Zobrazeno 1 - 10
of 13
pro vyhledávání: '"P M Quinton"'
Autor:
Orsolya Dobay, Krisztina Laub, Balázs Stercz, Adrienn Kéri, Bernadett Balázs, Adrienn Tóthpál, Szilvia Kardos, Pongsiri Jaikumpun, Kasidid Ruksakiet, Paul M. Quinton, Ákos Zsembery
Publikováno v:
Frontiers in Microbiology, Vol 9 (2018)
We investigated the effects of bicarbonate on the growth of several different bacteria as well as its effects on biofilm formation and intracellular cAMP concentration in Pseudomonas aeruginosa. Biofilm formation was examined in 96-well plates, with
Externí odkaz:
https://doaj.org/article/79880d0a049f4a04b5e4e6de889fc285
Autor:
J.A. Stryker, R. Fisher, Q. You, M.M. Or-Rashid, H.J. Boermans, M. Quinton, B.W. McBride, N.A. Karrow
Publikováno v:
Animal, Vol 7, Iss 1, Pp 151-159 (2013)
In recent years, livestock producers have been supplementing animal diets with fish meal (FM) to produce value-added products for health conscious consumers. As components of FM have unique neuroendocrine–immunomodulatory properties, we hypothesize
Externí odkaz:
https://doaj.org/article/18f4e22bacb44f2ab114d9ce6f21859d
Publikováno v:
Experimental physiology. 93(8)
With the advent of numerous candidate drugs for therapy in cystic fibrosis (CF), there is an urgent need for easily interpretable assays for testing their therapeutic value. Defects in the cystic fibrosis transmembrane conductance regulator (CFTR) ab
Autor:
John Adam, Best, P M, Quinton
Publikováno v:
Experimental physiology. 90(2)
Computerized assays on cultured cells ex vivo have been used to screen thousands of compounds for their effectiveness in correcting the basic physiological defect in cystic fibrosis (CF). While a number of these compounds appear promising, their effe
Publikováno v:
Experimental physiology. 89(4)
Effective and specific inhibition of the cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channel in epithelia has long been needed to better understand the role of anion movements in fluid and electrolyte transport. Until now, availabl
Autor:
M M, Reddy, P M, Quinton
Publikováno v:
JOP : Journal of the pancreas. 2
While cystic fibrosis transmembrane conductance regulator (CFTR) is well known to function as a Cl(-) channel, some mutations in the channel protein causing cystic fibrosis (CF) disrupt another vital physiological function, HCO(3)(-) transport. Patho
Autor:
P M, Quinton, M M, Reddy
Publikováno v:
The Japanese journal of physiology. 44
In contrast to fluid secretion which in many tissues is well known to be regulated by phosphorylation, little is known of phosphorylation regulation of electrolyte absorption. It is now well established that CFTR (cystic fibrosis transmembrane regula
Autor:
P M, Quinton, M M, Reddy
Publikováno v:
Advances in experimental medicine and biology. 290
Publikováno v:
Gene Therapy. 14:281-281
Autor:
P M, Quinton
Publikováno v:
Kidney international. Supplement. 21