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The effect of vitamin D supplementation on the muscle damage after eccentric exercise in young men: a randomized, control trial

Journal of the International Society of Sports Nutrition, 2020-11, Vol.17 (1), p.53-53

2020

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Comparison of physiological reactions and physiological strain in healthy men under heat stress in dry and steam heat saunas

Biology of sport, 2014, Vol.31 (2), p.145-149

2014

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The Impact of Vibration Therapy Interventions on Skin Condition and Skin Temperature Changes in Young Women with Lipodystrophy: A Pilot Study

Evidence-based complementary and alternative medicine, 2019-01, Vol.2019 (2019), p.1-9

2019

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Pharmacological characterization of a recently described human beta 3-adrenergic receptor mutant

Endocrinology (Philadelphia), 1996-06, Vol.137 (6), p.2638-2641

1996

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Human β 3-adrenergic receptor agonists containing 1,2,3-triazole-substituted benzenesulfonamides

Bioorganic & medicinal chemistry letters, 2000-09, Vol.10 (18), p.2111-2114

2000

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Substituted oxazole benzenesulfonamides as potent human β3 adrenergic receptor agonists

Bioorganic & medicinal chemistry letters, 2000-07, Vol.10 (14), p.1531-1534

2000

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A Novel Glucagon Receptor Antagonist Inhibits Glucagon-Mediated Biological Effects

Diabetes (New York, N.Y.), 2004-12, Vol.53 (12), p.3267-3273

2004

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Potent and selective human beta(3)-adrenergic receptor antagonists

The Journal of pharmacology and experimental therapeutics, 1999-08, Vol.290 (2), p.649

1999

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Discovery and investigation of a novel class of thiophene-derived antagonists of the human glucagon receptor

Bioorganic & medicinal chemistry letters, 2005-03, Vol.15 (5), p.1401-1405

2005

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Discovery of a Potent, Orally Bioavailable β3 Adrenergic Receptor Agonist, (R)-N-[4-[2-[[2-Hydroxy-2-(3-pyridinyl)ethyl]amino]ethyl]phenyl]-4-[4-[4-(trifluoromethyl)phenyl]thiazol-2-yl]benzenesulfonamide

Journal of medicinal chemistry, 2000-10, Vol.43 (21), p.3832-3836

2000

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Endocardial endothelium in the avascular heart of the frog: morphology and role of nitric oxide

Journal of experimental biology, 1997-12, Vol.200 (Pt 24), p.3109-3118

1997

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Potent, selective human β3 adrenergic receptor agonists containing a substituted indoline-5-sulfonamide pharmacophore

Bioorganic & medicinal chemistry letters, 1999-07, Vol.9 (13), p.1869-1874

1999

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Discovery of a potent, orally bioavailable beta(3) adrenergic receptor agonist, (R)-N-[4-[2-[[2-hydroxy-2-(3-pyridinyl)ethyl]amino]ethyl]phenyl]-4-[4 -[4-(trifluoromethyl)phenyl]thiazol-2-yl]benzenesulfonamide

Journal of medicinal chemistry, 2000-10, Vol.43 (21), p.3832-3836

2000

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Discovery of novel, potent, and orally active spiro-urea human glucagon receptor antagonists

Bioorganic & medicinal chemistry letters, 2005-10, Vol.15 (20), p.4564-4569

2005

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L-770,644: A potent and selective human β3 adrenergic receptor agonist with improved oral bioavailability

Bioorganic & medicinal chemistry letters, 1999-05, Vol.9 (9), p.1251-1254

1999

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Pharmacological characterization of a recently described human beta 3-adrenergic receptor mutant

Endocrinology (Philadelphia), 1996-06, Vol.137 (6), p.2638-2641

1996

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Phytosphingosine 1-phosphate: a high affinity ligand for the S1P(4)/Edg-6 receptor

Biochemical and biophysical research communications, 2002-09, Vol.297 (3), p.600-606

2002

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Direct observation (NMR) of the efficacy of glucagon receptor antagonists in murine liver expressing the human glucagon receptor

Bioorganic & medicinal chemistry, 2006-03, Vol.14 (5), p.1506-1517

2006

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Discovery of L-755,507: A subnanomolar human β3 adrenergic receptor agonist

