-
4
-
-
0028960378
-
Cellular schwannoma A. clinicopathologic, DNA flow cytometric, and proliferation marker study of 70 patients
-
Casadei G.P., Scheithauer B.W., Hirose T., Manfrini M., Van Houton C., Wood M.B. Cellular schwannoma A. clinicopathologic, DNA flow cytometric, and proliferation marker study of 70 patients. Cancer. 75:(5):1995;1109-1119
-
(1995)
Cancer
, vol.75
, Issue.5
, pp. 1109-1119
-
-
Casadei, G.P.1
Scheithauer, B.W.2
Hirose, T.3
Manfrini, M.4
Van Houton, C.5
Wood, M.B.6
-
5
-
-
0022468790
-
Benign plexiform (multinodular) schwannoma: A rare tumour unassociated with neurofibromatosis
-
Fletcher C.D., Davies S.E. Benign plexiform (multinodular) schwannoma: a rare tumour unassociated with neurofibromatosis. Histopathology. 10:(9):1986;971-980
-
(1986)
Histopathology
, vol.10
, Issue.9
, pp. 971-980
-
-
Fletcher, C.D.1
Davies, S.E.2
-
6
-
-
0031911172
-
Phenotypic diversity of neurofibromatosis 2: Association with plexiform schwannoma
-
Ishida T., Kuroda M., Motoi T., Oka T., Imamura T., Machinami R. Phenotypic diversity of neurofibromatosis 2: association with plexiform schwannoma. Histopathology. 32:(3):1998;264-270
-
(1998)
Histopathology
, vol.32
, Issue.3
, pp. 264-270
-
-
Ishida, T.1
Kuroda, M.2
Motoi, T.3
Oka, T.4
Imamura, T.5
MacHinami, R.6
-
8
-
-
0032466098
-
Spinal malignant melanotic schwannoma. Case report
-
Noubari B.A., Chiaramonte I., Magro G., Tropea R., Mancuso P. Spinal malignant melanotic schwannoma. Case report. J Neurosurg Sci. 42:(4):1998;245-249
-
(1998)
J Neurosurg Sci
, vol.42
, Issue.4
, pp. 245-249
-
-
Noubari, B.A.1
Chiaramonte, I.2
Magro, G.3
Tropea, R.4
Mancuso, P.5
-
9
-
-
0027405720
-
A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor
-
Trofatter J.A., MacCollin M.M., Rutter J.L., Murrell J.R., Duyao M.P., Parry D.M., et al. A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor. Cell. 72:(5):1993;791-800
-
(1993)
Cell
, vol.72
, Issue.5
, pp. 791-800
-
-
Trofatter, J.A.1
MacCollin, M.M.2
Rutter, J.L.3
Murrell, J.R.4
Duyao, M.P.5
Parry, D.M.6
-
10
-
-
0028091283
-
The neurofibromatosis type 2 gene is inactivated in schwannomas
-
Twist E.C., Ruttledge M.H., Rousseau M., Sanson M., Papi L., Merel P., et al. The neurofibromatosis type 2 gene is inactivated in schwannomas. Hum Mol Genet. 3:(1):1994;147-151
-
(1994)
Hum Mol Genet
, vol.3
, Issue.1
, pp. 147-151
-
-
Twist, E.C.1
Ruttledge, M.H.2
Rousseau, M.3
Sanson, M.4
Papi, L.5
Merel, P.6
-
12
-
-
15144359418
-
Universal absence of merlin, but not other ERM family members, in schwannomas
-
Stemmer-Rachamimov A.O., Xu L., Gonzalez-Agosti C., Burwick J.A., Pinney D., Beauchamp R., et al. Universal absence of merlin, but not other ERM family members, in schwannomas. Am J Pathol. 151:(6):1997;1649-1654
-
(1997)
Am J Pathol
, vol.151
, Issue.6
, pp. 1649-1654
-
-
Stemmer-Rachamimov, A.O.1
Xu, L.2
Gonzalez-Agosti, C.3
Burwick, J.A.4
Pinney, D.5
Beauchamp, R.6
-
13
-
-
18044399847
-
The NF2 tumor suppressor, merlin, functions in Rac-dependent signaling
-
Shaw R.J., Paez J.G., Curto M., Yaktine A., Pruitt W.M., Saotome I., et al. The NF2 tumor suppressor, merlin, functions in Rac-dependent signaling. Dev Cell. 1:(1):2001;63-72
