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Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1993
The multidrug resistance (mdr1) gene product functions as an ATP channel
E H Abraham, A G Prat, L Gerweck, et al.
The American Journal of Physiology
|
December 22, 1999
Actin filament organization is required for proper cAMP-dependent activation of CFTR
A G Prat, C C Cunningham, G R Jackson, et al.
Clinical Physiology (Oxford, England)
|
September 6, 2000
Increased circulating levels of plasma ATP in cystic fibrosis patients
A S Lader, A G Prat, G R Jackson, et al.
Annales De Medecine Interne
|
August 1, 1973
[Hepato-splenic thorotrastome (spectrogammametric study)]
R Duriez, R Delahaye, H Frossard, et al.
The Journal of Biological Chemistry
|
August 12, 1994
The cystic fibrosis transmembrane conductance regulator is a dual ATP and chloride channel
I L Reisin, A G Prat, E H Abraham, et al.
The Journal of Biological Chemistry
|
July 26, 1996
Regulation of epithelial sodium channels by short actin filaments
B K Berdiev, A G Prat, H F Cantiello, et al.
The Journal of Biological Chemistry
|
April 15, 1994
External ATP and its analogs activate the cystic fibrosis transmembrane conductance regulator by a cyclic AMP-independent mechanism
H F Cantiello, A G Prat, I L Reisin, et al.
The American Journal of Physiology
|
April 1, 1997
Role of actin in regulation of epithelial sodium channels by CFTR
I I Ismailov, B K Berdiev, V G Shlyonsky, et al.
Intensive Care Medicine
|
September 25, 2019
Feasibility and safety of ultra-low tidal volume ventilation without extracorporeal circulation in moderately severe and severe ARDS patients
J C Richard, S Marque, A Gros, et al.
The American Journal of Physiology
|
April 8, 1998
Electrodiffusional ATP movement through the cystic fibrosis transmembrane conductance regulator
H F Cantiello, G R Jackson, C F Grosman, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 81) with videos related to
Sort By:
Page
of 9
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1993
The multidrug resistance (mdr1) gene product functions as an ATP channel
E H Abraham, A G Prat, L Gerweck, et al.
The American Journal of Physiology
|
December 22, 1999
Actin filament organization is required for proper cAMP-dependent activation of CFTR
A G Prat, C C Cunningham, G R Jackson, et al.
Clinical Physiology (Oxford, England)
|
September 6, 2000
Increased circulating levels of plasma ATP in cystic fibrosis patients
A S Lader, A G Prat, G R Jackson, et al.
Annales De Medecine Interne
|
August 1, 1973
[Hepato-splenic thorotrastome (spectrogammametric study)]
R Duriez, R Delahaye, H Frossard, et al.
The Journal of Biological Chemistry
|
August 12, 1994
The cystic fibrosis transmembrane conductance regulator is a dual ATP and chloride channel
I L Reisin, A G Prat, E H Abraham, et al.
The Journal of Biological Chemistry
|
July 26, 1996
Regulation of epithelial sodium channels by short actin filaments
B K Berdiev, A G Prat, H F Cantiello, et al.
The Journal of Biological Chemistry
|
April 15, 1994
External ATP and its analogs activate the cystic fibrosis transmembrane conductance regulator by a cyclic AMP-independent mechanism
H F Cantiello, A G Prat, I L Reisin, et al.
The American Journal of Physiology
|
April 1, 1997
Role of actin in regulation of epithelial sodium channels by CFTR
I I Ismailov, B K Berdiev, V G Shlyonsky, et al.
Intensive Care Medicine
|
September 25, 2019
Feasibility and safety of ultra-low tidal volume ventilation without extracorporeal circulation in moderately severe and severe ARDS patients
J C Richard, S Marque, A Gros, et al.
The American Journal of Physiology
|
April 8, 1998
Electrodiffusional ATP movement through the cystic fibrosis transmembrane conductance regulator
H F Cantiello, G R Jackson, C F Grosman, et al.
Page
of 9