Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sorin, Fedeles"'
Publikováno v:
Kidney Medicine, Vol 5, Iss 3, Pp 100596- (2023)
Autosomal dominant polycystic kidney disease (ADPKD) is part of a spectrum of inherited diseases that also includes autosomal recessive polycystic kidney disease, autosomal dominant polycystic liver disease, and an expanding group of recessively inhe
Externí odkaz:
https://doaj.org/article/a51b69e5577e4313966d6d84ac980f92
Autor:
Sorin Fedeles, Ronald D. Perrone
Publikováno v:
Clinical journal of the American Society of Nephrology : CJASN.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48aaa978ffc250083339dc1008ac704e
https://pubmed.ncbi.nlm.nih.gov/35998972
https://pubmed.ncbi.nlm.nih.gov/35998972
Autor:
Matteus Krappitz, Rishi Bhardwaj, Ke Dong, Tobias Staudner, Duygu Elif Yilmaz, Carlotta Pioppini, Parisa Westergerling, David Ruemmele, Till Hollmann, Thuy Anh Nguyen, Yiqiang Cai, Anna-Rachel Gallagher, Stefan Somlo, Sorin Fedeles
Publikováno v:
Journal of the American Society of Nephrology. 34:110-121
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::498d5f7b92153529bc205f06f6541fd8
https://doi.org/10.1681/asn.2021091180
https://doi.org/10.1681/asn.2021091180
Autor:
Matteus, Krappitz, Rishi, Bhardwaj, Ke, Dong, Tobias, Staudner, Duygu Elif, Yilmaz, Carlotta, Pioppini, Parisa, Westergerling, David, Ruemmele, Till, Hollmann, Thuy Anh, Nguyen, Yiqiang, Cai, Anna-Rachel, Gallagher, Stefan, Somlo, Sorin, Fedeles
Publikováno v:
Journal of the American Society of Nephrology : JASN.
Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations inWe engineered aExpression of active XBP1 in cultured cells bearing PC1Modulating ER chaperone function through XBP1 activity improved Pkd in a murine model of PC1, suggesti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f4eb46d50a8c36dea54862cbb897c17c
https://pubmed.ncbi.nlm.nih.gov/36270750
https://pubmed.ncbi.nlm.nih.gov/36270750
Autor:
Thuy N, Vien, Leo C T, Ng, Jessica M, Smith, Ke, Dong, Matteus, Krappitz, Vladimir G, Gainullin, Sorin, Fedeles, Peter C, Harris, Stefan, Somlo, Paul G, DeCaen
Publikováno v:
Journal of Cell Science
article-version (VoR) Version of Record
article-version (VoR) Version of Record
Approximately 15% of autosomal dominant polycystic kidney disease (ADPKD) is caused by variants in PKD2. PKD2 encodes polycystin-2, which forms an ion channel in primary cilia and endoplasmic reticulum (ER) membranes of renal collecting duct cells. E
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e79f9690076b452b083a2e7eecaf5ee9
https://pubmed.ncbi.nlm.nih.gov/33199522
https://pubmed.ncbi.nlm.nih.gov/33199522
Autor:
Yasunobu, Ishikawa, Sorin, Fedeles, Arnaud, Marlier, Chao, Zhang, Anna-Rachel, Gallagher, Ann-Hwee, Lee, Stefan, Somlo
Publikováno v:
Journal of the American Society of Nephrology : JASN.
BACKGROUND: SEC63 encodes a resident protein in the endoplasmic reticulum membrane that, when mutated, causes human autosomal dominant polycystic liver disease. Selective inactivation of Sec63 in all distal nephron segments in embryonic mouse kidney
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8e00a341fe33ddfccca6ad134bc59386
https://pubmed.ncbi.nlm.nih.gov/30745418
https://pubmed.ncbi.nlm.nih.gov/30745418