(Q41019659)

25 September 2017

title

Molecular definition of chromosome translocations involving 10q24 and 19q13 in human malignant glioma cells (English)

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25 September 2017

2

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25 September 2017

Chernova O

1

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25 September 2017

language of work or name

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1 August 1998

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Cancer Genetics and Cytogenetics

25 September 2017

published in

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25 September 2017

volume

105

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25 September 2017

issue

1

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25 September 2017

page(s)

60-68

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Genetic alterations in gliomas

25 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900479-2

7 January 2021

Cytogenetics of malignant gliomas: I. The autosomes with reference to rearrangements

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7 January 2021

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

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7 January 2021

Loss of heterozygosity for 10q loci in human gliomas

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7 January 2021

Correlation of cytogenetic analysis and loss of heterozygosity studies in human diffuse astrocytomas and mixed oligo‐astrocytomas

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https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900479-2

7 January 2021

Loss of heterozygosity in malignant gliomas involves at least three distinct regions on chromosome 10.

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https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900479-2

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900479-2

7 January 2021

Two tumor suppressive loci on chromosome 10 involved in human glioblastomas

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https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900479-2

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900479-2

7 January 2021

Region-specific loss of heterozygosity on chromosome 19 is related to the morphologic type of human glioma

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https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900479-2

7 January 2021

Chromosomal translocations in human cancer.

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7 January 2021

Localization of the synovial sarcoma t(X;18)(p11.2;q11.2) breakpoint by fluorescence in situ hybridization

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https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900479-2

7 January 2021

Identification of novel genes, SYT and SSX, involved in the t(X;18)(p11.2;q11.2) translocation found in human synovial sarcoma

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https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900479-2

7 January 2021

Fusion of SYT to two genes, SSX1 and SSX2, encoding proteins with homology to the Kruppel-associated box in human synovial sarcoma

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7 January 2021

The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers

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https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900479-2

7 January 2021

Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours

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7 January 2021

Fusion of a fork head domain gene to PAX3 in the solid tumour alveolar rhabdomyosarcoma

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7 January 2021

Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11)

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7 January 2021

Fine structure physical mapping of a 1.9 Mb region of chromosome 13q12.

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7 January 2021

Molecular characterization of the 1p22 breakpoint region spanning the constitutional translocation breakpoint in a neuroblastoma patient with a t(1;10)(p22;q21)

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7 January 2021

Localization of the 8;13 translocation breakpoint associated with myeloproliferative disease to a 1.5 mbp region of chromosome 13

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https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900479-2

7 January 2021

T98G: An anchorage-independent human tumor cell line that exhibits stationary phase G1 arrest in vitro

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7 January 2021

An integrated metric physical map of human chromosome 19.

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7 January 2021

PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer

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https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900479-2

7 January 2021

Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers

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https://api.crossref.org/works/10.1016%2FS0165-4608%2897%2900479-2

7 January 2021

10.1016/S0165-4608(97)00479-2

Identifiers

DOI

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25 September 2017

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