-
(2001)
Dev Cell
, vol.1
, Issue.1
, pp. 63-72
-
-
Shaw, R.J.1
Paez, J.G.2
Curto, M.3
Yaktine, A.4
Pruitt, W.M.5
Saotome, I.6
-
14
-
-
0029880526
-
Schwannomatosis: A clinical and pathologic study
-
MacCollin M., Woodfin W., Kronn D., Short M.P. Schwannomatosis: a clinical and pathologic study. Neurology. 46:(4):1996;1072-1079
-
(1996)
Neurology
, vol.46
, Issue.4
, pp. 1072-1079
-
-
MacCollin, M.1
Woodfin, W.2
Kronn, D.3
Short, M.P.4
-
15
-
-
0031440868
-
Molecular analysis of the NF2 tumor-suppressor gene in schwannomatosis
-
Jacoby L.B., Jones D., Davis K., Kronn D., Short M.P., Gusella J., et al. Molecular analysis of the NF2 tumor-suppressor gene in schwannomatosis. Am J Hum Genet. 61:(6):1997;1293-1302
-
(1997)
Am J Hum Genet
, vol.61
, Issue.6
, pp. 1293-1302
-
-
Jacoby, L.B.1
Jones, D.2
Davis, K.3
Kronn, D.4
Short, M.P.5
Gusella, J.6
-
16
-
-
0038714575
-
Familial schwannomatosis: Exclusion of the NF2 locus as the germline event
-
MacCollin M., Willett C., Heinrich B., Jacoby L.B., Acierno J.S. Jr., Perry A., et al. Familial schwannomatosis: exclusion of the NF2 locus as the germline event. Neurology. 60:(12):2003;1968-1974
-
(2003)
Neurology
, vol.60
, Issue.12
, pp. 1968-1974
-
-
MacCollin, M.1
Willett, C.2
Heinrich, B.3
Jacoby, L.B.4
Acierno Jr., J.S.5
Perry, A.6
-
17
-
-
0033812849
-
Mutations of the gene encoding the protein kinase a type I-alpha regulatory subunit in patients with the Carney complex
-
Kirschner L.S., Carney J.A., Pack S.D., Taymans S.E., Giatzakis C., Cho Y.S., et al. Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex. Nat Genet. 26:(1):2000;89-92
-
(2000)
Nat Genet
, vol.26
, Issue.1
, pp. 89-92
-
-
Kirschner, L.S.1
Carney, J.A.2
Pack, S.D.3
Taymans, S.E.4
Giatzakis, C.5
Cho, Y.S.6
-
18
-
-
0038538463
-
Human tumors associated with Carney complex and germline PRKAR1A mutations: A protein kinase a disease
-
Stergiopoulos S.G., Stratakis C.A. Human tumors associated with Carney complex and germline PRKAR1A mutations: a protein kinase A disease. FEBS Lett. 546:(1):2003;59-64
-
(2003)
FEBS Lett
, vol.546
, Issue.1
, pp. 59-64
-
-
Stergiopoulos, S.G.1
Stratakis, C.A.2
-
19
-
-
0026319619
-
CDNA cloning of the type 1 neurofibromatosis gene: Complete sequence of the NF1 gene product
-
Marchuk D.A., Saulino A.M., Tavakkol R., Swaroop M., Wallace M.R., Andersen L.B., et al. cDNA cloning of the type 1 neurofibromatosis gene: complete sequence of the NF1 gene product. Genomics. 11:(4):1991;931-940
-
(1991)
Genomics
, vol.11
, Issue.4
, pp. 931-940
-
-
Marchuk, D.A.1
Saulino, A.M.2
Tavakkol, R.3
Swaroop, M.4
Wallace, M.R.5
Andersen, L.B.6
-
20
-
-
0026093769
-
Identification of the neurofibromatosis type 1 gene product
-
Gutmann D.H., Wood D.L., Collins F.S. Identification of the neurofibromatosis type 1 gene product. Proc Natl Acad Sci USA. 88:(21):1991;9658-9662
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, Issue.21
, pp. 9658-9662
-
-
Gutmann, D.H.1
Wood, D.L.2
Collins, F.S.3
-
21
-
-
0027396684
-
Tumour suppressors and the regulation of GTP-binding protein activity
-
