Fuxin Zhao

发表

Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families.

Jia Qu, Yi Tong, Min-Xin Guan, 2013, Mitochondrion.

Very low penetrance of Leber's hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutation.

J. Qu, Xiangtian Zhou, M. Guan, 2010, Molecular genetics and metabolism.

Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation.

W. Cai, J. Qu, Lifei Wang, 2010, Molecular genetics and metabolism.

Increased Connexin36 Phosphorylation in AII Amacrine Cell Coupling of the Mouse Myopic Retina

F. Pan, C. To, Xiangtian Zhou, 2020, Frontiers in Cellular Neuroscience.

Metagenomic Profiling of Ocular Surface Microbiome Changes in Meibomian Gland Dysfunction

Changqing Zeng, X. Tian, Chengcheng Tao, 2020, Investigative ophthalmology & visual science.

Exome sequencing reveals CCDC111 mutation associated with high myopia

Jinyu Wu, J. Qu, Xiangtian Zhou, 2013, Human Genetics.

Exome sequencing reveals CCDC111 mutation associated with high myopia

Jinyu Wu, J. Qu, Xiangtian Zhou, 2013, Human Genetics.

Conjunctival Microbiome Changes Associated With Soft Contact Lens and Orthokeratology Lens Wearing.

Changqing Zeng, N. Ajami, J. Petrosino, 2017, Investigative ophthalmology & visual science.

cAMP Level Modulates Scleral Collagen Remodeling, a Critical Step in the Development of Myopia

J. Qu, Chanyi Lu, Shufeng Liu, 2013, PloS one.

Common Postzygotic Mutational Signatures in Healthy Adult Tissues Related to Embryonic Hypoxia

Changqing Zeng, Y. Ke, H. Qu, 2021, Genom. Proteom. Bioinform..

Common postzygotic mutational signature in multiple healthy adult tissues related to embryonic hypoxia

Changqing Zeng, Y. Ke, H. Qu, 2020, bioRxiv.

The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation.

J. Qu, Xiaoling Liu, Taosheng Huang, 2016, Human molecular genetics.

Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation.

Ronghua Li, Yaping Qian, Zhihua Tao, 2010, Mitochondrion.

Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population.

Dean Y. Li, Liangdan Sun, X. Zuo, 2011, American journal of human genetics.

Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population

Changqing Zeng, Chaohua Li, Wei Chen, 2010, Molecular vision.

Scleral HIF-1α is a prominent regulatory candidate for genetic and environmental interactions in human myopia pathogenesis

Changqing Zeng, M. He, Lulin Huang, 2020, EBioMedicine.

Experimental murine myopia induces collagen type Iα1 (COL1A1) DNA methylation and altered COL1A1 messenger RNA expression in sclera

J. Qu, Xiangtian Zhou, Fuxin Zhao, 2012, Molecular vision.

Prevalence of Mitochondrial ND4 Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy.

J. Qu, Xiaoling Liu, Taosheng Huang, 2015, Investigative ophthalmology & visual science.

Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathy.

J. Qu, Xiaoling Liu, J. Mo, 2014, Investigative ophthalmology & visual science.

Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation.

J. Qu, F. Lu, Yu Zhang, 2010, Molecular genetics and metabolism.

Declines in PDE4B activity promote myopia progression through downregulation of scleral collagen expression.

Changqing Zeng, J. Qu, P. Reinach, 2021, Experimental eye research.

A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population.

Liangdan Sun, X. Zuo, Xuejun Zhang, 2013, Human molecular genetics.

PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathy.

Taosheng Huang, Xiangtian Zhou, Cheng Ai, 2020, The Journal of clinical investigation.

Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families.

W. Cai, Yan Wang, J. Qu, 2010, Biochemical and biophysical research communications.

Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation.

J. Qu, Xiaoling Liu, Xiangtian Zhou, 2010, Biochimica et biophysica acta.

Leber's hereditary optic neuropathy affects only female matrilineal relatives in two Chinese families.

