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Neurogastroenterology and Motility
|
September 11, 2004
Preclinical studies of opioids and opioid antagonists on gastrointestinal function
B Greenwood-Van Meerveld, C J Gardner, P J Little, et al.
Diabetologia
|
April 9, 2004
Thiazolidinediones reduce the LDL binding affinity of non-human primate vascular cell proteoglycans
L R Tannock, P J Little, C Tsoi, et al.
Cardiovascular Research
|
February 1, 1995
Intracellular pH in vascular smooth muscle: regulation by sodium-hydrogen exchange and multiple sodium dependent HCO3- mechanisms
P J Little, C B Neylon, C A Farrelly, et al.
Diabetologia
|
December 14, 2004
Fenofibrate modifies human vascular smooth muscle proteoglycans and reduces lipoprotein binding
J Nigro, M L Ballinger, R J Dilley, et al.
British Journal of Pharmacology
|
December 2, 2015
Integrating the GPCR transactivation-dependent and biased signalling paradigms in the context of PAR1 signalling
P J Little, M D Hollenberg, D Kamato, et al.
British Journal of Urology
|
December 1, 1976
Diagnosis of gross vesico-ureteric reflux using ultrasonography
R N Tremewan, R R Bailey, P J Little, et al.
FEBS Letters
|
October 7, 1997
Urokinase plasminogen activator induces smooth muscle cell migration: key role of growth factor-like domain
V Stepanova, A Bobik, R Bibilashvily, et al.
Biochemical and Biophysical Research Communications
|
June 15, 1993
Leu143 in the putative fourth membrane spanning domain is critical for amiloride inhibition of an epithelial Na+/H+ exchanger isoform (NHE-2)
C H Yun, P J Little, S K Nath, et al.
The Journal of Biological Chemistry
|
June 5, 1993
Cloning and expression of a rabbit cDNA encoding a serum-activated ethylisopropylamiloride-resistant epithelial Na+/H+ exchanger isoform (NHE-2)
C M Tse, S A Levine, C H Yun, et al.
Journal of Medicinal Chemistry
|
May 1, 1990
Synthesis and pharmacological evaluation of amino, azido, and nitrogen mustard analogues of 10-substituted cannabidiol and 11- or 12-substituted delta 8-tetrahydrocannabinol
D R Compton, P J Little, B R Martin, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 103) with videos related to
Sort By:
Page
of 11
Neurogastroenterology and Motility
|
September 11, 2004
Preclinical studies of opioids and opioid antagonists on gastrointestinal function
B Greenwood-Van Meerveld, C J Gardner, P J Little, et al.
Diabetologia
|
April 9, 2004
Thiazolidinediones reduce the LDL binding affinity of non-human primate vascular cell proteoglycans
L R Tannock, P J Little, C Tsoi, et al.
Cardiovascular Research
|
February 1, 1995
Intracellular pH in vascular smooth muscle: regulation by sodium-hydrogen exchange and multiple sodium dependent HCO3- mechanisms
P J Little, C B Neylon, C A Farrelly, et al.
Diabetologia
|
December 14, 2004
Fenofibrate modifies human vascular smooth muscle proteoglycans and reduces lipoprotein binding
J Nigro, M L Ballinger, R J Dilley, et al.
British Journal of Pharmacology
|
December 2, 2015
Integrating the GPCR transactivation-dependent and biased signalling paradigms in the context of PAR1 signalling
P J Little, M D Hollenberg, D Kamato, et al.
British Journal of Urology
|
December 1, 1976
Diagnosis of gross vesico-ureteric reflux using ultrasonography
R N Tremewan, R R Bailey, P J Little, et al.
FEBS Letters
|
October 7, 1997
Urokinase plasminogen activator induces smooth muscle cell migration: key role of growth factor-like domain
V Stepanova, A Bobik, R Bibilashvily, et al.
Biochemical and Biophysical Research Communications
|
June 15, 1993
Leu143 in the putative fourth membrane spanning domain is critical for amiloride inhibition of an epithelial Na+/H+ exchanger isoform (NHE-2)
C H Yun, P J Little, S K Nath, et al.
The Journal of Biological Chemistry
|
June 5, 1993
Cloning and expression of a rabbit cDNA encoding a serum-activated ethylisopropylamiloride-resistant epithelial Na+/H+ exchanger isoform (NHE-2)
C M Tse, S A Levine, C H Yun, et al.
Journal of Medicinal Chemistry
|
May 1, 1990
Synthesis and pharmacological evaluation of amino, azido, and nitrogen mustard analogues of 10-substituted cannabidiol and 11- or 12-substituted delta 8-tetrahydrocannabinol
D R Compton, P J Little, B R Martin, et al.
Page
of 11