Mindin serves as a tumour suppressor gene during colon cancer progression through MAPK/ERK signalling pathway in mice
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
Published in Journal of cellular and molecular medicine (01.08.2020)
Published in Journal of cellular and molecular medicine (01.08.2020)
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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
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
Published in Journal of cellular and molecular medicine (01.05.2019)
Published in Journal of cellular and molecular medicine (01.05.2019)
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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 carcinoma
He, Ke-Jie, Zhang, Yang-fan, Liang, Lai-ying, Cheng, Xiao-Shen, Gong, Guoyu, Ouyang, Xiao-Mei, Lin, Ying, Guleng, Bayasi
Published in Molecular therapy. Nucleic acids (13.12.2022)
Published in Molecular therapy. Nucleic acids (13.12.2022)
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Glycerol monolaurate ameliorates DSS-induced acute colitis by inhibiting infiltration of Th17, neutrophils, macrophages and altering the gut microbiota
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
Published in Frontiers in nutrition (Lausanne) (12.08.2022)
Published in Frontiers in nutrition (Lausanne) (12.08.2022)
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The genetic bases for non-syndromic hearing loss among Chinese
Ouyang, Xiao Mei, Yan, Denise, Yuan, Hui Jun, Pu, Dai, Du, Li Lin, Han, Don Yi, Liu, Xue Zhong
Published in Journal of human genetics (01.03.2009)
Published in Journal of human genetics (01.03.2009)
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Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31
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
Published in Human genetics (01.02.2009)
Published in Human genetics (01.02.2009)
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Refinement of the DFNA41 locus and candidate genes analysis
Yan, Denise, Ouyang, Xiao Mei, Zhu, Xiaofeng, Du, Li Lin, Chen, Zheng Yi, Liu, Xue Zhong
Published in Journal of human genetics (01.10.2005)
Published in Journal of human genetics (01.10.2005)
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Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans
Zheng, Qing Yin, Yan, Denise, Ouyang, Xiao Mei, Du, Li Lin, Yu, Heping, Chang, Bo, Johnson, Kenneth R., Liu, Xue Zhong
Published in Human molecular genetics (01.01.2005)
Published in Human molecular genetics (01.01.2005)
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Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss
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
Published in Human molecular genetics (15.05.2003)
Published in Human molecular genetics (15.05.2003)
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Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population
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
Published in Human genetics (01.03.2005)
Published in Human genetics (01.03.2005)
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The prevalence of connexin 26 (GJB2) mutations in the Chinese population
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
Published in Human genetics (01.10.2002)
Published in Human genetics (01.10.2002)
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Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east Asians
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
Published in Human genetics (01.12.2003)
Published in Human genetics (01.12.2003)
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Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness
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
Published in Human molecular genetics (01.12.2001)
Published in Human molecular genetics (01.12.2001)
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Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness
XIAO MEI OUYANG, XIA JUAN XIA, VERPY, Elisabeth, LI LIN DU, PANDYA, Arti, PETIT, Christine, BALKANY, Thomas, NANCE, Walter E, XUE ZHONG LIU
Published in Human genetics (01.07.2002)
Published in Human genetics (01.07.2002)
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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
Yan, Denise, Kamiya, Kazusaku, Ouyang, Xiao Mei, Liu, Xue Zhong
Published in International journal of experimental pathology (01.02.2011)
Published in International journal of experimental pathology (01.02.2011)
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Mutation screening of the GJA7 (Cx45) gene in a large international series of probands with nonsyndromic hearing impairment
Ouyang, Xiao Mei, Yan, Denise, Aslan, Idil, Du, Li Lin, Tekin, Mustafa, Liu, Xue-Zhong
Published in Genetic testing and molecular biomarkers (01.05.2011)
Published in Genetic testing and molecular biomarkers (01.05.2011)
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Evidence of a founder effect for the 235delC mutation of GJB2
Yan, Denise, Park, Hong-Joon, Ouyang, Xiao Mei, Pandya, Arti, Doi, Katsumi, Erdenetungalag, Raadnabazar, Du, Li Lin
Published in Human genetics (01.12.2003)
Published in Human genetics (01.12.2003)
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