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The Journal of Oral Implantology
|
February 8, 2002
Immediate postextraction implants: a histologic and histometric analysis in monkeys
A Scarano, G Iezzi, G Petrone, et al.
Journal of Medicinal Chemistry
|
October 14, 1994
Selective kappa-opioid agonists: synthesis and structure-activity relationships of piperidines incorporating on oxo-containing acyl group
G Giardina, G D Clarke, G Dondio, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
July 1, 1994
Contribution of alpha-2 adrenoceptors to kappa opioid agonist-induced water diuresis in the rat
Y X Wang, G D Clarke, M Sbacchi, et al.
Chronobiologia
|
January 1, 1982
Circadian rhythm of plasma tryptophan in clinically healthy subjects and patients with endogenous depression
L S Malatino, C E Fiore, M Costa, et al.
Rivista Di Patologia Nervosa E Mentale
|
November 1, 1979
[24 hours plasma tryptophan levels in patients with endogenous depression (author's transl)]
L S Malatino, C Calandra, M Costa, et al.
International Journal of Immunopathology and Pharmacology
|
October 13, 2012
Pulmonary malacoplakia at early stage: use of polymerase chain reaction for detection of Rhodococcus equi
A Mulè, G Petrone, A Santoro, et al.
Chirality
|
January 1, 1992
Enantiospecificity of kappa receptors: comparison of racemic compounds and active enantiomers in two novel series of kappa agonist analgesics
R Colle, G D Clarke, G Dondio, et al.
Journal of Medical Microbiology
|
June 1, 1996
The effects of inhibitors of vacuolar acidification on the release of Listeria monocytogenes from phagosomes of Caco-2 cells
M P Conte, G Petrone, C Longhi, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
June 1, 1996
Spinal intramedullary angiolipoma
G Maggi, F Aliberti, M R Colucci, et al.
Journal of Medicinal Chemistry
|
August 7, 1992
Substituted 1-(aminomethyl)-2-(arylacetyl)-1,2,3,4-tetrahydroisoquinolines: a novel class of very potent antinociceptive agents with varying degrees of selectivity for kappa and mu opioid receptors
V Vecchietti, G D Clarke, R Colle, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 65) with videos related to
Sort By:
Page
of 7
The Journal of Oral Implantology
|
February 8, 2002
Immediate postextraction implants: a histologic and histometric analysis in monkeys
A Scarano, G Iezzi, G Petrone, et al.
Journal of Medicinal Chemistry
|
October 14, 1994
Selective kappa-opioid agonists: synthesis and structure-activity relationships of piperidines incorporating on oxo-containing acyl group
G Giardina, G D Clarke, G Dondio, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
July 1, 1994
Contribution of alpha-2 adrenoceptors to kappa opioid agonist-induced water diuresis in the rat
Y X Wang, G D Clarke, M Sbacchi, et al.
Chronobiologia
|
January 1, 1982
Circadian rhythm of plasma tryptophan in clinically healthy subjects and patients with endogenous depression
L S Malatino, C E Fiore, M Costa, et al.
Rivista Di Patologia Nervosa E Mentale
|
November 1, 1979
[24 hours plasma tryptophan levels in patients with endogenous depression (author's transl)]
L S Malatino, C Calandra, M Costa, et al.
International Journal of Immunopathology and Pharmacology
|
October 13, 2012
Pulmonary malacoplakia at early stage: use of polymerase chain reaction for detection of Rhodococcus equi
A Mulè, G Petrone, A Santoro, et al.
Chirality
|
January 1, 1992
Enantiospecificity of kappa receptors: comparison of racemic compounds and active enantiomers in two novel series of kappa agonist analgesics
R Colle, G D Clarke, G Dondio, et al.
Journal of Medical Microbiology
|
June 1, 1996
The effects of inhibitors of vacuolar acidification on the release of Listeria monocytogenes from phagosomes of Caco-2 cells
M P Conte, G Petrone, C Longhi, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
June 1, 1996
Spinal intramedullary angiolipoma
G Maggi, F Aliberti, M R Colucci, et al.
Journal of Medicinal Chemistry
|
August 7, 1992
Substituted 1-(aminomethyl)-2-(arylacetyl)-1,2,3,4-tetrahydroisoquinolines: a novel class of very potent antinociceptive agents with varying degrees of selectivity for kappa and mu opioid receptors
V Vecchietti, G D Clarke, R Colle, et al.
Page
of 7