Li JJ - Search Results

1

Modeling the phenotype of spinal muscular atrophy by the direct conversion of human fibroblasts to motor neurons.

Zhang QJ, Li JJ, Lin X, Lu YQ, Guo XX, Dong EL, Zhao M, He J, Wang N, Chen WJ. Zhang QJ, et al. Among authors: li jj. Oncotarget. 2017 Feb 14;8(7):10945-10953. doi: 10.18632/oncotarget.14641. Oncotarget. 2017. PMID: 28099929 Free PMC article.

2

Clinical and genetic spectra in a series of Chinese patients with Charcot-Marie-Tooth disease.

Wang R, He J, Li JJ, Ni W, Wu ZY, Chen WJ, Wang Y. Wang R, et al. Among authors: li jj. Clin Chim Acta. 2015 Dec 7;451(Pt B):263-70. doi: 10.1016/j.cca.2015.10.007. Epub 2015 Oct 8. Clin Chim Acta. 2015. PMID: 26454100

3

Modeling the differential phenotypes of spinal muscular atrophy with high-yield generation of motor neurons from human induced pluripotent stem cells.

Lin X, Li JJ, Qian WJ, Zhang QJ, Wang ZF, Lu YQ, Dong EL, He J, Wang N, Ma LX, Chen WJ. Lin X, et al. Among authors: li jj. Oncotarget. 2017 Jun 27;8(26):42030-42042. doi: 10.18632/oncotarget.14925. Oncotarget. 2017. PMID: 28159932 Free PMC article.

4

Application of urine cells in drug intervention for spinal muscular atrophy.

Zhang QJ, Lin X, Li JJ, Lu YQ, Guo XX, Dong EL, Zhao M, He J, Wang N, Chen WJ. Zhang QJ, et al. Among authors: li jj. Exp Ther Med. 2017 Sep;14(3):1993-1998. doi: 10.3892/etm.2017.4791. Epub 2017 Jul 12. Exp Ther Med. 2017. PMID: 28962115 Free PMC article.

5

c.835-5T>G Variant in SMN1 Gene Causes Transcript Exclusion of Exon 7 and Spinal Muscular Atrophy.

Wu S, Li YL, Cheng NY, Wang C, Dong EL, Lu YQ, Li JJ, Guo XX, Lin X, Lai LL, Liu ZW, Wang N, Chen WJ. Wu S, et al. Among authors: li jj, li yl. J Mol Neurosci. 2018 Jun;65(2):196-202. doi: 10.1007/s12031-018-1079-1. Epub 2018 May 24. J Mol Neurosci. 2018. PMID: 29799103

6

Identification of a Novel Homozygous Splice-Site Mutation in SCARB2 that Causes Progressive Myoclonus Epilepsy with or without Renal Failure.

He J, Lin H, Li JJ, Su HZ, Wang DN, Lin Y, Wang N, Chen WJ. He J, et al. Among authors: li jj. Chin Med J (Engl). 2018 Jul 5;131(13):1575-1583. doi: 10.4103/0366-6999.235113. Chin Med J (Engl). 2018. PMID: 29941711 Free PMC article.

7

Advances in detecting and reducing off-target effects generated by CRISPR-mediated genome editing.

Li J, Hong S, Chen W, Zuo E, Yang H. Li J, et al. J Genet Genomics. 2019 Nov 20;46(11):513-521. doi: 10.1016/j.jgg.2019.11.002. Epub 2019 Nov 22. J Genet Genomics. 2019. PMID: 31911131 Review.

8

Cryptic exon activation causes dystrophinopathy in two Chinese families.

Jin M, Li JJ, Xu GR, Wang N, Wang ZQ. Jin M, et al. Among authors: li jj. Eur J Hum Genet. 2020 Jul;28(7):947-955. doi: 10.1038/s41431-020-0578-z. Epub 2020 Feb 11. Eur J Hum Genet. 2020. PMID: 32047267 Free PMC article.

9

Base editing-mediated splicing correction therapy for spinal muscular atrophy.

Lin X, Chen H, Lu YQ, Hong S, Hu X, Gao Y, Lai LL, Li JJ, Wang Z, Ying W, Ma L, Wang N, Zuo E, Yang H, Chen WJ. Lin X, et al. Among authors: li jj. Cell Res. 2020 Jun;30(6):548-550. doi: 10.1038/s41422-020-0304-y. Epub 2020 Mar 24. Cell Res. 2020. PMID: 32210360 Free PMC article. No abstract available.

10

Genetic screening method for analyzing survival motor neuron copy number in spinal muscular atrophy by multiplex ligation-dependent probe amplification and droplet digital polymerase chain reaction.

Hong JM, Zhao M, He J, Huang XJ, Zhao ZY, Chen WJ, Wang N, Li JJ. Hong JM, et al. Among authors: li jj. Chin Med J (Engl). 2020 Oct 20;133(20):2510-2511. doi: 10.1097/CM9.0000000000001102. Chin Med J (Engl). 2020. PMID: 32960844 Free PMC article. No abstract available.

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