(Q40686977)

22 September 2017

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title

Genetics of primary brain tumors: a review (English)

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22 September 2017

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M Bondy

1

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22 September 2017

J Wiencke

series ordinal

2

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22 September 2017

M Wrensch

series ordinal

3

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22 September 2017

A P Kyritsis

series ordinal

4

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22 September 2017

publication date

1 January 1994

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Journal of Neuro-Oncology

22 September 2017

published in

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22 September 2017

volume

18

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22 September 2017

issue

1

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22 September 2017

page(s)

69-81

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Causes of Death in Patients With Tuberous Sclerosis

22 September 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01324606

Amplification of the structurally and functionally altered epidermal growth factor receptor gene (c-erbB) in human brain tumors

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01324606

Amplified cellular oncogenes in neoplasms of the human central nervous system

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01324606

Deletion-mutant epidermal growth factor receptor in human gliomas: Effect of type II mutation on receptor function

21 January 2018

1 reference

12 December 2020

Neurofibromatosis and childhood tumors

1 reference

12 December 2020

Wild-type p53 is a cell cycle checkpoint determinant following irradiation

1 reference

12 December 2020

Amplification of the c-erbB oncogene is associated with malignancy in primary tumours of neuroepithelial tissue

1 reference

12 December 2020

p53: the ultimate tumor suppressor gene?

1 reference

12 December 2020

Expression of the p53 protein in a spectrum of astrocytic tumours

1 reference

12 December 2020

Amplification of Epidermal Growth Factor Receptor Gene in Gliomas: Histopathology and Prognosis

1 reference

12 December 2020

Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus.

1 reference

12 December 2020

An exploratory case-control study of brain tumors in adults

1 reference

12 December 2020

Amplification, enhanced expression and possible rearrangement of EGF receptor gene in primary human brain tumours of glial origin

1 reference

12 December 2020

Genetic and pathologic findings in a kindred with hereditary sarcoma, breast cancer, brain tumors, leukemia, lung, laryngeal, and adrenal cortical carcinoma

1 reference

12 December 2020

On the measurement of susceptibility to genetic factors

1 reference

12 December 2020

Interphase cytogenetics: a new tool for the study of genetic changes in brain tumors

1 reference

12 December 2020

Neurofibromatosis. A review of the clinical problem

1 reference

12 December 2020

Loss of heterozygosity on chromosome 10 in human glioblastoma multiforme.

1 reference

12 December 2020

Risk factors for gliomas and meningiomas in males in Los Angeles County

1 reference

12 December 2020

Turcot's syndrome. Evidence for autosomal dominant inheritance.

1 reference

12 December 2020

Localization of the gene for familial adenomatous polyposis on chromosome 5.

1 reference

12 December 2020

A cytogenetic study of 53 human gliomas.

1 reference

12 December 2020

Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17

1 reference

12 December 2020

Neurofibromatosis type 1 (NF1) gene: implication in neuroectodermal differentiation and genesis of brain tumors

1 reference

12 December 2020

Von Hippel-Lindau disease: a genetic study

1 reference

12 December 2020

Chromosomal patterns in human malignant astrocytomas

1 reference

12 December 2020

Oncogenesis in ovarian cancer

1 reference

12 December 2020

Cancer in Relatives of Children with Central-Nervous-System Neoplasms

1 reference

12 December 2020

Amplified and rearranged epidermal growth factor receptor genes in human glioblastomas reveal deletions of sequences encoding portions of the N- and/or C-terminal tails

1 reference

12 December 2020

p53 mutation and loss of heterozygosity on chromosomes 17 and 10 during human astrocytoma progression

1 reference

12 December 2020

Gestational and familial risk factors for childhood astrocytoma: results of a case-control study

1 reference

12 December 2020

Interphase cytogenetics of brain tumors

1 reference

12 December 2020

Von Recklinghausen neurofibromatosis

1 reference

12 December 2020

Mitotic recombination of chromosome 17 in astrocytomas

1 reference

12 December 2020

The GLI gene is a member of the Kruppel family of zinc finger proteins

1 reference

12 December 2020

Evidence for a 17p tumor related locus distinct from p53 in pediatric primitive neuroectodermal tumors.

