Mindin serves as a tumour suppressor gene during colon cancer progression through MAPK/ERK signalling pathway in mice von Cheng, Xiao‐Shen, Huo, Ya‐Ni, Fan, Yan‐Yun, Xiao, Chuan‐Xing, Ouyang, Xiao‐Mei, Liang, Lai‐Ying, Lin, Ying, Wu, Jian‐Feng, Ren, Jian‐Lin, Guleng, Bayasi

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The pattern‐recognition molecule mindin binds integrin Mac‐1 to promote macrophage phagocytosis via Syk activation and NF‐κB p65 translocation von Liu, Yuan‐sheng, Wang, Li‐fen, Cheng, Xiao‐Shen, Huo, Ya‐Ni, Ouyang, Xiao‐Mei, Liang, Lai‐Ying, Lin, Ying, Wu, Jian‐Feng, Ren, Jian‐Lin, Guleng, Bayasi

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ncRNAs-mediated high expression of TICRR promotes tumor cell proliferation and migration and is correlated with poor prognosis and tumor immune infiltration of hepatocellular carci... von He, Ke-Jie, Zhang, Yang-fan, Liang, Lai-ying, Cheng, Xiao-Shen, Gong, Guoyu, Ouyang, Xiao-Mei, Lin, Ying, Guleng, Bayasi

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Glycerol monolaurate ameliorates DSS-induced acute colitis by inhibiting infiltration of Th17, neutrophils, macrophages and altering the gut microbiota von He, Ke-Jie, Dong, Jia-Hui, Ouyang, Xiao-Mei, Huo, Ya-Ni, Cheng, Xiao-Shen, Lin, Ying, Li, Yue, Gong, Guoyu, Liu, Jingjing, Ren, Jian-Lin, Guleng, Bayasi

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The genetic bases for non-syndromic hearing loss among Chinese von Ouyang, Xiao Mei, Yan, Denise, Yuan, Hui Jun, Pu, Dai, Du, Li Lin, Han, Don Yi, Liu, Xue Zhong

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Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31 von Liu, Xue-Zhong, Yuan, Yongyi, Yan, Denise, Ding, Emilie Hong, Ouyang, Xiao Mei, Fei, Yu, Tang, Wenxue, Yuan, Huijun, Chang, Qing, Du, Li Lin, Zhang, Xin, Wang, Guojian, Ahmad, Shoeb, Kang, Dong Yang, Lin, Xi, Dai, Pu

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Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans von Zheng, Qing Yin, Yan, Denise, Ouyang, Xiao Mei, Du, Li Lin, Yu, Heping, Chang, Bo, Johnson, Kenneth R., Liu, Xue Zhong

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Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the GJB2 gene and hearing loss von Yan, Denise, Ouyang, Xiao Mei, Angeli, Simon I., Du, Li Lin, Liu, Xue Zong

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The prevalence of connexin 26 (GJB2) mutations in the Chinese population von XUE ZHONG LIU, XIA JUAN XIA, LI RONG XU, XIAO MEI KE, XIAO MEI OUYANG, LI LIN DU, YU HE LIU, ANGELI, Simon, TELISCHI, Fred F, NANCE, Walter E, BALKANY, Thomas

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Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss von Liu, Xue Zhong, Ouyang, Xiao Mei, Xia, Xia Juan, Zheng, Jing, Pandya, Arti, Li, Fang, Du, Li Lin, Welch, Katherine O., Petit, Christine, Smith, Richard J.H., Webb, Bradley T., Yan, Denise, Arnos, Kathleen S., Corey, David, Dallos, Peter, Nance, Walter E., Chen, Zheng Yi

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Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population von XIAO MEI OUYANG, YAN, Denise, BROWN, Steve D. M, BALKANY, Thomas, XUE ZHONG LIU, LI LIN DU, FIELDING HEJTMANCIK, J, JACOBSON, Samuel G, NANCE, Walter E, LI, An Ren, ANGELI, Simon, KAISER, Muriel, NEWTON, Valerie

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Refinement of the DFNA41 locus and candidate genes analysis von Yan, Denise, Ouyang, Xiao Mei, Zhu, Xiaofeng, Du, Li Lin, Chen, Zheng Yi, Liu, Xue Zhong

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Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness von XUE ZHONG LIU, XIA JUAN XIA, ARNOS, Kathleen S, NANCE, Walter E, ADAMS, Joe, ZHENG YI CHEN, WELCH, Katherine O, TEKIN, Mustafa, XIAO MEI OUYANG, KRISTIANSEN, Arther, PANDYA, Arti, BALKANY, Thomas

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Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east Asians von YAN, Denise, PARK, Hong-Joon, XUE ZHONG LIU, XIAO MEI OUYANG, PANDYA, Arti, DOI, Katsumi, ERDENETUNGALAG, Raadnabazar, LI LIN DU, MATSUSHIRO, Naoki, NANCE, Walter E, GRIFFITH, Andrew J

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Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness von XIAO MEI OUYANG, XIA JUAN XIA, VERPY, Elisabeth, LI LIN DU, PANDYA, Arti, PETIT, Christine, BALKANY, Thomas, NANCE, Walter E, XUE ZHONG LIU

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Application of the combination of 1,3-dichloropropene and dimethyl disulfide by soil injection or chemigation： effects against soilborne pests in cucumber in China von MAO, Lian-gang, WANG, Qiu-xia, YAN, Dong-dong, LIU, Peng-fei, SHEN, Jin, FANG, Wen-sheng, HU, Xiao-mei, LI, Yuan, OUYANG, Can-bin, GUO, Mei-xia, CAO, Ao-cheng

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Analysis of subcellular localization of Myo7a, Pcdh15 and Sans in Ush1c knockout mice von Yan, Denise, Kamiya, Kazusaku, Ouyang, Xiao Mei, Liu, Xue Zhong

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Analysis of subcellular localization of Myo7a, Pcdh15 and Sans in Ush1c knockout mice: Analysis of USH proteins in Ush1c knockout mice von Yan, Denise, Kamiya, Kazusaku, Ouyang, Xiao Mei, Liu, Xue Zhong

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Mutation screening of the GJA7 (Cx45) gene in a large international series of probands with nonsyndromic hearing impairment von Ouyang, Xiao Mei, Yan, Denise, Aslan, Idil, Du, Li Lin, Tekin, Mustafa, Liu, Xue-Zhong

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Evidence of a founder effect for the 235delC mutation of GJB2 von Yan, Denise, Park, Hong-Joon, Ouyang, Xiao Mei, Pandya, Arti, Doi, Katsumi, Erdenetungalag, Raadnabazar, Du, Li Lin

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