Yi Tong - Publications

Affiliations: 
Beijing Normal University, Beijing, Beijing Shi, China 
Area:
Visual system, fMRI

87 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Lian X, Shen X, Lu L, He N, Wan X, Samanta S, Tong Y. Resistance Switching Statistics and Mechanisms of Pt Dispersed Silicon Oxide-Based Memristors. Micromachines. 10. PMID 31159392 DOI: 10.3390/mi10060369  0.56
2018 Ji Y, Zhang J, Yu J, Wang Y, Lu Y, Liang M, Li Q, Jin X, Wei Y, Meng F, Gao Y, Cang X, Tong Y, Liu X, Zhang M, et al. Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy. Human Molecular Genetics. PMID 30597069 DOI: 10.1093/hmg/ddy450  0.64
2018 Li HM, Tong Y, Xia X, Huang J, Song PW, Zhang RJ, Shen CL. Bone Mesenchymal Stem Cell-Conditioned Medium Regulates the Differentiation of Neural Stem Cells Via Notch Pathway Activation. Cellular Reprogramming. PMID 30589560 DOI: 10.1089/cell.2018.0042  0.6
2018 Zhu J, Li Y, Wang J, Yu Z, Liu Y, Tong Y, Han W. Adaptive Steered Molecular Dynamics Combined With Protein Structure Networks Revealing the Mechanism of Y68I/G109P Mutations That Enhance the Catalytic Activity of D-psicose 3-Epimerase From . Frontiers in Chemistry. 6: 437. PMID 30320068 DOI: 10.3389/fchem.2018.00437  0.52
2018 Tong Y, Jiao Q, Liu Y, Lv J, Wang R, Zhu L. Maprotiline Prevents Monocrotaline-Induced Pulmonary Arterial Hypertension in Rats. Frontiers in Pharmacology. 9: 1032. PMID 30298002 DOI: 10.3389/fphar.2018.01032  0.52
2018 Shen X, Wang J, Zhang Y, Wang X, Ding Z, Li Y, Chen B, Tong Y. [Research progress of D-psicose: function and its biosynthesis]. Sheng Wu Gong Cheng Xue Bao = Chinese Journal of Biotechnology. 34: 1419-1431. PMID 30255676 DOI: 10.13345/j.cjb.170526  0.64
2018 Tian D, Xiao Y, Tong Y, Fu N, Liu Q, Li C. Diversity and conservation of Chinese wild begonias. Plant Diversity. 40: 75-90. PMID 30175289 DOI: 10.1016/j.pld.2018.06.002  0.4
2018 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. Novel mutations in HSF4 cause congenital cataracts in Chinese families. Bmc Medical Genetics. 19: 150. PMID 30143024 DOI: 10.1186/s12881-018-0636-3  0.68
2018 Yang B, Li H, Ruan Q, Tong Y, Liu Z, Xuan S, Jin J, Zhao Z. Rapid profiling and pharmacokinetic studies of multiple potential bioactive triterpenoids in rat plasma using UPLC/Q-TOF-MS/MS after oral administration of Ilicis Rotundae Cortex extract. Fitoterapia. PMID 29981874 DOI: 10.1016/j.fitote.2018.07.005  0.44
2018 Hao Y, Lyu J, Qu R, Tong Y, Sun D, Feng F, Tong L, Yang T, Zhao Z, Zhu L, Ding J, Xu Y, Xie H, Li H. Design, Synthesis, and Biological Evaluation of Pyrimido[4,5- d]pyrimidine-2,4(1 H,3 H)-diones as Potent and Selective Epidermal Growth Factor Receptor (EGFR) Inhibitors against L858R/T790M Resistance Mutation. Journal of Medicinal Chemistry. PMID 29906114 DOI: 10.1021/acs.jmedchem.8b00346  0.52
2018 Tong YF, Zhang NN, Zhang XR, Zhang QF. [Discussion on the micro-plastic operative treatment of nasal-septum deviation combined with crooked nose]. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology, Head, and Neck Surgery. 32: 462-464. PMID 29737745 DOI: 10.13201/j.issn.1001-1781.2018.06.015  0.6
