryonal tumors originating in the kidney and in the brain. Cancer 1984;54:2137-46.
-
(1984)
Cancer
, vol.54
, pp. 2137-2146
-
-
Bonnin, J.M.1
Rubinstein, L.J.2
Palmer, N.F.3
-
53
-
-
0029682255
-
Narrowing the critical region for a rhabdoid tumor locus in 22q11
-
Biegel JA, Allen CS, Kawasaki K, et al. Narrowing the critical region for a rhabdoid tumor locus in 22q11. Genes Chromosomes Cancer 1996;16:94-105.
-
(1996)
Genes Chromosomes Cancer
, vol.16
, pp. 94-105
-
-
Biegel, J.A.1
Allen, C.S.2
Kawasaki, K.3
-
54
-
-
0030032087
-
Loss of heterozygosity at chromosome regions 22q11-12 and 11p15.5 in renal rhabdoid tumors
-
Schofield DE, Beckwith JlB, Sklar J. Loss of heterozygosity at chromosome regions 22q11-12 and 11p15.5 in renal rhabdoid tumors. Genes Chromosomes Cancer 1996;15:10-7.
-
(1996)
Genes Chromosomes Cancer
, vol.15
, pp. 10-17
-
-
Schofield, D.E.1
Beckwith, J.L.B.2
Sklar, J.3
-
55
-
-
0026329588
-
Establishment of a rhabdoid tumor cell line with a specific chromosomal abnormality. 46,XY,t(11;22) (p15.5;q11.23)
-
Karnes PS, Tran TN, Cui MY, et al. Establishment of a rhabdoid tumor cell line with a specific chromosomal abnormality. 46,XY,t(11;22) (p15.5;q11.23). Cancer Genet Cytogenet 1991;56:31-8.
-
(1991)
Cancer Genet Cytogenet
, vol.56
, pp. 31-38
-
-
Karnes, P.S.1
Tran, T.N.2
Cui, M.Y.3
-
56
-
-
0031046285
-
Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Widemann syndrome chromosomal rearrangements
-
Lee MP, Hu RJ, Johnson LA, et al. Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Widemann syndrome chromosomal rearrangements. Nat Genet 1997;15:181-5.
-
(1997)
Nat Genet
, vol.15
, pp. 181-185
-
-
Lee, M.P.1
Hu, R.J.2
Johnson, L.A.3
-
58
-
-
0020395760
-
Cytological and cytogenetical studies on human meningioma
-
Zang KD. Cytological and cytogenetical studies on human meningioma. Cancer Genet Cytogenet 1982;6:249-74.
-
(1982)
Cancer Genet Cytogenet
, vol.6
, pp. 249-274
-
-
Zang, K.D.1
-
59
-
-
0026676710
-
Cytogenetic and loss of heterozygosity studies in ependyinomas, pilocytic astrocytomas, and oligodendrogliomas
-
Ransom DT, Ritland SR, Kimmel DW, et al. Cytogenetic and loss of heterozygosity studies in ependyinomas, pilocytic astrocytomas, and oligodendrogliomas. Genes Chromosomes Cancer 1992;5: 348-56.
-
(1992)
Genes Chromosomes Cancer
, vol.5
, pp. 348-356
-
-
Ransom, D.T.1
Ritland, S.R.2
Kimmel, D.W.3
-
60
-
-
0028144439
-
Analysis of the neurofibromatosis 2 gene in human ependymomas and astrocytomas
-
Rubio MP, Correa KM, Ramesh V, et al. Analysis of the neurofibromatosis 2 gene in human ependymomas and astrocytomas. Cancer Res 1994;54:45-57.
-
(1994)
Cancer Res
, vol.54
, pp. 45-57
-
-
Rubio, M.P.1
Correa, K.M.2
Ramesh, V.3
-
61
-
-
0029123934
-
Exon scanning for mutations of the NF2 gene in pediatric ependymomas, rhabdoid tumors and meningiomas
-
Slave I, MacCollin MM, Dunn M, et al. Exon scanning for mutations of the NF2 gene in pediatric ependymomas, rhabdoid tumors and meningiomas. Int J Cancer 1995;64:243-7.
