BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 21983717)

  • 1. [Identification of mutations in PKD1 and PKD2 genes in two Chinese families with autosomal dominant polycystic kidney disease].
    Yu CW; Yang Y; Zhang SZ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Oct; 28(5):485-9. PubMed ID: 21983717
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 12():164. PubMed ID: 22185115
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of novel mutations of PKD1 gene in Chinese patients with autosomal dominant polycystic kidney disease by targeted next-generation sequencing.
    Yang T; Meng Y; Wei X; Shen J; Zhang M; Qi C; Wang C; Liu J; Ma M; Huang S
    Clin Chim Acta; 2014 Jun; 433():12-9. PubMed ID: 24582653
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A comprehensive search for mutations in the PKD1 and PKD2 in Japanese subjects with autosomal dominant polycystic kidney disease.
    Kurashige M; Hanaoka K; Imamura M; Udagawa T; Kawaguchi Y; Hasegawa T; Hosoya T; Yokoo T; Maeda S
    Clin Genet; 2015 Mar; 87(3):266-72. PubMed ID: 24611717
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 15():129. PubMed ID: 25491204
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 18(3):240-2. PubMed ID: 21332816
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 5():17468. PubMed ID: 26632257
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A new PKD1 mutation discovered in a Chinese family with autosomal polycystic kidney disease.
    Wang Z; Wang Y; Xiong J
    Kidney Blood Press Res; 2014; 39(1):1-8. PubMed ID: 24821069
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel method for genomic analysis of PKD1 and PKD2 mutations in autosomal dominant polycystic kidney disease.
    Tan YC; Blumenfeld JD; Anghel R; Donahue S; Belenkaya R; Balina M; Parker T; Levine D; Leonard DG; Rennert H
    Hum Mutat; 2009 Feb; 30(2):264-73. PubMed ID: 18837007
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel splicing mutation in the PKD1 gene causes autosomal dominant polycystic kidney disease in a Chinese family: a case report.
    Xu P; Huang S; Li J; Zou Y; Gao M; Kang R; Yan J; Gao X; Gao Y
    BMC Med Genet; 2018 Nov; 19(1):198. PubMed ID: 30424739
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 6():35945. PubMed ID: 27782177
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification and Characterization of Novel Mutations in Chronic Kidney Disease (CKD) and Autosomal Dominant Polycystic Kidney Disease (ADPKD) in Saudi Subjects by Whole-Exome Sequencing.
    Alzahrani OR; Alatwi HE; Alharbi AA; Alessa AH; Al-Amer OM; Alanazi AFR; Shams AM; Alomari E; Naser AY; Alzahrani FA; Hosawi S; Alghamdi SM; Abdali WA; Elfaki I; Hawsawi YM
    Medicina (Kaunas); 2022 Nov; 58(11):. PubMed ID: 36422197
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 7():6. PubMed ID: 16430766
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel PKD1 and PKD2 mutations in autosomal dominant polycystic kidney disease (ADPKD).
    Hoefele J; Mayer K; Scholz M; Klein HG
    Nephrol Dial Transplant; 2011 Jul; 26(7):2181-8. PubMed ID: 21115670
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutational analysis of PKD1 gene in a Chinese family with autosomal dominant polycystic kidney disease.
    Liu J; Li L; Liu Q
    Int J Clin Exp Pathol; 2015; 8(10):13289-92. PubMed ID: 26722532
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutational Screening of PKD1 and PKD2 Genes in Iranian Population Diagnosed with Autosomal Dominant Polycystic Kidney Disease.
    Ranjzad F; Tara A; Basiri A; Aghdami N; Moghadasali R
    Clin Lab; 2017 Jul; 63(7):1261-1267. PubMed ID: 28792715
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic analysis of Iranian autosomal dominant polycystic kidney disease: new insight to haplotype analysis.
    Entezam M; Khatami MR; Saddadi F; Ayati M; Roozbeh J; Saghafi H; Keramatipour M
    Cell Mol Biol (Noisy-le-grand); 2016 Feb; 62(2):15-20. PubMed ID: 26950445
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutational screening of PKD1 and PKD2 in Indian ADPKD patients identified 95 genetic variants.
    Raj S; Singh RG; Das P
    Mutat Res; 2020; 821():111718. PubMed ID: 32823016
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.