1 reference

12 December 2020

Relationship between gene amplification and chromosomal deviations in malignant human gliomas

1 reference

12 December 2020

Mutations in the p53 gene occur in diverse human tumour types

1 reference

12 December 2020

Oncogenes: cause or consequence in the development of glial tumors

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12 December 2020

Cellular localization and cell cycle regulation by a temperature-sensitive p53 protein

1 reference

12 December 2020

Location of gene for Gorlin syndrome

1 reference

12 December 2020

Molecular analysis of deletions of the short arm of chromosome 9 in human gliomas

1 reference

12 December 2020

Trisomy 7 and sex chromosome loss in human brain tissue

1 reference

12 December 2020

Epidemiology of primary central nervous system neoplasms. II. Case-control study.

1 reference

12 December 2020

Detection of p53 gene mutations in human brain tumors by single-strand conformation polymorphism analysis of polymerase chain reaction products

1 reference

12 December 2020

Germ-line mutations of the p53 tumor suppressor gene in patients with high risk for cancer inactivate the p53 protein

1 reference

12 December 2020

Involvement of multiple chromosome 17p loci in medulloblastoma tumorigenesis

1 reference

12 December 2020

Retinoblastoma gene deletions in human glioblastomas

1 reference

12 December 2020

From gene to carcinogen: a rapidly evolving field in molecular epidemiology

1 reference

12 December 2020

Soft-tissue sarcomas, breast cancer, and other neoplasms. A familial syndrome?

1 reference

12 December 2020

Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms

1 reference

12 December 2020

Nevoid basal-cell carcinoma syndrome

1 reference

12 December 2020

Occurrence of childhood cancers among sibs and estimation of familial risks.

1 reference

12 December 2020

Genetic epidemiology of childhood brain tumors

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12 December 2020

Amplification and/or overexpression of platelet-derived growth factor receptors and epidermal growth factor receptor in human glial tumors

1 reference

12 December 2020

p53 mutations in nonastrocytic human brain tumors

1 reference

12 December 2020

Loss of heterozygosity at chromosome 1q22 in basal cell carcinomas and exclusion of the basal cell nevus syndrome gene from this site.

1 reference

12 December 2020

Differential expression of two types of the neurofibromatosis type 1 (NF1) gene transcripts related to neuronal differentiation

1 reference

12 December 2020

Loss of heterozygosity for loci on chromosome 17p in human malignant astrocytoma.

1 reference

12 December 2020

Hodgkin's disease: case control epidemiological study in Yorkshire

1 reference

12 December 2020

Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of Von Hippel Lindau disease

1 reference

12 December 2020

A detailed deletion mapping of the short arm of chromosome 3 in sporadic renal cell carcinoma

1 reference

12 December 2020

[Subependymal giant cell astrocytoma]

1 reference

12 December 2020

Karyotypes in 90 human gliomas

1 reference

12 December 2020

Familial Breast Cancer, Soft-Tissue Sarcomas, and Other Neoplasms

1 reference

12 December 2020

Proto-oncogene analyses in brain tumors

1 reference

12 December 2020

Mapping of the von Hippel-Lindau disease locus to a small region of chromosome 3p by genetic linkage analysis

1 reference

12 December 2020

p53 mutations in human malignant gliomas: comparison of loss of heterozygosity with mutation frequency

1 reference

12 December 2020

Genetic evidence that Turcot syndrome is not allelic to familial adenomatous polyposis

1 reference

12 December 2020

Long-term follow-up of von Recklinghausen neurofibromatosis. Survival and malignant neoplasms

1 reference

12 December 2020

Human hypervariable sequences in risk assessment: rare Ha-ras alleles in cancer patients

1 reference

12 December 2020

Brain tumors with tuberous sclerosis

1 reference

12 December 2020

Gene Amplification in Malignant Human Gliomas: Clinical and Histopathologic Aspects

1 reference

12 December 2020

Analysis of chromosome 22 deletions in neurofibromatosis type 2-related tumors

1 reference

12 December 2020

Malignancy in neurofibromatosis.

1 reference

12 December 2020

Paternal origin of new mutations in von Recklinghausen neurofibromatosis.

1 reference

12 December 2020

Loss of heterozygosity for 10q loci in human gliomas

1 reference

12 December 2020

On the heredity of glioblastoma.