2017 Hu X, Wang D, Tong Y, Tong L, Wang X, Zhu L, Xie H, Li S, Yang Y, Xu Y. Design, Synthesis, and Evaluation of Ribose-Modified Anilinopyrimidine Derivatives as EGFR Tyrosine Kinase Inhibitors. Frontiers in Chemistry. 5: 101. PMID 29250520 DOI: 10.3389/fchem.2017.00101  0.52
2017 Zhang S, Tong YX, Xu XS, Lin H, Chao TF. Prognostic significance of SATB1 in gastrointestinal cancer: a meta-analysis and literature review. Oncotarget. PMID 28430598 DOI: 10.18632/oncotarget.16867  0.48
2017 Wang C, He W, Tong Y, Zhang Y, Huang K, Song L, Zhong S, Ganeshkumar R, Zhao R. Memristive Devices with Highly Repeatable Analog States Boosted by Graphene Quantum Dots. Small (Weinheim An Der Bergstrasse, Germany). PMID 28296020 DOI: 10.1002/smll.201603435  0.64
2017 Lai CC, Wang KY, Chen R, Zhang AJ, Gu HJ, Yin YB, Wang DD, Liu LL, Xing L, Tong YG, Ma ZJ, Yang PH, Wang XL. Characterization of Highly Pathogenic Avian Influenza H5N1 Viruses Isolated from Domestic Poultry in China. Biomedical and Environmental Sciences : Bes. 30: 68-74. PMID 28245902 DOI: 10.3967/bes2017.009  0.48
2016 Tong Y, Luo X, Wu G, Shi W. [COMPARATIVE STUDY ON FIXATION WITH PERCUTANEOUS CANNULATED SCREWS ASSISTED BY ROBOT NAVIGATION AND CONVENTIONAL SURGERY WITH MANUAL POSITIONING FOR FEMORAL NECK FRACTURES]. Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi = Zhongguo Xiufu Chongjian Waike Zazhi = Chinese Journal of Reparative and Reconstructive Surgery. 30: 685-689. PMID 29786276 DOI: 10.7507/1002-1892.20160139  0.48
2016 Li Y, Tong Y, Xing F. DNA Barcoding Evaluation and Its Taxonomic Implications in the Recently Evolved Genus Oberonia Lindl. (Orchidaceae) in China. Frontiers in Plant Science. 7: 1791. PMID 27994608 DOI: 10.3389/fpls.2016.01791  0.52
2016 Zhang J, Zhang Z, Fu R, Ji Y, Jiang P, Tong Y, Qu J, Guan M. [The role of MT-ND1 m.3635G>A mutation in Leber's hereditary optic neuropathy]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 33: 747-751. PMID 27984598 DOI: 10.3760/cma.j.issn.1003-9406.2016.06.001  0.64
2016 Cai XB, Huang XF, Tong Y, Lu QK, Jin ZB. Novel CHM mutations identified in Chinese families with Choroideremia. Scientific Reports. 6: 35360. PMID 27739455 DOI: 10.1038/srep35360  0.36
2016 Pan Y, Zhao G, Cai Z, Chen F, Xu D, Huang S, Lan H, Tong Y. Synergistic Effect of Ferulic Acid and Z-Ligustilide, Major Components of A. sinensis, on Regulating Cold-Sensing Protein TRPM8 and TPRA1 In Vitro. Evidence-Based Complementary and Alternative Medicine : Ecam. 2016: 3160247. PMID 27413384 DOI: 10.1155/2016/3160247  0.52
2016 Hao Y, Wang X, Zhang T, Sun D, Tong Y, Xu Y, Chen H, Tong L, Zhu L, Zhao Z, Chen Z, Ding J, Xie H, Xu Y, Li H. Discovery and Structural Optimization of N5-Substituted 6,7-dioxo-6,7-dihydropteridines as Potent and Selective Epidermal Growth Factor Receptor (EGFR) Inhibitors Against L858R/T790M Resistance Mutation. Journal of Medicinal Chemistry. PMID 27396610 DOI: 10.1021/acs.jmedchem.6b00403  0.52
2016 Han X, Hou J, Xie J, Yin J, Tong Y, Lu C, Möhwald H. Synergism of Dewetting and Self-Wrinkling to Create Two-Dimensional Ordered Arrays of Functional Microspheres. Acs Applied Materials & Interfaces. PMID 27300307 DOI: 10.1021/acsami.6b03036  0.44
2016 Pan Y, Huang S, Cai Z, Lan H, Tong Y, Yu X, Zhao G, Chen F. TRPA1 and TRPM8 receptors may promote local vasodilation that aggravates oxaliplatin-induced peripheral neuropathy amenable to 17β-estradiol treatment. Current Neurovascular Research. PMID 27262300  0.52
