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1245 ROLE OF INNATE AND ADAPTIVE IMMUNITY IN THE DEVELOPMENT OF NON ALCOHOLIC FATTY LIVER DISEASE IN MORBIDLY OBESE PATIENTS

Journal of hepatology, 2013-04, Vol.58, p.S504-S505

2013

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Characteristics of pica practice during pregnancy in a sample of Argentine women

Journal of obstetrics and gynaecology, 2012-02, Vol.32 (2), p.150-153

2012

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Epidemiology of mucopolysaccharidoses (MPS) in United States: challenges and opportunities

Orphanet journal of rare diseases, 2021-05, Vol.16 (1), p.241-241, Article 241

2021

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N-Desmethylclozapine, an Allosteric Agonist at Muscarinic 1 Receptor, Potentiates N-Methyl-D-Aspartate Receptor Activity

Proceedings of the National Academy of Sciences - PNAS, 2003-11, Vol.100 (23), p.13674-13679

2003

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The Glycine Transporter Type 1 Inhibitor N-[3-(4'-Fluorophenyl)-3-(4'-Phenylphenoxy)Propyl]Sarcosine Potentiates NMDA Receptor-Mediated Responses In Vivo and Produces an Antipsychotic Profile in Rodent Behavior

The Journal of neuroscience, 2003-08, Vol.23 (20), p.7586-7591

2003

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The effects of deleting the mouse neurotensin receptor NTR1 on central and peripheral responses to neurotensin

The Journal of pharmacology and experimental therapeutics, 2002-01, Vol.300 (1), p.305-313

2002

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Effects of muscarinic cholinergic receptor antagonists on postnatal eye growth of rhesus monkeys

Optometry and vision science, 1999-06, Vol.76 (6), p.397-407

1999

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Pharmacology and expression analysis of glycine transporter GlyT1 with [ 3H]-(N-[3-(4′-fluorophenyl)-3-(4′phenylphenoxy)propyl])sarcosine

Neuropharmacology, 2003-10, Vol.45 (5), p.585-593

2003

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New isomeric classes of topically active ocular hypotensive carbonic anhydrase inhibitors: 5-substituted thieno[2,3-b]thiophene-2-sulfonamides and 5-substituted thieno[3,2-b]thiophene-2-sulfonamides

Journal of medicinal chemistry, 1991-06, Vol.34 (6), p.1805-1818

1991

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Sulfonylmethanesulfonamide inhibitors of carbonic anhydrase

Journal of medicinal chemistry, 1993-07, Vol.36 (15), p.2134-2141

1993

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Thienothiopyran-2-sulfonamides: novel topically active carbonic anhydrase inhibitors for the treatment of glaucoma

Journal of medicinal chemistry, 1989-12, Vol.32 (12), p.2510-2513

1989

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Pharmacology and expression analysis of glycine transporter GlyT1 with [ super(3)H]-(N-[3-(4'-fluorophenyl)-3-(4'phenylphenoxy)propyl])sarc osine

Neuropharmacology, 2003-10, Vol.45 (5), p.585-593

2003

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4-Substituted thiophene- and furan-2-sulfonamides as topical carbonic anhydrase inhibitors

Journal of medicinal chemistry, 1992-10, Vol.35 (21), p.3822-3831

1992

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A comparison of L-671,152 and MK-927, two topically effective ocular hypotensive carbonic anhydrase inhibitors, in experimental animals

Current eye research, 1990, Vol.9 (6), p.607-615

1990

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Effects of Muscarinic Cholinergic Receptor Antagonists on Postnatal Eye Growth of Rhesus Monkeys

Optometry and vision science, 1999-11, Vol.76 (11), p.804

1999

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Thieno[2,3-b]furan-2-sulfonamides as topical carbonic anhydrase inhibitors

Journal of medicinal chemistry, 1992-08, Vol.35 (16), p.3027-3033

1992

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Effects of muscarinic cholinergic receptor antagonists on postnatal eye growth of rhesus monkeys: Feature Issue on Myopia: Part 2

Optometry and vision science, 1999, Vol.76 (6), p.397-407

1999

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L‐662,583 is a topically effective ocular hypotensive carbonic anhydrase inhibitor in experimental animals

British journal of pharmacology, 1990-01, Vol.99 (1), p.59-64

1990

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Characterization of serotonin receptors in the iris + ciliary body of the albino rabbit