Rey I., Hall A. Tumour suppressors and the regulation of GTP-binding protein activity. Trends Cell Biol. 3:(2):1993;43-46
-
(1993)
Trends Cell Biol
, vol.3
, Issue.2
, pp. 43-46
-
-
Rey, I.1
Hall, A.2
-
22
-
-
0025244911
-
The catalytic domain of the neurofibromatosis type 1 gene product stimulates ras GTPase and complements ira mutants of S. cerevisiae
-
Xu G.F., Lin B., Tanaka K., Dunn D., Wood D., Gesteland R., et al. The catalytic domain of the neurofibromatosis type 1 gene product stimulates ras GTPase and complements ira mutants of S. cerevisiae. Cell. 63:(4):1990;835-841
-
(1990)
Cell
, vol.63
, Issue.4
, pp. 835-841
-
-
Xu, G.F.1
Lin, B.2
Tanaka, K.3
Dunn, D.4
Wood, D.5
Gesteland, R.6
-
23
-
-
0036159132
-
Neurofibromin regulates G protein-stimulated adenylyl cyclase activity
-
Tong J., Hannan F., Zhu Y., Bernards A., Zhong Y. Neurofibromin regulates G protein-stimulated adenylyl cyclase activity. Nat Neurosci. 5:(2):2002;95-96
-
(2002)
Nat Neurosci
, vol.5
, Issue.2
, pp. 95-96
-
-
Tong, J.1
Hannan, F.2
Zhu, Y.3
Bernards, A.4
Zhong, Y.5
-
24
-
-
0037310530
-
Neurofibromatosis 1: Closing the GAP between mice and men
-
Dasgupta B., Gutmann D.H. Neurofibromatosis 1: closing the GAP between mice and men. Curr Opin Genet Dev. 13:(1):2003;20-27
-
(2003)
Curr Opin Genet Dev
, vol.13
, Issue.1
, pp. 20-27
-
-
Dasgupta, B.1
Gutmann, D.H.2
-
25
-
-
0028349997
-
Targeted disruption of the neurofibromatosis type-1 gene leads to developmental abnormalities in heart and various neural crest-derived tissues
-
Brannan C.I., Perkins A.S., Vogel K.S., Ratner N., Nordlund M.L., Reid S.W., et al. Targeted disruption of the neurofibromatosis type-1 gene leads to developmental abnormalities in heart and various neural crest-derived tissues. Genes Dev. 8:(9):1994;1019-1029
-
(1994)
Genes Dev
, vol.8
, Issue.9
, pp. 1019-1029
-
-
Brannan, C.I.1
Perkins, A.S.2
Vogel, K.S.3
Ratner, N.4
Nordlund, M.L.5
Reid, S.W.6
-
26
-
-
0032786494
-
Mouse tumor model for neurofibromatosis type 1
-
Vogel K.S., Klesse L.J., Velasco-Miguel S., Meyers K., Rushing E.J., Parada L.F. Mouse tumor model for neurofibromatosis type 1. Science. 286:(5447):1999;2176-2179
-
(1999)
Science
, vol.286
, Issue.5447
, pp. 2176-2179
-
-
Vogel, K.S.1
Klesse, L.J.2
Velasco-Miguel, S.3
Meyers, K.4
Rushing, E.J.5
Parada, L.F.6
-
27
-
-
0037012848
-
Neurofibromas in NF1: Schwann cell origin and role of tumor environment
-
Zhu Y., Ghosh P., Charnay P., Burns D.K., Parada L.F. Neurofibromas in NF1: Schwann cell origin and role of tumor environment. Science. 296:(5569):2002;920-922
-
(2002)
Science
, vol.296
, Issue.5569
, pp. 920-922
-
-
Zhu, Y.1
Ghosh, P.2
Charnay, P.3
Burns, D.K.4
Parada, L.F.5
-
28
-
-
0346059618
-
Optic nerve glioma in mice requires astrocyte NF1 gene inactivation and NF1 brain heterozygosity
-
Bajenaru M.L., Hernandez M.R., Perry A., Zhu Y., Parada L.F., Garbow J.R., et al. Optic nerve glioma in mice requires astrocyte NF1 gene inactivation and NF1 brain heterozygosity. Cancer Res. 63:(24):2003;8573-8577
-
(2003)
Cancer Res
, vol.63
, Issue.24
, pp. 8573-8577
-
-
Bajenaru, M.L.1
Hernandez, M.R.2
Perry, A.3
Zhu, Y.4
Parada, L.F.5
