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Infliximab vs. adalimumab in Crohn's disease: results from 327 patients in an Australian and New Zealand observational cohort study

Alimentary pharmacology & therapeutics, 2017-02, Vol.45 (4), p.542-552

2017

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Comparative pharmacokinetics of diaveridine in pigs and chickens following single intravenous and oral administration

Journal of veterinary pharmacology and therapeutics, 2017-10, Vol.40 (5), p.500-504

2017

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MicroRNA-92a regulates the development of cutaneous malignant melanoma by mediating FOXP1

European review for medical and pharmacological sciences, 2019-10, Vol.23 (20), p.8991

2019

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Bioequivalence of Sarpogrelate in Healthy Chinese Subjects Under Fasting and Fed Conditions: A 4‐Way Replicate Crossover Investigation by a Reference‐Scaled Average Bioequivalence Approach

Clinical pharmacology in drug development, 2019-08, Vol.8 (6), p.713-720

2019

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Arsenite Causes DNA Damage in Keratinocytes Via Generation of Hydroxyl Radicals

Chemical research in toxicology, 2004-07, Vol.17 (7), p.871-878

2004

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Novel biomolecule lycopene-reduced graphene oxide-silver nanoparticle enhances apoptotic potential of trichostatin A in human ovarian cancer cells (SKOV3)

International journal of nanomedicine, 2017-01, Vol.12, p.7551-7575

2017

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An efficient PEGylated liposomal nanocarrier containing cell-penetrating peptide and pH-sensitive hydrazone bond for enhancing tumor-targeted drug delivery

International journal of nanomedicine, 2015-10, Vol.10 (default), p.6199-6214

2015

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In vivo study of doxorubicin-loaded cell-penetrating peptide-modified pH-sensitive liposomes: biocompatibility, bio-distribution, and pharmacodynamics in BALB/c nude mice bearing human breast tumors

Drug design, development and therapy, 2017-01, Vol.11, p.3105-3117

2017

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Protocatechuic aldehyde inhibits hepatitis B virus replication both in vitro and in vivo

Antiviral research, 2007-04, Vol.74 (1), p.59-64

2007

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Consolidation therapy for HBeAg-positive Asian chronic hepatitis B patients receiving lamivudine treatment: a multicentre study

Journal of antimicrobial chemotherapy, 2013-10, Vol.68 (10), p.2332-2338

2013

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Cardioselective Antiischemic ATP-Sensitive Potassium Channel (KATP) Openers. 5. Identification of 4-(N-Aryl)-Substituted Benzopyran Derivatives with High Selectivity

Journal of medicinal chemistry, 1997-01, Vol.40 (1), p.24-34

1997

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Effects of SCN1A and GABA Receptor Genetic Polymorphisms on Carbamazepine Tolerability and Efficacy in Chinese Patients with Partial Seizures: 2-Year Longitudinal Clinical Follow-Up

CNS neuroscience & therapeutics, 2012-07, Vol.18 (7), p.566-572

2012

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Pharmacokinetics of sarafloxacin in pigs and broilers following intravenous, intramuscular, and oral single-dose applications

Journal of veterinary pharmacology and therapeutics, 2001-10, Vol.24 (5), p.303-308

2001

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5-Cyanopyrimidine Derivatives as a Novel Class of Potent, Selective, and Orally Active Inhibitors of p38α MAP Kinase

Journal of medicinal chemistry, 2005-10, Vol.48 (20), p.6261-6270

2005

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Discovery of 2-amino-heteroaryl-benzothiazole-6-anilides as potent p56(lck) inhibitors

Bioorganic & medicinal chemistry letters, 2003-08, Vol.13 (15), p.2587-2590

2003

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Pharmacokinetic interactions of flunixin meglumine and doxycycline in broiler chickens

Journal of veterinary pharmacology and therapeutics, 2013-02, Vol.36 (1), p.85-88

2013

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α-ADDUCIN GENE AND ESSENTIAL HYPERTENSION IN CHINA

Clinical and experimental hypertension (1993), 2001, Vol.23 (7), p.579-589

2001

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Discovery of novel 2-(aminoheteroaryl)-thiazole-5-carboxamides as potent and orally active Src-family kinase p56(Lck) inhibitors

Bioorganic & medicinal chemistry letters, 2004-12, Vol.14 (24), p.6061-6066

2004

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Benzodiazepine-based selective inhibitors of mitochondrial F1F0 ATP hydrolase

Bioorganic & medicinal chemistry letters, 2004-02, Vol.14 (4), p.1031-1034

2004

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Cytotoxic triterpenoid saponins from Vaccaria segetalis

