Hwang DY - Search Results

1

HDAC6 involves in regulating the lncRNA-microRNA-mRNA network to promote the proliferation of glioblastoma cells.

Wu AC, Yang WB, Chang KY, Lee JS, Liou JP, Su RY, Cheng SM, Hwang DY, Kikkawa U, Hsu TI, Wang CY, Chang WC, Chen PY, Chuang JY. Wu AC, et al. Among authors: hwang dy. J Exp Clin Cancer Res. 2022 Feb 2;41(1):47. doi: 10.1186/s13046-022-02257-w. J Exp Clin Cancer Res. 2022. PMID: 35109908 Free PMC article.

2

PKD2 founder mutation is the most common mutation of polycystic kidney disease in Taiwan.

Yu CC, Lee AF, Kohl S, Lin MY, Cheng SM, Hung CC, Chang JM, Chiu YW, Hwang SJ, Otto EA, Hildebrandt F; Taiwan PKD Consortium; Hwang DY. Yu CC, et al. Among authors: hwang dy, hwang sj. NPJ Genom Med. 2022 Jul 1;7(1):40. doi: 10.1038/s41525-022-00309-w. NPJ Genom Med. 2022. PMID: 35778421 Free PMC article.

3

Chien CH, Yang WB, Chuang JY, Lee JS, Liao WA, Huang CY, Chen PY, Wu AC, Yang ST, Lai CC, Chi PI, Chu JM, Cheng SM, Liu CC, Hwang DY, Chen SH, Chang KY. Chien CH, et al. Among authors: hwang dy. J Exp Clin Cancer Res. 2022 Jul 13;41(1):220. doi: 10.1186/s13046-022-02429-8. J Exp Clin Cancer Res. 2022. PMID: 35831908 Free PMC article.

4

Whole-exome sequencing identified mutational profiles of urothelial carcinoma post kidney transplantation.

Lim LM, Chung WY, Hwang DY, Yu CC, Ke HL, Liang PI, Lin TW, Cheng SM, Huang AM, Kuo HT. Lim LM, et al. Among authors: hwang dy. J Transl Med. 2022 Jul 21;20(1):324. doi: 10.1186/s12967-022-03522-4. J Transl Med. 2022. PMID: 35864526 Free PMC article.

5

Germline mutations of homologous recombination genes and clinical outcomes in pancreatic cancer: a multicenter study in Taiwan.

Cheng SM, Su YY, Chiang NJ, Wang CJ, Chao YJ, Huang CJ, Tsai HJ, Chen SH, Chang CY, Tsai CR, Li YJ, Yen CJ, Chuang SC, Chang JS, Shan YS, Hwang DY, Chen LT. Cheng SM, et al. Among authors: hwang dy. J Biomed Sci. 2024 Feb 13;31(1):21. doi: 10.1186/s12929-024-01008-7. J Biomed Sci. 2024. PMID: 38350919 Free PMC article.

6

AUY922 induces retinal toxicity through attenuating TRPM1.

Shen CH, Hsieh CC, Jiang KY, Lin CY, Chiang NJ, Li TW, Yen CT, Chen WJ, Hwang DY, Chen LT. Shen CH, et al. Among authors: hwang dy. J Biomed Sci. 2021 Jul 23;28(1):55. doi: 10.1186/s12929-021-00751-5. J Biomed Sci. 2021. PMID: 34301262 Free PMC article.

7

Generation of induced pluripotent stem cells derived from an autosomal dominant polycystic kidney disease patient with a p.Ser1457fs mutation in PKD1.

Huang CY, Ho MC, Lee JJ, Hwang DY, Ko HW, Cheng YC, Hsu YH, Lu HE, Chen HC, Hsieh PCH. Huang CY, et al. Among authors: hwang dy. Stem Cell Res. 2017 Oct;24:139-143. doi: 10.1016/j.scr.2017.09.004. Epub 2017 Sep 15. Stem Cell Res. 2017. PMID: 29034881 Free article.

8

The rs1014290 polymorphism of the SLC2A9 gene is associated with type 2 diabetes mellitus in Han Chinese.

Liu WC, Hung CC, Chen SC, Lin MY, Chen LI, Hwang DY, Chang JM, Tsai JC, Chen HC, Hwang SJ. Liu WC, et al. Among authors: hwang dy, hwang sj. Exp Diabetes Res. 2011;2011:527520. doi: 10.1155/2011/527520. Epub 2011 Apr 14. Exp Diabetes Res. 2011. PMID: 21584282 Free PMC article.

9

PRRT2 missense mutations cluster near C-terminus and frequently lead to protein mislocalization.

Tsai MH, Nian FS, Hsu MH, Liu WS, Liu YT, Liu C, Lin PH, Hwang DY, Chuang YC, Tsai JW. Tsai MH, et al. Among authors: hwang dy. Epilepsia. 2019 May;60(5):807-817. doi: 10.1111/epi.14725. Epub 2019 Apr 13. Epilepsia. 2019. PMID: 30980674

10

CYP17A1 intron mutation causing cryptic splicing in 17α-hydroxylase deficiency.

Hwang DY, Hung CC, Riepe FG, Auchus RJ, Kulle AE, Holterhus PM, Chao MC, Kuo MC, Hwang SJ, Chen HC. Hwang DY, et al. Among authors: hwang sj. PLoS One. 2011;6(9):e25492. doi: 10.1371/journal.pone.0025492. Epub 2011 Sep 26. PLoS One. 2011. PMID: 21966534 Free PMC article.

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