- A Case of Cystinuria with Multiple Renal Stones in an 8-month-old Girl
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Kang EG, Lee JH, Lee BH, Kim GH, Park YS
- KMID: 2098920
- J Korean Soc Pediatr Nephrol.
- 2013 Oct;17(2):122-126.
Cystinuria is an autosomal recessive disease characterized by impaired transport of cystine and dibasic amino acids in the proximal renal tubule, resulting in the formation of cystine stones. It is... -
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- Genotype and Phenotype Analysis in Pediatric Patients with Cystinuria
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Kim JH, Park E, Hyun HS, Lee BH, Kim GH, Lee JH, Park YS, Kang HG, Ha IS, Cheong HI
- KMID: 2364176
- J Korean Med Sci.
- 2017 Feb;32(2):310-314.
- doi: 10.3346/jkms.2017.32.2.310
Cystinuria is an inherited disorder characterized by defective renal reabsorption of cystine and dibasic amino acids leading to nephrolithiasis. This study was conducted to analyze the genotypes and phenotypes of... -
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- The adaptor protein LAD/TSAd mediates laminin-dependent T cell migration via association with the 67 kDa laminin binding protein
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Park E, Choi Y, Ahn E, Park I, Yun Y
- KMID: 1009394
- Exp Mol Med.
- 2009 Oct;41(10):728-736.
- doi: 10.3858/emm.2009.41.10.079
The adaptor protein, LAD/TSAd, plays essential roles in T cell activation. To further understand the functions of this protein, we performed yeast two-hybrid screening using TSAd as bait and identified... -
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