2016 Wang C, He W, Tong Y, Zhao R. Investigation and Manipulation of Different Analog Behaviors of Memristor as Electronic Synapse for Neuromorphic Applications. Scientific Reports. 6: 22970. PMID 26971394 DOI: 10.1038/srep22970  0.32
2015 Yang J, Huang XF, Tong Y, Jin ZB. Targeted exome sequencing identified two novel truncation mutations in GPR98 causing Usher syndrome. Clinical & Experimental Ophthalmology. PMID 26432996 DOI: 10.1111/ceo.12664  0.36
2015 Qin J, Zhou Q, Xie W, Xu Y, Yu S, Liu Z, Tong YT, Dong Y, Hu W. Coherence enhancement of a chirped DFB laser for frequency-modulated continuous-wave reflectometry using a composite feedback loop. Optics Letters. 40: 4500-4503. PMID 26421566  0.44
2015 Gao M, Zhang S, Zhang Z, Zhao F, Zhang J, Liang M, Liu X, Wei Q, Tong Y, Qu J, Guan M. [A novel mutation T8821G in mitochondrial DNA may be associated with Leber's hereditary optic neuropathy]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 32: 485-9. PMID 26252090 DOI: 10.3760/cma.j.issn.1003-9406.2015.04.007  0.68
2015 Jiang P, Liang M, Zhang J, Gao Y, He Z, Yu H, Zhao F, Ji Y, Liu X, Zhang M, Fu Q, Tong Y, Sun Y, Zhou X, Huang T, et al. Prevalence of Mitochondrial ND4 Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy. Investigative Ophthalmology & Visual Science. 56: 4778-88. PMID 26218905 DOI: 10.1167/iovs.14-16158  0.68
2015 Xu Q, Chen Y, Zhao WM, Huang ZY, Duan XJ, Tong YY, Zhang Y, Li X, Chang GB, Chen GH. The CD8α gene in duck (Anatidae): cloning, characterization, and expression during viral infection. Molecular Biology Reports. 42: 431-9. PMID 25332128 DOI: 10.1007/s11033-014-3784-3  0.68
2014 Zhang J, Jiang P, Jin X, Liu X, Zhang M, Xie S, Gao M, Zhang S, Sun YH, Zhu J, Ji Y, Wei QP, Tong Y, Guan MX. Leber's hereditary optic neuropathy caused by the homoplasmic ND1 m.3635G>A mutation in nine Han Chinese families. Mitochondrion. 18: 18-26. PMID 25194554 DOI: 10.1016/j.mito.2014.08.008  0.64
2014 Xu Q, Chen Y, Zhang Y, Tong YY, Huang ZY, Zhao WM, Duan XJ, Li X, Chang GB, Chen GH. Molecular cloning and expression analysis of ferritin, heavy polypeptide 1 gene from duck (Anas platyrhynchos). Molecular Biology Reports. 41: 6233-40. PMID 24981929 DOI: 10.1007/s11033-014-3503-0  0.68
2014 Meng X, Zhu J, Gao M, Zhang S, Zhao F, Zhang J, Liu X, Wei Q, Tong Y, Zhang M, Qu J, Guan M. [The analysis of mitochondrial DNA haplogroups and variants for Leber's hereditary optic neuropathy in Chinese families carrying the m.14484T >C mutation]. Yi Chuan = Hereditas / Zhongguo Yi Chuan Xue Hui Bian Ji. 36: 336-45. PMID 24846978  0.68
2014 Zhang X, Ge X, Shi W, Huang P, Min Q, Li M, Yu X, Wu Y, Zhao G, Tong Y, Jin ZB, Qu J, Gu F. Molecular diagnosis of putative Stargardt disease by capture next generation sequencing. Plos One. 9: e95528. PMID 24763286 DOI: 10.1371/journal.pone.0095528  0.52
2014 Xing DJ, Zhang HX, Huang N, Wu KC, Huang XF, Huang F, Tong Y, Pang CP, Qu J, Jin ZB. Comprehensive molecular diagnosis of Bardet-Biedl syndrome by high-throughput targeted exome sequencing. Plos One. 9: e90599. PMID 24608809 DOI: 10.1371/journal.pone.0090599  0.64
