Similar articles for PMID: 29358698

Year	Number of Results
2003	1
2006	1
2009	1
2015	2
2016	1
2017	4
2018	8
2019	3
2020	2
2021	2
2022	1
2024	0

1

Production of Wilson Disease Model Rabbits with Homology-Directed Precision Point Mutations in the ATP7B Gene Using the CRISPR/Cas9 System.

Jiang W, Liu L, Chang Q, Xing F, Ma Z, Fang Z, Zhou J, Fu L, Wang H, Huang X, Chen X, Li Y, Li S. Jiang W, et al. Sci Rep. 2018 Jan 22;8(1):1332. doi: 10.1038/s41598-018-19774-4. Sci Rep. 2018. PMID: 29358698 Free PMC article.

2

CRISPR/Cas9-mediated correction of mutated copper transporter ATP7B.

Pöhler M, Guttmann S, Nadzemova O, Lenders M, Brand E, Zibert A, Schmidt HH, Sandfort V. Pöhler M, et al. PLoS One. 2020 Sep 30;15(9):e0239411. doi: 10.1371/journal.pone.0239411. eCollection 2020. PLoS One. 2020. PMID: 32997714 Free PMC article.

3

A Gene Therapy Approach to Improve Copper Metabolism and Prevent Liver Damage in a Mouse Model of Wilson Disease.

Greig JA, Nordin JML, Smith MK, Ashley SN, Draper C, Zhu Y, Bell P, Buza EL, Wilson JM. Greig JA, et al. Hum Gene Ther Clin Dev. 2019 Mar;30(1):29-39. doi: 10.1089/humc.2018.219. Epub 2019 Feb 25. Hum Gene Ther Clin Dev. 2019. PMID: 30693797

4

[Research progress in gene therapy for Wilson's disease].

Tang S, Bai L, Zheng SJ. Tang S, et al. Zhonghua Gan Zang Bing Za Zhi. 2021 Jan 20;29(1):21-24. doi: 10.3760/cma.j.cn501113-20201104-00598. Zhonghua Gan Zang Bing Za Zhi. 2021. PMID: 33541020 Chinese.

5

Spectrum of ATP7B mutations and genotype-phenotype correlation in large-scale Chinese patients with Wilson Disease.

Cheng N, Wang H, Wu W, Yang R, Liu L, Han Y, Guo L, Hu J, Xu L, Zhao J, Han Y, Liu Q, Li K, Wang X, Chen W. Cheng N, et al. Clin Genet. 2017 Jul;92(1):69-79. doi: 10.1111/cge.12951. Epub 2017 Feb 16. Clin Genet. 2017. PMID: 27982432

6

Epigenetic changes of the thioredoxin system in the tx-j mouse model and in patients with Wilson disease.

Mordaunt CE, Shibata NM, Kieffer DA, Czlonkowska A, Litwin T, Weiss KH, Gotthardt DN, Olson K, Wei D, Cooper S, Wan YY, Ali MR, LaSalle JM, Medici V. Mordaunt CE, et al. Hum Mol Genet. 2018 Nov 15;27(22):3854-3869. doi: 10.1093/hmg/ddy262. Hum Mol Genet. 2018. PMID: 30010856 Free PMC article.

7

Animal models of Wilson disease.

Medici V, Huster D. Medici V, et al. Handb Clin Neurol. 2017;142:57-70. doi: 10.1016/B978-0-444-63625-6.00006-9. Handb Clin Neurol. 2017. PMID: 28433110 Review.

8

Animal models of Wilson disease.

Reed E, Lutsenko S, Bandmann O. Reed E, et al. J Neurochem. 2018 Aug;146(4):356-373. doi: 10.1111/jnc.14323. Epub 2018 Jun 26. J Neurochem. 2018. PMID: 29473169 Free PMC article. Review.

9

Liver Expression of a MiniATP7B Gene Results in Long-Term Restoration of Copper Homeostasis in a Wilson Disease Model in Mice.

Murillo O, Moreno D, Gazquez C, Barberia M, Cenzano I, Navarro I, Uriarte I, Sebastian V, Arruebo M, Ferrer V, Bénichou B, Combal JP, Prieto J, Hernandez-Alcoceba R, Gonzalez Aseguinolaza G. Murillo O, et al. Hepatology. 2019 Jul;70(1):108-126. doi: 10.1002/hep.30535. Epub 2019 Mar 20. Hepatology. 2019. PMID: 30706949

10

Disease-causing point-mutations in metal-binding domains of Wilson disease protein decrease stability and increase structural dynamics.

Kumar R, Ariöz C, Li Y, Bosaeus N, Rocha S, Wittung-Stafshede P. Kumar R, et al. Biometals. 2017 Feb;30(1):27-35. doi: 10.1007/s10534-016-9976-7. Epub 2016 Oct 15. Biometals. 2017. PMID: 27744583 Free PMC article.

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