J. Qu, Ying Wang, Xiangtian Zhou, 2010, Investigative ophthalmology & visual science.

Dysfunction of VIPR2 leads to myopia in humans and mice

Changqing Zeng, M. He, Zhenglin Yang, 2020, Journal of Medical Genetics.

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

J. Qu, F. Lu, Xiangtian Zhou, 2009, Biochemical and biophysical research communications.

Leber's hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation.

J. Qu, Yan Liu, M. Liang, 2009, Biochemical and biophysical research communications.

Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation.

J. Qu, Xiangtian Zhou, M. Guan, 2009, Ophthalmology.

Leber's hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families.

J. Qu, F. Lu, Yaping Qian, 2006, Biochemical and biophysical research communications.

Genetic Interaction between Mfrp and Adipor1 Mutations Affect Retinal Disease Phenotypes

J. Naggert, G. Carter, Navdeep Gogna, 2021, International journal of molecular sciences.

Leber's hereditary optic neuropathy is associated with the T3866C mutation in mitochondrial ND1 gene in three Han Chinese Families.

J. Qu, Yaping Qian, J. Mo, 2012, Investigative ophthalmology & visual science.

PDE4B Proposed as a High Myopia Susceptibility Gene in Chinese Population

Changqing Zeng, S. Juo, Zhenglin Yang, 2022, Frontiers in Genetics.

Abnormal morphology and function in retinal ganglion cells derived from patients-specific iPSCs generated from individuals with Leber’s hereditary optic neuropathy

Xiangtian Zhou, M. Guan, Yanchun Ji, 2022, Human molecular genetics.

Mitochondrial haplogroup D4j specific variant m.11696G > a(MT-ND4) may increase the penetrance and expressivity of the LHON-associated m.11778G > a mutation in Chinese pedigrees

Xiaoling Liu, Xiangtian Zhou, M. Guan, 2017, Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis.

Mitochondrial ND1 Variants in 1281 Chinese Subjects With Leber's Hereditary Optic Neuropathy.

Xiaoling Liu, M. Guan, Y. Tong, 2016, Investigative ophthalmology & visual science.

[The analysis of mitochondrial DNA haplogroups and variants for Leber's hereditary optic neuropathy in Chinese families carrying the m.14484T >C mutation].

J. Qu, Xiaoling Liu, M. Guan, 2014, Yi chuan = Hereditas.

Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation in Chinese families

Xiaoling Liu, J. Mo, M. Guan, 2014, Journal of Human Genetics.

Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese families.

J. Qu, Xiangtian Zhou, Ying-zi Li, 2011, Ophthalmology.

Mitochondrial ND 1 Variants in 1281 Chinese Subjects With Leber ’ s Hereditary Optic Neuropathy

Xiaoling Liu, M. Guan, Y. Tong, 2016 .

Leber's hereditary optic neuropathy is associated with the T14502C mutation in mitochondrial ND6 gene in three Han Chinese families

J. Qu, Yaping Qian, J. Mo, 2012 .

[The mitochondrial ND5 T12338C mutation may be associated with Leber's hereditary optic neuropathy in two Chinese families].

J. Qu, Xiangtian Zhou, Xiao-ling Liu, 2011, Yi chuan = Hereditas.

[Leber's hereditary optic neuropathy may be associated with the mitochondrial tRNAGlu A14693G mutation in three Chinese families].

J. Qu, Yan Liu, Xiangtian Zhou, 2010, Yi chuan = Hereditas.

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

J. Qu, Yan Liu, Xiangtian Zhou, 2010, Yi chuan = Hereditas.

The mitochondrial tRNAGlu A14693G mutation may influence the phenotypic manifestation of ND1 G3460A mutation in a Chinese family with Leber’s hereditary optic neuropathy

Li Yang, W. Cai, J. Qu, 2007 .

Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family.

J. Qu, F. Lu, Ronghua Li, 2007, Mitochondrion.

Form-deprivation myopia downregulates calcium levels in retinal horizontal cells in mice.

J. Qu, Yuhan Wang, P. Reinach, 2022, Experimental eye research.

Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population.

Liangdan Sun, X. Zuo, Peiquan Zhao, 2011, American journal of human genetics.