Assistant Professor, Pediatric Emergency Medicine, Baylor College of Medicine
Pediatrics
Dr. Joe Tran, MD
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Joe Tran practices Pediatrics. He studied medicine at Baylor College of Medicine. He has 1 awards "Fellow (FAAP)". Tran has written publications. He has 30 publications published with PubMed. The lastest paper is: 'Retrospective cohort study evaluating liraglutide and exenatide in a veteran population.' He is registered with Medicare.
Publications
- Retrospective cohort study evaluating liraglutide and exenatide in a veteran population.
- Possible mechanisms of acquired resistance to anti-angiogenic drugs: implications for the use of combination therapy approaches.
- trans-1-[(2-Phenylcyclopropyl)methyl]-4-arylpiperazines: mixed dopamine D(2)/D(4) receptor antagonists as potential antipsychotic agents.
- Lead optimization of 2-(piperidin-3-yl)-1H-benzimidazoles: identification of 2-morpholin- and 2-thiomorpholin-2-yl-1H-benzimidazoles as selective and CNS penetrating H...
- Characterization of thien-2-yl 1S,2R-milnacipran analogues as potent norepinephrine/serotonin transporter inhibitors for the treatment of neuropathic pain.
- Structure-activity relationship studies on a series of piperazinebenzylalcohols and their ketone and amine analogs as melanocortin-4 receptor ligands.
- Studies on the structure-activity relationship of bicifadine analogs as monoamine transporter inhibitors.
- Identification of 1S,2R-milnacipran analogs as potent norepinephrine and serotonin transporter inhibitors.
- Pharmacological and pharmacokinetic characterization of 2-piperazine-alpha-isopropyl benzylamine derivatives as melanocortin-4 receptor antagonists.
- Design and synthesis of 3-arylpyrrolidine-2-carboxamide derivatives as melanocortin-4 receptor ligands.
- Studies on the structure-activity relationship of the basic amine of phenylpiperazines as melanocortin-4 receptor antagonists.
- Syntheses of tetrahydrothiophenes and tetrahydrofurans and studies of their derivatives as melanocortin-4 receptor ligands.
- Identification and characterization of pyrrolidine diastereoisomers as potent functional agonists and antagonists of the human melanocortin-4 receptor.
- Design, synthesis, in vitro, and in vivo characterization of phenylpiperazines and pyridinylpiperazines as potent and selective antagonists of the melanocortin-4 recep...
- Synthesis and characterization of trans-4-(4-chlorophenyl)pyrrolidine-3-carboxamides of piperazinecyclohexanes as ligands for the melanocortin-4 receptor.
- Synthesis and characterization of pyrrolidine derivatives as potent agonists of the human melanocortin-4 receptor.
- Discovery of 1-[2-[(1S)-(3-dimethylaminopropionyl)amino-2-methylpropyl]-4-methylphenyl]-4-[(2R)-methyl-3-(4-chlorophenyl)-propionyl]piperazine as an orally active anta...
- Pyrrolidinones as potent functional antagonists of the human melanocortin-4 receptor.
- Pyrrolidines as potent functional agonists of the human melanocortin-4 receptor.
- Pyrrolidinones as orally bioavailable antagonists of the human melanocortin-4 receptor with anti-cachectic activity.
- Propionylpiperazines as human melanocortin-4 receptor ligands.
- Arylpropionylpiperazines as antagonists of the human melanocortin-4 receptor.
- Design, synthesis, and SAR studies on a series of 2-pyridinylpiperazines as potent antagonists of the melanocortin-4 receptor.
- Practical asymmetric synthesis of alpha-branched 2-piperazinylbenzylamines by 1,2-additions of organometallic reagents to N-tert-butanesulfinyl imines.
- Structure-activity relationship studies on a series of cyclohexylpiperazines bearing a phanylacetamide as ligands of the human melanocortin-4 receptor.
- Optimization of piperazinebenzylamines with a N-(1-methoxy-2-propyl) side chain as potent and selective antagonists of the human melanocortin-4 receptor.
- Potent and orally active non-peptide antagonists of the human melanocortin-4 receptor based on a series of trans-2-disubstituted cyclohexylpiperazines.
- Identification of agonists and antagonists of the human melanocortin-4 receptor from piperazinebenzylamines.
- 4-{(2R)-[3-Aminopropionylamido]-3-(2,4-dichlorophenyl)propionyl}-1-{2-[(2-thienyl)ethylaminomethyl]phenyl}piperazine as a potent and selective melanocortin-4 receptor ...
Schools
Baylor University
Baylor College Of Med
Doctors Specialties
- Pediatrics
Accepted Insurances
Awards
- Fellow (FAAP)
Education
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Baylor College of Medicine
Hospital
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Texas Children's Hospital -
Baylor University Medical Center
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