-
1
-
-
0030016383
-
Epidemiology and etiology of intracranial meningiomas: A review
-
Bondy M and Lignon BL Epidemiology and etiology of intracranial meningiomas: a review. J Neurooncol 1996, 29:197-205
-
(1996)
J. Neurooncol.
, vol.29
, pp. 197-205
-
-
Bondy, M.1
Lignon, B.L.2
-
2
-
-
0034053970
-
Incidence and clinical features of asymptomatic meningiomas
-
Kuratsu J, Kochi M and Ushio Y Incidence and clinical features of asymptomatic meningiomas. J Neurosurg 2000, 92:766-770
-
(2000)
J. Neurosurg.
, vol.92
, pp. 766-770
-
-
Kuratsu, J.1
Kochi, M.2
Ushio, Y.3
-
3
-
-
0029875198
-
Molecular genetic investigation of the neurofibromatosis type 2 tumor suppressor gene in sporadic meningioma
-
Harada T, Irving RM, Xuereb JH, Barton DE, Hardy DG, Moffat DA and Maher ER Molecular genetic investigation of the neurofibromatosis type 2 tumor suppressor gene in sporadic meningioma. J Neurosurg 1996, 84:847-851
-
(1996)
J. Neurosurg.
, vol.84
, pp. 847-851
-
-
Harada, T.1
Irving, R.M.2
Xuereb, J.H.3
Barton, D.E.4
Hardy, D.G.5
Moffat, D.A.6
Maher, E.R.7
-
4
-
-
0034120650
-
Allelic loses in neurofibromatosis 2-associated meningiomas
-
Lamszus K, Vahldiek F, Mautner VF, Schichor C, Tonn J, Stavron D, Fillbrandt , Westphal M and Kluwe L Allelic loses in neurofibromatosis 2-associated meningiomas. J Neuropathol Exp Neurol 2000, 59:504-512
-
(2000)
J. Neuropathol. Exp. Neurol.
, vol.59
, pp. 504-512
-
-
Lamszus, K.1
Vahldiek, F.2
Mautner, V.F.3
Schichor, C.4
Tonn, J.5
Stavron, D.6
Fillbrandt, A.7
Westphal, M.8
Kluwe, L.9
-
5
-
-
0033119495
-
NF2 mutations and allelic status of 1p, 14q and 22q in sporadic meningiomas
-
Leone PE, Bello MJ, de Campos JM, Vaquero J, Sarasa JL, Pestaña A and Rey JA NF2 mutations and allelic status of 1p, 14q and 22q in sporadic meningiomas. Oncogene 1999, 18:2231-2239
-
(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
-
6
-
-
0032146093
-
Identification of a consistent region of allelic loss on 1p32 in meningiomas: Correlation with increased morbidity
-
Sulman EP, Dumanski JP, White PS, Khao H, Maris JM, Mathiesen T, Bruder C, Cnaan A and Brodeur GM Identification of a consistent region of allelic loss on 1p32 in meningiomas: correlation with increased morbidity. Cancer Res 1998, 58:3226-3230
-
(1998)
Cancer Res.
, vol.58
, pp. 3226-3230
-
-
Sulman, E.P.1
Dumanski, J.P.2
White, P.S.3
Khao, H.4
Maris, J.M.5
Mathiesen, T.6
Bruder, C.7
Cnaan, A.8
Brodeur, G.M.9
-
7
-
-
0030698270
-
1p and 3p deletions in meningiomas without detectable aberrations of chromosoma 22 identified by comparative genomic hybridization
-
Carlson KM, Bruder C, Nordenskjöld M and Dumanski JP 1p and 3p deletions in meningiomas without detectable aberrations of chromosoma 22 identified by comparative genomic hybridization. Genes Chromosomes Cancer 1997, 20:419-424
-
(1997)
Genes Chromosomes Cancer
, vol.20
, pp. 419-424
-
-
Carlson, K.M.1
Bruder, C.2
Nordenskjöld, M.3
Dumanski, J.P.4
-
8
-
-
0028348101
-
Chromosomal deletion in anaplastic meningiomas suggest multiple regions outside chromosome 22 as important in tumor progression
-
Lindblom A, Ruttledge M, Collins VP, Nordenskjöld M and Dumanski JP Chromosomal deletion in anaplastic meningiomas suggest multiple regions outside chromosome 22 as important in tumor progression. Int J Cancer 1994, 56:354-357
-
(1994)
Int. J. Cancer
, vol.56
, pp. 354-357
-
-
Lindblom, A.1
Ruttledge, M.2
Collins, V.P.3
Nordenskjöld, M.4
Dumanski, J.P.5
-
9
-
-
0034474968
-
Frequent loss of 1p32 region but no mutation of the p18 tumor suppressor gene in meningioma
-
Leuraud P, Marie Y, Robin E, Huguet S, He J, Mokhtari K, Cornu P, Hoang-Xuan K and Sanson M Frequent loss of 1p32 region but no mutation of the p18 tumor suppressor gene in meningioma. J Neurooncol 2000, 50:207-213
-
(2000)
