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Two novel α7 nicotinic acetylcholine receptor ligands: in vitro properties and their efficacy in collagen-induced arthritis in mice
PloS one, 2015, Vol.10 (1), p.e0116227-e0116227
2015
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Open Access
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Sustained Correction of a Murine Model of Phenylketonuria following a Single Intravenous Administration of AAVHSC15-PAH
Molecular therapy. Methods & clinical development, 2020-06, Vol.17, p.568-580
2020
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Microtubule-active drugs taxol, vinblastine, and nocodazole increase the levels of transcriptionally active p53
Cancer research (Chicago, Ill.), 1995-12, Vol.55 (24), p.6021-6025
1995
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The pheNIX trial: first-in-human gene therapy trial for PKU due to phenylalanine hydroxylase (PAH) deficiency
Molecular genetics and metabolism, 2021-04, Vol.132, p.S166-S167
2021
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eP265 - The pheNIX trial: first-in-human gene therapy trial for PKU due to phenylalanine hydroxylase (PAH) deficiency
Molecular genetics and metabolism, 2021-04, Vol.132, p.S166-S167
2021
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5-year retrospective analysis of patients with phenylketonuria (PKU) and hyperphenylalaninemia treated at two specialized clinics
Molecular genetics and metabolism, 2020-03, Vol.129 (3), p.177-185
2020
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Discovery of Novel 2‑((Pyridin-3-yloxy)methyl)piperazines as α7 Nicotinic Acetylcholine Receptor Modulators for the Treatment of Inflammatory Disorders
Journal of medicinal chemistry, 2014-05, Vol.57 (10), p.3966-3983
2014
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Single intravenous dose of AAVHSC15 vector with human phenylalanine hydroxylase transgene results in sustained correction of phenylketonuria in the PAH mouse model
Molecular genetics and metabolism, 2019-02, Vol.126 (2), p.S56
2019
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Single intravenous dose of AAVHSC15 vector with human phenylalanine hydroxylase transgene results in sustained correction of phenylketonuria in the PAHenu2 mouse model
Molecular genetics and metabolism, 2019-02, Vol.126 (2), p.S56-S56
2019
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Two Novel [alpha]7 Nicotinic Acetylcholine Receptor Ligands: In Vitro Properties and Their Efficacy in Collagen-Induced Arthritis in Mice
PloS one, 2015-01, Vol.10 (1)
2015
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Identification of 2-{2-[2-(5-Bromo-2- methoxyphenyl)-ethyl]-3-fluorophenyl}-4,5-dihydro-1H-imidazole (ML00253764), a Small Molecule Melanocortin 4 Receptor Antagonist That Effectively Reduces Tumor-Induced Weight Loss in a Mouse Model
Journal of medicinal chemistry, 2004-03, Vol.47 (7), p.1602-1604
2004
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Identification of 2-[2-[2-(5-bromo-2- methoxyphenyl)-ethyl]-3-fluorophenyl]-4,5-dihydro-1H-imidazole (ML00253764), a small molecule melanocortin 4 receptor antagonist that effectively reduces tumor-induced weight loss in a mouse model
Journal of medicinal chemistry, 2004-03, Vol.47 (7), p.1602-1604
2004
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Identification of 2-{2-[2-(5-Bromo-2- methoxyphenyl)-ethyl]-3-fluorophenyl}-4,5-dihydro-1 H -imidazole (ML00253764), a Small Molecule Melanocortin 4 Receptor Antagonist That Effectively Reduces Tumor-Induced Weight Loss in a Mouse Model
Journal of medicinal chemistry, 2004-03, Vol.47 (7), p.1602-1604
2004
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Identification of 2-{2-[2-(5-bromo-2-methoxyphenyl)-ethyl]-3-fluorophenyl}-4,5-dihydro-1H-imidazol e (ML00253764), a small molecule melanocortin 4 receptor antagonist that effectively reduces tumor-induced weight loss in a mouse model
Journal of medicinal chemistry, 2004, Vol.47 (7), p.1602-1604
2004
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