Works matching AU Shu, Xinhua

Results: 66
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    RPGR mutation analysis and disease: an update.

    Published in:
    Human Mutation, 2007, v. 28, n. 4, p. 322, doi. 10.1002/humu.20461
    By:
    • Shu, Xinhua;
    • Black, Graeme C.;
    • Rice, Jacqueline M.;
    • Hart-Holden, Niki;
    • Jones, Alison;
    • O'Grady, Anna;
    • Ramsden, Simon;
    • Wright, Alan F.
    Publication type:
    Article
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    Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome.

    Published in:
    Human Mutation, 2004, v. 24, n. 5, p. 439, doi. 10.1002/humu.9285
    By:
    • Wright, Alan F.;
    • Reddick, Adam C.;
    • Schwartz, Sharon B.;
    • Ferguson, Julie S.;
    • Aleman, Tomas S.;
    • Kellner, Ulrich;
    • Jurklies, Bernhard;
    • Schuster, Andreas;
    • Zrenner, Eberhart;
    • Wissinger, Bernd;
    • Lennon, Alan;
    • Shu, Xinhua;
    • Cideciyan, Artur V.;
    • Stone, Edwin M.;
    • Jacobson, Samuel G.;
    • Swaroop, Anand
    Publication type:
    Article
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    SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout.

    Published in:
    Nature Genetics, 2008, v. 40, n. 4, p. 437, doi. 10.1038/ng.106
    By:
    • Vitart, Veronique;
    • Rudan, Igor;
    • Hayward, Caroline;
    • Gray, Nicola K.;
    • Floyd, James;
    • Palmer, Colin N. A.;
    • Knott, Sara A.;
    • Kolcic, Ivana;
    • Polasek, Ozren;
    • Graessler, Juergen;
    • Wilson, James F.;
    • Marinaki, Anthony;
    • Riches, Philip L.;
    • Xinhua Shu;
    • Janicijevic, Branka;
    • Smolej-Narancic, Nina;
    • Gorgoni, Barbara;
    • Morgan, Joanne;
    • Campbell, Susan;
    • Biloglav, Zrinka
    Publication type:
    Article
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    Lifespan and mitochondrial control of neurodegeneration.

    Published in:
    Nature Genetics, 2004, v. 36, n. 11, p. 1153, doi. 10.1038/ng1448
    By:
    • Wright, Alan F.;
    • Jacobson, Samuel G.;
    • Cideciyan, Artur V.;
    • Roman, Alejandro J;
    • Shu, Xinhua;
    • Vlachantoni, Dafni;
    • McInnes, Roderick R.;
    • Riemersma, Rudolph A.
    Publication type:
    Article
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    Cover Image.

    Published in:
    2018
    By:
    • Patibandla, Srinath;
    • Zhang, Yinan;
    • Tohari, Ali Mohammad;
    • Gu, Peng;
    • Reilly, James;
    • Chen, Yu;
    • Shu, Xinhua
    Publication type:
    Cover Art
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    Oxysterols and retinal degeneration.

    Published in:
    British Journal of Pharmacology, 2021, v. 178, n. 16, p. 3205, doi. 10.1111/bph.15391
    By:
    • Zhang, Xun;
    • Alhasani, Reem Hasaballah;
    • Zhou, Xinzhi;
    • Reilly, James;
    • Zeng, Zhihong;
    • Strang, Niall;
    • Shu, Xinhua
    Publication type:
    Article
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    Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degeneration.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 23, p. 4857, doi. 10.1093/hmg/ddt336
    By:
    • Ansari, Morad;
    • Mckeigue, Paul M.;
    • Skerka, Christine;
    • Hayward, Caroline;
    • Rudan, Igor;
    • Vitart, Veronique;
    • Polasek, Ozren;
    • Armbrecht, Ana-Maria;
    • Yates, John R.W.;
    • Vatavuk, Zoran;
    • Bencic, Goran;
    • Kolcic, Ivana;
    • Oostra, Ben A.;
    • Van Duijn, Cornelia M.;
    • Campbell, Susan;
    • Stanton, Chloe M.;
    • Huffman, Jennifer;
    • Shu, Xinhua;
    • Khan, Jane C.;
    • Shahid, Humma
    Publication type:
    Article
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    CERKL regulates autophagy via the NAD-dependent deacetylase SIRT1.

    Published in:
    Autophagy, 2019, v. 15, n. 3, p. 453, doi. 10.1080/15548627.2018.1520548
    By:
    • Hu, Xuebin;
    • Lu, Zhaojing;
    • Yu, Shanshan;
    • Reilly, James;
    • Liu, Fei;
    • Jia, Danna;
    • Qin, Yayun;
    • Han, Shanshan;
    • Liu, Xiliang;
    • Qu, Zhen;
    • Lv, Yuexia;
    • Li, Jingzhen;
    • Huang, Yuwen;
    • Jiang, Tao;
    • Jia, Haibo;
    • Wang, Qing;
    • Liu, Jingyu;
    • Shu, Xinhua;
    • Tang, Zhaohui;
    • Liu, Mugen
    Publication type:
    Article
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    Metabolomics in Retinal Diseases: An Update.

    Published in:
    Biology (2079-7737), 2021, v. 10, n. 10, p. 944, doi. 10.3390/biology10100944
    By:
    • Li, Xing;
    • Cai, Shichang;
    • He, Zhiming;
    • Reilly, James;
    • Zeng, Zhihong;
    • Strang, Niall;
    • Shu, Xinhua
    Publication type:
    Article
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    Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration.

    Published in:
    Human Molecular Genetics, 2003, v. 12, n. 20, p. 2657, doi. 10.1093/hmg/ddg289
    By:
    • Hayward, Caroline;
    • Shu, Xinhua;
    • Cideciyan, Artur V.;
    • Lennon, Alan;
    • Barran, Perdita;
    • Zareparsi, Sepideh;
    • Sawyer, Lindsay;
    • Hendry, Grace;
    • Dhillon, Baljean;
    • Milam, Ann H.;
    • Luthert, Philip J.;
    • Swaroop, Anand;
    • Hastie, Nicholas D.;
    • Jacobson, Samuel G.;
    • Wright, Alan F.
    Publication type:
    Article
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    Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2.

    Published in:
    Nephrology Dialysis Transplantation, 2012, v. 27, n. 3, p. 1035, doi. 10.1093/ndt/gfr419
    By:
    • Dinour, Dganit;
    • Gray, Nicola K.;
    • Ganon, Liat;
    • Knox, Andrew J.S.;
    • Shalev, Hanna;
    • Sela, Ben-Ami;
    • Campbell, Susan;
    • Sawyer, Lindsay;
    • Shu, Xinhua;
    • Valsamidou, Evgenia;
    • Landau, Daniel;
    • Wright, Alan F.;
    • Holtzman, Eliezer J.
    Publication type:
    Article
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