2014 Wang J, He C, Hsi JH, Xu X, Liu Y, He J, Ling H, Ding P, Tong Y, Zou X, Zhou Q, Liao L, Wang X, Ruan Y, Shao Y, et al. Virological outcomes and drug resistance in Chinese patients after 12 months of 3TC-based first-line antiretroviral treatment, 2011-2012. Plos One. 9: e88305. PMID 24516631 DOI: 10.1371/journal.pone.0088305  0.52
2014 Xu Q, Chen Y, Zhao WM, Huang ZY, Zhang Y, Li X, Tong YY, Chang GB, Chang GB, Duan XJ, Chen GH. DNA methylation and regulation of the CD8A after duck hepatitis virus type 1 infection. Plos One. 9: e88023. PMID 24505360 DOI: 10.1371/journal.pone.0088023  0.68
2014 Ji Y, Liang M, Zhang J, Zhang M, Zhu J, Meng X, Zhang S, Gao M, Zhao F, Wei QP, Jiang P, Tong Y, Liu X, Qin Mo J, Guan MX. Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation in Chinese families. Journal of Human Genetics. 59: 134-40. PMID 24430572 DOI: 10.1038/jhg.2013.134  0.68
2014 Liang M, Jiang P, Li F, Zhang J, Ji Y, He Y, Xu M, Zhu J, Meng X, Zhao F, Tong Y, Liu X, Sun Y, Zhou X, Mo JQ, et al. Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathy. Investigative Ophthalmology & Visual Science. 55: 1321-31. PMID 24398099 DOI: 10.1167/iovs.13-13011  0.68
2014 Xu Q, Chen Y, Tong YY, Huang ZY, Zhao WM, Duan XJ, Zhang Y, Li X, Chang GB, Chen GH. Identification and expression analysis of the leukocyte cell-derived chemotaxin-2 (LECT2) gene in duck (Anas platyrhynchos). Gene. 533: 280-5. PMID 24076354 DOI: 10.1016/j.gene.2013.09.047  0.68
2013 Huang XF, Xiang P, Chen J, Xing DJ, Huang N, Min Q, Gu F, Tong Y, Pang CP, Qu J, Jin ZB. Targeted exome sequencing identified novel USH2A mutations in Usher syndrome families. Plos One. 8: e63832. PMID 23737954 DOI: 10.1371/journal.pone.0063832  0.68
2013 Zhang J, Zhao F, Fu Q, Liang M, Tong Y, Liu X, Lin B, Mi H, Zhang M, Wei QP, Xue L, Jiang P, Zhou X, Mo JQ, Huang T, et al. Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families. Mitochondrion. 13: 772-81. PMID 23665487 DOI: 10.1016/j.mito.2013.05.002  0.68
2012 Li XJ, Tong Y, Zhang SK. [The clinical outcomes of idiopathic optic neuritis with no light perception in 21 eyes]. [Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology. 48: 1060-4. PMID 23336407  0.6
2012 Liu Z, Sun CB, Tong Y, Zhang HJ, Zhao GJ, Qu J. [Measurement of retinal nerve fiber layer thickness in Leber hereditary optic neuropathy by optical coherence tomography]. [Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology. 48: 888-92. PMID 23302242  0.64
2012 Zhou X, Qian Y, Zhang J, Tong Y, Jiang P, Liang M, Dai X, Zhou H, Zhao F, Ji Y, Mo JQ, Qu J, Guan MX. Leber's hereditary optic neuropathy is associated with the T3866C mutation in mitochondrial ND1 gene in three Han Chinese Families. Investigative Ophthalmology & Visual Science. 53: 4586-94. PMID 22577081 DOI: 10.1167/iovs.11-9109  0.68
2012 Wu RQ, Qiao C, Tong Y, Ge Z, Zhang JF, Wu YJ, Qiu HR, Wang Z, Liu P. [Study of immunoglobulin and T-cell receptor gene rearrangements in patients with non-Hodgkin's lymphoma]. Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi. 33: 10-5. PMID 22575185  0.56
2012 Li XQ, Cai HC, Zhou SY, Yang JH, Xi YB, Gao XB, Zhao WJ, Li P, Zhao GY, Tong Y, Bao FC, Ma Y, Wang S, Yan YB, Lu CL, et al. A novel mutation impairing the tertiary structure and stability of γC-crystallin (CRYGC) leads to cataract formation in humans and zebrafish lens. Human Mutation. 33: 391-401. PMID 22052681 DOI: 10.1002/humu.21648  0.68
