Works matching AU Guo, Xiangming

Results: 41

Numerical modeling of electromagnetic wave propagation in spatially-varying evaporation duct conditions via 3D parabolic equation method.

Published in:

Frontiers in Marine Science, 2025, p. 1, doi. 10.3389/fmars.2025.1611884

By:

Ji, Hanjie;
Guo, Lixin;
Zhang, Yan;
Nie, Tianhang;
Wei, Yiwen;
Zhang, Jinpeng;
Li, Qingliang;
Guo, Xiangming;
Zhang, Yusheng

Publication type:

Article

Molecular characterization of six Chinese families with m.3460G>A and Leber hereditary optic neuropathy.

Published in:

Neurogenetics, 2010, v. 11, n. 3, p. 349, doi. 10.1007/s10048-010-0236-7

By:

Yu, Dandan;
Jia, Xiaoyun;
Zhang, A-Mei;
Guo, Xiangming;
Zhang, Ya-Ping;
Zhang, Qingjiong;
Yao, Yong-Gang

Publication type:

Article

Flexible epoxy composite coatings modified by reactive rubber with improvements in water and corrosive resistances.

Published in:

Journal of Polymer Engineering, 2020, v. 40, n. 1, p. 57, doi. 10.1515/polyeng-2019-0276

By:

Wang, Jinwei;
Guo, Xiangming;
Wu, Di

Publication type:

Article

Screening for CRX gene mutations in Chinese patients with Lebercongenital amaurosis and mutational phenotype.

Published in:

Ophthalmic Genetics, 2001, v. 22, n. 2, p. 89, doi. 10.1076/opge.22.2.89.2227

By:

Zhang, Qingjiong;
Li, Shiqiang;
Guo, Xiangming;
Guo, Li;
Xiao, Xueshan;
Jia, Xiaoyun;
Kuang, Zhihe

Publication type:

Article

Evaporation Duct Anomalies Caused by Mesoscale Eddies in the Kuroshio Extension.

Published in:

Geophysical Research Letters, 2024, v. 51, n. 12, p. 1, doi. 10.1029/2024GL108404

By:

Gao, Yuan;
Zhang, Yongchui;
Zhao, Xiaofeng;
Shi, Yang;
Guo, Xiangming;
Wang, Bo

Publication type:

Article

Identification of Genetic Defects in 33 Probands with Stargardt Disease by WES-Based Bioinformatics Gene Panel Analysis.

Published in:

PLoS ONE, 2015, v. 10, n. 7, p. 1, doi. 10.1371/journal.pone.0132635

By:

Xin, Wei;
Xiao, Xueshan;
Li, Shiqiang;
Jia, Xiaoyun;
Guo, Xiangming;
Zhang, Qingjiong

Publication type:

Article

Exome Sequencing of 18 Chinese Families with Congenital Cataracts: A New Sight of the <i>NHS</i> Gene.

Published in:

PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0100455

By:

Sun, Wenmin;
Xiao, Xueshan;
Li, Shiqiang;
Guo, Xiangming;
Zhang, Qingjiong

Publication type:

Article

Exome Sequencing of 47 Chinese Families with Cone-Rod Dystrophy: Mutations in 25 Known Causative Genes.

Published in:

PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0065546

By:

Huang, Li;
Zhang, Qingyan;
Li, Shiqiang;
Guan, Liping;
Xiao, Xueshan;
Zhang, Jianguo;
Jia, Xiaoyun;
Sun, Wenmin;
Zhu, Zhihong;
Gao, Yang;
Yin, Ye;
Wang, Panfeng;
Guo, Xiangming;
Wang, Jun;
Zhang, Qingjiong

Publication type:

Article

Mitochondrial DNA Haplogroup Background Affects LHON, but Not Suspected LHON, in Chinese Patients.

Published in:

PLoS ONE, 2011, v. 6, n. 11, p. 1, doi. 10.1371/journal.pone.0027750

By:

A-Mei Zhang;
Xiaoyun Jia;
Rui Bi;
Antonio Salas;
Shiqiang Li;
Xueshan Xiao;
Panfeng Wang;
Xiangming Guo;
Qing-Peng Kong;
Qingjiong Zhang;
Yong-Gang Yao1

Publication type:

Article

Detection of Variants in 15 Genes in 87 Unrelated Chinese Patients with Leber Congenital Amaurosis.

