Lectin binding in Meth-A cells polyploidized by different mechanisms

Cytologia

Volumn 65, Issue 4, 2000, Pages 389-395

  Fujikawa Yamamoto, K ^a   Ohdoi, C ^a   Yamagishi, H ^a   Zong, Z ^a   Wang, S ^a  

^a KANAZAWA MEDICAL UNIVERSITY   (Japan)

Author keywords

Cells; Demecolcine; K 252a; Lectin; Meth A; Polyploidization

Indexed keywords

RICINUS COMMUNIS;

EID: 0034496713     PISSN: 00114545     EISSN: None     Source Type: Journal    
DOI: 10.1508/cytologia.65.389     Document Type: Article

References (12)

1. 2 block caused by staurosporine, a potent inhibitor of protein kinases
2. Hyperploidization of V79 cells by K-252a in comparison with demecolcine
3. Hyperploidization of Meth-A and B16F10 cells by K-252a and staurosporine
4. Spontaneous polyploidization results in apoptosis in a Meth-A tumor cell line
5. Lack of synchrony among multiple nuclei induces partial DNA fragmentation in V79 Cells polyploidized by demecolcine
6. Cell division and the mitotic spindle
7. K-252 compounds, novel and potent inhibitors of protein kinase C and cyclic nucleotide-dependent protein kinases
8. Rapid flow cytofluorometric analysis of mammalian cell cycle by propidium iodide staining
9. Transmembrane control of the receptors on normal and tumor cells. I. Cytoplasmic influence over cell surface components
10. Development of polyploidization in taxol-resistant human leukemia cells in vitro
11. Uncoupled cell cycle without mitosis induced by a protein kinase inhibitor, K-252a