2011 Tong Y, Qiao C, Wu RQ, Liu P, Zhou X. [Detection of gene rearrangement in bone marrow of patients with non Hodgkin's lymphoma by BIOMED-2 protocols]. Zhongguo Shi Yan Xue Ye Xue Za Zhi / Zhongguo Bing Li Sheng Li Xue Hui = Journal of Experimental Hematology / Chinese Association of Pathophysiology. 19: 1409-14. PMID 22169293  0.52
2011 Zhang Y, Zhang JJ, Ji YC, Zhang ML, Tong Y, Zhao FX, Qu J, Zhou XT, Guan MX. [The mitochondrial tRNA(Thr) A15951G mutation may be associated with Leber's hereditary optic neuropathy in two Chinese families]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 28: 501-6. PMID 21983721 DOI: 10.3760/cma.j.issn.1003-9406.2011.05.006  0.68
2011 Zhang X, Zhang Q, Tong Y, Dai H, Zhao X, Bai F, Xu L, Li Y. Large novel deletions detected in Chinese families with aniridia: correlation between genotype and phenotype. Molecular Vision. 17: 548-57. PMID 21364908  0.52
2011 Shen Y, Zhou X, Wang Z, Yang G, Jiang Y, Sun C, Wang J, Tong Y, Guo H. Coagulation profiles and thromboembolic events of bortezomib plus thalidomide and dexamethasone therapy in newly diagnosed multiple myeloma. Leukemia Research. 35: 147-51. PMID 20832859 DOI: 10.1016/j.leukres.2010.08.007  0.56
2010 Zhao X, Yang C, Tong Y, Zhang X, Xu L, Li Y. Identification a novel MYOC gene mutation in a Chinese family with juvenile-onset open angle glaucoma. Molecular Vision. 16: 1728-35. PMID 20806035  0.52
2010 Zhang M, Zhou X, Li C, Zhao F, Zhang J, Yuan M, Sun YH, Wang J, Tong Y, Liang M, Yang L, Cai W, Wang L, Qu J, Guan MX. Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation. Molecular Genetics and Metabolism. 101: 192-9. PMID 20728388 DOI: 10.1016/j.ymgme.2010.07.014  0.68
2010 Zhang J, Zhou X, Zhou J, Li C, Zhao F, Wang Y, Meng Y, Wang J, Yuan M, Cai W, Tong Y, Sun YH, Yang L, Qu J, Guan MX. Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families. Biochemical and Biophysical Research Communications. 399: 647-53. PMID 20691156 DOI: 10.1016/j.bbrc.2010.07.135  0.68
2010 Yang J, Han X, Huang D, Yu L, Zhu Y, Tong Y, Zhu B, Li C, Weng M, Ma X. Analysis of TGFBI gene mutations in Chinese patients with corneal dystrophies and review of the literature. Molecular Vision. 16: 1186-93. PMID 20664689  0.68
2010 Zhou X, Zhang H, Zhao F, Ji Y, Tong Y, Zhang J, Zhang Y, Yang L, Qian Y, Lu F, Qu J, Guan MX. Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation. Molecular Genetics and Metabolism. 100: 379-84. PMID 20627642 DOI: 10.1016/j.ymgme.2010.04.013  0.68
2010 Qu J, Wang Y, Tong Y, Zhou X, Zhao F, Yang L, Zhang S, Zhang J, West CE, Guan MX. Leber's hereditary optic neuropathy affects only female matrilineal relatives in two Chinese families. Investigative Ophthalmology & Visual Science. 51: 4906-12. PMID 20435583 DOI: 10.1167/iovs.09-5027  0.52
2010 Liu Y, Zhuang SL, Tong Y, Qu J, Zhou XT, Zhao FX, Zhang JJ, Zhang YM, Zhang Y, Guan MX. [Leber's hereditary optic neuropathy and limbs abnormity claudication may be associated with the mitochondrial ND1 T3866C mutation]. Yi Chuan = Hereditas / Zhongguo Yi Chuan Xue Hui Bian Ji. 32: 141-7. PMID 20176558  0.68
