Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis.
about
Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors.The neurofibroma in von Recklinghausen neurofibromatosis has a unicellular origin.A murine model of neurofibromatosis type 2 that accurately phenocopies human schwannoma formationNeurofibromatosis type 2.Loss of heterozygosity on long arm of chromosome 22 in sporadic colorectal carcinomaMolecular biology of unreresectable meningiomas: implications for new treatments and review of the literature.A prospective study of cavernous sinus surgery for meningiomas and resultant common ophthalmic complications (an American Ophthalmological Society thesis)Molecular mechanisms promoting the pathogenesis of Schwann cell neoplasmsDNA amplification by polymerase chain reaction from brain tissues embedded in paraffin.Molecular genetic aspects of human cancers: the 1993 Frank Rose Lecture.Noise trauma in the aetiology of acoustic neuromas in men in Los Angeles County, 1978-1985Recessive mechanisms of malignancy.Constitutional ring chromosomes and tumour suppressor genes.Further exclusion data for the Von Recklinghausen neurofibromatosis gene: a genetic linkage study of 19 polymorphic markers.DNA linkage analysis in Von Recklinghausen neurofibromatosis.The von Recklinghausen neurofibromatosis region on chromosome 17--genetic and physical maps come into focusA t(4;22) in a meningioma points to the localization of a putative tumor-suppressor gene.Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningiomaMolecular genetic approach to human meningioma: loss of genes on chromosome 22Frequent NF2 gene transcript mutations in sporadic meningiomas and vestibular schwannomas.Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of diseaseClinical and genetic patterns of neurofibromatosis 1 and 2.Bilateral optic nerve sheath meningiomas in a patient with neurofibromatosis type 2Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis.Analysis of chromosome 22 deletions in neurofibromatosis type 2-related tumorsFlanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22.High frequency of inactivating mutations in the neurofibromatosis type 2 gene (NF2) in primary malignant mesotheliomas.Abnormalities in structure and expression of the human retinoblastoma gene in SCLC.Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification.Calpain-dependent proteolysis of NF2 protein: involvement in schwannomas and meningiomas.Loss of distinct regions on the short arm of chromosome 17 associated with tumorigenesis of human astrocytomasCytogenetics and molecular genetics of malignant gliomas and medulloblastoma.Progress toward the isolation and characterization of the genes causing neurofibromatosis.The molecular genetics of meningiomas.Tumor suppressor genes and cancer of the human nervous system.Gastrointestinal manifestations of type 1 neurofibromatosis (von Recklinghausen's disease).Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of Von Hippel Lindau disease.Schwannomas and their pathogenesis.The neurofibromatoses. What do we know about them?Neuropathology and molecular genetics of neurofibromatosis 2 and related tumors.
P2860
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P2860
Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis.
description
1987 nî lūn-bûn
@nan
1987 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1987 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
name
Common pathogenetic mechanism ...... al acoustic neurofibromatosis.
@ast
Common pathogenetic mechanism ...... al acoustic neurofibromatosis.
@en
Common pathogenetic mechanism ...... al acoustic neurofibromatosis.
@nl
type
label
Common pathogenetic mechanism ...... al acoustic neurofibromatosis.
@ast
Common pathogenetic mechanism ...... al acoustic neurofibromatosis.
@en
Common pathogenetic mechanism ...... al acoustic neurofibromatosis.
@nl
prefLabel
Common pathogenetic mechanism ...... al acoustic neurofibromatosis.
@ast
Common pathogenetic mechanism ...... al acoustic neurofibromatosis.
@en
Common pathogenetic mechanism ...... al acoustic neurofibromatosis.
@nl
P2093
P356
P1433
P1476
Common pathogenetic mechanism ...... al acoustic neurofibromatosis.
@en
P2093
Martuza RL
Ozelius LJ
Seizinger BR
St George-Hyslop P
P304
P356
10.1126/SCIENCE.3105060
P407
P577
1987-04-01T00:00:00Z