Published in:

PLoS ONE, 2011, v. 6, n. 5, p. 1, doi. 10.1371/journal.pone.0019458

By:

Lin Li;
Xueshan Xiao;
Shiqiang Li;
Xiaoyun Jia;
Panfeng Wang;
Xiangming Guo;
Xiaodong Jiao;
Qingjiong Zhang;
Hejtmancik, J. Fielding

Publication type:

Article

Confirmation and refinement of an autosomal dominant congenital motor nystagmus locus in chromosome 1q31.3-q32.1.

Published in:

Journal of Human Genetics, 2012, v. 57, n. 12, p. 756, doi. 10.1038/jhg.2012.103

By:

Li, Lin;
Xiao, Xueshan;
Yi, Changxian;
Jiao, Xiaodong;
Guo, Xiangming;
Hejtmancik, James Fielding;
Zhang, Qingjiong

Publication type:

Article

Confirmation of a genetic locus for X-linked recessive high myopia outside MYP1.

Published in:

Journal of Human Genetics, 2007, v. 52, n. 5, p. 469, doi. 10.1007/s10038-007-0130-9

By:

Qingjiong Zhang;
Shiqiang Li;
Xueshan Xiao;
Xiaoyun Jia;
Xiangming Guo

Publication type:

Article

Cataracts, ataxia, short stature, and mental retardation in a Chinese family mapped to Xpter-q13.1.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 8, p. 695, doi. 10.1007/s10038-006-0009-1

By:

Xiangming Guo;
Huangxuan Shen;
Xueshan Xiao;
Qilin Dai;
Shiqiang Li;
Xiaoyun Jia;
Hejtmancik, J.;
Qingjiong Zhang

Publication type:

Article

Molecular epidemiology of mtDNA mutations in 903 Chinese families suspected with Leber hereditary optic neuropathy.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 10, p. 851, doi. 10.1007/s10038-006-0032-2

By:

Xiaoyun Jia;
Shiqiang Li;
Xueshan Xiao;
Xiangming Guo;
Qingjiong Zhang

Publication type:

Article

CSNB1 in Chinese families associated with novel mutations in NYX.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 7, p. 634, doi. 10.1007/s10038-006-0406-5

By:

Xueshan Xiao;
Xiaoyun Jia;
Xiangming Guo;
Shiqiang Li;
Zhikuan Yang;
Qingjiong Zhang

Publication type:

Article

Linkage analysis of two families with X-linked recessive congenital motor nystagmus.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 1, p. 76, doi. 10.1007/s10038-005-0316-y

By:

Xiangming Guo;
Shiqiang Li;
Xiaoyun Jia;
Xueshan Xiao;
Panfeng Wang;
Qingjiong Zhang

Publication type:

Article

Mutation analysis of the genes associated with anterior segment dysgenesis, microcornea and microphthalmia in 257 patients with glaucoma.

Published in:

International Journal of Molecular Medicine, 2015, v. 36, n. 4, p. 1111, doi. 10.3892/ijmm.2015.2325

By:

XIAOBO HUANG;
XUESHAN XIAO;
XIAOYUN JIA;
SHIQIANG LI;
MIAOLING LI;
XIANGMING GUO;
XING LIU;
QINGJIONG ZHANG

Publication type:

Article

Exome sequencing reveals CHM mutations in six families with atypical choroideremia initially diagnosed as retinitis pigmentosa.

Published in:

International Journal of Molecular Medicine, 2014, v. 34, n. 2, p. 573, doi. 10.3892/ijmm.2014.1797

By:

SHIQIANG LI;
LIPING GUAN;
SHAOHUA FANG;
HUI JIANG;
XUESHAN XIAO;
JIANHUA YANG;
PANFENG WANG;
YE YIN;
XIANGMING GUO;
JUN WANG;
JIANGUO ZHANG;
QINGJIONG ZHANG

Publication type:

Article

Detection of CRB1 mutations in families with retinal dystrophy through phenotype-oriented mutational screening.

Published in:

International Journal of Molecular Medicine, 2014, v. 33, n. 4, p. 913, doi. 10.3892/ijmm.2014.1655

By:

SHIQIANG LI;
TAO SHEN;
XUESHAN XIAO;
XIANGMING GUO;
QINGJIONG ZHANG

Publication type:

Article

Mutation survey and genotype-phenotype analysis of COL2A1 and COL11A1 genes in 16 Chinese patients with Stickler syndrome.