J. Neurooncol.
, vol.50
, pp. 207-213
-
-
Leuraud, P.1
Marie, Y.2
Robin, E.3
Huguet, S.4
He, J.5
Mokhtari, K.6
Cornu, P.7
Hoang-Xuan, K.8
Sanson, M.9
-
10
-
-
14444278729
-
Characterization of the human homologue of RAD54: A gene located on chromosome 1p32 at a region of high loss of heterozygosity in breast tumors
-
Rasio D, Murakum Y, Robbins D, Roth T, Silver A, Negrini M, Schmidt C, Burczak J, Fishel R and Croce CM Characterization of the human homologue of RAD54: a gene located on chromosome 1p32 at a region of high loss of heterozygosity in breast tumors. Cancer Res 1997, 57:2378-2383
-
(1997)
Cancer Res.
, vol.57
, pp. 2378-2383
-
-
Rasio, D.1
Murakum, Y.2
Robbins, D.3
Roth, T.4
Silver, A.5
Negrini, M.6
Schmidt, C.7
Burczak, J.8
Fishel, R.9
Croce, C.M.10
-
11
-
-
0033519702
-
Mutations in the RAD54 recombination gene in primary cancers
-
Matsuda M, Miyagawa K, Takahashi M, Fukuda T, Kataoka T, Asahara T, Inui H, Watatani M, Yasutomi M, Kamada N, Dohi K and Kamiya K Mutations in the RAD54 recombination gene in primary cancers. Oncogene 1999, 18:3427-3430
-
(1999)
Oncogene
, vol.18
, pp. 3427-3430
-
-
Matsuda, M.1
Miyagawa, K.2
Takahashi, M.3
Fukuda, T.4
Kataoka, T.5
Asahara, T.6
Inui, H.7
Watatani, M.8
Yasutomi, M.9
Kamada, N.10
Dohi, K.11
Kamiya, K.12
-
12
-
-
0032925350
-
Search for mutations of the hRAD54 gene in sporadic meningiomas with deletion at 1p32
-
Mendiola M, Bello MJ, Alonso J, Leone PE, Vaquero J, Sarasa JL, Kusak ME, de Campos JM, Pestaña A and Rey JA Search for mutations of the hRAD54 gene in sporadic meningiomas with deletion at 1p32. Molecular Carcinogenesis 1999, 24:300-304
-
(1999)
Molecular Carcinogenesis
, vol.24
, pp. 300-304
-
-
Mendiola, M.1
Bello, M.J.2
Alonso, J.3
Leone, P.E.4
Vaquero, J.5
Sarasa, J.L.6
Kusak, M.E.7
de Campos, J.M.8
Pestaña, A.9
Rey, J.A.10
-
13
-
-
0007808928
-
Diagnostic Molecular Pathology: A Practical Approach
-
Oxford, IRL Press
-
Herrington CS and McGee OD Diagnostic Molecular Pathology: A Practical Approach. The Practical Approach Series. Oxford, IRL Press 1992, 93-94
-
(1992)
The Practical Approach Series
, pp. 93-94
-
-
Herrington, C.S.1
McGee, O.D.2
-
14
-
-
16044374874
-
Human and mouse homologs of the Saccharomyces cerevisiae RAD54 DNA repair gene: Evidence for functional conservation
-
Kanaar R, Toelstra C, SMA , Swagemakers Essers J, Smit B, Franssen JH, Pastink A, Bezzubova OY, Buerstedde JM, Clever B, Heyer WD and Hoeijmakers HJ Human and mouse homologs of the Saccharomyces cerevisiae RAD54 DNA repair gene: evidence for functional conservation. Curr Biol 1996, 6:828-838
-
(1996)
Curr. Biol.
, vol.6
, pp. 828-838
-
-
Kanaar, R.1
Toelstra, C.S.M.A.2
Swagemakers Essers, J.3
Smit, B.4
Franssen, J.H.5
Pastink, A.6
Bezzubova, O.Y.7
Buerstedde, J.M.8
Clever, B.9
Heyer, W.D.10
Hoeijmakers, H.J.11
-
15
-
-
0034721088
-
Gros1, a potential grwth suppresor on chromosome 1: Its identity to basement membrane-associated proteoglycan, leprecan
-
Kaul SC, Sugihara T, Yoshida A, Nomura H and Wahwa R Gros1, a potential grwth suppresor on chromosome 1: its identity to basement membrane-associated proteoglycan, leprecan. Oncogene 2000, 19:3576-3583
-
(2000)
Oncogene
, vol.19
, pp. 3576-3583
-
-
Kaul, S.C.1
Sugihara, T.2
Yoshida, A.3
Nomura, H.4
Wahwa, R.5
-
16
-
-
0032499621
-
Structure of the gene encoding the human cyclin-dependent kinase inhibitor p18 and mutational analysis in breast cancer
-
Blais A, Labrie Y, Pouliot F, Lachance Y and Labrie C Structure of the gene encoding the human cyclin-dependent kinase inhibitor p18 and mutational analysis in breast cancer. Biochem Biophys Res Commun 1998, 247:146-153
-
(1998)
Biochem. Biophys. Res. Commun.
