Search Results - "Yan, L. K."

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  1. 1

    The tunable negative permittivity and negative permeability of percolative Fe/Al2O3 composites in radio frequency range by Sun, K., Fan, R. H., Zhang, Z. D., Yan, K. L., Zhang, X. H., Xie, P. T., Yu, M. X., Pan, S. B.

    Published in Applied physics letters (27-04-2015)
    “…The electromagnetic properties including ac conductivity, permittivity, and permeability of percolative Fe/Al2O3 composites, which were prepared by in-situ…”
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    Journal Article
  2. 2

    Newly identified respiratory viruses associated with acute lower respiratory tract infections in children in Lanzou, China, from 2006 to 2009 by Jin, Y., Zhang, R.-F., Xie, Z.-P., Yan, K.-L., Gao, H.-C., Song, J.-R., Yuan, X.-H., Cheng, W.-X., Hou, Y.-D., Duan, Z.-J.

    Published in Clinical microbiology and infection (01-01-2012)
    “…Nasopharyngeal aspirates were collected from 813 children <14 years old with acute lower respiratory tract infections in Lanzhou, China, from December 2006 to…”
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    Journal Article
  3. 3

    Childhood psoriasis: a study of 277 patients from China by Fan, X, Xiao, F-L, Yang, S, Liu, J-B, Yan, K-L, Liang, Y-H, Sun, L-D, Du, W-H, Jin, Y-T, Zhang, X-J

    “…Objectives  Psoriasis is common in childhood. The aim of this study was to present the clinical and epidemiological profile of childhood psoriasis in China…”
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    Journal Article
  4. 4

    9-Cis-retinoic acid exhibits antifibrotic activity via the induction of cyclooxygenase-2 expression and prostaglandin E2 production in scleroderma fibroblasts by Xiao, R., Kanekura, T., Yoshida, N., Higashi, Y., Yan, K. -L., Fukushige, T., Kanzaki, T.

    Published in Clinical and experimental dermatology (01-07-2008)
    “…Summary Background.  The pathogenesis of scleroderma (SSc) is not fully understood, and there is no effective treatment for this chronic disease. Retinoic acid…”
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    Journal Article
  5. 5

    Effect of small interfering RNA on the expression of connective tissue growth factor and type I and III collagen in skin fibroblasts of patients with systemic sclerosis by Xiao, R., Liu, F-Y., Luo, J-Y., Yang, X-J., Wen, H-Q., Su, Y-W., Yan, K-L., Li, Y-P., Liang, Y-S.

    Published in British journal of dermatology (1951) (01-12-2006)
    “…Summary Background  Systemic sclerosis (SSc) is characterized by an excessive production of extracellular matrix. It is widely accepted that fibrosis is…”
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    Journal Article
  6. 6

    Effectiveness of adenosine triphosphate to monitor manual cleaning and disinfection efficacy of flexible endoscopes in Hong Kong by Chan, Ada S F, Chan, Henry L Y, Yan, Bruno K L, Lai, Mooris K C

    Published in JGH open (01-02-2023)
    “…Background and Aim Adenosine triphosphate (ATP) bioluminescence assay is widely adopted in the West to allow rapid evaluation of endoscopes for…”
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    Journal Article
  7. 7

    Milk glucosidase activity enables suckled pup starch digestion by Nichols, B. L., Diaz-Sotomayor, M., Avery, S. E., Chacko, S. K., Hadsell, D. L., Baker, S. S., Hamaker, B. R., Yan, L. K., Lin, H. M., Quezada-Calvillo, R.

    Published in Molecular and cellular pediatrics (01-02-2016)
    “…ᅟ Starch requires six enzymes for digestion to free glucose: two amylases (salivary and pancreatic) and four mucosal maltase activities; sucrase-isomaltase and…”
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    Journal Article
  8. 8

    A novel mutation of the DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria by Li, M., Jiang, Y. X., Liu, J. B., Yang, S., He, P. P., Gao, M., Wei, S. C., Yan, K. L., Huang, W., Zhang, X. J.