Published in:

Molecular Vision, 2016, v. 22, p. 1

By:

Xun Wang;
Xiaoyun Jia;
Xueshan Xiao;
Shiqiang Li;
Jie Li;
Yadi Li;
Yantao Wei;
Xiaoling Liang;
Xiangming Guo

Publication type:

Article

Xlinked-heterozygous mutations in ARR3 cause female-limited early onset high myopia.

Published in:

Molecular Vision, 2016, v. 22, p. 1

By:

Xueshan Xiao;
Shiqiang Li;
Xiaoyun Jia;
Xiangming Guo;
Qingjiong Zhang

Publication type:

Article

Exome sequencing identified null mutations in LOXL3 associated with early-onset high myopia.

Published in:

Molecular Vision, 2016, v. 22, p. 1

By:

Jiali Li;
Bei Gao;
Xueshan Xiao;
Shiqiang Li;
Xiaoyun Jia;
Wenmin Sun;
Xiangming Guo;
Qingjiong Zhang

Publication type:

Article

Genetic and Clinical Analyses of DOA and LHON in 304 Chinese Patients with Suspected Childhood-Onset Hereditary Optic Neuropathy.

Published in:

PLoS ONE, 2017, v. 12, n. 1, p. 1, doi. 10.1371/journal.pone.0170090

By:

Li, Yadi;
Li, Jie;
Jia, Xiaoyun;
Xiao, Xueshan;
Li, Shiqiang;
Guo, Xiangming

Publication type:

Article

Further evidence of autosomal-dominant Leber congenital amaurosis caused by heterozygous CRX mutation.

Published in:

Graefe's Archive of Clinical & Experimental Ophthalmology, 2007, v. 245, n. 9, p. 1401, doi. 10.1007/s00417-007-0554-0

By:

Panfeng Wang;
Xiangming Guo

Publication type:

Article

Novel PITX2 Mutations including a Mutation Causing an Unusual Ophthalmic Phenotype of Axenfeld-Rieger Syndrome.

Published in:

Journal of Ophthalmology, 2019, p. 1, doi. 10.1155/2019/5642126

By:

Huang, Liqin;
Meng, Yong;
Guo, Xiangming

Publication type:

Article

Identification of CNGA3 Mutations in 46 Families: Common Cause of Achromatopsia and Cone-Rod Dystrophies in Chinese Patients.

Published in:

2014

By:

Li, Shiqiang;
Huang, Li;
Xiao, Xueshan;
Jia, Xiaoyun;
Guo, Xiangming;
Zhang, Qingjiong

Publication type:

Journal Article

Identification of CNGA3 Mutations in 46 Families.

Published in:

JAMA Ophthalmology, 2014, v. 132, n. 9, p. 1076, doi. 10.1001/jamaophthalmol.2014.1032

By:

Shiqiang Li;
Li Huang;
Xueshan Xiao;
Xiaoyun Jia;
Xiangming Guo;
Qingjiong Zhang

Publication type:

Article

Novel mutations of FRMD7 in Chinese patients with congenital motor nystagmus.

Published in:

Molecular Medicine Reports, 2017, v. 16, n. 2, p. 1753, doi. 10.3892/mmr.2017.6824

By:

XIUHUA JIA;
XIANG ZHU;
QIGEN LI;
XIAOYUN JIA;
SHIQIANG LI;
XIANGMING GUO

Publication type:

Article

GPR143 mutations in Chinese patients with ocular albinism type 1.

Published in:

Molecular Medicine Reports, 2017, v. 15, n. 5, p. 3069, doi. 10.3892/mmr.2017.6366

By:

XIUHUA JIA;
JIN YUAN;
XIAOYUN JIA;
SHIQI LING;
SHIQIANG LI;
XIANGMING GUO

Publication type:

Article

RGR variants in different forms of retinal diseases: The undetermined role of truncation mutations.

Published in:

Molecular Medicine Reports, 2016, v. 14, n. 5, p. 4811, doi. 10.3892/mmr.2016.5847

By:

JIALI LI;
XUESHAN XIAO;
SHIQIANG LI;
XIAOYUN JIA;
XIANGMING GUO;
QINGJIONG ZHANG

Publication type:

Article

Mutation analysis of Leber congenital amaurosis-associated genes in patients with retinitis pigmentosa.

Published in:

Molecular Medicine Reports, 2015, v. 11, n. 3, p. 1827, doi. 10.3892/mmr.2014.2894

By:

TAO SHEN;
LIPING GUAN;
SHIQIANG LI;
JIANGUO ZHANG;
XUESHAN XIAO;
HUI JIANG;
JIANHUA YANG;
XIANGMING GUO;
JUN WANG;
QINGJIONG ZHANG

Publication type:

Article

Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome.

