Biomonitoring of occupational exposure to PAH through analysis of DNA adducts in human white blood cells by quantitative immunofluorescence microscopy and 32P-postlabelling

Author(s):  
R. Roggeband ◽  
P.T.M. van den Berg ◽  
M.-J.-S.T. Steenwinkel ◽  
R.A. Baan ◽  
C.J.M. van der Wulp
2015 ◽  
Vol 49 (9) ◽  
pp. 1049-1054 ◽  
Author(s):  
H. Li ◽  
S. Cui ◽  
S. Wang ◽  
X. Jiang ◽  
S. Zhang ◽  
...  

2014 ◽  
Vol 1364 ◽  
pp. 183-191 ◽  
Author(s):  
Nathalie Grova ◽  
Guillaume Salquèbre ◽  
Emilie M. Hardy ◽  
Henri Schroeder ◽  
Brice M.R. Appenzeller

1994 ◽  
Vol 15 (3) ◽  
pp. 557-560 ◽  
Author(s):  
Margarita Rojas ◽  
Kroum Alexandrov ◽  
Frederik-Jan van Schooten ◽  
Michel Hillebrand ◽  
Erik Kriek ◽  
...  

Author(s):  
Dorota Butkiewicz ◽  
Ewa Grzybowska ◽  
David H. Phillips ◽  
Kari Hemminki ◽  
Mieczys?aw Chor??y

1980 ◽  
Vol 97 (3) ◽  
pp. 1103-1107 ◽  
Author(s):  
Edward I. Ginns ◽  
Roscoe O. Brady ◽  
Daniel W. Stowens ◽  
F.Scott Furbish ◽  
John A. Barranger

1990 ◽  
Vol 269 (3) ◽  
pp. 723-728 ◽  
Author(s):  
M Wolf ◽  
M Baggiolini

Cytosol and membrane fractions from human neutrophils, monocytes, lymphocytes and platelets were separated by SDS/PAGE, blotted on to nitrocellulose and assayed for selective binding of phosphatidylserine (PS). Two PS-binding proteins with apparent molecular masses of 115 kDa and 100 kDa were identified in the cytosol of neutrophils, monocytes and lymphocytes. Corresponding bands along with other PS-binding proteins were detected in platelets in both cytosol and membrane fractions. These proteins were also found to bind protein kinase C (PKC) provided that PS was present. The 115 kDa and 100 kDa proteins (PS-p115/110) were partially purified from neutrophils and were used for the study of PS and PKC binding. The binding of PS did not require Ca2+ or Mg2+ and was inhibited by phosphatidic acid, by 1-alkyl-2-acetylphosphocholine and, to a lesser extent, by other lipids. The binding of PKC, however, was strictly PS- and Ca2(+)-dependent and seems to occur secondarily to PS binding.


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