Tong Y - Search Results

1

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. Among authors: tong y. 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

2

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. Among authors: tong y. Mitochondrion. 2009 Jul;9(4):273-8. doi: 10.1016/j.mito.2009.04.003. Epub 2009 Apr 24. Mitochondrion. 2009. PMID: 19394449

3

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. Among authors: tong y. 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

4

[Rapid genetic screening of Leber's hereditary optic neuropathy with mtDNA G11778A mutation by AS-PCR with whole blood].

Yang JH, Tong Y, Li BH, Chen YK. Yang JH, et al. Among authors: tong y. Zhonghua Yan Ke Za Zhi. 2005 Mar;41(3):243-5. Zhonghua Yan Ke Za Zhi. 2005. PMID: 15840367 Chinese.

5

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. Among authors: tong y. Mol Vis. 2008 Apr 18;14:727-31. Mol Vis. 2008. PMID: 18432316 Free PMC article.

6

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. Among authors: tong y. Mol Vis. 2010 Jun 30;16:1186-93. Mol Vis. 2010. PMID: 20664689 Free PMC article. Review.

7

Mutation screening of crystallin genes in Chinese families with congenital cataracts.

Zhuang J, Cao Z, Zhu Y, Liu L, Tong Y, Chen X, Wang Y, Lu C, Ma X, Yang J. Zhuang J, et al. Among authors: tong y. Mol Vis. 2019 Aug 9;25:427-437. eCollection 2019. Mol Vis. 2019. PMID: 31523120 Free PMC article.

8

[Leber's hereditary optic neuropathy and limbs abnormity claudication may be associated with the mitochondrial ND1 T3866C mutation].

Liu Y, Zhuang SL, Tong Y, Qu J, Zhou XT, Zhao FX, Zhang JJ, Zhang YM, Zhang Y, Guan MX. Liu Y, et al. Among authors: tong y. Yi Chuan. 2010 Feb;32(2):141-7. doi: 10.3724/sp.j.1005.2010.00141. Yi Chuan. 2010. PMID: 20176558 Chinese.

9

Novel mutations in HSF4 cause congenital cataracts in Chinese families.

Cao Z, Zhu Y, Liu L, Wu S, Liu B, Zhuang J, Tong Y, Chen X, Xie Y, Nie K, Lu C, Ma X, Yang J. Cao Z, et al. Among authors: tong y. BMC Med Genet. 2018 Aug 24;19(1):150. doi: 10.1186/s12881-018-0636-3. BMC Med Genet. 2018. PMID: 30143024 Free PMC article.

10

Leber's hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation.

Liang M, Guan M, Zhao F, Zhou X, Yuan M, Tong Y, Yang L, Wei QP, Sun YH, Lu F, Qu J, Guan MX. Liang M, et al. Among authors: tong y. Biochem Biophys Res Commun. 2009 Jun 5;383(3):286-92. doi: 10.1016/j.bbrc.2009.03.097. Epub 2009 Mar 24. Biochem Biophys Res Commun. 2009. PMID: 19324017 Free PMC article.

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