Results 1 to 10 of about 53,957 (281)

EGR1 Nuclear Condensates Promote Renal Cyst Development in Polycystic Kidney Disease. [PDF]

Exploration (Beijing)
Ren C, Wu Z, Li M, Du Y, Zhou H, Quan Y, Xiong M, Wang Y, Qiu Z, Zhu S, Li X, He J, Gao C, Cai H, Li T, Yang B.   +15 more
europepmc   +1 more source

Mechanistic Insights into the Pathogenesis of Polycystic Kidney Disease. [PDF]

Cells
Al-Orjani Q, Alshriem LA, Gallagher G, Buqaileh R, Azizi N, AbouAlaiwi W.   +5 more
europepmc   +1 more source

Coincidence of autosomal dominant polycystic kidney disease and Alport syndrome: a case report and literature review. [PDF]

CEN Case Rep
Liu R, Liu F.
europepmc   +1 more source

Inferior Vena Cava Thrombosis After Nephrectomy of the Native Kidneys in Patients With Autosomal Dominant Polycystic Kidney Disease. [PDF]

IJU Case Rep
Matsushita Y, Watanabe K, Aoki T, Tsuyuki H, Watanabe H, Tamura K, Katahashi K, Isobe S, Motoyama D, Inamoto T.   +9 more
europepmc   +1 more source

Autosomal dominant polycystic kidney disease is not a risk factor for scoliosis. [PDF]

Int Urol Nephrol
Jankowska Z, Niemczyk M.
europepmc   +1 more source

Polycystic Kidney Disease [PDF]

Comprehensive Physiology, 2017
ABSTRACT Renal cysts, which arise from renal tubules, can be seen in a variety of hereditary and nonhereditary entities. Common mechanisms associated with renal cyst formation include increased cell proliferation, epithelial fluid secretion, and extracellular matrix remodeling. Hereditary polycystic kidney disease
Joseph, Ghata, Benjamin D, Cowley
core   +5 more sources

Kynurenines in polycystic kidney disease

Journal of Nephrology, 2022
Abstract Background Autosomal dominant polycystic kidney disease (ADPKD) is a common hereditary disorder, characterized by kidney cyst formation. A major pathological feature of ADPKD is the development of interstitial inflammation.
Jost, Klawitter, Matthew J, Jackson, Peter H, Smith, Katharina, Hopp, Michel, Chonchol, Berenice Y, Gitomer, Melissa A, Cadnapaphornchai, Uwe, Christians, Jelena, Klawitter   +8 more
openaire   +2 more sources

Polycystic Kidney/Liver Disease

Clinics in Liver Disease, 2022
Autosomal dominant polycystic kidney disease (ADPKD) is a genetic disorder that leads to chronic kidney disease and end-stage kidney disease (ESKD). Polycystic liver disease (PCLD) is the most common extrarenal manifestation of ADPKD. Though isolated PCLD and PCLD due to ADPKD are genetically distinct, they follow a similar clinical course of ...
Rebecca, Roediger, Douglas, Dieterich, Pramodh, Chanumolu, Priya, Deshpande   +3 more
openaire   +2 more sources