نتایج جستجو برای: calyculin a

تعداد نتایج: 13431803  

Journal: :American journal of physiology. Cell physiology 2008
Alejandro Ortiz-Acevedo Robert R Rigor Hector M Maldonado Peter M Cala

Alteration in cell volume of vertebrates results in activation of volume-sensitive ion flux pathways. Fine control of the activity of these pathways enables cells to regulate volume following osmotic perturbation. Protein phosphorylation and dephosphorylation have been reported to play a crucial role in the control of volume-sensitive ion flux pathways. Exposing Amphiuma tridactylu red blood ce...

Journal: :Mutagenesis 2007
Peter E Bryant Hossein Mozdarani

To study the possible influence of cell-cycle delay on cells reaching mitosis during conventional radiation-induced chromatid break experiments using colcemid as a blocking agent, we have compared the chromatid break kinetics following a single dose of gamma rays (0.75 Gy) in metaphase CHO cells using calyculin-induced premature chromosome condensation (PCC), with those using colcemid block. Ca...

Journal: :Andrologia 2001
M L Hortas J A Castilla M T Gil F Samaniego M Morell M Redondo

Protein phosphorylation is involved in sperm capacitation, so the effect of protein phosphatase inhibitors on the capacitation of spermatozoa of males with unexplained infertility was investigated. d-mannose ligand specific receptor expression in fresh, living spermatozoa, capacitated or treated with calyculin A (an inhibitor of protein phosphatases 1 and 2A), was studied in three groups of men...

H. Mozdarani, S. Hosseini,

Background: Premature chromosome condensation (PCC) is a method for interphase chromosome analysis in biodosimetry. This study was performed to verify the usefulness of PCC induced by calyculin A in human peripheral blood lymphocytes (pbl) for biological dosimetry and possible construction of dose-response curve. Materials and Methods: Peripheral blood was obtained from a healthy donor and expo...

Journal: :Cardiovascular research 2011
Young-Eun Cho Duck-Sun Ahn Kathleen G Morgan Young-Ho Lee

AIMS The role of Ca(2+) sensitization induced by a Ca(2+)-independent myosin light chain kinase (MLCK) in hypertension has not been determined. The aim of this study was to clarify the role of possible Ca(2+)-independent MLCK activity in hypertension. METHODS AND RESULTS We compared increases in contractile force and phosphorylation of myosin light chain (MLC) evoked by calyculin A, a phospha...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2005
Eliane El Achkar Michelle Gerbault-Seureau Martine Muleris Bernard Dutrillaux Michelle Debatisse

Various studies suggest a tight relationship between chromosome rearrangements driving tumor progression and breaks at loci called common fragile sites. Most of these sites are induced after perturbation of the replication dynamics, notably by aphidicolin treatment. We have mapped the majority of these sites to the interface of R and G bands, which calls into question the previous assignment of...

Journal: :Lab on a chip 2013
Phrabha S Raman Colin D Paul Kimberly M Stroka Konstantinos Konstantopoulos

Cells migrate in vivo within three-dimensional (3D) extracellular matrices. Cells also migrate through 3D longitudinal channels formed between the connective tissue and the basement membrane of muscle, nerve, and epithelium. Although traction forces have been measured during 2D cell migration, no assay has been developed to probe forces during migration through confined microenvironments. We th...

Journal: :Journal of Histochemistry & Cytochemistry 2005

Journal: :The Journal of pharmacology and experimental therapeutics 1998
M H Kim S H Kim H S Kim J W Chang Y S Hong H W Kim C S Park

Possible involvement of reversible phosphorylation and dephosphorylation of myosin light chain (MLC) by myosin light chain kinase (MLCK) and protein phosphatases (PPases), respectively, in the Ca++-calmodulin-dependent inhibition of renin secretion was investigated with the use of putative MLCK inhibitor ML-7 [1-(5-iodonaphthalene-1-sulfonyl)-1H-hexahydro-1,4-diazepine] and PPase type1 (PPase-1...

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