- Deep learning outperforms kidney organoid experts
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Yu S, Gee HY
- KMID: 2540178
- Kidney Res Clin Pract.
- 2023 Jan;42(1):1-3.
- doi: 10.23876/j.krcp.22.174
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- Genetic Characteristics and Audiological Performance After Cochlear Implantation in Patients With Incomplete Partition Type III
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Jung J, Lee SA, Kim UK, Moon IS, Gee HY, Choi JY
- KMID: 2548369
- Clin Exp Otorhinolaryngol.
- 2023 Nov;16(4):403-406.
- doi: 10.21053/ceo.2023.00864
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- Effects of Cold Agglutinin on the Accuracy of Complete Blood Count Results and Optimal Sample Pretreatment Protocols for Eliminating Such Effects
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Rim JH, Chang MH, Oh J, Gee HY, Kim JH, Yoo J
- KMID: 2408078
- Ann Lab Med.
- 2018 Jul;38(4):371-374.
- doi: 10.3343/alm.2018.38.4.371
No abstract available. -
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- Genetics of vesicoureteral reflux and congenital anomalies of the kidney and urinary tract
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Lee KH, Gee HY, Shin JI
- KMID: 2379890
- Investig Clin Urol.
- 2017 Jun;58(Suppl 1):S4-S13.
- doi: 10.4111/icu.2017.58.S1.S4
The definition of congenital anomalies of the kidney and urinary tract (CAKUT) is the disease of structural malformations in the kidney and/or urinary tract containing vesicoureteral reflux (VUR). These anomalies... -
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- Uridine-5'-Triphosphate Stimulates Chloride Secretion via Cystic Fibrosis Transmembrane Conductance Regulator and Ca2+-Activated Chloride Channels in Cultured Human Middle Ear Epithelial Cells
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Son EJ, Gee HY, Lee MG, Lee WS, Choi JY
- KMID: 2277285
- Korean J Otorhinolaryngol-Head Neck Surg.
- 2011 Dec;54(12):840-846.
- doi: 10.3342/kjorl-hns.2011.54.12.840
BACKGROUND AND OBJECTIVES: Nucleotide binding to purinergic P2Y receptors contributes to the regulation of fluid and ion transport in the middle ear epithelial cells. Here, we investigated the regulatory mechanism... -
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- The L441P Mutation of Cystic Fibrosis Transmembrane conductance Regulator and its Molecular Pathogenic Mechanisms in a Korean Patient with Cystic Fibrosis
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Gee HY, Kim CK, Kim SW, Lee JH, Kim JH, Kim KH, Lee MG
- KMID: 1713852
- J Korean Med Sci.
- 2010 Jan;25(1):166-171.
- doi: 10.3346/jkms.2010.25.1.166
Cystic fibrosis (CF) is an autosomal recessive disorder usually found in populations of white Caucasian descent. CF is caused by mutations in the Cystic Fibrosis Transmembrane conductance Regulator (CFTR) gene.... -
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