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Nutricion Hospitalaria
|
November 21, 2012
[Nutritional support response in critically ill patients; differences between medical and surgical patients]
M Zamora Elson, C Serón Arbeloa, L Labarta Monzón, et al.
Nutricion Hospitalaria
|
March 14, 2012
[Nutritional support outcomes in critical care]
C Serón Arbeloa, M Zamora Elson, L Labarta Monzón, et al.
Paediatric Anaesthesia
|
June 17, 2025
Perspectives in Perioperative Quality Improvement: Case Studies in Positive Deviance Using Real-World Data
Aaron B Low, Jill R Maresh, Terri Jarvi, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 3, 2005
3,3-Bisaryloxindoles as mineralocorticoid receptor antagonists
David A Neel, Matthew L Brown, Peter A Lander, et al.
Biochemical Pharmacology
|
March 10, 2004
Evaluation of the binding of the tricyclic isoxazole photoaffinity label LY475776 to multidrug resistance associated protein 1 (MRP1) orthologs and several ATP- binding cassette (ABC) drug transporters
Anne H Dantzig, Robert L Shepard, Susan E Pratt, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 6, 2005
Cyclohexyl-linked tricyclic isoxazoles are potent and selective modulators of the multidrug resistance protein (MRP1)
Bryan H Norman, Peter A Lander, Joseph M Gruber, et al.
Nature Communications
|
January 31, 2024
Selective replication and vertical transmission of Ebola virus in experimentally infected Angolan free-tailed bats
S A Riesle-Sbarbaro, G Wibbelt, A Düx, et al.
Journal of Medicinal Chemistry
|
November 28, 2007
(S)-N-{3-[1-cyclopropyl-1-(2,4-difluoro-phenyl)-ethyl]-1H-indol-7-yl}-methanesulfonamide: a potent, nonsteroidal, functional antagonist of the mineralocorticoid receptor
Michael G Bell, Douglas L Gernert, Timothy A Grese, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 11, 2015
Design and synthesis of a novel series of [1-(4-hydroxy-benzyl)-1H-indol-5-yloxy]-acetic acid compounds as potent, selective, thyroid hormone receptor β agonists
Timothy P Burkholder, Brian E Cunningham, Joshua R Clayton, et al.
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of 8
Search research articles
Search
Showing results (71-80 of 79) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 79 results.
Nutricion Hospitalaria
|
November 21, 2012
[Nutritional support response in critically ill patients; differences between medical and surgical patients]
M Zamora Elson, C Serón Arbeloa, L Labarta Monzón, et al.
Nutricion Hospitalaria
|
March 14, 2012
[Nutritional support outcomes in critical care]
C Serón Arbeloa, M Zamora Elson, L Labarta Monzón, et al.
Paediatric Anaesthesia
|
June 17, 2025
Perspectives in Perioperative Quality Improvement: Case Studies in Positive Deviance Using Real-World Data
Aaron B Low, Jill R Maresh, Terri Jarvi, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 3, 2005
3,3-Bisaryloxindoles as mineralocorticoid receptor antagonists
David A Neel, Matthew L Brown, Peter A Lander, et al.
Biochemical Pharmacology
|
March 10, 2004
Evaluation of the binding of the tricyclic isoxazole photoaffinity label LY475776 to multidrug resistance associated protein 1 (MRP1) orthologs and several ATP- binding cassette (ABC) drug transporters
Anne H Dantzig, Robert L Shepard, Susan E Pratt, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 6, 2005
Cyclohexyl-linked tricyclic isoxazoles are potent and selective modulators of the multidrug resistance protein (MRP1)
Bryan H Norman, Peter A Lander, Joseph M Gruber, et al.
Nature Communications
|
January 31, 2024
Selective replication and vertical transmission of Ebola virus in experimentally infected Angolan free-tailed bats
S A Riesle-Sbarbaro, G Wibbelt, A Düx, et al.
Journal of Medicinal Chemistry
|
November 28, 2007
(S)-N-{3-[1-cyclopropyl-1-(2,4-difluoro-phenyl)-ethyl]-1H-indol-7-yl}-methanesulfonamide: a potent, nonsteroidal, functional antagonist of the mineralocorticoid receptor
Michael G Bell, Douglas L Gernert, Timothy A Grese, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 11, 2015
Design and synthesis of a novel series of [1-(4-hydroxy-benzyl)-1H-indol-5-yloxy]-acetic acid compounds as potent, selective, thyroid hormone receptor β agonists
Timothy P Burkholder, Brian E Cunningham, Joshua R Clayton, et al.
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