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Journal Abstract Search

225 related items for PubMed ID: 35619721

  • 41. Comprehensive functional characterization of complement factor I rare variant genotypes identified in the SCOPE geographic atrophy cohort.
    Hallam TM, Andreadi A, Sharp SJ, Brocklebank V, Gardenal E, Dreismann A, SCOPE Study Group, Lotery AJ, Marchbank KJ, Harris CL, Jones AV, Kavanagh D.
    J Biol Chem; 2024 Jul; 300(7):107452. PubMed ID: 38852887
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  • 43. Comprehensive Analysis of Complement Genes in Patients with Atypical Hemolytic Uremic Syndrome.
    Zhang T, Lu J, Liang S, Chen D, Zhang H, Zeng C, Liu Z, Chen H.
    Am J Nephrol; 2016 Jul; 43(3):160-9. PubMed ID: 27064621
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  • 44. [Analysis of variants in complement genes in Han Chinese children with atypical hemolytic uremic syndrome].
    Yi CL, Zhao F, Qiu HZ, Wang LM, Huang J, Nie XJ, Yu ZH.
    Zhonghua Er Ke Za Zhi; 2017 Aug 02; 55(8):624-627. PubMed ID: 28822440
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  • 51. Defining the genetics of thrombotic microangiopathies.
    Vieira-Martins P, El Sissy C, Bordereau P, Gruber A, Rosain J, Fremeaux-Bacchi V.
    Transfus Apher Sci; 2016 Apr 02; 54(2):212-9. PubMed ID: 27177491
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  • 55. Clinical and Genetic Characteristics of Atypical Hemolytic Uremic Syndrome in Children: A Chinese Cohort Study.
    Wu D, Chen J, Ling C, Chen Z, Fan J, Sun Q, Meng Q, Liu X.
    Nephron; 2021 Apr 02; 145(4):415-427. PubMed ID: 33873197
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  • 58. Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndrome.
    Kavanagh D, Richards A, Noris M, Hauhart R, Liszewski MK, Karpman D, Goodship JA, Fremeaux-Bacchi V, Remuzzi G, Goodship TH, Atkinson JP.
    Mol Immunol; 2008 Jan 02; 45(1):95-105. PubMed ID: 17597211
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