Comparative genomic hybridization of human malignant gliomas reveals multiple amplification sites and nonrandom chromosomal gains and losses (Q35834190)

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scientific article published in June 1994

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English	Comparative genomic hybridization of human malignant gliomas reveals multiple amplification sites and nonrandom chromosomal gains and losses	scientific article published in June 1994

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27 October 2019

Comparative genomic hybridization of human malignant gliomas reveals multiple amplification sites and nonrandom chromosomal gains and losses (English)

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27 October 2019

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Schröck E

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Thiel G

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Lozanova T

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du Manoir S

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Meffert MC

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Jauch A

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Speicher MR

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Nürnberg P

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Vogel S

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Jänisch W

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1 June 1994

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The American Journal of Pathology

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144

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1203-1218

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27 October 2019

Comparative genomic hybridization: a rapid new method for detecting and mapping DNA amplification in tumors

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Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization.

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Generation of band-specific painting probes from a single microdissected chromosome

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Detection of amplified DNA sequences by reverse chromosome painting using genomic tumor DNA as probe

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Age-related nonrandom chromosomal abnormalities in human low-grade astrocytomas.

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Molecular cytogenetic analysis of formalin-fixed, paraffin-embedded solid tumors by comparative genomic hybridization after universal DNA-amplification

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Deletion mapping of the long arm of chromosome 10 in glioblastoma multiforme

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Trisomy 7 in nonneoplastic cells.

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Relationship between gene amplification and chromosomal deviations in malignant human gliomas

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

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Specific chromosomal abnormalities in malignant human gliomas.

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Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes

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

1 reference

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Chromosomal patterns in human malignant astrocytomas

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Cytogenetics of human brain tumors

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Cancer statistics, 1990.

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Construction and characterization of plasmid libraries enriched in sequences from single human chromosomes

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Amplification of the epidermal growth factor receptor gene in human gliomas

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Coamplification of simple repetitive DNA fingerprint fragments and the EGFR gene in human gliomas.

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Cytogenetics and Molecular Genetics of Malignant Gliomas and Medulloblastoma

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11 July 2018

Coexpression of platelet-derived growth factor (PDGF) B chain and PDGF B-type receptor in human gliomas.

1 reference

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11 July 2018

Trisomy 7 and sex chromosome loss need not be representative of tumor parenchyma cells in malignant glioma.

1 reference

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11 July 2018

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

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Prognostic value of cytogenetic analysis in human cerebral astrocytomas

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Combined erbB gene overexpression and decreased H-ras gene expression in human gliomas

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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

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Metaphase and interphase cytogenetics with Alu-PCR-amplified yeast artificial chromosome clones containing the BCR gene and the protooncogenes c-raf-1, c-fms, and c-erbB-2.

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

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EGF receptor amplification and expression in human brain tumours

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Epidermal growth factor receptor in human brain tumors.

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

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Search for putative suppressor genes in meningioma: significance of chromosome 22

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Karyotypes in 90 human gliomas

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Abnormalities of chromosome 22 in meningiomas and confirmation of the origin of a dicentric 22 by in situ hybridization

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

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

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

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A cytogenetic study of 53 human gliomas.

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27 October 2019

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