Wu H - Search Results

1

Generation of an integration-free induced pluripotent stem cell line (PUMCHi001-A) from a patient with familial partial lipodystrophy type 2 (FPLD2) carrying a heterozygous p.R349W (c.1045C > T) mutation in the LMNA gene.

Xiao C, Yu M, Liu J, Wu H, Deng M, Zhang Q, Xiao X. Xiao C, et al. Among authors: wu h. Stem Cell Res. 2020 Jan;42:101651. doi: 10.1016/j.scr.2019.101651. Epub 2019 Nov 6. Stem Cell Res. 2020. PMID: 31794942 Free article.

2

Generation of an Abcc8 homozygous mutation human embryonic stem cell line using CRISPR/Cas9.

Guo D, Liu H, Gao G, Ruzi A, Wang K, Wu H, Lai K, Liu Y, Yang F, Lai L, Li YX. Guo D, et al. Among authors: wu h. Stem Cell Res. 2016 Nov;17(3):640-642. doi: 10.1016/j.scr.2016.11.011. Epub 2016 Nov 9. Stem Cell Res. 2016. PMID: 27934599 Free article.

3

Generation of an Abcc8 heterozygous mutation human embryonic stem cell line using CRISPR/Cas9.

Guo D, Liu H, Gao G, Ruzi A, Wang K, Wu H, Lai K, Liu Y, Yang F, Lai L, Li YX. Guo D, et al. Among authors: wu h. Stem Cell Res. 2016 Nov;17(3):670-672. doi: 10.1016/j.scr.2016.11.014. Epub 2016 Nov 5. Stem Cell Res. 2016. PMID: 27934605 Free article.

4

Generation of an ASGR1 homozygous mutant human embryonic stem cell line WAe001-A-6 using CRISPR/Cas9.

Xu Y, Wu Y, Guo D, Gao G, Lai K, Yang F, Wang K, Wu H, Lai L, Li J, Xu K, Li YX. Xu Y, et al. Among authors: wu y, wu h. Stem Cell Res. 2017 Jul;22:29-32. doi: 10.1016/j.scr.2017.05.006. Epub 2017 May 19. Stem Cell Res. 2017. PMID: 28952928 Free article.

5

Generation of two MEN1 knockout lines from a human embryonic stem cell line.

Liu Y, Ruzi A, Guo D, Wu F, Liu H, Wu H, Wu Y, Yuan F, Zhuang Y, Yang F, Lai K, Lai L, Li YX. Liu Y, et al. Among authors: wu y, wu h, wu f. Stem Cell Res. 2017 Oct;24:169-173. doi: 10.1016/j.scr.2017.06.005. Epub 2017 Jun 10. Stem Cell Res. 2017. PMID: 29034888 Free article.

6

Cardiotoxicity evaluation of nine alkaloids from Rhizoma Coptis.

Zhang MY, Yu YY, Wang SF, Zhang Q, Wu HW, Wei JY, Yang W, Li SY, Yang HJ. Zhang MY, et al. Among authors: wu hw. Hum Exp Toxicol. 2018 Feb;37(2):185-195. doi: 10.1177/0960327117695633. Epub 2017 Mar 1. Hum Exp Toxicol. 2018. PMID: 29233041

7

Targeted elimination of mutant mitochondrial DNA in MELAS-iPSCs by mitoTALENs.

Yang Y, Wu H, Kang X, Liang Y, Lan T, Li T, Tan T, Peng J, Zhang Q, An G, Liu Y, Yu Q, Ma Z, Lian Y, Soh BS, Chen Q, Liu P, Chen Y, Sun X, Li R, Zhen X, Liu P, Yu Y, Li X, Fan Y. Yang Y, et al. Among authors: wu h. Protein Cell. 2018 Mar;9(3):283-297. doi: 10.1007/s13238-017-0499-y. Epub 2018 Jan 9. Protein Cell. 2018. PMID: 29318513 Free PMC article.

8

Co-Occurrence of Multiple Endocrine Abnormalities Induced by the DIHS/DRESS.

Deng M, Wu H, Yu M, Tian Y, Li Y, Xiao X. Deng M, et al. Among authors: wu h. Int J Endocrinol. 2019 Oct 3;2019:7959615. doi: 10.1155/2019/7959615. eCollection 2019. Int J Endocrinol. 2019. PMID: 31687021 Free PMC article.

9

Generation of an isogenic gene-corrected iPSC line (PUMCHi001-A-1) from a familial partial lipodystrophy type 2 (FPLD2) patient with a heterozygous R349W mutation in the LMNA gene.

Xiao C, Yu M, Liu J, Wu H, Deng M, Zhang Q, Xiao X. Xiao C, et al. Among authors: wu h. Stem Cell Res. 2020 Apr;44:101753. doi: 10.1016/j.scr.2020.101753. Epub 2020 Mar 14. Stem Cell Res. 2020. PMID: 32213461 Free article.

10

Clinical characteristics of endocrinopathies in Chinese patients with hereditary haemochromatosis.

Wu H, Yu M, Xiao C, Zhang Q, Xiao X. Wu H, et al. Diabetes Metab Res Rev. 2021 May;37(4):e3448. doi: 10.1002/dmrr.3448. Epub 2021 Apr 4. Diabetes Metab Res Rev. 2021. PMID: 33738915

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