Gee HY - Search Results

1

A novel early truncation mutation in OTOG causes prelingual mild hearing loss without vestibular dysfunction.

Yu S, Choi HJ, Lee JS, Lee HJ, Rim JH, Choi JY, Gee HY, Jung J. Yu S, et al. Among authors: gee hy. Eur J Med Genet. 2019 Jan;62(1):81-84. doi: 10.1016/j.ejmg.2018.05.018. Epub 2018 May 22. Eur J Med Genet. 2019. PMID: 29800624

2

Shank2 mutant mice display a hypersecretory response to cholera toxin.

Jung ES, Park J, Gee HY, Jung J, Noh SH, Lee JS, Richter W, Namkung W, Lee MG. Jung ES, et al. Among authors: gee hy. J Physiol. 2014 Apr 15;592(8):1809-21. doi: 10.1113/jphysiol.2013.268631. Epub 2014 Jan 20. J Physiol. 2014. PMID: 24445315 Free PMC article.

3

The HSP70 co-chaperone DNAJC14 targets misfolded pendrin for unconventional protein secretion.

Jung J, Kim J, Roh SH, Jun I, Sampson RD, Gee HY, Choi JY, Lee MG. Jung J, et al. Among authors: gee hy. Nat Commun. 2016 Apr 25;7:11386. doi: 10.1038/ncomms11386. Nat Commun. 2016. PMID: 27109633 Free PMC article.

4

A novel missense mutation in NR0B1 causes delayed-onset primary adrenal insufficiency in adults.

Oh CM, Chun S, Lee JE, Lee JS, Park S, Gee HY, Kim SW. Oh CM, et al. Among authors: gee hy. Clin Genet. 2017 Sep;92(3):344-346. doi: 10.1111/cge.12966. Epub 2017 Mar 1. Clin Genet. 2017. PMID: 28075027

5

Fecal Occult Blood Test Results of the National Colorectal Cancer Screening Program in South Korea (2006-2013).

Rim JH, Youk T, Kang JG, Park BK, Gee HY, Kim JH, Yoo J. Rim JH, et al. Among authors: gee hy. Sci Rep. 2017 Jun 5;7(1):2804. doi: 10.1038/s41598-017-03134-9. Sci Rep. 2017. PMID: 28584248 Free PMC article.

6

Adult-Onset Vitelliform Macular Dystrophy caused by BEST1 p.Ile38Ser Mutation is a Mild Form of Best Vitelliform Macular Dystrophy.

Jun I, Lee JS, Lee JH, Lee CS, Choi SI, Gee HY, Lee MG, Kim EK. Jun I, et al. Among authors: gee hy. Sci Rep. 2017 Aug 22;7(1):9146. doi: 10.1038/s41598-017-09629-9. Sci Rep. 2017. PMID: 28831140 Free PMC article.

7

ANO9/TMEM16J promotes tumourigenesis via EGFR and is a novel therapeutic target for pancreatic cancer.

Jun I, Park HS, Piao H, Han JW, An MJ, Yun BG, Zhang X, Cha YH, Shin YK, Yook JI, Jung J, Gee HY, Park JS, Yoon DS, Jeung HC, Lee MG. Jun I, et al. Among authors: gee hy. Br J Cancer. 2017 Dec 5;117(12):1798-1809. doi: 10.1038/bjc.2017.355. Epub 2017 Oct 12. Br J Cancer. 2017. PMID: 29024940 Free PMC article.

8

Accuracy of Next-Generation Sequencing for Molecular Diagnosis in Patients With Infantile Nystagmus Syndrome.

Rim JH, Lee ST, Gee HY, Lee BJ, Choi JR, Park HW, Han SH, Han J. Rim JH, et al. Among authors: gee hy. JAMA Ophthalmol. 2017 Dec 1;135(12):1376-1385. doi: 10.1001/jamaophthalmol.2017.4859. JAMA Ophthalmol. 2017. PMID: 29145603 Free PMC article.

9

Whole-exome sequencing identified a missense mutation in WFS1 causing low-frequency hearing loss: a case report.

Choi HJ, Lee JS, Yu S, Cha DH, Gee HY, Choi JY, Lee JD, Jung J. Choi HJ, et al. Among authors: gee hy. BMC Med Genet. 2017 Dec 19;18(1):151. doi: 10.1186/s12881-017-0511-7. BMC Med Genet. 2017. PMID: 29258540 Free PMC article.

10

ZMYND10 stabilizes intermediate chain proteins in the cytoplasmic pre-assembly of dynein arms.

Cho KJ, Noh SH, Han SM, Choi WI, Kim HY, Yu S, Lee JS, Rim JH, Lee MG, Hildebrandt F, Gee HY. Cho KJ, et al. Among authors: gee hy. PLoS Genet. 2018 Mar 30;14(3):e1007316. doi: 10.1371/journal.pgen.1007316. eCollection 2018 Mar. PLoS Genet. 2018. PMID: 29601588 Free PMC article.

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