Deletion of IRF-1, mapping to chromosome 5q31.1, in human leukemia and preleukemic myelodysplasia (Q28266438)

2

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M G Pallavicini

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H Harada

4

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N Tanaka

5

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M L Slovak

6

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H Yamamoto

7

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K Harada

8

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T C Meeker

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A F List

https://api.crossref.org/works/10.1126/SCIENCE.8438156

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language of work or name

English

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publication date

12 February 1993

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published in

Science

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volume

259

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issue

5097

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page(s)

968-71

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.8438156

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.8438156

Identification of a Gene Located at Chromosome 5q21 that Is Mutated in Colorectal Cancers

21 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.8438156

Identification of FAP locus genes from chromosome 5q21

21 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.8438156

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.8438156

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.8438156

Somatic mutations in the neurofibromatosis 1 gene in human tumors

21 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.8438156

Sequence of a cDNA coding for human IRF-1

21 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.8438156

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.8438156

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.8438156

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.8438156

The neurofibromatosis type 1 gene encodes a protein related to GAP

21 April 2017

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.8438156

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

21 April 2017

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.8438156

The gene for human complement component C9 mapped to chromosome 5 by polymerase chain reaction

21 April 2017

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.8438156

Nucleotide sequence of cDNA and derived amino acid sequence of human complement component C9

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.8438156

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.8438156

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.8438156

Identification and characterization of the familial adenomatous polyposis coli gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.8438156

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.8438156

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.8438156

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.8438156

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.8438156

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.8438156

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.8438156

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.8438156