Journal of asian natural products research, 2008-02, Vol.10 (2), p.177-184

2008

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Molecular design, synthesis, and structure-Activity relationships leading to the potent and selective p56(lck) inhibitor BMS-243117

Bioorganic & medicinal chemistry letters, 2003-07, Vol.13 (13), p.2145-2149

2003

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Discovery and initial SAR of 2-amino-5-carboxamidothiazoles as inhibitors of the Src-family kinase p56(Lck)

Bioorganic & medicinal chemistry letters, 2003-11, Vol.13 (22), p.4007-4010

2003

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Design, synthesis, and evaluation of novel 3-amino-4-hydrazine-cyclobut-3-ene-1,2-diones as potent and selective CXCR2 chemokine receptor antagonists

Bioorganic & medicinal chemistry letters, 2009-10, Vol.19 (19), p.5741-5745

2009

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N-[1-aryl-2-(1-imidazolo)ethyl]-guanidine derivatives as potent inhibitors of the bovine mitochondrial F1F0 ATP hydrolase

Bioorganic & medicinal chemistry letters, 2004-02, Vol.14 (4), p.1027-1030

2004

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Angiotensin II type 2 receptor gene polymorphisms and essential hypertension

Acta pharmacologica Sinica, 2003-11, Vol.24 (11), p.1089-1093

2003

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Infliximab vs. adalimumab in Crohn's disease: results from 327 patients in an Australian and New Zealand observational cohort study

Comparative pharmacokinetics of diaveridine in pigs and chickens following single intravenous and oral administration

MicroRNA-92a regulates the development of cutaneous malignant melanoma by mediating FOXP1

Bioequivalence of Sarpogrelate in Healthy Chinese Subjects Under Fasting and Fed Conditions: A 4‐Way Replicate Crossover Investigation by a Reference‐Scaled Average Bioequivalence Approach

Arsenite Causes DNA Damage in Keratinocytes Via Generation of Hydroxyl Radicals

Novel biomolecule lycopene-reduced graphene oxide-silver nanoparticle enhances apoptotic potential of trichostatin A in human ovarian cancer cells (SKOV3)

An efficient PEGylated liposomal nanocarrier containing cell-penetrating peptide and pH-sensitive hydrazone bond for enhancing tumor-targeted drug delivery

In vivo study of doxorubicin-loaded cell-penetrating peptide-modified pH-sensitive liposomes: biocompatibility, bio-distribution, and pharmacodynamics in BALB/c nude mice bearing human breast tumors

Protocatechuic aldehyde inhibits hepatitis B virus replication both in vitro and in vivo

Consolidation therapy for HBeAg-positive Asian chronic hepatitis B patients receiving lamivudine treatment: a multicentre study

Cardioselective Antiischemic ATP-Sensitive Potassium Channel (KATP) Openers. 5. Identification of 4-(N-Aryl)-Substituted Benzopyran Derivatives with High Selectivity

Effects of SCN1A and GABA Receptor Genetic Polymorphisms on Carbamazepine Tolerability and Efficacy in Chinese Patients with Partial Seizures: 2-Year Longitudinal Clinical Follow-Up

Pharmacokinetics of sarafloxacin in pigs and broilers following intravenous, intramuscular, and oral single-dose applications

5-Cyanopyrimidine Derivatives as a Novel Class of Potent, Selective, and Orally Active Inhibitors of p38α MAP Kinase

Discovery of 2-amino-heteroaryl-benzothiazole-6-anilides as potent p56(lck) inhibitors

Pharmacokinetic interactions of flunixin meglumine and doxycycline in broiler chickens

α-ADDUCIN GENE AND ESSENTIAL HYPERTENSION IN CHINA

Discovery of novel 2-(aminoheteroaryl)-thiazole-5-carboxamides as potent and orally active Src-family kinase p56(Lck) inhibitors

Benzodiazepine-based selective inhibitors of mitochondrial F1F0 ATP hydrolase

Cytotoxic triterpenoid saponins from Vaccaria segetalis

Molecular design, synthesis, and structure-Activity relationships leading to the potent and selective p56(lck) inhibitor BMS-243117

Discovery and initial SAR of 2-amino-5-carboxamidothiazoles as inhibitors of the Src-family kinase p56(Lck)

Design, synthesis, and evaluation of novel 3-amino-4-hydrazine-cyclobut-3-ene-1,2-diones as potent and selective CXCR2 chemokine receptor antagonists

N-[1-aryl-2-(1-imidazolo)ethyl]-guanidine derivatives as potent inhibitors of the bovine mitochondrial F1F0 ATP hydrolase

Angiotensin II type 2 receptor gene polymorphisms and essential hypertension

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