Yang J - Search Results

1

Inhibiting the SARM1-NAD⁺ axis reduces oxidative stress-induced damage to retinal and nerve cells.

Zhang Y, Yao Y, Yang J, Zhou B, Zhu Y. Zhang Y, et al. Among authors: yang j. Int Immunopharmacol. 2024 Jun 15;134:112193. doi: 10.1016/j.intimp.2024.112193. Epub 2024 May 8. Int Immunopharmacol. 2024. PMID: 38723372 Free article.

2

Identification of candidate cancer genes involved in human retinoblastoma by data mining.

Yang J, Zhao JJ, Zhu Y, Xiong W, Lin JY, Ma X. Yang J, et al. Childs Nerv Syst. 2008 Aug;24(8):893-900. doi: 10.1007/s00381-008-0595-7. Epub 2008 Mar 19. Childs Nerv Syst. 2008. PMID: 18350306

3

A novel nonsense mutation in CRYBB1 associated with autosomal dominant congenital cataract.

Yang J, Zhu Y, Gu F, He X, Cao Z, Li X, Tong Y, Ma X. Yang J, et al. Mol Vis. 2008 Apr 18;14:727-31. Mol Vis. 2008. PMID: 18432316 Free PMC article.

4

The novel G10680A mutation is associated with complete penetrance of the LHON/T14484C family.

Yang J, Zhu Y, Tong Y, Zhang Z, Chen L, Chen S, Cao Z, Liu C, Xu J, Ma X. Yang J, et al. Mitochondrion. 2009 Jul;9(4):273-8. doi: 10.1016/j.mito.2009.04.003. Epub 2009 Apr 24. Mitochondrion. 2009. PMID: 19394449

5

Confirmation of the mitochondrial ND1 gene mutation G3635A as a primary LHON mutation.

Yang J, Zhu Y, Tong Y, Chen L, Liu L, Zhang Z, Wang X, Huang D, Qiu W, Zhuang S, Ma X. Yang J, et al. Biochem Biophys Res Commun. 2009 Aug 14;386(1):50-4. doi: 10.1016/j.bbrc.2009.05.127. Epub 2009 Jun 2. Biochem Biophys Res Commun. 2009. PMID: 19497304

6

Novel A14841G mutation is associated with high penetrance of LHON/C4171A family.

Yang J, Zhu Y, Chen L, Zhang H, Tong Y, Huang D, Zhang Z, Chen S, Han X, Ma X. Yang J, et al. Biochem Biophys Res Commun. 2009 Sep 4;386(4):693-6. doi: 10.1016/j.bbrc.2009.06.102. Epub 2009 Jun 23. Biochem Biophys Res Commun. 2009. PMID: 19555656

7

Analysis of TGFBI gene mutations in Chinese patients with corneal dystrophies and review of the literature.

Yang J, Han X, Huang D, Yu L, Zhu Y, Tong Y, Zhu B, Li C, Weng M, Ma X. Yang J, et al. Mol Vis. 2010 Jun 30;16:1186-93. Mol Vis. 2010. PMID: 20664689 Free PMC article. Review.

8

Identifcation of a novel mutation p.I240T in the FRMD7 gene in a family with congenital nystagmus.

Zhu Y, Zhuang J, Ge X, Zhang X, Wang Z, Sun J, Yang J, Gu F. Zhu Y, et al. Among authors: yang j. Sci Rep. 2013 Oct 30;3:3084. doi: 10.1038/srep03084. Sci Rep. 2013. PMID: 24169426 Free PMC article.

9

A novel de novo duplication mutation of PAX6 in a Chinese family with aniridia and other ocular abnormalities.

Zhuang J, Chen X, Tan Z, Zhu Y, Zhao K, Yang J. Zhuang J, et al. Among authors: yang j. Sci Rep. 2014 May 2;4:4836. doi: 10.1038/srep04836. Sci Rep. 2014. PMID: 24787241 Free PMC article.

10

A recurrent G367R mutation in MYOC associated with juvenile open angle glaucoma in a large Chinese family.

Yao YH, Wang YQ, Fang WF, Zhang L, Yang JH, Zhu YH. Yao YH, et al. Int J Ophthalmol. 2018 Mar 18;11(3):369-374. doi: 10.18240/ijo.2018.03.04. eCollection 2018. Int J Ophthalmol. 2018. PMID: 29600168 Free PMC article.

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