Bioorganic & medicinal chemistry letters, 1998-05, Vol.8 (9), p.1107-1112

1998

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Human β3 adrenergic receptor agonists containing imidazolidinone and imidazolone benzenesulfonamides

Bioorganic & medicinal chemistry letters, 1999-03, Vol.9 (5), p.755-758

1999

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Discovery of an orally bioavailable alkyl oxadiazole β3 adrenergic receptor agonist

Bioorganic & medicinal chemistry letters, 2000-07, Vol.10 (13), p.1427-1429

2000

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3-pyridylethanolamines : Potent and selective human β3 adrenergic receptor agonists

Bioorganic & medicinal chemistry letters, 1998-11, Vol.8 (21), p.3087-3092

1998

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Human beta3 adrenergic receptor agonists containing cyanoguanidine and nitroethylenediamine moieties

Bioorganic & medicinal chemistry letters, 2001-02, Vol.11 (3), p.379

2001

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‘When orff meets guinness’: music in advertising as a form of cultural hybrid

Poetics (Amsterdam), 2001-07, Vol.29 (2), p.109-123

Tota, Anna Lisa

2001

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Potent, selective 3-pyridylethanolamine β3 adrenergic receptor agonists possessing a thiazole benzenesulfonamide pharmacophore

Bioorganic & medicinal chemistry letters, 2000-09, Vol.10 (17), p.1971-1973

2000

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The effect of vitamin D supplementation on the muscle damage after eccentric exercise in young men: a randomized, control trial

Comparison of physiological reactions and physiological strain in healthy men under heat stress in dry and steam heat saunas

The Impact of Vibration Therapy Interventions on Skin Condition and Skin Temperature Changes in Young Women with Lipodystrophy: A Pilot Study

Pharmacological characterization of a recently described human beta 3-adrenergic receptor mutant

Human β 3-adrenergic receptor agonists containing 1,2,3-triazole-substituted benzenesulfonamides

Substituted oxazole benzenesulfonamides as potent human β3 adrenergic receptor agonists

A Novel Glucagon Receptor Antagonist Inhibits Glucagon-Mediated Biological Effects

Potent and selective human beta(3)-adrenergic receptor antagonists

Discovery and investigation of a novel class of thiophene-derived antagonists of the human glucagon receptor

Discovery of a Potent, Orally Bioavailable β3 Adrenergic Receptor Agonist, (R)-N-[4-[2-[[2-Hydroxy-2-(3-pyridinyl)ethyl]amino]ethyl]phenyl]-4-[4-[4-(trifluoromethyl)phenyl]thiazol-2-yl]benzenesulfonamide

Endocardial endothelium in the avascular heart of the frog: morphology and role of nitric oxide

Potent, selective human β3 adrenergic receptor agonists containing a substituted indoline-5-sulfonamide pharmacophore

Discovery of a potent, orally bioavailable beta(3) adrenergic receptor agonist, (R)-N-[4-[2-[[2-hydroxy-2-(3-pyridinyl)ethyl]amino]ethyl]phenyl]-4-[4 -[4-(trifluoromethyl)phenyl]thiazol-2-yl]benzenesulfonamide

Discovery of novel, potent, and orally active spiro-urea human glucagon receptor antagonists

L-770,644: A potent and selective human β3 adrenergic receptor agonist with improved oral bioavailability

Pharmacological characterization of a recently described human beta 3-adrenergic receptor mutant

Phytosphingosine 1-phosphate: a high affinity ligand for the S1P(4)/Edg-6 receptor

Direct observation (NMR) of the efficacy of glucagon receptor antagonists in murine liver expressing the human glucagon receptor

Discovery of L-755,507: A subnanomolar human β3 adrenergic receptor agonist

Human β3 adrenergic receptor agonists containing imidazolidinone and imidazolone benzenesulfonamides

Discovery of an orally bioavailable alkyl oxadiazole β3 adrenergic receptor agonist

3-pyridylethanolamines : Potent and selective human β3 adrenergic receptor agonists

Human beta3 adrenergic receptor agonists containing cyanoguanidine and nitroethylenediamine moieties

‘When orff meets guinness’: music in advertising as a form of cultural hybrid

Potent, selective 3-pyridylethanolamine β3 adrenergic receptor agonists possessing a thiazole benzenesulfonamide pharmacophore

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