Germline SMARCB1 mutation predisposes to multiple meningiomas and schwannomas with preferential location of cranial meningiomas at the falx cerebri.
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A heritable form of SMARCE1-related meningiomas with important implications for follow-up and family screening.SWI/SNF chromatin remodeling complexes and cancerTherapeutic advances for the tumors associated with neurofibromatosis type 1, type 2, and schwannomatosisChildhood neurofibromatosis type 2 (NF2) and related disorders: from bench to bedside and biologically targeted therapies.Chromatin-regulating proteins as targets for cancer therapy.Genetic profiling by single-nucleotide polymorphism-based array analysis defines three distinct subtypes of orbital meningiomaPathology and molecular genetics of meningioma: recent advances.The molecular pathogenesis of schwannomatosis, a paradigm for the co-involvement of multiple tumour suppressor genes in tumorigenesis.Neurocutaneous Syndromes and Brain Tumors.Cellular prion protein (PrP(C)) in the development of Merlin-deficient tumours.Atypical teratoid rhabdoid tumors of the posterior fossa in children.Integrated genomic analyses of de novo pathways underlying atypical meningiomasLoss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomas.Meningeal SWI/SNF related, matrix-associated, actin-dependent regulator of chromatin, subfamily B member 1 (SMARCB1)-deficient tumours: an emerging group of meningeal tumours.Use of clinical next-generation sequencing to identify melanomas harboring SMARCB1 mutations.Germline SMARCE1 mutations predispose to both spinal and cranial clear cell meningiomas.Systemic therapy for recurrent meningioma.High incidence of activating TERT promoter mutations in meningiomas undergoing malignant progression.Intracranial meningiomas and neurofibromatosis type 2.Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria.RNA-based analysis of two SMARCB1 mutations associated with familial schwannomatosis with meningiomas.Report of a patient with a constitutional missense mutation in SMARCB1, Coffin-Siris phenotype, and schwannomatosis.Somatic SMARCB1 Mutation in Sporadic Multiple Meningiomas: Case ReportMutational Landscapes and Phenotypic Spectrum of SWI/SNF-Related Intellectual Disability Disorders
P2860
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P2860
Germline SMARCB1 mutation predisposes to multiple meningiomas and schwannomas with preferential location of cranial meningiomas at the falx cerebri.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
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2011年學術文章
@zh-hant
name
Germline SMARCB1 mutation pred ...... ningiomas at the falx cerebri.
@en
Germline SMARCB1 mutation pred ...... ningiomas at the falx cerebri.
@nl
type
label
Germline SMARCB1 mutation pred ...... ningiomas at the falx cerebri.
@en
Germline SMARCB1 mutation pred ...... ningiomas at the falx cerebri.
@nl
prefLabel
Germline SMARCB1 mutation pred ...... ningiomas at the falx cerebri.
@en
Germline SMARCB1 mutation pred ...... ningiomas at the falx cerebri.
@nl
P2093
P2860
P1433
P1476
Germline SMARCB1 mutation pred ...... ningiomas at the falx cerebri.
@en
P2093
Imke Christiaans
Pepijn van den Munckhof
Susan B Kenter
Theo J M Hulsebos
P2860
P2888
P356
10.1007/S10048-011-0300-Y
P50
P577
2011-10-26T00:00:00Z