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Select record 21
ArticlesPeer ReviewedFull Text
Variants in the WDR44 WD40-repeat domain cause a spectrum of ciliopathy by impairing ciliogenesis initiation
Author / Creator:Accogli, Andrea ; Shakya, Saurabh ; Yang, Taewoo ; Insinna, Christine ; Kim, Soo Yeon ; Bell, David ; Butov, Kirill R. ; Severino, Mariasavina ; Niceta, Marcello ; Scala, Marcello ; Lee, Hyun Sik ; Yoo, Taekyeong ; Stauffer, Jimmy ; Zhao, Huijie ; Fiorillo, Chiara ; Pedemonte, Marina ; Diana, Maria C. ; Baldassari, Simona ; Zakharova, Viktoria ; Shcherbina, Anna ; Rodina, Yulia ; Fagerberg, Christina ; Roos, Laura Sønderberg ; Wierzba, Jolanta ; Dobosz, Artur ; Gerard, Amanda ; Potocki, Lorraine ; Rosenfeld, Jill A. ; Lalani, Seema R. ; Scott, Tiana M. ; Scott, Daryl ; Azamian, Mahshid S. ; Louie, Raymond ; Moore, Hannah W. ; Champaigne, Neena L. ; Hollingsworth, Grace ; Torella, Annalaura ; Nigro, Vincenzo ; Ploski, Rafal ; Salpietro, Vincenzo ; Zara, Federico ; Pizzi, Simone ; Chillemi, Giovanni ; Ognibene, Marzia ; Cooney, Erin ; Do, Jenny ; Linnemann, Anders ; Larsen, Martin J. ; Specht, Suzanne ; Walters, Kylie J. ; Choi, Hee-Jung ; Choi, Murim ; Tartaglia, Marco ; Youkharibache, Phillippe ; Chae, Jong-Hee ; Capra, Valeria ; Park, Sung-Gyoo ; Westlake, Christopher J.
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2024-01, Vol.15 (1), p.365-365, Article 365
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ArticlesPeer ReviewedFull Text
Polycystins recruit cargo to distinct ciliary extracellular vesicle subtypes in C. elegans
Author / Creator:Nikonorova, Inna A. ; desRanleau, Elizabeth ; Jacobs, Katherine C. ; Saul, Josh ; Walsh, Jonathon D. ; Wang, Juan ; Barr, Maureen M.
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2025-04, Vol.16 (1), p.2899-18, Article 2899
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ArticlesPeer ReviewedFull Text
Adult human kidney organoids: cellular origin and disease modeling
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2022-11, Vol.54 (11), p.1593-1594
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Ultra high frequency ultrasound enables real-time visualization of blood supply from chorioallantoic membrane to human autosomal dominant polycystic kidney tissue
Author / Creator:Schueler, Jan ; Kuenzel, Jonas ; Thuesing, Anna ; Pion, Eric ; Behncke, Rose Yinghan ; Haegerling, Rene ; Fuchs, Dieter ; Kraus, Andre ; Buchholz, Bjoern ; Huang, Boqiang ; Merhof, Dorit ; Werner, Jens M. ; Schmidt, Katharina M. ; Hackl, Christina ; Aung, Thiha ; Haerteis, Silke
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2024-05, Vol.14 (1), p.10063-10063, Article 10063
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Reliability of radiomic analysis on multiparametric MRI for patients affected by autosomal dominant polycystic kidney disease
Author / Creator:Lussana, Francesca ; Lanzarone, Ettore ; Villa, Giulia ; Mastropietro, Alfonso ; Caroli, Anna ; Scalco, Elisa
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2025-05, Vol.15 (1), p.16526-12, Article 16526
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PKD1 mutation perturbs morphogenesis in tubular epithelial organoids derived from human pluripotent stem cells
Author / Creator:Scarlat, Alexandru ; Trionfini, Piera ; Rizzo, Paola ; Conti, Sara ; Longaretti, Lorena ; Breno, Matteo ; Longhi, Lorenzo ; Xinaris, Christodoulos ; Remuzzi, Giuseppe ; Benigni, Ariela ; Tomasoni, Susanna
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2025-03, Vol.15 (1), p.10375-13, Article 10375
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ArticlesPeer ReviewedFull Text
The epidermal growth factor receptor pathway in chronic kidney diseases
Author / Creator:Harskamp, Laura R. ; Gansevoort, Ron T. ; van Goor, Harry ; Meijer, Esther
Publisher:London: Nature Publishing Group UK
Journal title:Nature reviews. Nephrology, 2016-08, Vol.12 (8), p.496-506
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Why kidneys fail in autosomal dominant polycystic kidney disease
Author / Creator:Grantham, Jared J. ; Mulamalla, Sumanth ; Swenson-Fields, Katherine I.
Publisher:London: Nature Publishing Group UK
Journal title:Nature reviews. Nephrology, 2011-10, Vol.7 (10), p.556-566
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mTORC1-mediated inhibition of polycystin-1 expression drives renal cyst formation in tuberous sclerosis complex
Author / Creator:Pema, Monika ; Drusian, Luca ; Chiaravalli, Marco ; Castelli, Maddalena ; Yao, Qin ; Ricciardi, Sara ; Somlo, Stefan ; Qian, Feng ; Biffo, Stefano ; Boletta, Alessandra
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2016-03, Vol.7 (1), p.10786-11, Article 10786