, vol.247
, pp. 146-153
-
-
Blais, A.1
Labrie, Y.2
Pouliot, F.3
Lachance, Y.4
Labrie, C.5
-
17
-
-
0025972272
-
Molecular cloning and chromosomal localization of the murine homolog of the human helix-loop-helix gene SCL
-
Begley CG, Visvader J, Green AR, Aplan PD, Metcalf D, Kirsch IR and Gough NM Molecular cloning and chromosomal localization of the murine homolog of the human helix-loop-helix gene SCL. Proc Natl Acad Sci USA 1991, 88:869-873
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 869-873
-
-
Begley, C.G.1
Visvader, J.2
Green, A.R.3
Aplan, P.D.4
Metcalf, D.5
Kirsch, I.R.6
Gough, N.M.7
-
18
-
-
0030921503
-
An scl gene product lacking the transactivation domain induces bony abnormalities and cooperates with LMO1 to generate T-cell malignancies in transgenic mice
-
Aplan PD, Jones CA, Chervinsky DS, Zhao X, Ellsworth M, Wu C, McGuire EA and Gross KW An scl gene product lacking the transactivation domain induces bony abnormalities and cooperates with LMO1 to generate T-cell malignancies in transgenic mice. EMBO J 1997, 16:2408-2419
-
(1997)
EMBO J.
, vol.16
, pp. 2408-2419
-
-
Aplan, P.D.1
Jones, C.A.2
Chervinsky, D.S.3
Zhao, X.4
Ellsworth, M.5
Wu, C.6
McGuire, E.A.7
Gross, K.W.8
-
19
-
-
0032898184
-
Isolation and characterization of human patched 2 (PTCH2), a putative tumour suppressor gene in basal cell carcinoma and medulloblastoma on chromosome 1p32
-
Smyth I, Narang MA, Evans T, Heimann C, Nakamura Y, Chenevix-Trench G, Pietsch T, Wicking C and Wainwright BJ Isolation and characterization of human patched 2 (PTCH2), a putative tumour suppressor gene in basal cell carcinoma and medulloblastoma on chromosome 1p32. Hum Mol Genet 1999, 8:291-297
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 291-297
-
-
Smyth, I.1
Narang, M.A.2
Evans, T.3
Heimann, C.4
Nakamura, Y.5
Chenevix-Trench, G.6
Pietsch, T.7
Wicking, C.8
Wainwright, B.J.9
-
20
-
-
0030004207
-
Cloning and sequencing a human homolog (hMYH) of the Escherichia coli mut Y gene whose function is required for the repais of oxidative DNA damage
-
Slupska MM, Baikalov C, Luther WM, Chiang JH, Wei P and Miller JH Cloning and sequencing a human homolog (hMYH) of the Escherichia coli mut Y gene whose function is required for the repais of oxidative DNA damage. J Bacteriol 1996, 178:3885-3892
-
(1996)
J. Bacteriol.
, vol.178
, pp. 3885-3892
-
-
Slupska, M.M.1
Baikalov, C.2
Luther, W.M.3
Chiang, J.H.4
Wei, P.5
Miller, J.H.6
-
21
-
-
0035839577
-
Muf1, a novel Elongin BC-interacting leucine-rich repeat protein that can assemble with Cul5 and Rbx1 to reconstitute a ubiquitin ligase
-
Kamura T, Burian D, Yan Q, Schmidt SL, Lane WS, Querido E, Branton PE, Shilatifard A, Conaway RC and Conaway JW Muf1, a novel Elongin BC-interacting leucine-rich repeat protein that can assemble with Cul5 and Rbx1 to reconstitute a ubiquitin ligase. J Biol Chem 2001, 276:29748-29753
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 29748-29753
-
-
Kamura, T.1
Burian, D.2
Yan, Q.3
Schmidt, S.L.4
Lane, W.S.5
Querido, E.6
Branton, P.E.7
Shilatifard, A.8
Conaway, R.C.9
Conaway, J.W.10
-
22
-
-
0035313837
-
Gene silencing by double-stranded RNA
-
Carthew RW Gene silencing by double-stranded RNA. Curr Opin Cell Biology 2001, 13:244-248
-
(2001)
Curr. Opin. Cell Biology
, vol.13
, pp. 244-248
-
-
Carthew, R.W.1
-
23
-
-
0035900635
-
A short primer on RNAi: RNA-directed RNA polymerase acts as a key catalist
-
Nishikura K A short primer on RNAi: RNA-directed RNA polymerase acts as a key catalist. Cell 2001, 107:415-418
-
(2001)
Cell
, vol.107
, pp. 415-418
-
-
Nishikura, K.1
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