Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Binu M. Paul"'
Autor:
Gregory B. Vanden Heuvel, Binu M. Paul
Publikováno v:
Wiley Interdisciplinary Reviews: Developmental Biology. 3:465-487
Polycystic kidney disease (PKD) is a life-threatening genetic disorder characterized by the presence of fluid-filled cysts primarily in the kidneys. PKD can be inherited as autosomal recessive (ARPKD) or autosomal dominant (ADPKD) traits. Mutations i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::738b1b685e24400196ba7020dda26ee8
https://doi.org/10.1002/wdev.152
https://doi.org/10.1002/wdev.152
Autor:
Moonnoh R. Lee, Mark B. Consugar, Vicente E. Torres, Daniel G. Bichet, Eliecer Coto, Edgar Almeida, Jamie L. Sundsbak, Maurizio Clementi, Katharina Hopp, Vickie J. Kubly, Sandro Rossetti, Peter C. Harris, Nadja Bogdanova, Christina M. Heyer, Binu M. Paul
Publikováno v:
Kidney International. 85:383-392
Mutations to PKD1 and PKD2 are associated with autosomal dominant polycystic kidney disease (ADPKD). The absence of apparent PKD1/PKD2 linkage in five published European or North American families with ADPKD suggested a third locus, designated PKD3 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ca9d521855023ad28c7ffdf664854c7
https://doi.org/10.1038/ki.2013.227
https://doi.org/10.1038/ki.2013.227
Autor:
Gregory G. Germino, Lynn Magenheimer, Carol G. Carlton, Gregory B. Vanden Heuvel, Dianne Vassmer, Binu M. Paul, Klaus Piontek, Aaron Taylor
Publikováno v:
Developmental Dynamics. 240:1493-1501
Polycystic kidney diseases (PKD) are inherited disorders characterized by fluid-filled cysts primarily in the kidneys. We previously reported differences between the expression of Cux1, p21, and p27 in the cpk and Pkd1 null mouse models of PKD. Embry
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d5020797cd5fff714a5a83e00e9402d
https://doi.org/10.1002/dvdy.22625
https://doi.org/10.1002/dvdy.22625
Autor:
Richard C. Baybutt, Joshua C. Wright, Greg Vanden Heuvel, Binu M. Paul, Erica L. Andres, Anna Woo
Publikováno v:
The FASEB Journal. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7b18bde0ee3525a5df307266cb0f527
https://doi.org/10.1096/fasebj.29.1_supplement.663.3
https://doi.org/10.1096/fasebj.29.1_supplement.663.3
Autor:
Binu M, Paul, Gregory B, Vanden Heuvel
Publikováno v:
Wiley interdisciplinary reviews. Developmental biology. 3(6)
Polycystic kidney disease (PKD) is a life-threatening genetic disorder characterized by the presence of fluid-filled cysts primarily in the kidneys. PKD can be inherited as autosomal recessive (ARPKD) or autosomal dominant (ADPKD) traits. Mutations i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a08460fa9bfcac72238c66490e0f74cb
https://pubmed.ncbi.nlm.nih.gov/25186187
https://pubmed.ncbi.nlm.nih.gov/25186187
Autor:
Darren P. Wallace, Jing Zhou, Jennifer G. Brantley, Brandon Chapman, Binu M. Paul, Neal I. Alcalay, Gregory B. Vanden Heuvel, Dianne Vassmer, Madhulika Sharma, Robin L. Maser
Publikováno v:
American journal of physiology. Renal physiology. 295(6)
Polycystic kidney diseases (PKD) are inherited as autosomal dominant (ADPKD) or autosomal recessive (ARPKD) traits and are characterized by progressive enlargement of renal cysts. Aberrant cell proliferation is a key feature in the progression of PKD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a82708bc5b3109d11d0eff78fad85ff1
https://pubmed.ncbi.nlm.nih.gov/18829740
https://pubmed.ncbi.nlm.nih.gov/18829740