Results 191 to 200 of about 462,629 (365)
Autosomal dominant polycystic kidney disease. [PDF]
John C. Lieske, F. Gary Toback
openalex +1 more source
ABSTRACT Chloride channels are involved in many cellular processes, including cell volume regulation, modulation of cell excitability, and electrolyte and water secretion. Mutations of these proteins are associated with heterogeneous diseases such as myotonia, cystic fibrosis, epilepsy, deafness, lysosomal storage disease, and various kinds of renal ...
Paola Laghetti+4 more
wiley +1 more source
Importance of IFT140 in Patients with Polycystic Kidney Disease Without a Family History
Introduction: Recently, the monoallelic loss-of-function IFT140 variant was identified as a causative gene for autosomal dominant polycystic kidney disease (ADPKD).
Takuya Fujimaru+19 more
doaj
Adult polycystic kidney disease: Studies of the defect in urine concentration
Manuel Martínez–Maldonado+3 more
openalex +1 more source
Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene. [PDF]
M.H. Breuning+6 more
openalex +1 more source
Abstract Aims To evaluate whether type 2 diabetes status modifies the efficacy and safety of combining zibotentan (zibo), a selective endothelin receptor antagonist, and dapagliflozin (dapa) compared to placebo plus dapagliflozin in individuals with chronic kidney disease (CKD).
Victor Wasehuus+7 more
wiley +1 more source
Exclusion of autosomal dominant polycystic kidney disease type II (ADPKD2) from 160 cM of chromosome 1. [PDF]
Sushil Kumar+4 more
openalex +1 more source
Our study demonstrates the feasibility of using diffusion tensor imaging (DTI) to evaluate pediatric kidney transplants. Significant differences in fractional anisotropy (FA) and track length were observed between transplanted and healthy kidneys, reflecting altered microstructural organization.
Suraj D. Serai+5 more
wiley +1 more source