Deletions on the long arm of chromosome 17 in pilocytic astrocytoma. (Q48386167)

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25 October 2019

title

Deletions on the long arm of chromosome 17 in pilocytic astrocytoma (English)

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25 October 2019

1

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25 October 2019

author name string

D N Louis

2

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25 October 2019

A G Menon

3

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25 October 2019

K von Ammon

4

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25 October 2019

I Petersen

5

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25 October 2019

D Ellison

6

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25 October 2019

O D Wiestler

7

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25 October 2019

B R Seizinger

8

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25 October 2019

publication date

1 January 1993

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25 October 2019

published in

Acta Neuropathologica

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25 October 2019

volume

86

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25 October 2019

issue

1

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25 October 2019

page(s)

81-85

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Detection of frequent allelic loss on proximal chromosome 17q in sporadic breast carcinoma using microsatellite length polymorphisms

25 October 2019

cites work

1 reference

12 December 2020

A small deletion and an adjacent base exchange in a potential stem-loop region of the neurofibromatosis 1 gene

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12 December 2020

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

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Somatic mutations in the neurofibromatosis 1 gene in human tumors

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

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Mitotic recombination of chromosome 17 in astrocytomas

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Association of epidermal growth factor receptor gene amplification with loss of chromosome 10 in human glioblastoma multiforme

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Reduction to homozygosity involving p53 in esophageal cancers demonstrated by the polymerase chain reaction

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Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma

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Dictyostelium nucleoside diphosphate kinase highly homologous to Nm23 and Awd proteins involved in mammalian tumor metastasis and Drosophila development

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Regulation of Ras-GAP and the neurofibromatosis-1 gene product by eicosanoids

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Loss of genetic information in central nervous system tumors common to children and young adults

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12 December 2020

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

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12 December 2020

TP53 Gene Mutations and 17p Deletions in Human Astrocytomas

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12 December 2020

Karyotypes in 90 human gliomas

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von Recklinghausen neurofibromatosis. II. Incidence of optic gliomata

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Somatic allelic deletion of nm23 in human cancer

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

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Gene Amplification in Malignant Human Gliomas: Clinical and Histopathologic Aspects

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Evidence for a novel gene associated with low tumor metastatic potential

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12 December 2020

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

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

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12 December 2020

The neurofibromatosis type 1 gene encodes a protein related to GAP

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12 December 2020

A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations

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12 December 2020

Abnormal regulation of mammalian p21ras contributes to malignant tumor growth in von Recklinghausen (type 1) neurofibromatosis

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12 December 2020

Linkage of early-onset familial breast cancer to chromosome 17q21

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12 December 2020

Cytogenetic analysis of 39 pediatric central nervous system tumors

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12 December 2020

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

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12 December 2020

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

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Clonal genomic alterations in glioma malignancy stages.

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Identifiers

DOI

10.1007/BF00454903

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8103960%20AND%20SRC:MED&resulttype=core&format=json

release_35lhsmavvrbjfka4b7kw6a6viu

25 October 2019

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/35lhsmavvrbjfka4b7kw6a6viu

24 November 2022

mapped directly with Wikidata item

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