- Identification of a Fibrillin-1 Gene Mutation in a Monozygotic Twin Presenting with Bilateral Juvenile-onset Ectopia Lentis
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Yum HR, Kim SE, Shin SY, Park SH
- KMID: 2360145
- Korean J Ophthalmol.
- 2015 Feb;29(1):77-78.
- doi: 10.3341/kjo.2015.29.1.77
No abstract available. -
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- Concomitant AID Expression and BCL7A Loss Associates With Accelerated Phase Progression and Imatinib Resistance in Chronic Myeloid Leukemia
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Yu N, Shin S, Choi JR, Kim Y, Lee KA
- KMID: 2373641
- Ann Lab Med.
- 2017 Mar;37(2):177-179.
- doi: 10.3343/alm.2017.37.2.177
No abstract available. -
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- Polymorphisms of COTL1 gene identified by proteomic approach and their association with autoimmune disorders
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Jin EH, Shim SC, Kim HG, Chae SC, Chung HT
- KMID: 1123810
- Exp Mol Med.
- 2009 May;41(5):354-361.
- doi: 10.3858/emm.2009.41.5.040
To select candidate genes, we attempted to comparative analysis of protein levels between rheumatoid arthritis (RA) patients and healthy controls by two-dimensional electrophoresis (2-DE) and matrix-assisted laser desorption ionization mass... -
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- The enabled homolog gene polymorphisms are associated with susceptibility and progression of childhood IgA nephropathy
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Hahn WH, Suh JS, Cho BS, Kim SD
- KMID: 1122280
- Exp Mol Med.
- 2009 Nov;41(11):793-801.
- doi: 10.3858/emm.2009.41.11.085
The enabled homolog gene (ENAH, hMena) is abundantly expressed in mesangial tissue, and might play an important role in inflammatory processes of IgA nephropathy (IgAN). The present study was conducted... -
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