Molecular genetic approach to human meningioma: loss of genes on chromosome 22 - Wikidata - wikimedia - TriplyDB

Molecular genetic approach to human meningioma: loss of genes on chromosome 22

Molecular genetic approach to human meningioma: loss of genes on chromosome 22

http://www.wikidata.org/entity/Q30502412

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The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family Maternally expressed gene 3, an imprinted noncoding RNA gene, is associated with meningioma pathogenesis and progression Meningiomas and Proteomics: Focus on New Potential Biomarkers and Molecular Pathways.Update on meningiomas.DNA amplification by polymerase chain reaction from brain tissues embedded in paraffin.The ninth Gordon Hamilton-Fairley memorial lecture. Hereditary cancers: clues to mechanisms of carcinogenesis.Recessive mechanisms of malignancy.Molecular genetics of neurological tumours Mifepristone (RU 486) treatment of meningiomas.Analysis of the neurofibromatosis 2 gene reveals molecular variants of meningioma.Deletion of Alu sequences in the fifth c-sis intron in individuals with meningiomas.Equal parental origin of chromosome 22 losses in human sporadic meningioma: no evidence for genomic imprinting.Homozygous deletion of the alpha- and beta 1-interferon genes in human leukemia and derived cell lines Frequent NF2 gene transcript mutations in sporadic meningiomas and vestibular schwannomas.Clinical and genetic patterns of neurofibromatosis 1 and 2.Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis.Distal deletion of chromosome Ip in ductal carcinoma of the breast.Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22.Comprehensive genetic and epigenetic analysis of sporadic meningioma for macro-mutations on 22q and micro-mutations within the NF2 locus.Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification.Differential DNA sequence deletions from chromosomes 3, 11, 13, and 17 in squamous-cell carcinoma, large-cell carcinoma, and adenocarcinoma of the human lung Loss of distinct regions on the short arm of chromosome 17 associated with tumorigenesis of human astrocytomas Molecular cloning and chromosomal mapping of DNA rearranged with the parathyroid hormone gene in a parathyroid adenoma.Genetic profiling by single-nucleotide polymorphism-based array analysis defines three distinct subtypes of orbital meningioma Endocrine aspects of the diagnosis and treatment of primary brain tumours.Alterations of the tumor suppressor genes CDKN2A (p16(INK4a)), p14(ARF), CDKN2B (p15(INK4b)), and CDKN2C (p18(INK4c)) in atypical and anaplastic meningiomas Meningioma pathology, genetics, and biology.NF2 gene analysis distinguishes hemangiopericytoma from meningioma.XH1--a new cervical carcinoma cell line and xenograft model of tumour invasion, 'metastasis' and regression.Cytogenetics and molecular genetics of malignant gliomas and medulloblastoma.Progress toward the isolation and characterization of the genes causing neurofibromatosis.Modeling NF2 with human arachnoidal and meningioma cell culture systems: NF2 silencing reflects the benign character of tumor growth.Tumor suppressor genes and cancer of the human nervous system.Molecular genetics of neurofibromatosis 2 and related tumors (acoustic neuroma and meningioma).Fine needle aspiration cytology of ectopic meningioma presenting as a neck mass: a case report and a review of the literature.Molecular probes in neuro-oncology: a review.Activation of multiple growth factor signalling pathways is frequent in meningiomas.Molecular genetic approaches to the analysis of human ophthalmic disease.Regulation of expression of the c-sis proto-oncogene Neuropathology and molecular genetics of neurofibromatosis 2 and related tumors.

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P2860

Molecular genetic approach to human meningioma: loss of genes on chromosome 22

http://www.wikidata.org/entity/Q30502412

description

1987 nî lūn-bûn

@nan

1987 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

1987 թվականի օգոստոսին հրատարակված գիտական հոդված

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1987年の論文

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1987年論文

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1987年論文

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1987年論文

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1987年論文

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1987年論文

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1987年论文

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name

Molecular genetic approach to human meningioma: loss of genes on chromosome 22

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Molecular genetic approach to human meningioma: loss of genes on chromosome 22

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type

label

Molecular genetic approach to human meningioma: loss of genes on chromosome 22

@ast

Molecular genetic approach to human meningioma: loss of genes on chromosome 22

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prefLabel

Molecular genetic approach to human meningioma: loss of genes on chromosome 22

@ast

Molecular genetic approach to human meningioma: loss of genes on chromosome 22

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PNAS.84.15.5419

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Proceedings of the National Academy of Sciences of the United States of America

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Molecular genetic approach to human meningioma: loss of genes on chromosome 22

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B R Seizinger

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L Atkins

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R L Martuza

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P2860

A highly polymorphic locus in human DNA

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.

Chromosome preparations of leukocytes cultured from human peripheral blood.

A polymorphic DNA marker genetically linked to Huntington's disease.

Exact significance testing to establish treatment equivalence with ordered categorical data.

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma.

Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis.

Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13.

A discordant sibship analysis between beta-NGF and neurofibromatosis.

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James F. Gusella

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