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Journal Abstract Search

360 related items for PubMed ID: 29529603

  • 1. Novel Mutations in the PKD1 and PKD2 Genes of Chinese Patients with Autosomal Dominant Polycystic Kidney Disease.
    Xu D, Ma Y, Gu X, Bian R, Lu Y, Xing X, Mei C.
    Kidney Blood Press Res; 2018; 43(2):297-309. PubMed ID: 29529603
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  • 2. Identification of novel mutations and risk assessment of Han Chinese patients with autosomal dominant polycystic kidney disease.
    Zhang M, Liu S, Xia X, Cui Y, Li X.
    Nephrology (Carlton); 2019 May; 24(5):504-510. PubMed ID: 29633482
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  • 3. Identification of novel PKD1 and PKD2 mutations in a Chinese population with autosomal dominant polycystic kidney disease.
    Liu B, Chen SC, Yang YM, Yan K, Qian YQ, Zhang JY, Hu YT, Dong MY, Jin F, Huang HF, Xu CM.
    Sci Rep; 2015 Dec 03; 5():17468. PubMed ID: 26632257
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  • 4. 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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  • 5. 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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  • 6. Mutational analysis in patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD): Identification of five mutations in the PKD1 gene.
    Abdelwahed M, Hilbert P, Ahmed A, Mahfoudh H, Bouomrani S, Dey M, Hachicha J, Kamoun H, Keskes-Ammar L, Belguith N.
    Gene; 2018 Sep 10; 671():28-35. PubMed ID: 29860066
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  • 7. Novel mutations of PKD genes in Chinese patients suffering from autosomal dominant polycystic kidney disease and seeking assisted reproduction.
    He WB, Xiao WJ, Tan YQ, Zhao XM, Li W, Zhang QJ, Zhong CG, Li XR, Hu L, Lu GX, Lin G, Du J.
    BMC Med Genet; 2018 Oct 17; 19(1):186. PubMed ID: 30333007
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  • 11. Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease - a case report.
    Elisakova V, Merta M, Reiterova J, Baxova A, Kotlas J, Hirschfeldova K, Obeidova L, Tesar V, Stekrova J.
    BMC Nephrol; 2018 Jul 04; 19(1):163. PubMed ID: 29973168
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  • 12. Novel PKD1 and PKD2 mutations in Taiwanese patients with autosomal dominant polycystic kidney disease.
    Chang MY, Chen HM, Jenq CC, Lee SY, Chen YM, Tian YC, Chen YC, Hung CC, Fang JT, Yang CW, Wu-Chou YH.
    J Hum Genet; 2013 Nov 04; 58(11):720-7. PubMed ID: 23985799
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  • 13. Genotype-phenotype of autosomal dominant polycystic kidney disease in Malta.
    Ciantar N, Zahra G, Delicata J, Sammut F, Calleja-Agius J, Farrugia E, Said E.
    Eur J Med Genet; 2024 Jun 04; 69():104934. PubMed ID: 38537868
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  • 16. Identification of novel mutations in Chinese Hans with autosomal dominant polycystic kidney disease.
    Yu C, Yang Y, Zou L, Hu Z, Li J, Liu Y, Ma Y, Ma M, Su D, Zhang S.
    BMC Med Genet; 2011 Dec 20; 12():164. PubMed ID: 22185115
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  • 17. Technical Evaluation: Identification of Pathogenic Mutations in PKD1 and PKD2 in Patients with Autosomal Dominant Polycystic Kidney Disease by Next-Generation Sequencing and Use of a Comprehensive New Classification System.
    Kinoshita M, Higashihara E, Kawano H, Higashiyama R, Koga D, Fukui T, Gondo N, Oka T, Kawahara K, Rigo K, Hague T, Katsuragi K, Sudo K, Takeshi M, Horie S, Nutahara K.
    PLoS One; 2016 Dec 20; 11(11):e0166288. PubMed ID: 27835667
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  • 18. Putative mutation of PKD1 gene responsible for autosomal dominant polycystic kidney disease in a Chinese family.
    Li J, Yu C, Tao Y, Yang Y, Hu Z, Zhang S.
    Int J Urol; 2011 Mar 20; 18(3):240-2. PubMed ID: 21332816
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  • 19. Exome sequencing of Saudi Arabian patients with ADPKD.
    Al-Muhanna FA, Al-Rubaish AM, Vatte C, Mohiuddin SS, Cyrus C, Ahmad A, Shakil Akhtar M, Albezra MA, Alali RA, Almuhanna AF, Huang K, Wang L, Al-Kuwaiti F, Elsalamouni TSA, Al Hwiesh A, Huang X, Keating B, Li J, Lanktree MB, Al-Ali AK.
    Ren Fail; 2019 Nov 20; 41(1):842-849. PubMed ID: 31488014
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