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Cited by 571

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Terminal differentiation of human promyelocytic leukemic cells in primary culture in response to retinoic acid

Open access
Breitman, TR, Collins, SJ, Keene, BR·1981·Blood

Abstract

The recent finding that retinoic acid induces terminal granulocytic differentiation of the human promyelocytic leukemia cell line, HL-60, prompted an investigation of the sensitivity to this inducer of human myelocytic leukemia cells in primary suspension culture. Of the 21 leukemic specimens, only cells from the two patients with acute promyelocytic leukemia differentiated in response to retinoic acid. After an incubation period of 5--7 days in 1 microM retinoic acid, the cells from these two patients showed extensive morphological and functional maturation. Thus, because it appears that retinoic acid specifically induces granulocytic differentiation of leukemic promyelocytes, this compound may have therapeutic utility in the treatment of acute promyelocytic leukemia.

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Crossref · 10.1182/blood.v57.6.1000.1000

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Metadata

Authors
Breitman, T., Collins, S., & Keene, B.
Venue
Blood
Published
1981-06-01
Volume
57
Issue
6
Pages
1000-1004
ISSN
  • 0006-4971 (ISSN-L)
  • 1528-0020
OpenAlex
W92934419
Cited by
571
References
1
FWCI
7.28
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Terminal differentiation of human promyelocytic leukemic cells in primary culture in response to retinoic acid. https://app.cochat.ai/papers/10.1182/blood.v57.6.1000.1000
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Breitman, T., Collins, S., & Keene, B. (1981). Terminal differentiation of human promyelocytic leukemic cells in primary culture in response to retinoic acid. Blood. https://doi.org/10.1182/blood.v57.6.1000.1000

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.