Works by Mao, Youying


Results: 15
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    Mutations in transcription factor CP2-like 1 may cause a novel syndrome with distal renal tubulopathy in humans.

    Published in:
    Nephrology Dialysis Transplantation, 2021, v. 36, n. 2, p. 237, doi. 10.1093/ndt/gfaa215
    By:
    • Klämbt, Verena;
    • Werth, Max;
    • Onuchic-Whitford, Ana C;
    • Getwan, Maike;
    • Kitzler, Thomas M;
    • Buerger, Florian;
    • Mao, Youying;
    • Deutsch, Konstantin;
    • Mann, Nina;
    • Majmundar, Amar J;
    • Kaminski, Michael M;
    • Shen, Tian;
    • Schmidt-Ott, Kai M;
    • Shalaby, Mohamed;
    • Desoky, Sherif El;
    • Kari, Jameela A;
    • Shril, Shirlee;
    • Lienkamp, Soeren S;
    • Barasch, Jonathan;
    • Hildebrandt, Friedhelm
    Publication type:
    Article
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    Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models.

    Published in:
    American Journal of Medical Genetics. Part A, 2022, v. 188, n. 5, p. 1355, doi. 10.1002/ajmg.a.62644
    By:
    • Wang, Chunyan;
    • Seltzsam, Steve;
    • Zheng, Bixia;
    • Wu, Chen‐Han Wilfred;
    • Nicolas‐Frank, Camille;
    • Yousef, Kirollos;
    • Au, Kit Sing;
    • Mann, Nina;
    • Pantel, Dalia;
    • Schneider, Sophia;
    • Schierbaum, Luca;
    • Kitzler, Thomas M.;
    • Connaughton, Dervla M.;
    • Mao, Youying;
    • Dai, Rufeng;
    • Nakayama, Makiko;
    • Kari, Jameela A.;
    • El Desoky, Sherif;
    • Shalaby, Mohammed;
    • Eid, Loai A.
    Publication type:
    Article
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