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Year | Number of Results |
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1996 | 2 |
1999 | 1 |
2024 | 0 |
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Page 1
The RAR-RXR as well as the RXR-RXR pathway is involved in signaling growth inhibition of human CD34+ erythroid progenitor cells.
Blood. 1996 Mar 1;87(5):1728-36.
Blood. 1996.
PMID: 8634418
Free article.
Transactivation studies showed that both the RAR (Ro 13-7410) and RXR (Ro 25-6603 and Ro 25-7386) ligands were highly selective at 100 nmol/L. At this concentration, Ro 13-7410 potently inhibited G-CSF-stimulated myeloid as well as SCF + Epo-induced erythroid …
Transactivation studies showed that both the RAR (Ro 13-7410) and RXR (Ro 25-6603 and Ro 25-7386) ligands were highly s …
Myeloid differentiation and retinoblastoma phosphorylation changes in HL-60 cells induced by retinoic acid receptor- and retinoid X receptor-selective retinoic acid analogs.
Brooks SC 3rd, Kazmer S, Levin AA, Yen A.
Brooks SC 3rd, et al.
Blood. 1996 Jan 1;87(1):227-37.
Blood. 1996.
PMID: 8547646
Free article.
RA analogs that selectively bind only to RARs (Am580 and/or TTNPB) or to RXRs (Ro 25-6603, SR11237, and/or SR11234) did not elicit the above-mentioned three cellular responses. In contrast, simultaneous treatment with both an RAR-selective ligand (Am580 or TT …
RA analogs that selectively bind only to RARs (Am580 and/or TTNPB) or to RXRs (Ro 25-6603, SR11237, and/or SR11234) did …
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Retinoic acid induces apoptosis of human CD34+ hematopoietic progenitor cells: involvement of retinoic acid receptors and retinoid X receptors depends on lineage commitment of the hematopoietic progenitor cells.
Josefsen D, Blomhoff HK, Lømo J, Blystad AK, Smeland EB.
Josefsen D, et al.
Exp Hematol. 1999 Apr;27(4):642-53. doi: 10.1016/s0301-472x(98)00073-3.
Exp Hematol. 1999.
PMID: 10210322
Free article.
To explore the receptor signaling pathways involved in RA-induced apoptosis, we used selective ligands for retinoic acid receptors (RARs; RO13-7410) and retinoid X receptors (RXRs; RO 25-6603). We found that RARs were involved in RA-mediated apoptosis of myel …
To explore the receptor signaling pathways involved in RA-induced apoptosis, we used selective ligands for retinoic acid receptors (RARs; RO …
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