1 reference

12 December 2020

Familial glioma: occurrence within the "familial cancer syndrome" and systemic malformations

1 reference

12 December 2020

Childhood cancer deaths in California-born twins. A further report on types of cancer found.

1 reference

12 December 2020

Comparative study of p53 gene and protein alterations in human astrocytic tumors

1 reference

12 December 2020

Increased expression of the epidermal growth factor receptor gene in malignant gliomas is invariably associated with gene amplification

1 reference

12 December 2020

Brain Tumor in a Pedigree of Cancer Family Syndrome

1 reference

12 December 2020

Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22

1 reference

12 December 2020

Familial pheochromocytomas with unusual associations

1 reference

12 December 2020

Participation of p53 protein in the cellular response to DNA damage

1 reference

12 December 2020

Loss of distinct regions on the short arm of chromosome 17 associated with tumorigenesis of human astrocytomas

1 reference

12 December 2020

Turcot syndrome. Autosomal dominant or recessive transmission?

1 reference

12 December 2020

Prospective study of a family cancer syndrome

1 reference

12 December 2020

Alternative splicing of neurofibromatosis type 1 gene transcript in malignant brain tumors: PCR analysis of frozen-section mRNA

1 reference

12 December 2020

Risk factors for tumors of the brain and meninges: results from the Adelaide Adult Brain Tumor Study

1 reference

12 December 2020

A cytoplasmic protein stimulates normal N-ras p21 GTPase, but does not affect oncogenic mutants

1 reference

12 December 2020

Turcot syndrome (glioma polyposis). Case report

1 reference

12 December 2020

Familial factors associated with malignant gliomas

1 reference

12 December 2020

Evidence for the involvement of a potential second tumor suppressor gene on chromosome 17 distinct from p53 in malignant astrocytomas

1 reference

12 December 2020

Molecular genetics of neurological tumours

1 reference

12 December 2020

Cytogenetic and loss of heterozygosity studies in ependymomas, pilocytic astrocytomas, and oligodendrogliomas

1 reference

12 December 2020

Evidence for a tumor suppressor gene on chromosome 19q associated with human astrocytomas, oligodendrogliomas, and mixed gliomas

1 reference

12 December 2020

Changes of telomere lengths in human intracranial tumours

1 reference

12 December 2020

The neurofibromatosis type 1 gene encodes a protein related to GAP

1 reference

12 December 2020

Identification and characterization of transcripts from the neurofibromatosis 1 region: the sequence and genomic structure of EVI2 and mapping of other transcripts

1 reference

12 December 2020

Deaths from childhood leukemia and solid tumors among twins and other sibs in the United States, 1960-67

1 reference

12 December 2020

Chromosome 11p15 deletions in human malignant astrocytomas and primitive neuroectodermal tumors

1 reference

12 December 2020

Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene

1 reference

12 December 2020

Subependymal giant cell astrocytoma: a clinical, pathological, and flow cytometric study

1 reference

12 December 2020

Neurofibromatosis 2 (bilateral acoustic neurofibromatosis).

1 reference

12 December 2020

von Hippel-Lindau disease (angiomatosis of the retina and cerebellum)

1 reference

12 December 2020

Renal cell cancer: oncogenes and tumor suppressor genes

1 reference

12 December 2020

Allelotype of colorectal carcinomas

1 reference

12 December 2020

Structural alterations of the epidermal growth factor receptor gene in human gliomas

1 reference

12 December 2020

Hereditary gastrointestinal polyposis syndromes

1 reference

12 December 2020

Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients

1 reference

12 December 2020

p53 mutations are associated with 17p allelic loss in grade II and grade III astrocytoma

1 reference

12 December 2020

Familial cancer syndromes: A survey

1 reference

12 December 2020

Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneity

1 reference

12 December 2020

A cancer family syndrome in twenty-four kindreds

1 reference

12 December 2020

Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9

1 reference

12 December 2020

Cytogenetics of human brain tumors

1 reference

12 December 2020

Clonal genomic alterations in glioma malignancy stages.

1 reference

12 December 2020

Turcot's syndrome of glioma and polyposis occurs in the absence of germ line mutations of exons 5 to 9 of the p53 gene.

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01324606

1 reference

Dimensions Publication ID

22 September 2017

1025900919

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