Search Results - "Wang, Pei‐Guang"

Novel mutations in Chinese Han patients with tuberous sclerosis complex: Case series and review of the published work by Zheng, Li‐Yun, LEE, Yu‐Wei, Han, Yang, Tang, Li‐Li, Cheng, Yu‐Yan, Dou, Jin‐Fa, Zhou, Fu‐Sheng, Zheng, Xiao‐Dong, Wang, Hong‐Yan, Wang, Pei‐Guang, Gao, Min

“…Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disease characterized by hamartomas in multiple organ systems. This study was performed in…”
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Association of HLA-DQA1 and DQB1 alleles with keloids in Chinese Hans by Lu, Wen-Sheng, Wang, Jian-Feng, Yang, Sen, Xiao, Feng-Li, Quan, Cheng, Cheng, Hui, Wang, Pei-Guang, Zhang, An-Ping, Cai, Li-Qiong, Zhang, Xue-Jun

“…Summary Background Some studies have suggested that human HLA status might potentiate development of keloids phenotype, and exists ethnic differences. No…”
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Decreased Serum Level of Interferon-γ in Patients with Pityriasis Rosea by Zeng, Ming, Zhao, Shi-Xiang, Liu, Ling-Hua, Zuo, Xian-Bo, Zheng, Xiao-Dong, Li, Tao, Zhang, Min, Wang, Pei-Guang, Yang, Sen

“…KCI Citation Count: 3…”
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A novel U2HR non-synonymous mutation in a Chinese patient with Marie Unna Hereditary Hypotrichosis by Cai, Li-Qiong, Wang, Pei-Guang, Gao, Min, Lu, Wen-Sheng, Xu, Sheng-Xin, Fang, Qiao-Yun, Zhou, Wen-Ming, Lin, Da, Du, Wen-Hui, Zhang, Shu-Mei, Yang, Sen, Zhang, Xue-Jun

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Association of HLA class I alleles with aloplecia areata in Chinese Hans by Xiao, Feng-Li, Yang, Sen, Yan, Kai-lin, Cui, Yong, Liang, Yan-Hua, Zhou, Fu-Sheng, Du, Wen-Hui, Gao, Min, Sun, Liang-Dan, Fan, Xing, Chen, Jian-Jun, Wang, Pei-Guang, Zhu, Ya-Gang, Zhou, Shun-Ming, Zhang, Xue-Jun

“…Some studies suggested that human HLA status may potentiate development of the AA phenotype and exists ethic differences. No report has been published about…”
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HLA haplotypic association with different phenotype of alopecia areata in Chinese Hans by Xiao, Feng-Li, Yang, Sen, Lin, Guo-Shu, Gao, Min, Cui, Yong, Yin, Xian-Yong, Wang, Pei-Guang, Xu, Shengxin, Zhang, Xue-Jun

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Polymorphisms in Interleukin-15 Gene on Chromosome 4q31.2 Are Associated with Psoriasis Vulgaris in Chinese Population by Zhang, Xue-Jun, Yan, Kai-Lin, Wang, Zhi-Min, Yang, Sen, Zhang, Guo-Long, Fan, Xing, Xiao, Feng-Li, Gao, Min, Cui, Yong, Wang, Pei-Guang, Sun, Liang-dan, Zhang, Kai-Yue, Wang, Beilan, Wang, Da-Zhi, Xu, Shi-Jie, Huang, Wei, Liu, Jian-Jun

“…Through a series of linkage analyses in a large Chinese family cohort of psoriasis, we previously identified and confirmed a non-HLA psoriasis linkage locus…”
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Inversa Acne (Hidradenitis Suppurativa): A Case Report and Identification of the Locus at Chromosome 1p21.1–1q25.3 by Gao, Min, Wang, Pei-Guang, Cui, Yong, Yang, Sen, Zhang, Yu-Hui, Lin, Da, Zhang, Kai-Yue, Liang, Yan-Hua, Sun, Liang-Dan, Yan, Kai-Lin, Xiao, Feng-Li, Huang, Wei, Zhang, Xue-Jun

“…Acne inversa (hidradenitis suppurativa) is a chronic relapsing inflammatory skin disease characterized by recurrent draining sinuses and abscesses,…”
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Exome sequencing identified a missense mutation of EPS8L3 in Marie Unna hereditary hypotrichosis by Zhang, Xin, Guo, Bi-Rong, Cai, Li-Qiong, Jiang, Tao, Sun, Liang-Dan, Cui, Yong, Hu, Jing-Chu, Zhu, Jun, Chen, Gang, Tang, Xian-Fa, Sun, Guang-Qing, Tang, Hua-Yang, Liu, Yuan, Li, Min, Li, Qi-Bin, Cheng, Hui, Gao, Min, Li, Ping, Yang, Xu, Zuo, Xian-Bo, Zheng, Xiao-Dong, Wang, Pei-Guang, Wang, Jian, Wang, Jun, Liu, Jian-Jun, Yang, Sen, Li, Ying-Rui, Zhang, Xue-Jun