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Select record 30
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Ketosis slows the progression of PKD: POLYCYSTIC KIDNEY DISEASE
Author / Creator:Carney, Ellen F.
Publisher:London: Nature Publishing Group UK
Journal title:Nature reviews. Nephrology, 2020-01, Vol.16 (1), p.1-1
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ArticlesPeer ReviewedFull Text
A genetic interaction network of five genes for human polycystic kidney and liver diseases defines polycystin-1 as the central determinant of cyst formation
Author / Creator:Fedeles, Sorin V ; Tian, Xin ; Gallagher, Anna-Rachel ; Mitobe, Michihiro ; Nishio, Saori ; Lee, Seung Hun ; Cai, Yiqiang ; Geng, Lin ; Crews, Craig M ; Somlo, Stefan
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2011-07, Vol.43 (7), p.639-647
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Select record 32
ArticlesPeer ReviewedFull Text
New treatment paradigms for ADPKD: moving towards precision medicine
Author / Creator:Lanktree, Matthew B. ; Chapman, Arlene B.
Publisher:London: Nature Publishing Group UK
Journal title:Nature reviews. Nephrology, 2017-12, Vol.13 (12), p.750-768
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ArticlesPeer ReviewedFull Text
Evaluation of tolvaptan-associated hepatic disorder using different national pharmacovigilance databases
Author / Creator:Uno, Takaya ; Hosomi, Kouichi ; Yokoyama, Satoshi
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2024-10, Vol.14 (1), p.25943-10, Article 25943
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Reversing polycystic kidney disease
Author / Creator:Boletta, Alessandra
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2021-12, Vol.53 (12), p.1623-1624
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ArticlesPeer ReviewedFull Text
The cilia protein IFT88 is required for spindle orientation in mitosis
Author / Creator:Delaval, Benedicte ; Bright, Alison ; Lawson, Nathan D. ; Doxsey, Stephen
Publisher:London: Nature Publishing Group UK
Journal title:Nature cell biology, 2011-04, Vol.13 (4), p.461-468
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ArticlesPeer ReviewedFull Text
Cystin genetic variants cause autosomal recessive polycystic kidney disease associated with altered Myc expression
Author / Creator:Yang, Chaozhe ; Harafuji, Naoe ; O’Connor, Amber K. ; Kesterson, Robert A. ; Watts, Jacob A. ; Majmundar, Amar J. ; Braun, Daniela A. ; Lek, Monkol ; Laricchia, Kristen M. ; Fathy, Hanan M. ; Mane, Shrikant ; Shril, Shirlee ; Hildebrandt, Friedhelm ; Guay-Woodford, Lisa M.
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2021-09, Vol.11 (1), p.18274-18274, Article 18274
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A high-throughput screening platform for Polycystic Kidney Disease (PKD) drug repurposing utilizing murine and human ADPKD cells
Author / Creator:Asawa, Rosita R. ; Danchik, Carina ; Zakharov, Alexey ; Chen, Yuchi ; Voss, Ty ; Jadhav, Ajit ; Wallace, Darren P. ; Trott, Josephine F. ; Weiss, Robert H. ; Simeonov, Anton ; Martinez, Natalia J.
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2020-03, Vol.10 (1), p.4203-4203, Article 4203
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Select record 38
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Inhibition of glucosylceramide accumulation results in effective blockade of polycystic kidney disease in mouse models
Author / Creator:Natoli, Thomas A ; Smith, Laurie A ; Rogers, Kelly A ; Wang, Bing ; Komarnitsky, Svetlana ; Budman, Yeva ; Belenky, Alexei ; Bukanov, Nikolay O ; Dackowski, William R ; Husson, Hervé ; Russo, Ryan J ; Shayman, James A ; Ledbetter, Steven R ; Leonard, John P ; Ibraghimov-Beskrovnaya, Oxana
Publisher:New York: Nature Publishing Group US
Journal title:Nature medicine, 2010-07, Vol.16 (7), p.788-792
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The tyrosine-kinase inhibitor Nintedanib ameliorates autosomal-dominant polycystic kidney disease
Author / Creator:Jamadar, Abeda ; Suma, Sreenath M. ; Mathew, Sijo ; Fields, Timothy A. ; Wallace, Darren P. ; Calvet, James P. ; Rao, Reena
Publisher:London: Nature Publishing Group UK
Journal title:Cell death & disease, 2021-10, Vol.12 (10), p.947-8, Article 947
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Translational research in ADPKD: lessons from animal models
Author / Creator:Happé, Hester ; Peters, Dorien J. M.
Publisher:London: Nature Publishing Group UK
Journal title:Nature reviews. Nephrology, 2014-10, Vol.10 (10), p.587-601
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Showing 21 to 40 of 91 results

