Dr. Yoon Taik Kwon M.D.
Allergist and Immunologist
1100 Sir Francis Drake Blvd Greenbrae CA, 94904About
Dr. Yoon Kwon practices Allergy and Immunology care in Greenbrae, CA. Dr. Kwon specializes in the diagnosis and treatment of asthma and other allergic diseases. Allergist-Immunologists are trained and certified to treat each patients sensitivity and response to allergens of varying severity. Dr. Kwon provides several means of testing and treatment to increase immunity to potentially harmful substances.
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Data provided by the National Library of Medicine- Bivalent inhibitor of the N-end rule pathway.
- Regulation of N-cadherin-mediated adhesion by the p35-Cdk5 kinase.
- Altered activity, social behavior, and spatial memory in mice lacking the NTAN1p amidase and the asparagine branch of the N-end rule pathway.
- The role of the p35/cdk5 kinase in cortical development.
- Varying intertrial interval reveals temporally defined memory deficits and enhancements in NTAN1-deficient mice.
- Loss of Ubr1 promotes aneuploidy and accelerates B-cell lymphomagenesis in TLX1/HOX11-transgenic mice.
- Hyperthermia enhances mapatumumab-induced apoptotic death through ubiquitin-mediated degradation of cellular FLIP(long) in human colon cancer cells.
- Role of AMP-activated protein kinase in cross-talk between apoptosis and autophagy in human colon cancer.
- Cloning and characterization of the gene encoding an extracellular alkaline serine protease from Vibrio metschnikovii strain RH530.
- Cloning, sequencing, and expression of a minor protease-encoding gene from Serratia marcescens ATCC21074.
- The cdk5/p35 kinase is essential for neurite outgrowth during neuronal differentiation.
- Mice lacking p35, a neuronal specific activator of Cdk5, display cortical lamination defects, seizures, and adult lethality.
- A novel disruption of cortical development in p35(-/-) mice distinct from reeler.
- p35, the neuronal-specific activator of cyclin-dependent kinase 5 (Cdk5) is degraded by the ubiquitin-proteasome pathway.
- Alternative splicing results in differential expression, activity, and localization of the two forms of arginyl-tRNA-protein transferase, a component of the N-end rule pathway.
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