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                                                                                  發佈時間:2019-03-25        瀏覽次數:29

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                                                                                         趣赢附屬兒科醫院 ,副主任醫師 ,碩士生導師。入選2018年“國家自然趣赢基金-優秀青年趣赢基金”項目資助。在長期的臨牀和科研工作中 ,致力於探索小兒遺傳性性腎臟疾病的機制研究  ,聚焦神經系統發育缺陷合併腎臟發育障礙及功能損害的綜合徵型疾病的突變譜系及分子機制。多篇研究發表於Nature Genetics、Journal of Clinical Investigation 等學術專刊。曾獲上海市科技進步一等獎(第四完成人) 。

                                                                                  教育研究經歷
                                                                                  2014/09 - 2016/09 美國哈佛醫學院,波士頓兒童醫院,博士後
                                                                                  2010/09 - 2010/05 悉尼兒童醫院,Clinical fellow
                                                                                  2001/09 - 2006/06 趣赢附屬兒科醫院 兒趣赢,博士
                                                                                  1996/09 - 2001/06 趣赢上海醫學院 臨牀醫學專業  ,學士

                                                                                  研究方向

                                                                                  兒童遺傳性腎臟疾病

                                                                                  代表性論文

                                                                                  1. Ashraf S, Kudo H, Rao J, Kikuchi A, Widmeier E, Lawson JA, Tan W, Hermle T, Warejko JK, Shril S, Airik M, Jobst-Schwan T, Lovric S, Braun DA, Gee HY, Schapiro D, Majmundar AJ, Sadowski CE, Pabst WL, Daga A, van der Ven AT, Schmidt JM, Low BC, Gupta AB, Tripathi BK, Wong J, Campbell K, Metcalfe K, Schanze D, Niihori T, Kaito H, Nozu K, Tsukaguchi H, Tanaka R, Hamahira K, Kobayashi Y, Takizawa T, Funayama R, Nakayama K, Aoki Y, Kumagai N, Iijima K, Fehrenbach H, Kari JA, El Desoky S, Jalalah S, Bogdanovic R, Stajić N, Zappel H, Rakhmetova A,  Wassmer SR, Jungraithmayr T, Strehlau J, Kumar AS, Bagga A, Soliman NA, Mane SM, Kaufman L, Lowy DR, Jairajpuri MA, Lifton RP, Pei Y, Zenker M, Kure S, Hildebrandt F(2018). Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment. Nat Commun. 17;9(1):1960

                                                                                  2. Rao J*, Ashraf S*, Tan W, van der Ven AT, Gee HY, Braun DA, Fehér K, George SP, Esmaeilniakooshkghazi A, Choi WI, Jobst-Schwan T, Schneider R, Schmidt JM, Widmeier E, Warejko JK, Hermle T, Schapiro D, Lovric S, Shril S, Daga A, Nayir A, Shenoy M, Tse Y, Bald M, Helmchen U, Mir S, Berdeli A, Kari JA, El Desoky S, Soliman NA, Bagga A, Mane S, Jairajpuri MA, Lifton RP, Khurana S, Martins JC, Hildebrandt F (2017). Advillin acts upstream of phospholipase C ϵ1 in steroid-resistant  nephrotic syndrome. J Clin Invest. 127(12):4257-4269.

                                                                                  3. Braun DA*, Rao J*, Mollet G, Schapiro D, Daugeron MC, Tan W, Gribouval O, Boyer O, Revy P, Jobst-Schwan T, Schmidt JM, Lawson JA, Schanze D, Ashraf S, Ullmann JFP, Hoogstraten CA, Boddaert N, Collinet B, Martin G, Liger D, Lovric S, Furlano M, Guerrera IC, Sanchez-Ferras O, Hu JF, Boschat AC, Sanquer S, Menten B, Vergult S, De Rocker N, Airik M, Hermle T, Shril S, Widmeier E, Gee HY, Choi WI, Sadowski CE, Pabst WL, Warejko JK, Daga A, Basta T, Matejas V, Scharmann K, Kienast SD, Behnam B, Beeson B, Begtrup A, Bruce M, Ch'ng GS, Lin SP, Chang JH, Chen CH, Cho MT, Gaffney PM, Gipson PE, Hsu CH, Kari JA, Ke YY, Kiraly-Borri C, Lai WM, Lemyre E, Littlejohn RO, Masri A, Moghtaderi M, Nakamura K, Ozaltin F, Praet M, Prasad C, Prytula A, Roeder ER, Rump P, Schnur RE, Shiihara T, Sinha MD, Soliman NA, Soulami K, Sweetser DA, Tsai WH, Tsai JD, Topaloglu R, Vester U, Viskochil DH, Vatanavicharn N, Waxler JL, Wierenga KJ, Wolf MTF, Wong SN, Leidel SA, Truglio G, Dedon PC, Poduri A, Mane S, Lifton RP, Bouchard M, Kannu P, Chitayat D, Magen D, Callewaert B, van Tilbeurgh H, Zenker M, Antignac C, Hildebrandt F(2017). Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly. Nat. Genet.;49(10):1529-1538

                                                                                  4. Lin Y, Rao J# Zha XL, Xu H#(2013). Angiopoietin-like 3 induces podocyte F-actin rearrangement through integrin α(V)β3/FAK/PI3K pathway-mediated Rac1 activation. Biomed Res Int.;2013:135608

                                                                                  5. Rao J, Kennedy SE, Cohen S, Rosenberg AR(2012). A systematic review of interventions for reducing pain and distress in children undergoing voiding cystourethrography. Acta Paediatr.; 101(3):224-229

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