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Variants in the WDR44 WD40-repeat domain cause a spectrum of ciliopathy by impairing ciliogenesis initiation

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Polycystins recruit cargo to distinct ciliary extracellular vesicle subtypes in C. elegans

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Adult human kidney organoids: cellular origin and disease modeling

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Ultra high frequency ultrasound enables real-time visualization of blood supply from chorioallantoic membrane to human autosomal dominant polycystic kidney tissue

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Reliability of radiomic analysis on multiparametric MRI for patients affected by autosomal dominant polycystic kidney disease

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PKD1 mutation perturbs morphogenesis in tubular epithelial organoids derived from human pluripotent stem cells

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The epidermal growth factor receptor pathway in chronic kidney diseases

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Why kidneys fail in autosomal dominant polycystic kidney disease

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mTORC1-mediated inhibition of polycystin-1 expression drives renal cyst formation in tuberous sclerosis complex

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Ketosis slows the progression of PKD: POLYCYSTIC KIDNEY DISEASE

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A genetic interaction network of five genes for human polycystic kidney and liver diseases defines polycystin-1 as the central determinant of cyst formation

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New treatment paradigms for ADPKD: moving towards precision medicine

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Evaluation of tolvaptan-associated hepatic disorder using different national pharmacovigilance databases

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Reversing polycystic kidney disease

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The cilia protein IFT88 is required for spindle orientation in mitosis

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Cystin genetic variants cause autosomal recessive polycystic kidney disease associated with altered Myc expression

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A high-throughput screening platform for Polycystic Kidney Disease (PKD) drug repurposing utilizing murine and human ADPKD cells

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Inhibition of glucosylceramide accumulation results in effective blockade of polycystic kidney disease in mouse models

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The tyrosine-kinase inhibitor Nintedanib ameliorates autosomal-dominant polycystic kidney disease

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Translational research in ADPKD: lessons from animal models

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