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Journal Abstract Search

325 related items for PubMed ID: 35031424

  • 21. Mutation Analysis of Autosomal-Dominant Polycystic Kidney Disease Patients.
    Suzuki Y, Katayama K, Saiki R, Hirabayashi Y, Murata T, Ishikawa E, Ito M, Dohi K.
    Genes (Basel); 2023 Feb 09; 14(2):. PubMed ID: 36833371
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  • 25. Somatic Mutations in Renal Cyst Epithelium in Autosomal Dominant Polycystic Kidney Disease.
    Tan AY, Zhang T, Michaeel A, Blumenfeld J, Liu G, Zhang W, Zhang Z, Zhu Y, Rennert L, Martin C, Xiang J, Salvatore SP, Robinson BD, Kapur S, Donahue S, Bobb WO, Rennert H.
    J Am Soc Nephrol; 2018 Aug 09; 29(8):2139-2156. PubMed ID: 30042192
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  • 27. Targeted Next Generation Sequencing Revealed Novel Variants in the PKD1 and PKD2 Genes of Iranian Patients with Autosomal Dominant Polycystic Kidney Disease.
    Hosseinpour M, Ardalani F, Mohseni M, Beheshtian M, Arzhangi S, Ossareh S, Najmabadi H, Nobakht A, Kahrizi K, Broumand B.
    Arch Iran Med; 2022 Sep 01; 25(9):600-608. PubMed ID: 37543885
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  • 28. Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney disease.
    Magistroni R, He N, Wang K, Andrew R, Johnson A, Gabow P, Dicks E, Parfrey P, Torra R, San-Millan JL, Coto E, Van Dijk M, Breuning M, Peters D, Bogdanova N, Ligabue G, Albertazzi A, Hateboer N, Demetriou K, Pierides A, Deltas C, St George-Hyslop P, Ravine D, Pei Y.
    J Am Soc Nephrol; 2003 May 01; 14(5):1164-74. PubMed ID: 12707387
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  • 31. Identification of novel PKD1 and PKD2 mutations in Korean patients with autosomal dominant polycystic kidney disease.
    Choi R, Park HC, Lee K, Lee MG, Kim JW, Ki CS, Hwang YH, Ahn C.
    BMC Med Genet; 2014 Dec 10; 15():129. PubMed ID: 25491204
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  • 32. Effect of genotype on the severity and volume progression of polycystic liver disease in autosomal dominant polycystic kidney disease.
    Chebib FT, Jung Y, Heyer CM, Irazabal MV, Hogan MC, Harris PC, Torres VE, El-Zoghby ZM.
    Nephrol Dial Transplant; 2016 Jun 10; 31(6):952-60. PubMed ID: 26932689
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  • 33. Mutation analyses by next-generation sequencing and multiplex ligation-dependent probe amplification in Japanese autosomal dominant polycystic kidney disease patients.
    Mochizuki T, Teraoka A, Akagawa H, Makabe S, Akihisa T, Sato M, Kataoka H, Mitobe M, Furukawa T, Tsuchiya K, Nitta K.
    Clin Exp Nephrol; 2019 Aug 10; 23(8):1022-1030. PubMed ID: 30989420
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  • 36. PKD1 and PKD2 mutations in Slovenian families with autosomal dominant polycystic kidney disease.
    Vouk K, Strmecki L, Stekrova J, Reiterova J, Bidovec M, Hudler P, Kenig A, Jereb S, Zupanic-Pajnic I, Balazic J, Haarpaintner G, Leskovar B, Adamlje A, Skoflic A, Dovc R, Hojs R, Komel R.
    BMC Med Genet; 2006 Jan 23; 7():6. PubMed ID: 16430766
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  • 37. System analysis of gene mutations and clinical phenotype in Chinese patients with autosomal-dominant polycystic kidney disease.
    Jin M, Xie Y, Chen Z, Liao Y, Li Z, Hu P, Qi Y, Yin Z, Li Q, Fu P, Chen X.
    Sci Rep; 2016 Oct 26; 6():35945. PubMed ID: 27782177
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  • 38. Novel mutations of PKD genes in the Czech population with autosomal dominant polycystic kidney disease.
    Obeidova L, Elisakova V, Stekrova J, Reiterova J, Merta M, Tesar V, Losan F, Kohoutova M.
    BMC Med Genet; 2014 Apr 03; 15():41. PubMed ID: 24694054
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