2010 Tong Y, Sun YH, Zhou X, Zhao F, Mao Y, Wei QP, Yang L, Qu J, Guan MX. Very low penetrance of Leber's hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutation. Molecular Genetics and Metabolism. 99: 417-24. PMID 20053576 DOI: 10.1016/j.ymgme.2009.12.004  0.68
2010 Qu J, Zhou X, Zhao F, Liu X, Zhang M, Sun YH, Liang M, Yuan M, Liu Q, Tong Y, Wei QP, Yang L, Guan MX. Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation. Biochimica Et Biophysica Acta. 1800: 305-12. PMID 19733221 DOI: 10.1016/j.bbagen.2009.08.010  0.68
2009 Liu Z, Sun CB, Tong Y, Qu J. [Evaluation of serum levels of SOD and MDA in patients with Leber's hereditary optic neuropathy carrying the mitochondrial DNA G11778A mutation]. [Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology. 45: 719-23. PMID 20021885  0.64
2009 Zhao F, Guan M, Zhou X, Yuan M, Liang M, Liu Q, Liu Y, Zhang Y, Yang L, Tong Y, Wei QP, Sun YH, Qu J, Guan MX. Leber's hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation. Biochemical and Biophysical Research Communications. 389: 466-72. PMID 19732751 DOI: 10.1016/j.bbrc.2009.08.168  0.68
2009 Yang J, Zhu Y, Chen L, Zhang H, Tong Y, Huang D, Zhang Z, Chen S, Han X, Ma X. Novel A14841G mutation is associated with high penetrance of LHON/C4171A family. Biochemical and Biophysical Research Communications. 386: 693-6. PMID 19555656 DOI: 10.1016/j.bbrc.2009.06.102  0.68
2009 Yang J, Zhu Y, Tong Y, Chen L, Liu L, Zhang Z, Wang X, Huang D, Qiu W, Zhuang S, Ma X. Confirmation of the mitochondrial ND1 gene mutation G3635A as a primary LHON mutation. Biochemical and Biophysical Research Communications. 386: 50-4. PMID 19497304 DOI: 10.1016/j.bbrc.2009.05.127  0.68
2009 Yang J, Zhu Y, Tong Y, Zhang Z, Chen L, Chen S, Cao Z, Liu C, Xu J, Ma X. The novel G10680A mutation is associated with complete penetrance of the LHON/T14484C family. Mitochondrion. 9: 273-8. PMID 19394449 DOI: 10.1016/j.mito.2009.04.003  0.68
2009 Liang M, Guan M, Zhao F, Zhou X, Yuan M, Tong Y, Yang L, Wei QP, Sun YH, Lu F, Qu J, Guan MX. Leber's hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation. Biochemical and Biophysical Research Communications. 383: 286-92. PMID 19324017 DOI: 10.1016/j.bbrc.2009.03.097  0.68
2009 Qu J, Zhou X, Zhang J, Zhao F, Sun YH, Tong Y, Wei QP, Cai W, Yang L, West CE, Guan MX. Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation. Ophthalmology. 116: 558-564.e3. PMID 19167085 DOI: 10.1016/j.ophtha.2008.10.022  0.52
2008 Li Y, Deng T, Tong Y, Peng S, Dong B, He D. Identification of two novel OPA1 mutations in Chinese families with autosomal dominant optic atrophy. Molecular Vision. 14: 2451-7. PMID 19112530  0.52
2008 He X, Gu F, Wang Z, Wang C, Tong Y, Wang Y, Yang J, Liu W, Zhang M, Ma X. A novel frameshift mutation in FRMD7 causing X-linked idiopathic congenital nystagmus. Genetic Testing. 12: 607-13. PMID 19072571 DOI: 10.1089/gte.2008.0070  0.68
2008 Cai W, Fu Q, Zhou X, Qu J, Tong Y, Guan MX. Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation. Journal of Genetics and Genomics = Yi Chuan Xue Bao. 35: 649-55. PMID 19022198 DOI: 10.1016/S1673-8527(08)60086-7  0.68
