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Deletion of IRF-1, mapping to chromosome 5q31.1, in human leukemia and preleukemic myelodysplasia

Author

Cheryl L. Willman

1954 -

Published in: Science

Date of publication: February 12, 1993

Language: English

Main subject: leukemia

Bibliographic databases:

Cites articles 26

Date

Title

Authors

October 1, 1974

Distinct haematological disorder with deletion of long arm of no. 5 chromosome

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December 1984

Nucleotide sequence of cDNA and derived amino acid sequence of human complement component C9
December 13, 1985

The human gene encoding GM-CSF is at 5q21-q32, the chromosome region deleted in the 5q- anomaly
September 1, 1985

Expression of the human c-fms proto-oncogene in hematopoietic cells and its deletion in the 5q- syndrome
July 1, 1985

The 5q-anomaly
February 28, 1986

Evidence for the involvement of GM-CSF and FMS in the deletion (5q) in myeloid disorders

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May 1986

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization
March 1986

Clinical and cytogenetic correlations in 63 patients with therapy-related myelodysplastic syndromes and acute nonlymphocytic leukemia: further evidence for characteristic abnormalities of chromosomes no. 5 and 7

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August 1987

The interleukin 3 gene is located on human chromosome 5 and is deleted in myeloid leukemias with a deletion of 5q

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September 9, 1988

Regulated expression of a gene encoding a nuclear factor, IRF-1, that specifically binds to IFN-beta gene regulatory elements,Regulated expression of a gene encoding a nuclear factor, IRF-1, that specifically binds to IFN-β gene regulatory elements
December 1, 1988

Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.
August 25, 1989

Structurally similar but functionally distinct factors, IRF-1 and IRF-2, bind to the same regulatory elements of IFN and IFN-inducible genes
April 25, 1989

Sequence of a cDNA coding for human IRF-1
May 1, 1989

The gene for human complement component C9 mapped to chromosome 5 by polymerase chain reaction
January 1, 1989

Induction of endogenous IFN-alpha and IFN-beta genes by a regulatory transcription factor, IRF-1.
December 1, 1989

Induction of the transcription factor IRF-1 and interferon-beta mRNAs by cytokines and activators of second-messenger pathways
August 10, 1990

The neurofibromatosis type 1 gene encodes a protein related to GAP
June 1, 1990

An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor
March 15, 1991

Identification of a gene located at chromosome 5q21 that is mutated in colorectal cancers,Identification of a Gene Located at Chromosome 5q21 that Is Mutated in Colorectal Cancers

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August 9, 1991

Identification of FAP locus genes from chromosome 5q21

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Identification and characterization of the familial adenomatous polyposis coli gene
January 1, 1991

Specific depletion of the B-cell population induced by aberrant expression of human interferon regulatory factor 1 gene in transgenic mice

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April 17, 1992

Somatic mutations in the neurofibromatosis 1 gene in human tumors
July 1992

Assignment of two human cell cycle genes, CDC25C and CCNB1, to 5q31 and 5q12, respectively
July 1992

A radiation hybrid map of 18 growth factor, growth factor receptor, hormone receptor, or neurotransmitter receptor genes on the distal region of the long arm of chromosome 5
February 12, 1993

Anti-oncogenic and oncogenic potentials of interferon regulatory factors-1 and -2

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