-
(1995)
Int J Cancer
, vol.64
, pp. 243-247
-
-
Slave, I.1
MacCollin, M.M.2
Dunn, M.3
-
62
-
-
0030293102
-
Loss of heterozygosity on chromosome 22 in human gliomas does not inactivate the neurofibromatosis type-2 gene
-
Watkins D, Ruttledge MH, Sarrazin J, et al. Loss of heterozygosity on chromosome 22 in human gliomas does not inactivate the neurofibromatosis type-2 gene. Cancer Genet Cytogenet 1996; 92:73-8.
-
(1996)
Cancer Genet Cytogenet
, vol.92
, pp. 73-78
-
-
Watkins, D.1
Ruttledge, M.H.2
Sarrazin, J.3
-
64
-
-
0029133473
-
Intracranial ependymomas of childhood: Long-term outcome and prognostic factors
-
Pollack IF, Gerszten PC, Martinez AJ, et al. Intracranial ependymomas of childhood: Long-term outcome and prognostic factors. Neurosurg 1995;37:655-66.
-
(1995)
Neurosurg
, vol.37
, pp. 655-666
-
-
Pollack, I.F.1
Gerszten, P.C.2
Martinez, A.J.3
-
65
-
-
0029865075
-
Constitutional de novo t(1:22)(p22;11.2) and ependymoma
-
Park JP, Chaffee S, Noll WW, et al. Constitutional de novo t(1:22)(p22;11.2) and ependymoma. Cancer Genet Cytogenet 1996;86:150-2.
-
(1996)
Cancer Genet Cytogenet
, vol.86
, pp. 150-152
-
-
Park, J.P.1
Chaffee, S.2
Noll, W.W.3
-
67
-
-
0029820302
-
Molecular genetic analysis of chromosome arm 17p and chromosome arm 22q DNA sequences in sporadic pediatric ependymomas
-
von Haken MS, White EC, Daneshvar-Shyesther L, et al. Molecular genetic analysis of chromosome arm 17p and chromosome arm 22q DNA sequences in sporadic pediatric ependymomas. Genes Chromosomes Cancer 1996;17:37-44.
-
(1996)
Genes Chromosomes Cancer
, vol.17
, pp. 37-44
-
-
Von Haken, M.S.1
White, E.C.2
Daneshvar-Shyesther, L.3
-
68
-
-
0021183267
-
Transgenic mice harboring SV40 T-antigen genes develop characteristic brain tumors
-
Brinster RI, Chen HY, Messing A, et al. Transgenic mice harboring SV40 T-antigen genes develop characteristic brain tumors. Cell 1984;37:367-79.
-
(1984)
Cell
, vol.37
, pp. 367-379
-
-
Brinster, R.I.1
Chen, H.Y.2
Messing, A.3
-
69
-
-
0026566559
-
DNA sequences similar to those of simian virus 40 in ependymomas and choroid plexus tumors of childhood
-
Bergsagel DJ, Finegold MJ, Butel JS, et al. DNA sequences similar to those of simian virus 40 in ependymomas and choroid plexus tumors of childhood N Engl J Med 1992;326:988-93.
-
(1992)
N Engl J Med
, vol.326
, pp. 988-993
-
-
Bergsagel, D.J.1
Finegold, M.J.2
Butel, J.S.3
-
70
-
-
0030910239
-
A molecular genetic model of astrocytoma histopathology
-
Louis DN. A molecular genetic model of astrocytoma histopathology. Brain Pathol 1997;7:755-64.
-
(1997)
Brain Pathol
, vol.7
, pp. 755-764
-
-
Louis, D.N.1
-
71
-
-
0029736653
-
Human glioblastomas with no alterations of the CDKN2A, P16(INK4A, MTS1) and CDK4 genes have frequent mutations of the retinoblastoma gene
-
Ichimura K, Schmidt EE, Goike HM, et al. Human glioblastomas with no alterations of the CDKN2A, P16(INK4A, MTS1) and CDK4 genes have frequent mutations of the retinoblastoma gene. Oncogene 1996;13:1065-72.
