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Novel pancreatic endocrine maturation pathways identified by genomic profiling and causal reasoning

PloS one, 2013-02, Vol.8 (2), p.e56024-e56024

2013

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GLUT4 Overexpression in db/db Mice Dose-Dependently Ameliorates Diabetes But Is Not a Lifelong Cure

Diabetes (New York, N.Y.), 2001-03, Vol.50 (3), p.593-600

2001

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Discovery of potent and orally bioavailable heterocycle-based β3-adrenergic receptor agonists, potential therapeutics for the treatment of obesity

Bioorganic & medicinal chemistry letters, 2007-09, Vol.17 (18), p.5245-5250

2007

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Discovery of N-benzyl-2-[(4S)-4-(1H-indol-3-ylmethyl)-5-oxo-1-phenyl-4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6-yl]-N-isopropylacetamide, an orally active, gut-selective CCK1 receptor agonist for the potential treatment of obesity

Bioorganic & medicinal chemistry letters, 2010-11, Vol.20 (22), p.6797-6801

2010

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Potent and selective, sulfamide-based human β3-adrenergic receptor agonists

Bioorganic & medicinal chemistry letters, 2004-06, Vol.14 (12), p.3235-3240

2004

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Limited Structure-Activity Relationships for Carboxy and AminoTerminal Substitutions of Peptide YY 25–36

Advances in experimental medicine and biology, 2009, Vol.611, p.551-552

2009

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Distribution of β3-adrenoceptor mRNA in human tissues

European journal of pharmacology. Molecular pharmacology section, 1995-04, Vol.289 (2), p.223-228

1995

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Discovery of N-benzyl-2-[(4S)-4-(1H-indol-3-ylmethyl)-5-oxo-1-phenyl -4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6- y l]-N-isopropylacetamide, an orally active, gut-selective CCK1 receptor agonist for the potential treatment of obesity

Bioorganic & medicinal chemistry letters, 2010-11, Vol.20 (22), p.6797-6801

2010

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Discovery of potent and orally bioavailable heterocycle-based beta3-adrenergic receptor agonists, potential therapeutics for the treatment of obesity

Bioorganic & medicinal chemistry letters, 2007-09, Vol.17 (18), p.5245-5250

2007

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Discovery of potent and orally bioavailable heterocycle-based β 3-adrenergic receptor agonists, potential therapeutics for the treatment of obesity

Bioorganic & medicinal chemistry letters, 2007, Vol.17 (18), p.5245-5250

2007

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Enhanced peripheral glucose utilization in transgenic mice expressing the human GLUT4 gene

The Journal of biological chemistry, 1994-11, Vol.269 (47), p.29956-29961

1994

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Modulation of Insulin Secretion and Glycemia by Selective Inhibition of Cyclic AMP Phosphodiesterase III

Biochemical and biophysical research communications, 1997-07, Vol.236 (3), p.665-669

1997

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Potent and selective, sulfamide-based human beta 3-adrenergic receptor agonists

Bioorganic & medicinal chemistry letters, 2004-06, Vol.14 (12), p.3235-3240

2004

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Potent and selective, sulfamide-based human β 3-adrenergic receptor agonists

Bioorganic & medicinal chemistry letters, 2004, Vol.14 (12), p.3235-3240

2004

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Glucose-dependent action of glucagon-like peptide-1(7-37) in vivo during short- or long-term administration

Metabolism, clinical and experimental, 1995-09, Vol.44 (9), p.1231-1237

1995

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Comparison of the glucose dependency of glucagon-like peptide-1(7–37) and glyburide in vitro and in vivo

Metabolism, clinical and experimental, 1996-03, Vol.45 (3), p.404-409

1996

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Potent and Selective, Sulfamide-Based Human β3-Adrenergic Receptor Agonists

ChemInform, 2004-10, Vol.35 (40), p.no-no

2004

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Potent and Selective, Sulfamide‐Based Human β 3 ‐Adrenergic Receptor Agonists

ChemInform, 2004-10, Vol.35 (40)

