Results 41 to 50 of about 7,104 (202)

Mapping of the podocin proximity-dependent proteome reveals novel components of the kidney podocyte foot process

open access: yesFrontiers in Cell and Developmental Biology, 2023
Introduction: The unique architecture of glomerular podocytes is integral to kidney filtration. Interdigitating foot processes extend from the podocyte cell body, wrap around fenestrated capillaries, and form specialized junctional complexes termed slit ...
Gary F. Gerlach   +4 more
doaj   +1 more source

Podocin and Nephrotic Syndrome [PDF]

open access: yesJournal of the American Society of Nephrology, 2004
Idiopathic nephrotic syndrome (INS) is the most frequent glomerular disease in childhood. Most of the children respond to corticosteroid therapy whereas 10% of them fail to respond to this treatment.
openaire   +1 more source

Evaluation of Tryptic Podocin Peptide in Urine Sediment Using LC-MS-MRM Method as a Potential Biomarker of Glomerular Injury in Dogs with Clinical Signs of Renal and Cardiac Disorders

open access: yesMolecules, 2019
The early asymptomatic stage of glomerular injury is a diagnostic challenge in the course of renal and extra-renal disease, e.g., heart insufficiency. It was found that podocin, a podocyte-specific protein present in the urine, may serve as a biomarker ...
Barbara Szczepankiewicz   +6 more
doaj   +1 more source

Familial Focal Segmental Glomerulosclerosis With Late-Onset Presentation and R229Q/R291W Podocin Mutations

open access: yesFrontiers in Genetics, 2020
IntroductionPathogenic variants in different genes have been described as involved in the development of familial focal segmental glomerulosclerosis (FSGS).
Michelle T. P. Riguetti   +6 more
doaj   +1 more source

Endoplasmic reticulum–retained podocin mutants are massively degraded by the proteasome [PDF]

open access: yesJournal of Biological Chemistry, 2018
Podocin is a key component of the slit diaphragm in the glomerular filtration barrier, and mutations in the podocin-encoding gene NPHS2 are a common cause of hereditary steroid-resistant nephrotic syndrome. A mutant allele encoding podocin with a p.R138Q amino acid substitution is the most frequent pathogenic variant in European and North American ...
Maria-Carmen, Serrano-Perez   +8 more
openaire   +3 more sources

The insect nephrocyte is a podocyte-like cell with a filtration slit diaphragm. [PDF]

open access: yes, 2008
The nephron is the basic structural and functional unit of the vertebrate kidney. It is composed of a glomerulus, the site of ultrafiltration, and a renal tubule, along which the filtrate is modified. Although widely regarded as a vertebrate adaptation, '
Bader, Augustinus   +16 more
core   +1 more source

Molecular Mechanisms of Proteinuria in Focal Segmental Glomerulosclerosis

open access: yesFrontiers in Medicine, 2018
Focal segmental glomerulosclerosis (FSGS) is the most common primary glomerular disease resulting in end-stage renal disease in the USA and is increasing in prevalence worldwide.
Yumeng Wen, Sapna Shah, Kirk N. Campbell
doaj   +1 more source

mRNA Expression of Podocyte Associated Proteins in Peripheral Blood Mononuclear Cells of Type 2 Diabetes Mellitus Patients with and without Nephropathy [PDF]

open access: yesJournal of Krishna Institute of Medical Sciences University, 2020
Background: Diabetic nephropathy is the leading cause of End-Stage Renal Disease (ESRD) emerging in developed as well as developing countries, with the complicated pathogenesis.
Gouri M. Bhoite   +4 more
doaj  

Containing anti-PLA2R IgG antibody induces podocyte injury in idiopathic membranous nephropathy

open access: yesRenal Failure, 2023
Background Idiopathic membranous nephropathy is widely recognized as an autoimmune kidney disease that is accompanied by the discovery of several autoantibodies, and the antibody subclass in the circulation of patients with iMN is mainly IgG.
Ying Zhang   +8 more
doaj   +1 more source

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