Garbow, J.R.6
-
29
-
-
0036675901
-
The molecular and genetic basis of neurological tumours
-
Zhu Y., Parada L.F. The molecular and genetic basis of neurological tumours. Nat Rev Cancer. 2:(8):2002;616-626
-
(2002)
Nat Rev Cancer
, vol.2
, Issue.8
, pp. 616-626
-
-
Zhu, Y.1
Parada, L.F.2
-
30
-
-
0032763861
-
Mouse models of tumor development in neurofibromatosis type 1
-
Cichowski K., Shih T.S., Schmitt E., Santiago S., Reilly K., McLaughlin M.E., et al. Mouse models of tumor development in neurofibromatosis type 1. Science. 286:(5447):1999;2172-2176
-
(1999)
Science
, vol.286
, Issue.5447
, pp. 2172-2176
-
-
Cichowski, K.1
Shih, T.S.2
Schmitt, E.3
Santiago, S.4
Reilly, K.5
McLaughlin, M.E.6
-
31
-
-
9144260570
-
Neurofibromin-deficient Schwann cells secrete a potent migratory stimulus for Nf1+/- mast cells
-
Yang F.C., Ingram D.A., Chen S., Hingtgen C.M., Ratner N., Monk K.R., et al. Neurofibromin-deficient Schwann cells secrete a potent migratory stimulus for Nf1+/- mast cells. J Clin Invest. 112:(12):2003;1851-1861
-
(2003)
J Clin Invest
, vol.112
, Issue.12
, pp. 1851-1861
-
-
Yang, F.C.1
Ingram, D.A.2
Chen, S.3
Hingtgen, C.M.4
Ratner, N.5
Monk, K.R.6
-
32
-
-
0347985298
-
It takes two to tango: Mast cell and Schwann cell interactions in neurofibromas
-
Viskochil D.H. It takes two to tango: mast cell and Schwann cell interactions in neurofibromas. J Clin Invest. 112:(12):2003;1791-1793
-
(2003)
J Clin Invest
, vol.112
, Issue.12
, pp. 1791-1793
-
-
Viskochil, D.H.1
-
33
-
-
0026680340
-
Perineurioma: An uncommon soft tissue neoplasm distinct from localized hypertrophic neuropathy and neurofibroma
-
Tsang W.Y., Chan J.K., Chow L.T., Tse C.C. Perineurioma: an uncommon soft tissue neoplasm distinct from localized hypertrophic neuropathy and neurofibroma. Am J Surg Pathol. 16:(8):1992;756-763
-
(1992)
Am J Surg Pathol
, vol.16
, Issue.8
, pp. 756-763
-
-
Tsang, W.Y.1
Chan, J.K.2
Chow, L.T.3
Tse, C.C.4
-
34
-
-
0029066876
-
Intraneural perineurioma. a clonal neoplasm associated with abnormalities of chromosome 22
-
Emory T.S., Scheithauer B.W., Hirose T., Wood M., Onofrio B.M., Jenkins R.B. Intraneural perineurioma. A clonal neoplasm associated with abnormalities of chromosome 22. Am J Clin Pathol. 103:(6):1995;696-704
-
(1995)
Am J Clin Pathol
, vol.103
, Issue.6
, pp. 696-704
-
-
Emory, T.S.1
Scheithauer, B.W.2
Hirose, T.3
Wood, M.4
Onofrio, B.M.5
Jenkins, R.B.6
-
35
-
-
0031051644
-
Soft-tissue perineurioma. Evidence for an abnormality of chromosome 22, criteria for diagnosis, and review of the literature
-
Giannini C., Scheithauer B.W., Jenkins R.B., Erlandson R.A., Perry A., Borell T.J., et al. Soft-tissue perineurioma. Evidence for an abnormality of chromosome 22, criteria for diagnosis, and review of the literature. Am J Surg Pathol. 21:(2):1997;164-173
-
(1997)
Am J Surg Pathol
, vol.21
, Issue.2
, pp. 164-173
-
-
Giannini, C.1
Scheithauer, B.W.2
Jenkins, R.B.3
Erlandson, R.A.4
Perry, A.5
Borell, T.J.6
-
36
-
-
0023099684
-
Malignant peripheral nerve sheath tumor. An immunohistochemical study of 62 cases
-
