Dr. Charles Qing Huang M.D.
Ophthalmologist
3700 Vaca Valley Pkwy Kaiser Permanente Op Vacaville CA, 95688About
Dr. Charles Huang is an ophthalmologist practicing in Vacaville, CA. Dr. Huang specializes in eye and vision care. As an ophthalmologist, Dr. Huang can practice medicine as well as surgery. Opthalmologists can perform surgeries because they have their medical degrees along with at least eight years of additional training. Dr. Huang can diagnose and treat diseases, perform eye operations and prescribe eye glasses and contacts. Ophthalmologists can also specialize even further in a specific area of eye care.
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Electrical stimulation of the auditory nerve: direct current measurement in vivo.
- Reduction in excitability of the auditory nerve following electrical stimulation at high stimulus rates. IV. Effects of stimulus intensity.
- Reduction in excitability of the auditory nerve following electrical stimulation at high stimulus rates: V. Effects of electrode surface area.
- Stimulus induced pH changes in cochlear implants: an in vitro and in vivo study.
- 1-Alkyl-3-amino-5-aryl-1H-[1,2,4]triazoles: novel synthesis via cyclization of N-acyl-S-methylisothioureas with alkylhydrazines and their potent corticotropin-releasing factor-1 (CRF(1)) receptor antagonist activities.
- 6,7-dihydroxyisoquinoline-3-carboxylic acids are potent inhibitors on the binding of insulin-like growth factor (IGF) to IGF-binding proteins: optimization of the 1-position benzoyl side chain.
- Synthesis of 3-phenylpyrazolo[4,3-b]pyridines via a convenient synthesis of 4-amino-3-arylpyrazoles and SAR of corticotropin-releasing factor receptor type-1 antagonists.
- Synthesis of 1-methyl-3-phenylpyrazolo[4,3-b]pyridines via a methylation of 4-phthalimino-3-phenylpyrazoles and optimization toward highly potent corticotropin-releasing factor type-1 antagonists.
- Design, synthesis, and SAR of 2-dialkylamino-4-arylpyrimidines as potent and selective corticotropin-releasing factor(1) (CRF(1)) receptor antagonists.
- Optimization of 3-phenylpyrazolo[1,5-a]pyrimidines as potent
- Expression of testis specific ankyrin repeat and SOCS box-containing 17 gene.
- Synthesis of benzoylpyrimidines as antagonists of the corticotropin-releasing factor-1 receptor.
- Design and synthesis of 3-(2-pyridyl)pyrazolo[1,5-a]pyrimidines as potent CRF1 receptor antagonists.
- Uracils as potent antagonists of the human gonadotropin-releasing hormone receptor without atropisomers.
- 1-(4-Amino-phenyl)-pyrrolidin-3-yl-amine and 6-(3-amino-pyrrolidin-1-yl)-pyridin-3-yl-amine derivatives as melanin-concentrating hormone receptor-1 antagonists.
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