Current eye research, 1987, Vol.6 (3), p.527-532

1987

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3H-pirenzepine and 3H-AFDX-384 binding sites in the rabbit ciliary process

Experimental eye research, 1992-09, Vol.55, p.51-51

1992

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Preclinical studies on L-671,152, a topically effective ocular hypotensive carbonic anhydrase inhibitor

British journal of pharmacology, 1989-12, Vol.98 Suppl, p.820P-820P

1989

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Characterization of [ 3H]forskolin binding sites in the iris-ciliary body of the albino rabbit

Life sciences (1973), 1988, Vol.42 (13), p.1307-1314

1988

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Muscarinic receptors of the albino rabbit ciliary process

Experimental eye research, 1989-04, Vol.48 (4), p.509-522

1989

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Ontogenetic changes in GABA modulation of brain benzodiazepine binding

Neuropharmacology, 1980-04, Vol.19 (4), p.405-408

1980

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Alpha 1-adrenoceptors in the albino rabbit ciliary process

Journal of ocular pharmacology, 1988, Vol.4 (3), p.203-214

1988

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1245 ROLE OF INNATE AND ADAPTIVE IMMUNITY IN THE DEVELOPMENT OF NON ALCOHOLIC FATTY LIVER DISEASE IN MORBIDLY OBESE PATIENTS

Characteristics of pica practice during pregnancy in a sample of Argentine women

Epidemiology of mucopolysaccharidoses (MPS) in United States: challenges and opportunities

N-Desmethylclozapine, an Allosteric Agonist at Muscarinic 1 Receptor, Potentiates N-Methyl-D-Aspartate Receptor Activity

The Glycine Transporter Type 1 Inhibitor N-[3-(4'-Fluorophenyl)-3-(4'-Phenylphenoxy)Propyl]Sarcosine Potentiates NMDA Receptor-Mediated Responses In Vivo and Produces an Antipsychotic Profile in Rodent Behavior

The effects of deleting the mouse neurotensin receptor NTR1 on central and peripheral responses to neurotensin

Effects of muscarinic cholinergic receptor antagonists on postnatal eye growth of rhesus monkeys

Pharmacology and expression analysis of glycine transporter GlyT1 with [ 3H]-(N-[3-(4′-fluorophenyl)-3-(4′phenylphenoxy)propyl])sarcosine

New isomeric classes of topically active ocular hypotensive carbonic anhydrase inhibitors: 5-substituted thieno[2,3-b]thiophene-2-sulfonamides and 5-substituted thieno[3,2-b]thiophene-2-sulfonamides

Sulfonylmethanesulfonamide inhibitors of carbonic anhydrase

Thienothiopyran-2-sulfonamides: novel topically active carbonic anhydrase inhibitors for the treatment of glaucoma

Pharmacology and expression analysis of glycine transporter GlyT1 with [ super(3)H]-(N-[3-(4'-fluorophenyl)-3-(4'phenylphenoxy)propyl])sarc osine

4-Substituted thiophene- and furan-2-sulfonamides as topical carbonic anhydrase inhibitors

A comparison of L-671,152 and MK-927, two topically effective ocular hypotensive carbonic anhydrase inhibitors, in experimental animals

Effects of Muscarinic Cholinergic Receptor Antagonists on Postnatal Eye Growth of Rhesus Monkeys

Thieno[2,3-b]furan-2-sulfonamides as topical carbonic anhydrase inhibitors

Effects of muscarinic cholinergic receptor antagonists on postnatal eye growth of rhesus monkeys: Feature Issue on Myopia: Part 2

L‐662,583 is a topically effective ocular hypotensive carbonic anhydrase inhibitor in experimental animals

Characterization of serotonin receptors in the iris + ciliary body of the albino rabbit

3H-pirenzepine and 3H-AFDX-384 binding sites in the rabbit ciliary process

Preclinical studies on L-671,152, a topically effective ocular hypotensive carbonic anhydrase inhibitor

Characterization of [ 3H]forskolin binding sites in the iris-ciliary body of the albino rabbit

Muscarinic receptors of the albino rabbit ciliary process

Ontogenetic changes in GABA modulation of brain benzodiazepine binding

Alpha 1-adrenoceptors in the albino rabbit ciliary process

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