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Biochemical and Biophysical Research Communications
|
March 2, 2005
Do drug substrates enter the common drug-binding pocket of P-glycoprotein through "gates"?
Tip W Loo, David M Clarke
Biochemical and Biophysical Research Communications
|
May 24, 2017
Thiol-reactive drug substrates of human P-glycoprotein label the same sites to activate ATPase activity in membranes or dodecyl maltoside detergent micelles
Tip W Loo, David M Clarke
Methods in Molecular Biology (Clifton, N.J.)
|
May 20, 2011
Repair of CFTR folding defects with correctors that function as pharmacological chaperones
Tip W Loo, David M Clarke
The Journal of Biological Chemistry
|
October 29, 2015
Mapping the Binding Site of the Inhibitor Tariquidar That Stabilizes the First Transmembrane Domain of P-glycoprotein
Tip W Loo, David M Clarke
Biochemical Pharmacology
|
December 3, 2014
Tariquidar inhibits P-glycoprotein drug efflux but activates ATPase activity by blocking transition to an open conformation
Tip W Loo, David M Clarke
Biochemical Pharmacology
|
January 14, 2014
The cystic fibrosis V232D mutation inhibits CFTR maturation by disrupting a hydrophobic pocket rather than formation of aberrant interhelical hydrogen bonds
Tip W Loo, David M Clarke
Australian Family Physician
|
April 3, 2002
A questionnaire to measure general practitioners' attitudes to their role in the management of patients with depression and anxiety
Louise McCall, David M Clarke, Glenn Rowley
Psychosomatic Medicine
|
November 21, 2015
Health Anxiety and Its Relationship to Disability and Service Use: Findings From a Large Epidemiological Survey
Irene Bobevski, David M Clarke, Graham Meadows
Biochemistry
|
April 28, 2011
Benzbromarone stabilizes ΔF508 CFTR at the cell surface
Tip W Loo, M Claire Bartlett, David M Clarke
The Journal of Biological Chemistry
|
July 4, 2008
Arginines in the first transmembrane segment promote maturation of a P-glycoprotein processing mutant by hydrogen bond interactions with tyrosines in transmembrane segment 11
Tip W Loo, M Claire Bartlett, David M Clarke
Page
of 13
Search research articles
Search
Showing results (31-40 of 123) with videos related to
Sort By:
Page
of 13
Biochemical and Biophysical Research Communications
|
March 2, 2005
Do drug substrates enter the common drug-binding pocket of P-glycoprotein through "gates"?
Tip W Loo, David M Clarke
Biochemical and Biophysical Research Communications
|
May 24, 2017
Thiol-reactive drug substrates of human P-glycoprotein label the same sites to activate ATPase activity in membranes or dodecyl maltoside detergent micelles
Tip W Loo, David M Clarke
Methods in Molecular Biology (Clifton, N.J.)
|
May 20, 2011
Repair of CFTR folding defects with correctors that function as pharmacological chaperones
Tip W Loo, David M Clarke
The Journal of Biological Chemistry
|
October 29, 2015
Mapping the Binding Site of the Inhibitor Tariquidar That Stabilizes the First Transmembrane Domain of P-glycoprotein
Tip W Loo, David M Clarke
Biochemical Pharmacology
|
December 3, 2014
Tariquidar inhibits P-glycoprotein drug efflux but activates ATPase activity by blocking transition to an open conformation
Tip W Loo, David M Clarke
Biochemical Pharmacology
|
January 14, 2014
The cystic fibrosis V232D mutation inhibits CFTR maturation by disrupting a hydrophobic pocket rather than formation of aberrant interhelical hydrogen bonds
Tip W Loo, David M Clarke
Australian Family Physician
|
April 3, 2002
A questionnaire to measure general practitioners' attitudes to their role in the management of patients with depression and anxiety
Louise McCall, David M Clarke, Glenn Rowley
Psychosomatic Medicine
|
November 21, 2015
Health Anxiety and Its Relationship to Disability and Service Use: Findings From a Large Epidemiological Survey
Irene Bobevski, David M Clarke, Graham Meadows
Biochemistry
|
April 28, 2011
Benzbromarone stabilizes ΔF508 CFTR at the cell surface
Tip W Loo, M Claire Bartlett, David M Clarke
The Journal of Biological Chemistry
|
July 4, 2008
Arginines in the first transmembrane segment promote maturation of a P-glycoprotein processing mutant by hydrogen bond interactions with tyrosines in transmembrane segment 11
Tip W Loo, M Claire Bartlett, David M Clarke
Page
of 13