A search for novel tumour suppressor genes for adult acute leukaemia by allelotyping at sub-telomeric chromosomal regions (Q74825196)

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scientific article published on 01 May 1998

Language	Label	Description	Also known as
English	A search for novel tumour suppressor genes for adult acute leukaemia by allelotyping at sub-telomeric chromosomal regions	scientific article published on 01 May 1998

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scholarly article

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13 November 2019

A search for novel tumour suppressor genes for adult acute leukaemia by allelotyping at sub-telomeric chromosomal regions (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9685700%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

Hanneke C Kluin-Nelemans

6

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13 November 2019

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M Giphart-Gassler

1

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13 November 2019

A De Nooij-Van Dalen

2

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13 November 2019

V Van Buuren-Van Seggelen

3

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13 November 2019

B Morolli

4

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13 November 2019

P Lohman

5

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13 November 2019

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1 May 1998

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13 November 2019

Mutation Research

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13 November 2019

400

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13 November 2019

1-2

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13 November 2019

409-419

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13 November 2019

Chromosomal translocations in human cancer.

1 reference

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Unique fusion of bcr and c-abl genes in Philadelphia chromosome positive acute lymphoblastic leukemia

1 reference

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Fusion of the leucine zipper gene HLF to the E2A gene in human acute B-lineage leukemia

1 reference

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7 January 2021

Involvement of a homolog of Drosophila trithorax by 11q23 chromosomal translocations in acute leukemias

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7 January 2021

Six-year follow-up of the clinical significance of karyotype in acute lymphoblastic leukemia

1 reference

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7 January 2021

The human leukemia oncogene bcr-abl abrogates the anchorage requirement but not the growth factor requirement for proliferation

1 reference

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7 January 2021

Cytogenetic deletion maps of hematologic neoplasms: circumstantial evidence for tumor suppressor loci

1 reference

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7 January 2021

Frequency of homozygous deletion at p16/CDKN2 in primary human tumours

1 reference

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7 January 2021

Overview: genes that predispose to cancer

1 reference

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7 January 2021

Loss of constitutional heterozygosity in human cancer.

1 reference

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7 January 2021

Homozygous deletions at 9p21 in childhood acute lymphoblastic leukemia detected by microsatellite analysis

1 reference

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7 January 2021

TEL is one of the targets for deletion on 12p in many cases of childhood B-lineage acute lymphoblastic leukemia

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2898%2900022-0

7 January 2021

The commonly deleted region at 9p21-22 in lymphoblastic leukemias spans at least 400 kb and includes p16 but not p15 or the IFN gene cluster

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2898%2900022-0

7 January 2021

Delineation of a 6 cM commonly deleted region in childhood acute lymphoblastic leukemia on the 6q chromosomal arm.

1 reference

https://api.crossref.org/works/10.1016%2FS0027-5107%2898%2900022-0

7 January 2021

ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia

1 reference

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7 January 2021

Isolation and molecular characterization of spontaneous mutants of lymphoblastoid cells with extended loss of heterozygosity

1 reference

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7 January 2021

Chromosome loss with concomitant duplication and recombination both contribute most to loss of heterozygosity in vitro

1 reference

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7 January 2021

Allelotype of colorectal carcinomas

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7 January 2021

The 1993-94 Généthon human genetic linkage map

1 reference

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A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

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7 January 2021

Microsatellite instability in childhood T cell acute lymphoblastic leukemia.

1 reference

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7 January 2021

Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers

1 reference

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7 January 2021

Acute lymphoblastic leukemia and chromosome 21.

1 reference

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7 January 2021

Molecular mechanisms of spontaneous and induced loss of heterozygosity in human cells in vitro

1 reference

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7 January 2021

Genetic instability on chromosome 16 in a human B lymphoblastoid cell line

1 reference

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7 January 2021

Clues to the pathogenesis of familial colorectal cancer

1 reference

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7 January 2021

Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis

1 reference

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7 January 2021

Instability of short tandem repeats (microsatellites) in human cancers.

1 reference

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7 January 2021

MSH2 deficient mice are viable and susceptible to lymphoid tumours

1 reference

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7 January 2021

Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer

1 reference

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7 January 2021

Rarity of microsatellite alterations in acute myeloid leukaemia.

1 reference

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7 January 2021

Identifiers

10.1016/S0027-5107(98)00022-0

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9685700%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9685700%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

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