Neuropathology and molecular genetics of neurofibromatosis 2 and related tumors.
about
Schwannomin isoform-1 interacts with syntenin via PDZ domainsSchwannomatosis involving peripheral nerves: a case report.Hereditary spinal neurofibromatosis: a rare form of NF1?A functional association between merlin and HEI10, a cell cycle regulator.Meningioma pathology, genetics, and biology.NF2 gene analysis distinguishes hemangiopericytoma from meningioma.A case of multiple cutaneous schwannomas; schwannomatosis or neurofibromatosis type 2?Evaluation of NF2 gene deletion in sporadic schwannomas, meningiomas, and ependymomas by chromogenic in situ hybridizationDiagnostic and molecular pathology of meningiomas.Antiangiogenic agents for nonmalignant brain tumors.Molecular Cytogenetic Study of the NF2 Gene Deletion in Meningioma in Sudanese PatientsNeurogenic tumors of soft tissue.The merlin tumor suppressor interacts with Ral guanine nucleotide dissociation stimulator and inhibits its activity.Germline SMARCB1 mutation predisposes to multiple meningiomas and schwannomas with preferential location of cranial meningiomas at the falx cerebri.Expression of the tumor suppressor genes NF2, 4.1B, and TSLC1 in canine meningiomas.Loss of SMARCE1 expression is a specific diagnostic marker of clear cell meningioma: a comprehensive immunophenotypical and molecular analysis.Merlin links to the cAMP neuronal signaling pathway by anchoring the RIbeta subunit of protein kinase A.Chromosomal and genetic abnormalities in benign and malignant meningiomas using DNA microarray.Aggressive phenotypic and genotypic features in pediatric and NF2-associated meningiomas: a clinicopathologic study of 53 cases.Unique intracerebral tumor with divergent differentiation in a patient presenting as NF2: report of a case with features of astrocytoma, ependymoma, and PNET.High-Grade Glioma is not a Feature of Neurofibromatosis Type 2 in the Unirradiated Patient.PTEN/PTENP1: 'Regulating the regulator of RTK-dependent PI3K/Akt signalling', new targets for cancer therapy.Ruptured posterior cerebral artery aneurysm in association with neurofibromatosis type 2--a case report.NF2 status of meningiomas is associated with tumour localization and histology.[Hereditary tumor syndromes in neuropathology].Cystic meningioangiomatosis in neurofibromatosis type 2: an MRI-pathological study.
P2860
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P2860
Neuropathology and molecular genetics of neurofibromatosis 2 and related tumors.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年学术文章
@wuu
1995年学术文章
@zh-cn
1995年学术文章
@zh-hans
1995年学术文章
@zh-my
1995年学术文章
@zh-sg
1995年學術文章
@yue
1995年學術文章
@zh
1995年學術文章
@zh-hant
name
Neuropathology and molecular genetics of neurofibromatosis 2 and related tumors.
@en
type
label
Neuropathology and molecular genetics of neurofibromatosis 2 and related tumors.
@en
prefLabel
Neuropathology and molecular genetics of neurofibromatosis 2 and related tumors.
@en
P2860
P1433
P1476
Neuropathology and molecular genetics of neurofibromatosis 2 and related tumors.
@en
P2093
P2860
P304
P356
10.1111/J.1750-3639.1995.TB00590.X
P577
1995-04-01T00:00:00Z