Wick M.R., Swanson P.E., Scheithauer B.W., Manivel J.C. Malignant peripheral nerve sheath tumor. An immunohistochemical study of 62 cases. Am J Clin Pathol. 87:(4):1987;425-433
-
(1987)
Am J Clin Pathol
, vol.87
, Issue.4
, pp. 425-433
-
-
Wick, M.R.1
Swanson, P.E.2
Scheithauer, B.W.3
Manivel, J.C.4
-
37
-
-
0021173624
-
Malignant peripheral nerve sheath tumors with divergent differentiation
-
Ducatman B.S., Scheithauer B.W. Malignant peripheral nerve sheath tumors with divergent differentiation. Cancer. 54:(6):1984;1049-1057
-
(1984)
Cancer
, vol.54
, Issue.6
, pp. 1049-1057
-
-
Ducatman, B.S.1
Scheithauer, B.W.2
-
38
-
-
0033605452
-
Pathology of tumors of the peripheral nerve sheath in type 1 neurofibromatosis
-
Woodruff J.M. Pathology of tumors of the peripheral nerve sheath in type 1 neurofibromatosis. Am J Med Genet. 89:(1):1999;23-30
-
(1999)
Am J Med Genet
, vol.89
, Issue.1
, pp. 23-30
-
-
Woodruff, J.M.1
-
39
-
-
0034979601
-
Rb and TP53 pathway alterations in sporadic and NF1-related malignant peripheral nerve sheath tumors
-
Birindelli S., Perrone F., Oggionni M., Lavarino C., Pasini B., Vergani B., et al. Rb and TP53 pathway alterations in sporadic and NF1-related malignant peripheral nerve sheath tumors. Lab Invest. 81:(6):2001;833-844
-
(2001)
Lab Invest
, vol.81
, Issue.6
, pp. 833-844
-
-
Birindelli, S.1
Perrone, F.2
Oggionni, M.3
Lavarino, C.4
Pasini, B.5
Vergani, B.6
-
40
-
-
0032762784
-
Malignant transformation of neurofibromas in neurofibromatosis 1 is associated with CDKN2A/p16 inactivation
-
Nielsen G.P., Stemmer-Rachamimov A.O., Ino Y., Moller M.B., Rosenberg A.E., Louis D.N. Malignant transformation of neurofibromas in neurofibromatosis 1 is associated with CDKN2A/p16 inactivation. Am J Pathol. 155:(6):1999;1879- 1884
-
(1999)
Am J Pathol
, vol.155
, Issue.6
, pp. 1879-1884
-
-
Nielsen, G.P.1
Stemmer-Rachamimov, A.O.2
Ino, Y.3
Moller, M.B.4
Rosenberg, A.E.5
Louis, D.N.6
-
41
-
-
0029781715
-
P53 expression in neurofibroma and malignant peripheral nerve sheath tumor. An immunohistochemical study of sporadic and NF1-associated tumors
-
Halling K.C., Scheithauer B.W., Halling A.C., Nascimento A.G., Ziesmer S.C., Roche P.C., et al. p53 expression in neurofibroma and malignant peripheral nerve sheath tumor. An immunohistochemical study of sporadic and NF1-associated tumors. Am J Clin Pathol. 106:(3):1996;282-288
-
(1996)
Am J Clin Pathol
, vol.106
, Issue.3
, pp. 282-288
-
-
Halling, K.C.1
Scheithauer, B.W.2
Halling, A.C.3
Nascimento, A.G.4
Ziesmer, S.C.5
Roche, P.C.6
-
42
-
-
0141571288
-
Malignant peripheral nerve sheath tumor: A comparison of grade, immunophenotype, and cell cycle/growth activation marker expression in sporadic and neurofibromatosis 1-related lesions
-
Zhou H., Coffin C.M., Perkins S.L., Tripp S.R., Liew M., Viskochil D.H. Malignant peripheral nerve sheath tumor: a comparison of grade, immunophenotype, and cell cycle/growth activation marker expression in sporadic and neurofibromatosis 1-related lesions. Am J Surg Pathol. 27:(10):2003;1337-1345
-
(2003)
Am J Surg Pathol
, vol.27
, Issue.10
, pp. 1337-1345
-
-
Zhou, H.1
Coffin, C.M.2
Perkins, S.L.3
Tripp, S.R.4
Liew, M.5
Viskochil, D.H.6
|