“…Marie Unna hereditary hypotrichosis (MUHH) is an autosomal dominant disorder characterised by coarse, wiry, twisted hair developed in early childhood and…”
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Oscillation Theorems for Even Order Damped Equations with Distributed Deviating Arguments by Gao, Chunxia, Wang, Pei-Guang

“…A class of even order damped differential equations with distributed deviating arguments are investigated. Several new criteria that ensure the oscillation of…”
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Real-time simulation study of fractional PID based on the RSLogix 5000 platform by Jiang Ping, Ma Xiao, Wang Pei-Guang

“…In order to apply fractional order PID controller to the reality engineering project, fractional PID controller is developed by limited memory digital…”
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A new image fusion algorithm based on fractional wavelet transform by Hua Tian, Pei-guang Wang, Wei Zheng

“…The fractional wavelet transform is a kind of signal analysis method established in the Fourier's analysis. It has multi-resolution and fractional domain…”
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The Gene for a Rare Autosomal Dominant Form of Pompholyx Maps to Chromosome 18q22.1–18q22.3 by Chen, Jian-Jun, Liang, Yan-Hua, Zhou, Fu-Sheng, Yang, Sen, Wang, Jian, Wang, Pei-Guang, Du, Wen-Hui, Xu, Shi-Jie, Huang, Wei, Zhang, Xue-Jun

“…Pompholyx is a rather common disorder characterized by recurrent crops of vesicles or bullae on the lateral aspects of the fingers, as well as the palms and…”
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Identification of a Novel Locus for Progressive Symmetric Erythrokeratodermia to a 19.02-cM Interval at 21q11.2–21q21.2 by Cui, Yong, Yang, Sen, Gao, Min, Zhou, Wen-Ming, Li, Ming, Wang, Ying, Chen, Jian-Jun, Yan, Kai-Lin, Niu, Zhen-Min, Wang, Pei-Guang, Xiao, Feng-Li, Liang, Yan-Hua, Sun, Liang-Dan, Fan, Xing, Huang, Wei, Zhang, Xue-Jun

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Existence of Positive Solutions for Second-Order m-Point Boundary Value Problems on Time Scales by Wang, Pei-guang, Wang, Ying

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novel KIT missense mutation in one Chinese family with piebaldism by Yin, Xian-Yong, Ren, Yun-Qing, Yang, Sen, Xu, Sheng-Xin, Zhou, Fu-Sheng, Du, Wen-Hui, Lin, Da, Wang, Pei-Guang, Zhang, Shu-Mei, Zhang, Xue-Jun

“…Piebaldism is an autosomal dominant disorder characterized by congenital leukoderma, mostly affecting forehead, abdomen and knee. Previous studies have…”
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Follow-Up Analysis of PSORS9 in 151 Chinese Families Confirmed the Linkage to 4q31–32 and Refined the Evidence to the Families of Early-Onset Psoriasis by Yan, Kai-Lin, Huang, Wei, Zhang, Xue-Jun, Yang, Sen, Chen, Yu-Ming, Xiao, Feng-Li, Fan, Xing, Gao, Min, Cui, Yong, Zhang, Guo-Long, Sun, Liang-dan, Wang, Pei-Guang, Chen, Jian-Jun, Li, Wei, Chen, Ze-hua, Wang, Zhi-Min, Wang, Da-zhi, Zhang, Kai-Yue, Liu, Jian-Jun

“…Psoriasis linkage to 4q28–32 (PSORS9) was initially identified by our genome-wide scan in 61 Chinese families and subsequently supported by a meta-analysis of…”
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Five mutations of ATP2A2 gene in Chinese patients with Darier's disease and a literature review of 86 cases reported in China by REN, Yun-Qing, MIN GAO, SHEN, Yu-Jun, SEN YANG, ZHANG, Xue-Jun, LIANG, Yan-Hua, HOU, Yan-Xia, WANG, Pei-Guang, SUN, Liang-Dan, XU, Sheng-Xin, WEI LI, DU, Wen-Hui, ZHOU, Fu-Sheng

“…Darier's disease (DD) is an autosomal dominantly inherited skin disorder characterized by loss of adhesion between epidermal cells (acantholysis) and abnormal…”
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Identification of a Novel Locus for Marie Unna Hereditary Hypotrichosis to a 17.5 cM Interval at 1p21.1–1q21.3 by Yang, Sen, Gao, Min, Cui, Yong, Yan, Kai-Lin, Ren, Yun-Qing, Zhang, Guo-Long, Wang, Pei-Guang, Xiao, Feng-Li, Du, Wen-Hui, Liang, Yan-Hua, Sun, Liang-Dan, Xu, Shi-Jie, Huang, Wei, Zhang, Xue-Jun

“…Marie Unna hereditary hypotrichosis (MUHH) is a rare autosomal dominant disorder characterized by coarse, wiry, twisted hair developed in early childhood and…”
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A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2 by Wang, Pei-Guang, Gao, Min, Cui, Yong, Xiao, Feng-Li, Zhu, Ya-Gang, Ren, Yun-Qing, Yan, Kai-Lin, Du, Wen-Hui, Zhang, Kai-Yue, Yang, Sen, Huang, Wei, Zhang, Xue-Jun

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