Results 1 to 10 of about 1,438 (134)

THSD7A-associated membranous nephropathy involves both complement-mediated and autonomous podocyte injury [PDF]

open access: yesFrontiers in Pharmacology
Membranous nephropathy (MN) continues to be a leading cause of nephrotic syndrome in non-diabetic adults. As a unique subtype in the serology-based classification of MN, thrombospondin type 1 domain containing 7A (THSD7A)-associated MN has attracted ...
Deepak Malhotra   +2 more
exaly   +7 more sources

THSD7A as a novel prognostic factor for colorectal carcinoma [PDF]

open access: yesBMC Gastroenterology
Background Thrombospondin type 1 domain-containing 7 A (THSD7A) expression, an angiogenesis-related protein, has been implicated in various aspects of cancer progression, reflecting its potential as a prognostic marker for various cancers.
Oktay Halit Aktepe   +8 more
doaj   +4 more sources

THSD7A Positivity Is Associated with High Expression of FAK in Prostate Cancer

open access: yesDiagnostics, 2023
Prostate cancer is one of the most common malignancies, and there are a wide range of treatment options after diagnosis. Most prostate cancers behave in an indolent manner.
Matthias Saar
exaly   +6 more sources

Expression of THSD7A in neoplasm tissues and its relationship with proteinuria [PDF]

open access: yesBMC Nephrology, 2019
Background Thrombospondin type 1 domain containing 7A (THSD7A) was recently identified target autoantigen in membranous nephropathy (MN). However, patients with positive THSD7A expression were prone to have malignancies.
Dandan Dong, Jiamei Luo, Ping Zhang
exaly   +5 more sources

Characterization of THSD7A-antibodies not binding to glomerular THSD7A in a patient with diabetes mellitus but no membranous nephropathy [PDF]

open access: yesScientific Reports, 2021
Membranous nephropathy (MN) is an autoimmune disease caused by autoantibodies against the podocyte antigens phospholipase A2 receptor 1 (PLA2R1) and thrombospondin type 1 domain containing protein 7A (THSD7A) in 80% and 2–3% of patients, respectively ...
Linda Reinhard   +8 more
doaj   +3 more sources

Clinical Features and Pathology of PLA2R and THSD7A-Associated Membranous Nephropathy: A Single-Center Study from China [PDF]

open access: yesImmunoTargets and Therapy
Yan Pan, Wei Dong Chen, Lei Liu, Huijuan Yang, Baochao Chang, Caixia Cui Department of Nephrology, First Affiliated Hospital of Bengbu Medical College, Bengbu, Anhui Province, People’s Republic of ChinaCorrespondence: Wei Dong Chen, Email cwd2012@163 ...
Baochao Chang
exaly   +4 more sources

An update on clinical significance of use of THSD7A in diagnosing idiopathic membranous nephropathy: a systematic review and meta-analysis of THSD7A in IMN [PDF]

open access: yesRenal Failure, 2018
Background: THSD7A is a new target antigen of idiopathic membranous nephropathy (IMN). Moreover, malignancies are also found in patients with THSD7A-positive membranous nephropathy.
Song Ren   +6 more
doaj   +4 more sources

The Alternative Pathway Is Necessary and Sufficient for Complement Activation by Anti-THSD7A Autoantibodies, Which Are Predominantly IgG4 in Membranous Nephropathy

open access: yesFrontiers in Immunology, 2022
Membranous nephropathy (MN) is an immune kidney disease characterized by glomerular subepithelial immune complexes (ICs) containing antigen, IgG, and products of complement activation. Whereas proteinuria is caused by complement-mediated podocyte injury,
Tiffany N Caza   +2 more
exaly   +3 more sources

THSD7A-positive membranous nephropathy after kidney transplantation: A case report

open access: yesNefrología (English Edition), 2023
Membranous nephropathy (MN) is a common cause of nephrotic syndrome after kidney transplantation (KT); however, scarce is known regarding post-KT thrombospondin type-1 domain-containing 7A (THSD7A)-positive MN.
Eulàlia Solà-Porta   +8 more
doaj   +6 more sources

A Novel Insight into the Role of PLA2R and THSD7A in Membranous Nephropathy [PDF]

open access: yesJournal of Immunology Research, 2021
Membranous nephropathy (MN) is an organ-restricted autoimmune disease mainly caused by circulating autoantibodies against podocyte antigens, including the M-type phospholipase A2 receptor (PLA2R) and thrombospondin domain-containing 7A (THSD7A ...
Pingna Zhang   +7 more
doaj   +4 more sources

Home - About - Disclaimer - Privacy