2008 Sun DG, Yang JH, Tong Y, Zhao GJ, Ma X. [A novel PAX6 mutation (c.1286delC) in the patients with hereditary congenital aniridia.]. Yi Chuan = Hereditas / Zhongguo Yi Chuan Xue Hui Bian Ji. 30: 1301-6. PMID 18930890  0.68
2008 Tong Y, Wang Y, Jiang F, Liu B, Zhang S, Yang W. [A pedigree of Leber's hereditary optic neuropathy with mtDNA 14484 mutation]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 25: 531-3. PMID 18841565  0.6
2008 Wang JY, Gu YS, Wang J, Tong Y, Wang Y, Shao JB, Qi M. MGB probe assay for rapid detection of mtDNA11778 mutation in the Chinese LHON patients by real-time PCR. Journal of Zhejiang University. Science. B. 9: 610-5. PMID 18763310 DOI: 10.1631/jzus.B0820058  0.6
2008 Yang J, Zhu Y, Gu F, He X, Cao Z, Li X, Tong Y, Ma X. A novel nonsense mutation in CRYBB1 associated with autosomal dominant congenital cataract. Molecular Vision. 14: 727-31. PMID 18432316  0.68
2007 Zhao FX, Zhou XT, Qu J, Wei QP, Tong Y, Yang L, Lv JX, Guan MX. [Leber's hereditary optic neuropathy is associated with the mitochondrial G11696A mutation in two Chinese families]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 24: 556-9. PMID 17922426  0.68
2007 Wang Y, Tong Y, Hu SX, Wang JY, Shao JB, Zhang HX. [Analysis on the effect of secondary mutations on Leber's hereditary optic neuropathy]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 24: 397-400. PMID 17680528  0.6
2007 Tong Y, Mao Y, Zhou X, Yang L, Zhang J, Cai W, Zhao F, Wang X, Lu F, Qu J, Guan MX. The mitochondrial tRNA(Glu) A14693G mutation may influence the phenotypic manifestation of ND1 G3460A mutation in a Chinese family with Leber's hereditary optic neuropathy. Biochemical and Biophysical Research Communications. 357: 524-30. PMID 17434142 DOI: 10.1016/j.bbrc.2007.03.189  0.68
2007 Qu J, Li R, Zhou X, Tong Y, Yang L, Chen J, Zhao F, Lu C, Qian Y, Lu F, Guan MX. Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family. Mitochondrion. 7: 140-6. PMID 17300996 DOI: 10.1016/j.mito.2006.11.015  0.68
2006 Li YM, Wang JY, Chen Y, Shao JB, Wang J, Tong Y. [Detection of mtDNA*LHON G11778A mutation by real-time polymerase chain reaction using TaqMan-MGB probe technology]. [Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology. 42: 728-32. PMID 17081446  0.6
2006 Li R, Qu J, Zhou X, Tong Y, Hu Y, Qian Y, Lu F, Mo JQ, West CE, Guan MX. The mitochondrial tRNA(Thr) A15951G mutation may influence the phenotypic expression of the LHON-associated ND4 G11778A mutation in a Chinese family. Gene. 376: 79-86. PMID 16624503 DOI: 10.1016/j.gene.2006.02.014  0.52
2006 Qu J, Li R, Zhou X, Tong Y, Lu F, Qian Y, Hu Y, Mo JQ, West CE, Guan MX. The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation. Investigative Ophthalmology & Visual Science. 47: 475-83. PMID 16431939 DOI: 10.1167/iovs.05-0665  0.52
2006 Zhou X, Wei Q, Yang L, Tong Y, Zhao F, Lu C, Qian Y, Sun Y, Lu F, Qu J, Guan MX. Leber's hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families. Biochemical and Biophysical Research Communications. 340: 69-75. PMID 16364244 DOI: 10.1016/j.bbrc.2005.11.150  0.68
2005 Wang JY, Zhang HY, Li YM, Yu HN, Wang J, Shen SR, Tong Y. Study on total cell antioxidant capacity in Leber's hereditary optic neuropathy. Shi Yan Sheng Wu Xue Bao. 38: 555-8. PMID 16416974  0.6
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