Cai A - Search Results

1

Development of CRISPR-Mediated Systems in the Study of Duchenne Muscular Dystrophy.

Cai A, Kong X. Cai A, et al. Hum Gene Ther Methods. 2019 Jun;30(3):71-80. doi: 10.1089/hgtb.2018.187. Epub 2019 May 27. Hum Gene Ther Methods. 2019. PMID: 31062609 Review.

2

[IDUA gene mutation analysis and prenatal diagnosis of two families affected with mucopolysaccharidosis type I].

Yang X, Mei S, Kong X, Zhao Z, Cai A, Yao J, Li Y, Qin Z. Yang X, et al. Among authors: cai a. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Jun 10;34(3):347-351. doi: 10.3760/cma.j.issn.1003-9406.2017.03.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28604952 Chinese.

3

[Progress in gene therapy for Duchenne muscular dystrophy].

Cui SY, Cai AJ, Kong XD. Cui SY, et al. Among authors: cai aj. Zhonghua Er Ke Za Zhi. 2017 Sep 2;55(9):717-719. doi: 10.3760/cma.j.issn.0578-1310.2017.09.022. Zhonghua Er Ke Za Zhi. 2017. PMID: 28881525 Chinese. No abstract available.

4

Exploring the cause of early miscarriage with SNP-array analysis and karyotyping.

Qu S, Wang L, Cai A, Cui S, Bai N, Liu N, Kong X. Qu S, et al. Among authors: cai a. J Matern Fetal Neonatal Med. 2019 Jan;32(1):1-10. doi: 10.1080/14767058.2017.1367379. Epub 2017 Oct 16. J Matern Fetal Neonatal Med. 2019. PMID: 29034762

5

[Analysis of non-invasive prenatal screening detection in fetal chromosome aneuploidy].

Cai AJ, Zhu CF, Xue SW, Cui SY, Qu SZ, Liu N, Kong XD. Cai AJ, et al. Zhonghua Fu Chan Ke Za Zhi. 2017 Nov 25;52(11):765-769. doi: 10.3760/cma.j.issn.0529-567X.2017.11.009. Zhonghua Fu Chan Ke Za Zhi. 2017. PMID: 29179272 Chinese.

6

Generation of ZZUi008-A, a transgene-free, induced pluripotent stem cell line derived from chorionic villi cells of a fetus with Duchenne muscular dystrophy.

Zhu X, Cai A, Meng J, Liu L, Cui S, Qu S, Zhao J, Liu N, Kong X. Zhu X, et al. Among authors: cai a. Stem Cell Res. 2018 Oct;32:47-50. doi: 10.1016/j.scr.2018.07.017. Epub 2018 Jul 17. Stem Cell Res. 2018. PMID: 30172907 Free article.

7

[Genetic testing of chorionic villi from abortuses during early pregnancy].

Yang Y, Qu S, Wang L, Guo Y, Xue S, Cai A, Cui S, Kong X. Yang Y, et al. Among authors: cai a. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jun 10;36(6):547-551. doi: 10.3760/cma.j.issn.1003-9406.2019.06.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31055802 Chinese.

8

A novel NAPB splicing mutation identified by Trio-based exome sequencing is associated with early-onset epileptic encephalopathy.

Zhao X, Wang Y, Cai A, Mei S, Liu N, Kong X. Zhao X, et al. Among authors: cai a. Eur J Med Genet. 2021 Jan;64(1):104101. doi: 10.1016/j.ejmg.2020.104101. Epub 2020 Nov 12. Eur J Med Genet. 2021. PMID: 33189936

9

Genetic analysis and identification of novel variations in Chinese patients with pediatric epilepsy by whole-exome sequencing.

Zhao X, Ning H, Wang Y, Zhao G, Mei S, Liu N, Wang C, Cai A, Wei E, Kong X. Zhao X, et al. Among authors: cai a. Neurol Sci. 2022 Jul;43(7):4439-4451. doi: 10.1007/s10072-022-05953-9. Epub 2022 Feb 26. Neurol Sci. 2022. PMID: 35217970

10

In Vitro Effects of Acitretin on Human Neuronal SH-SY5Y Cells.

Cai A, Liu N, Lin Z, Li X, Wang J, Wu Y, Gao K, Jiang Y. Cai A, et al. Neurochem Res. 2023 Jan;48(1):72-81. doi: 10.1007/s11064-022-03716-8. Epub 2022 Aug 20. Neurochem Res. 2023. PMID: 35987975 Free PMC article.

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