Literature DB >> 14551343

Autosomal dominant polycystic kidney disease: modifier genes and endothelial dysfunction.

Olivier Devuyst, Alexandre Persu, Minh-Truc Vo-Cong.   

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Year:  2003        PMID： 14551343     DOI： 10.1093/ndt/gfg351

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN： 0931-0509            Impact factor:   5.992


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  3 in total

1.  Role of endothelial nitric oxide synthase VNTR (intron 4 a/b) polymorphism on the progression of renal disease in autosomal dominant polycystic kidney disease.

Authors:  Ramprasad Elumalai; Soundararajan Periasamy; Gnanasambandan Ramanathan; Bhaskar Vks Lakkakula
Journal:  J Renal Inj Prev       Date:  2014-07-01

2.  Detection and impact of rare regulatory variants in human disease.

Authors:  Xin Li; Stephen B Montgomery
Journal:  Front Genet       Date:  2013-05-31       Impact factor: 4.599

3.  Human Evaluation of the Glu298Asp Polymorphism in NOS3 Gene and its Relationship with Onset age of ESRD in Iranian Patients Suffering from ADPKD.

Authors:  Negin Dasar; Sayyed Mohammad Hossein Ghaderian; Eznollah Azargashb
Journal:  Int J Mol Cell Med       Date:  2012
  3 in total

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