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Journal of the American Geriatrics Society
|
September 15, 1998
A prospective study of the efficacy of the physician order form for life-sustaining treatment
S W Tolle, V P Tilden, C A Nelson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
September 1, 1989
Second messengers involved in the mechanism of action of bradykinin in sensory neurons in culture
G M Burgess, I Mullaney, M McNeill, et al.
JAMA
|
October 9, 1987
Roentgenograms in pericardial effusion
P M Dunn, J MacNichol, M M Krekeler, et al.
Archives of Disease in Childhood
|
October 1, 1989
Classification of perinatal death
J W Keeling, I MacGillivray, J Golding, et al.
Journal of Medicinal Chemistry
|
September 1, 1995
Synthesis and quantitative structure-activity relationships of dequalinium analogues as K+ channel blockers: investigation into the role of the substituent at position 4 of the quinoline ring
D Galanakis, J A Calder, C R Ganellin, et al.
Journal of Medicinal Chemistry
|
September 23, 2000
bis-Quinolinium cyclophanes: 8,14-diaza-1,7(1, 4)-diquinolinacyclotetradecaphane (UCL 1848), a highly potent and selective, nonpeptidic blocker of the apamin-sensitive Ca(2+)-activated K(+) channel
J Q Chen, D Galanakis, C R Ganellin, et al.
Nursing Outlook
|
June 28, 2000
Nursing's perspective on improving communication about nursing home residents' preferences for medical treatments at end of life
V P Tilden, C A Nelson, P M Dunn, et al.
The Journal of Physiology
|
September 5, 2001
SK3 is an important component of K(+) channels mediating the afterhyperpolarization in cultured rat SCG neurones
R Hosseini, D C Benton, P M Dunn, et al.
Journal of Medicinal Chemistry
|
January 23, 1998
Bis-quinolinium cyclophanes: 6,10-diaza-3(1,3),8(1,4)-dibenzena-1,5(1,4)- diquinolinacyclodecaphane (UCL 1684), the first nanomolar, non-peptidic blocker of the apamin-sensitive Ca(2+)-activated K+ channel
J C Rosa, D Galanakis, C R Ganellin, et al.
British Journal of Pharmacology
|
January 1, 1996
Discrimination between subtypes of apamin-sensitive Ca(2+)-activated K+ channels by gallamine and a novel bis-quaternary quinolinium cyclophane, UCL 1530
P M Dunn, D C Benton, J Campos Rosa, et al.
Page
of 28
Search research articles
Search
Showing results (251-260 of 272) with videos related to
Sort By:
Page
of 28
Journal of the American Geriatrics Society
|
September 15, 1998
A prospective study of the efficacy of the physician order form for life-sustaining treatment
S W Tolle, V P Tilden, C A Nelson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
September 1, 1989
Second messengers involved in the mechanism of action of bradykinin in sensory neurons in culture
G M Burgess, I Mullaney, M McNeill, et al.
JAMA
|
October 9, 1987
Roentgenograms in pericardial effusion
P M Dunn, J MacNichol, M M Krekeler, et al.
Archives of Disease in Childhood
|
October 1, 1989
Classification of perinatal death
J W Keeling, I MacGillivray, J Golding, et al.
Journal of Medicinal Chemistry
|
September 1, 1995
Synthesis and quantitative structure-activity relationships of dequalinium analogues as K+ channel blockers: investigation into the role of the substituent at position 4 of the quinoline ring
D Galanakis, J A Calder, C R Ganellin, et al.
Journal of Medicinal Chemistry
|
September 23, 2000
bis-Quinolinium cyclophanes: 8,14-diaza-1,7(1, 4)-diquinolinacyclotetradecaphane (UCL 1848), a highly potent and selective, nonpeptidic blocker of the apamin-sensitive Ca(2+)-activated K(+) channel
J Q Chen, D Galanakis, C R Ganellin, et al.
Nursing Outlook
|
June 28, 2000
Nursing's perspective on improving communication about nursing home residents' preferences for medical treatments at end of life
V P Tilden, C A Nelson, P M Dunn, et al.
The Journal of Physiology
|
September 5, 2001
SK3 is an important component of K(+) channels mediating the afterhyperpolarization in cultured rat SCG neurones
R Hosseini, D C Benton, P M Dunn, et al.
Journal of Medicinal Chemistry
|
January 23, 1998
Bis-quinolinium cyclophanes: 6,10-diaza-3(1,3),8(1,4)-dibenzena-1,5(1,4)- diquinolinacyclodecaphane (UCL 1684), the first nanomolar, non-peptidic blocker of the apamin-sensitive Ca(2+)-activated K+ channel
J C Rosa, D Galanakis, C R Ganellin, et al.
British Journal of Pharmacology
|
January 1, 1996
Discrimination between subtypes of apamin-sensitive Ca(2+)-activated K+ channels by gallamine and a novel bis-quaternary quinolinium cyclophane, UCL 1530
P M Dunn, D C Benton, J Campos Rosa, et al.
Page
of 28