(Q40468663)

English

Fine mapping of chromosome 10q deletions in mycosis fungoides and sezary syndrome: identification of two discrete regions of deletion at 10q23.33-24.1 and 10q24.33-25.1.

scientific article published on February 2005

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scholarly article

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5 January 2020

Fine mapping of chromosome 10q deletions in mycosis fungoides and sezary syndrome: identification of two discrete regions of deletion at 10q23.33-24.1 and 10q24.33-25.1. (English)

1 reference

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5 January 2020

mycosis fungoides

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inferred from title

Tracey Mitchell

2

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5 January 2020

author name string

E Mary Wain

1

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5 January 2020

Robin Russell-Jones

3

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5 January 2020

Sean J Whittaker

4

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5 January 2020

publication date

1 February 2005

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5 January 2020

Genes, Chromosomes and Cancer

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5 January 2020

42

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5 January 2020

2

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5 January 2020

184-192

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5 January 2020

PTEN / MMAC1 mutation and frequent loss of heterozygosity identified in chromosome 10q in a subset of hepatocellular carcinomas.

1 reference

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Cytogenetics of T-cell malignant lymphoma. Report of 17 cases and review of the chromosomal breakpoints

1 reference

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A novel gene, LGI1, from 10q24 is rearranged and downregulated in malignant brain tumors

1 reference

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7 January 2021

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Infrequent Fas mutations but no Bax or p53 mutations in early mycosis fungoides: a possible mechanism for the accumulation of malignant T lymphocytes in the skin

1 reference

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7 January 2021

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Loss of heterozygosity on chromosome 10q is associated with earlier onset sporadic colorectal adenocarcinoma.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20115

7 January 2021

based on heuristic

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Detection of a Peripheral Blood T Cell Clone is an Independent Prognostic Marker in Mycosis Fungoides

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20115

7 January 2021

based on heuristic

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Cluster of allele losses within a 2.5 cM region of chromosome 10 in high-grade invasive bladder cancer

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20115

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20115

7 January 2021

based on heuristic

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Notable losses at specific regions of chromosomes 10q and 13q in the Sézary syndrome detected by comparative genomic hybridization

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20115

7 January 2021

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Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20115

7 January 2021

based on heuristic

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Chromosome aberrations, spontaneous SCE, and growth kinetics in PHA-stimulated lymphocytes of five cases with Sézary syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20115

7 January 2021

based on heuristic

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Molecular cytogenetic analysis of cutaneous T-cell lymphomas: identification of common genetic alterations in Sézary syndrome and mycosis fungoides

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20115

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular cytogenetic characterization of Sézary syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20115

7 January 2021

based on heuristic

inferred from DOI database lookup

DMBT1, a new member of the SRCR superfamily, on chromosome 10q25.3-26.1 is deleted in malignant brain tumours

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20115

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutational analysis of the PTEN/MMAC1 gene in non-Hodgkin's lymphoma.

1 reference

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7 January 2021

based on heuristic

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The most common chromosome change in 86 chronic B cell or T cell tumors: a 14q32 translocation

1 reference

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7 January 2021

based on heuristic

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Allelotyping in mycosis fungoides and Sézary syndrome: common regions of allelic loss identified on 9p, 10q, and 17p

1 reference

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7 January 2021

based on heuristic

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Microsatellite instability is associated with hypermethylation of the hMLH1 gene and reduced gene expression in mycosis fungoides

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20115

7 January 2021

based on heuristic

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Large cell transformation of Sézary syndrome. A conventional and molecular cytogenetic study

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20115

7 January 2021

based on heuristic

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Recurrent abnormalities of chromosome bands 10q23-25 in non-Hodgkin's lymphoma

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20115

7 January 2021

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Mechanisms underlying losses of heterozygosity in human colorectal cancers

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20115

7 January 2021

based on heuristic

inferred from DOI database lookup

Twenty-year trends in the reported incidence of mycosis fungoides and associated mortality

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20115

7 January 2021

based on heuristic

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Clinical implications of cytogenetic studies in cutaneous T-cell lymphoma (CTCL)

1 reference

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7 January 2021

based on heuristic

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Fine-structure deletion mapping of 10q22-24 identifies regions of loss of heterozygosity and suggests that sporadic follicular thyroid adenomas and follicular thyroid carcinomas develop along distinct neoplastic pathways

1 reference

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7 January 2021

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Prognosis in cutaneous T-cell lymphoma by skin stage: long-term survival in 489 patients

1 reference

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Identifiers

10.1002/GCC.20115

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15540164%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15540164%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

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