    Published in Clinical and experimental dermatology (01-09-2004)
    “…Summary Dyschromatosis symmetrica hereditaria (DSH) is a pigmentary genodermatosis of autosomal dominant inheritance characterized by a mixture of…”
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    Journal Article
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    Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3 by HE, P. P, ZHANG, X. J, SUN, L. D, DU, W. H, Y.J.SHEN, XU, S. J, HUANG, W, YANG, Q, LI, M, LIANG, Y. H, YANG, S, YAN, K. L, CUI, Y, SHEN, Y. Y, WANG, H. Y

    Published in British journal of dermatology (1951) (01-05-2004)
    “…Marie Unna hereditary hypotrichosis (MUHH) is a rare autosomal congenital alopecia with progressive hair loss starting in early childhood and accelerating at…”
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    Journal Article
  11. 11

    Theoretical investigation of electronic structure and spectroscopic properties of functionalized bis-silicon-bridged stilbene homologue by Kan, Y.H., Su, Z.M., Yan, L.K., Teng, Y.L., Yang, S.Y., Wang, R.S.

    Published in Synthetic metals (20-09-2005)
    “…Electronic structures of bis-sillicon-bridged trans-stilbene homologues were theoretically analyzed from the viewpoint of electronic effect occurring from…”
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    Journal Article Conference Proceeding
  12. 12

    Refined localization of a punctate palmoplantar keratoderma gene to a 506-cM region at 15q22.2-15q22.31 by GAO, M, YANG, S, XU, S. J, HUANG, W, ZHANG, X. J, LI, M, YAN, K. L, JIANG, Y. X, CUI, Y, XIAO, F. L, SHEN, Y. J, CHEN, J. J, LIU, J. B

    Published in British journal of dermatology (1951) (01-05-2005)
    “…Punctate palmoplantar keratoderma (PPK) is a rare autosomal dominant cutaneous disorder characterized by numerous hyperkeratotic papules distributed on the…”
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    Journal Article
  13. 13

    Marie Unna hereditary hypotrichosis: report of a Chinese family and evidence for genetic heterogeneity by Yan, K. L., He, P. P., Yang, S., Li, M., Yang, Q., Ren, Y. Q., Cui, Y., Gao, M., Xiao, F. L., Huang, W., Zhang, X. J.

    Published in Clinical and experimental dermatology (01-09-2004)
    “…Summary Marie Unna hereditary hypotrichosis (MUHH) is a rare autosomal dominant disorder with progressive hair loss starting in early childhood and aggravating…”
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    Journal Article
  14. 14

    UGT1A1 gene mutation spectrum with indirect hyperbilirubinemia in children by Shen, Y, Guo, H M, Zheng, Y C, Zheng, B X, Yan, K L, Kong, G P, Lin, Q, Jin, Y, Liu, Z F, Li, M

    Published in Zhonghua gan zang bing za zhi (20-02-2024)
    “…To explore the relevancy between the uridine diphosphate-glucuronylgly-cosyltransferase 1A1 (UGT1A1) gene mutation and the phenotype of indirect…”
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    Journal Article
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    Feasibility Study on the Polyethylene (PE) Waveguide Cable for Future Exploration in Terabit DSL by Yan, L. K., Seman, F. C., Khee, Y. S., Sohoo, A. A.

    “…Due to the demand for higher data rates and greater download speeds by users and increasing number of deployed devices providing content-rich data, new…”
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    Conference Proceeding
  18. 18

    ABO blood groups and platelet reactivity in patients with coronary artery disease undergoing percutaneous coronary intervention treated with clopidogrel by Liu, M L, Li, J W, Yan, K L, Yuan, J Q, Zhao, X Y

    Published in European heart journal (28-10-2024)
    “…Abstract Background The association between ABO blood groups and the risk of thrombosis and bleeding in patients with coronary artery disease has been of…”
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    Journal Article
  19. 19

    Remnant cholesterol is associated with platelet reactivity for patients with coronary artery disease underwent percutaneous coronary intervention by Liu, M L, Li, J W, Yan, K L, Yuan, J Q, Zhao, X Y

    Published in European heart journal (28-10-2024)
    “…Abstract Background In recent years, remnant cholesterol has received increasing attention and has been shown to be associated with thrombotic and bleeding…”
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    Journal Article
  20. 20

    A Novel Linkage to Generalized Vitiligo on 4q13-q21 Identified in a Genomewide Linkage Analysis of Chinese Families by Chen, Jian-Jun, Huang, Wei, Gui, Jin-Ping, Yang, Sen, Zhou, Fu-Sheng, Xiong, Quan-Geng, Wu, Hong-Bo, Cui, Yong, Gao, Min, Li, Wei, Li, Jin-Xian, Yan, Kai-Lin, Yuan, Wen-Tao, Xu, Shi-Jie, Liu, Jian-Jun, Zhang, Xue-Jun

    Published in American journal of human genetics (01-06-2005)
    “…Generalized vitiligo is a common, autoimmune, familial-clustering depigmentary disorder of the skin and hair that results from selective destruction of…”
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    Journal Article