-
(1996)
Oncogene
, vol.13
, pp. 1065-1072
-
-
Ichimura, K.1
Schmidt, E.E.2
Goike, H.M.3
-
72
-
-
17144436629
-
Identification of a candidate tumour suppressor gene, MMACI, at chromosome 10q23.3 that is mutated in multiple advanced cancers
-
Steck PA, Pershouse MA, Jasser SA, et al Identification of a candidate tumour suppressor gene, MMACI, at chromosome 10q23.3 that is mutated in multiple advanced cancers. Nat Genet 1997;15:356-62.
-
(1997)
Nat Genet
, vol.15
, pp. 356-362
-
-
Steck, P.A.1
Pershouse, M.A.2
Jasser, S.A.3
-
73
-
-
0030936323
-
PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast and prostate cancer
-
Li J, Yen C, Liaw D et al. PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast and prostate cancer. Science 1997;275:1943-7.
-
(1997)
Science
, vol.275
, pp. 1943-1947
-
-
Li, J.1
Yen, C.2
Liaw, D.3
-
74
-
-
0028800035
-
Frequent expression of a mutant EGF receptor in multiple human tumors
-
Moscatello DK, Holgado-Madruga M, Godwin AK, et al. Frequent expression of a mutant EGF receptor in multiple human tumors. Cancer Res 1995;55:5536-9.
-
(1995)
Cancer Res
, vol.55
, pp. 5536-5539
-
-
Moscatello, D.K.1
Holgado-Madruga, M.2
Godwin, A.K.3
-
75
-
-
0031032368
-
The relationship between TP53 mutations and overexpression of p53 and prognosis in malignant gliomas of childhood
-
Pollack, I.F., Hamilton, R.L., Finkelstein, S.D et al. The relationship between TP53 mutations and overexpression of p53 and prognosis in malignant gliomas of childhood. Cancer Res 1997;57:304-9.
-
(1997)
Cancer Res
, vol.57
, pp. 304-309
-
-
Pollack, I.F.1
Hamilton, R.L.2
Finkelstein, S.D.3
-
77
-
-
0025612530
-
Absence of isochromosome 12p in a pineal region malignant germ cell tumor
-
Shen V, Chapparo M, Choi BH, et al. Absence of isochromosome 12p in a pineal region malignant germ cell tumor. Cancer Genet Cytogenet 1990;50:153-60.
-
(1990)
Cancer Genet Cytogenet
, vol.50
, pp. 153-160
-
-
Shen, V.1
Chapparo, M.2
Choi, B.H.3
-
78
-
-
0028961918
-
Numerical sex chromosomal abnormalities in pineal teratomas by cytogenetic analysis and fluorescence in situ hybridization
-
Yu IT, Griffin CA, Phillips PC, et al. Numerical sex chromosomal abnormalities in pineal teratomas by cytogenetic analysis and fluorescence in situ hybridization. Lab Invest 1995;72:419-23.
-
(1995)
Lab Invest
, vol.72
, pp. 419-423
-
-
Yu, I.T.1
Griffin, C.A.2
Phillips, P.C.3
-
79
-
-
0029877937
-
Deletion of 1p36 in childhood endodermal sinus tumors by two-color fluorescence in situ hybridization: A pediatric oncology group study
-
Perlman EJ, Valentine MB, Griffin CA, et al. Deletion of 1p36 in childhood endodermal sinus tumors by two-color fluorescence in situ hybridization: a pediatric oncology group study. Genes Chromosomes Cancer 1996;16:15-20.
-
(1996)
Genes Chromosomes Cancer
, vol.16
, pp. 15-20
-
-
Perlman, E.J.1
Valentine, M.B.2
Griffin, C.A.3
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