Published in:

Current Eye Research, 2018, v. 43, n. 11, p. 1334, doi. 10.1080/02713683.2018.1493129

By:

Wang, Xun;
Liu, Xing;
Huang, Liqin;
Fang, Shaohua;
Jia, Xiaoyun;
Xiao, Xueshan;
Li, Shiqiang;
Guo, Xiangming

Publication type:

Article

Screening for NDP Mutations in 44 Unrelated Patients with Familial Exudative Vitreoretinopathy or Norrie Disease.

Published in:

Current Eye Research, 2012, v. 37, n. 8, p. 726, doi. 10.3109/02713683.2012.675615

By:

Yang, Huiqin;
Li, Shiqiang;
Xiao, Xueshan;
Guo, Xiangming;
Zhang, Qingjiong

Publication type:

Article

Mutations in RPGR and RP2 of Chinese Patients with X-Linked Retinitis Pigmentosa.

Published in:

Current Eye Research, 2010, v. 35, n. 1, p. 73, doi. 10.3109/02713680903395299

By:

Ji, Yanli;
Wang, Juan;
Xiao, Xueshan;
Li, Shiqiang;
Guo, Xiangming;
Zhang, Qingjiong

Publication type:

Article

Identification of Novel Mutations in the XLRS1 Gene in Chinese Patients with X-linked Juvenile Retinoschisis.

Published in:

Current Eye Research, 2007, v. 32, n. 7/8, p. 685, doi. 10.1080/02713680701486410

By:

Zeng, Meizhen;
Yi, Changxian;
Guo, Xiangming;
Jia, Xiaoyun;
Deng, Yan;
Wang, Juan;
Shen, Huangxuan

Publication type:

Article

Effects of Mechanical Stress on the Life and Insulation Performance of DC-Link Capacitors.

Published in:

Energies (19961073), 2024, v. 17, n. 3, p. 699, doi. 10.3390/en17030699

By:

Sun, Xiaowu;
Qiao, Ying;
Li, Yinda;
Guo, Xiangming;
Cao, Chongfeng

Publication type:

Article

Researching on the Deterministic Channel Models for Urban Microcells Considering Diffraction Effects.

Published in:

Energies (19961073), 2021, v. 14, n. 8, p. 2143, doi. 10.3390/en14082143

By:

Hou, Chunzhi;
Wu, Zhensen;
Wu, Jiaji;
Cao, Yunhua;
Lin, Leke;
Guo, Xiangming;
Lu, Changsheng;
Chehri, Abdellah;
Jeon, Gwanggil

Publication type:

Article

Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing.

Published in:

Human Genetics, 2014, v. 133, n. 10, p. 1255, doi. 10.1007/s00439-014-1460-2

By:

Xu, Yan;
Shen, Tao;
Xiao, Xueshan;
Li, Shiqiang;
Jia, Xiaoyun;
Guo, Xiangming;
Zhang, Qingjiong;
Guan, Liping;
Zhang, Jianguo;
Jiang, Hui;
Yang, Jianhua;
Yin, Ye;
Wang, Jun

Publication type:

Article

A novel locus for autosomal dominant congenital motor nystagmus mapped to 1q31-q32.2 between D1S2816 and D1S2692.

Published in:

Human Genetics, 2012, v. 131, n. 5, p. 697, doi. 10.1007/s00439-011-1113-7

By:

Xiao, Xueshan;
Li, Shiqiang;
Guo, Xiangming;
Zhang, Qingjiong

Publication type:

Article

Common variants in chromosome 4q25 are associated with myopia in Chinese adults.

Published in:

Ophthalmic & Physiological Optics, 2012, v. 32, n. 1, p. 68, doi. 10.1111/j.1475-1313.2011.00885.x

By:

Gao, Yang;
Wang, Panfeng;
Li, Shiqiang;
Xiao, Xueshan;
Jia, Xiaoyun;
Guo, Xiangming;
Zhang, Qingjiong

Publication type:

Article

EDH-STNet: An Evaporation Duct Height Spatiotemporal Prediction Model Based on Swin-Unet Integrating Multiple Environmental Information Sources.

Published in:

Remote Sensing, 2024, v. 16, n. 22, p. 4227, doi. 10.3390/rs16224227

By:

Ji, Hanjie;
Guo, Lixin;
Zhang, Jinpeng;
Wei, Yiwen;
Guo, Xiangming;
Zhang, Yusheng

Publication type:

Article