2004

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Distribution of β 3-adrenoceptor mRNA in human tissues

European journal of pharmacology. Molecular pharmacology section, 1995, Vol.289 (2), p.223-228

1995

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Microscopy Visualization of Carrier Transport in CdSeTe/CdTe Solar Cells

ACS applied materials & interfaces, 2022-09, Vol.14 (35), p.39976-39984

2022

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Pure estrogen receptor antagonists potentiate capecitabine activity in ESR1-mutant breast cancer

NPJ breast cancer, 2024-06, Vol.10 (1), p.42-12

2024

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Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss

American journal of human genetics, 2022-06, Vol.109 (6), p.1077-1091

2022

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Risk factors for postoperative wound dehiscence after skin repair: A case-control study

Journal of the American Academy of Dermatology, 2022-11, Vol.87 (5), p.1099-1102

2022

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A School-Based Intervention to Increase Lyme Disease Preventive Measures Among Elementary School-Aged Children

Vector borne and zoonotic diseases (Larchmont, N.Y.), 2016-08, Vol.16 (8), p.507-515

2016

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Dietary behaviour of children attending primary school in Italy found by the surveillance system "OKkio alla salute"

Epidemiologia e prevenzione, 2015-09, Vol.39 (5-6), p.380

2015

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Novel pancreatic endocrine maturation pathways identified by genomic profiling and causal reasoning

GLUT4 Overexpression in db/db Mice Dose-Dependently Ameliorates Diabetes But Is Not a Lifelong Cure

Discovery of potent and orally bioavailable heterocycle-based β3-adrenergic receptor agonists, potential therapeutics for the treatment of obesity

Discovery of N-benzyl-2-[(4S)-4-(1H-indol-3-ylmethyl)-5-oxo-1-phenyl-4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6-yl]-N-isopropylacetamide, an orally active, gut-selective CCK1 receptor agonist for the potential treatment of obesity

Potent and selective, sulfamide-based human β3-adrenergic receptor agonists

Limited Structure-Activity Relationships for Carboxy and AminoTerminal Substitutions of Peptide YY 25–36

Distribution of β3-adrenoceptor mRNA in human tissues

Discovery of N-benzyl-2-[(4S)-4-(1H-indol-3-ylmethyl)-5-oxo-1-phenyl -4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6- y l]-N-isopropylacetamide, an orally active, gut-selective CCK1 receptor agonist for the potential treatment of obesity

Discovery of potent and orally bioavailable heterocycle-based beta3-adrenergic receptor agonists, potential therapeutics for the treatment of obesity

Discovery of potent and orally bioavailable heterocycle-based β 3-adrenergic receptor agonists, potential therapeutics for the treatment of obesity

Enhanced peripheral glucose utilization in transgenic mice expressing the human GLUT4 gene

Modulation of Insulin Secretion and Glycemia by Selective Inhibition of Cyclic AMP Phosphodiesterase III

Potent and selective, sulfamide-based human beta 3-adrenergic receptor agonists

Potent and selective, sulfamide-based human β 3-adrenergic receptor agonists

Glucose-dependent action of glucagon-like peptide-1(7-37) in vivo during short- or long-term administration

Comparison of the glucose dependency of glucagon-like peptide-1(7–37) and glyburide in vitro and in vivo

Potent and Selective, Sulfamide-Based Human β3-Adrenergic Receptor Agonists

Potent and Selective, Sulfamide‐Based Human β 3 ‐Adrenergic Receptor Agonists

Distribution of β 3-adrenoceptor mRNA in human tissues

Microscopy Visualization of Carrier Transport in CdSeTe/CdTe Solar Cells

Pure estrogen receptor antagonists potentiate capecitabine activity in ESR1-mutant breast cancer

Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss

Risk factors for postoperative wound dehiscence after skin repair: A case-control study

A School-Based Intervention to Increase Lyme Disease Preventive Measures Among Elementary School-Aged Children

Dietary behaviour of children attending primary school in Italy found by the surveillance system "OKkio alla salute"

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