Disease: Glomerulopathy with fibronectin deposits
- A case of familial glomerulopathy with fibronectin deposits caused by the Y973C mutation in fibronectin
- A case of unexpected diagnosis of fibronectin glomerulopathy with histological features of membranoproliferative glomerulonephritis
- A child with genetic FN1 mutation in the absence of classic glomerulopathy with fibronectin deposits(GFND) findings on biopsy
- A high-impact FN1 variant correlates with fibronectin-mediated glomerulopathy via decreased binding to collagen type IV
- A novel single amino acid deletion impairs fibronectin function and causes familial glomerulopathy with fibronectin deposits: case report of a family
- A novel variant in <em>FN1</em> in a family with fibronectin glomerulopathy
- A Rare Cause of Nephrotic Syndrome in Adults - Collagenofibrotic Glomerulopathy
- A recurrent fibronectin glomerulopathy in a renal transplant patient: a case report
- Acute and chronic vascular rejection in nonhuman primate kidney transplantation
- AJKD Atlas of Renal Pathology: Fibronectin Glomerulopathy
- Alterations in extracellular matrix components in transplant glomerulopathy
- An aid to the diagnosis of genetic disorders underlying adult-onset renal failure: a literature review
- Anti-basement membrane glomerulopathy in experimental trypanosomiasis
- Antigenic specificities of glomerular-bound autoantibodies in membranous glomerulopathy induced by mercuric chloride
- Association of glomerulopathy with the 5'-end polymorphism of the aldose reductase gene and renal insufficiency in type 2 diabetic patients
- Bortezomib-containing regiment in treating glomerulopathy with fibronectin deposits combined with monoclonal gammopathy of undetermined significance: a case report and literature review
- Case Report: Recurrent Deposition in Renal Allografts: A Rare Case of Fibronectin Glomerulopathy Overlooked in Native Kidneys
- Characterization of glomerular diseases using proteomic analysis of laser capture microdissected glomeruli
- Clinical and morphological features of fibronectin glomerulopathy: a report of ten patients from a single institution
- Clinicopathologic characteristics of nodular glomerulosclerosis in Chinese patients with type 2 diabetes
- Clinicopathological analysis of glomerulopathy with fibronectin deposits (GFND): a case of sporadic, elderly-onset GFND with codeposition of IgA, C1q, and fibrinogen
- Clinicopathological and morphometrical analysis of 5 cases from 4 families of fibronectin glomerulopathy
- Detection of a Splice Site Variant in a Patient with Glomerulopathy and Fibronectin Deposits
- Extraglomerular Vascular Involvement of Glomerulopathy with Fibronectin Deposits
- Familial glomerulopathy with giant fibrillar (fibronectin-positive) deposits: 15-year follow-up in a large kindred
- Familial lobular glomerulopathy: first case report in Asia
- Fibronectin Conformation and Assembly: Analysis of Fibronectin Deletion Mutants and Fibronectin Glomerulopathy (GFND) Mutants
- Fibronectin expression in human mesangial cell cultures and its alterations by adriamycin
- Fibronectin glomerulopathy
- Fibronectin glomerulopathy - A sporadic case with unusual clinical manifestation
- Fibronectin Glomerulopathy Caused by the Y973C Mutation in Fibronectin: A Case Report and Literature Review
- Fibronectin glomerulopathy complicated with persistent cloaca and congenital esophageal atresia: a case report and literature review
- Fibronectin Glomerulopathy Confused with Glomerular Endothelial Injury in a Patient with Takotsubo Cardiomyopathy
- Fibronectin glomerulopathy in a 34-year-old man: a case report
- Fibronectin glomerulopathy in a 88 year-old male with acute kidney injury on chronic kidney disease: A case report and a review of the literature
- Fibronectin glomerulopathy in a kidney allograft biopsy
- Fibronectin glomerulopathy with monoclonal gammopathy responding to bortezomib plus dexamethasone: a case report
- Fibronectin glomerulopathy with nephrotic syndrome in a 3-year-old male
- Fibronectin Glomerulopathy: A Rare Autosomal Dominant Glomerular Disease
- Fibronectin glomerulopathy: an unusual cause of adult-onset nephrotic syndrome
- Fibronectin non-amyloid glomerulopathy
- Frequent COL4 mutations in familial microhematuria accompanied by later-onset Alport nephropathy due to focal segmental glomerulosclerosis
- Generation of an induced pluripotent stem cell line XJHi001-A from a fibronectin glomerulopathy patient carrying a heterozygous NM_212482.2(C.5888-1G > C) mutation in the FN1 gene
- Generation of the integration-free induced pluripotent stem cell line (FHUSTCi001-A) from a patient with glomerulopathy with fibronectin deposits harboring FN1 mutation
- Glomerular kidney disease in dysproteinemia and with organized deposits
- Glomerular matrix proteins in nodular glomerulosclerosis in association with light chain deposition disease and diabetes mellitus
- Glomerulopathies with organized deposits
- Glomerulopathy associated with predominant fibronectin deposits: a newly recognized hereditary disease
- Glomerulopathy associated with predominant fibronectin deposits: exclusion of the genes for fibronectin, villin and desmin as causative genes
- Glomerulopathy with fibronectin deposits: a clinicopathological study
- GLUT-1 overexpression: Link between hemodynamic and metabolic factors in glomerular injury?
- Identification of mutations in FN1 leading to glomerulopathy with fibronectin deposits
- Insight into the physiological function(s) of uteroglobin by gene-knockout and antisense-transgenic approaches
- Mechanical stretch-induced fibronectin and transforming growth factor-beta1 production in human mesangial cells is p38 mitogen-activated protein kinase-dependent
- Membranous glomerulonephritis in the Iberian lynx (Lynx pardinus)
- Molecular cloning of the critical region for glomerulopathy with fibronectin deposits (GFND) and evaluation of candidate genes
- Molecular genetics of familial hematuric diseases
- Morphology of basement membrane and associated matrix proteins in normal and pathological tissues
- Mutations in FN1 cause glomerulopathy with fibronectin deposits
- Newer glomerular diseases
- Pathogenesis of glomerulosclerosis in light chain deposition disease. Role for transforming growth factor-beta
- Pathologic-genomic correlation identified a novel variant in FN1 and established the diagnosis of recurrent fibronectin glomerulopathy in the kidney allograft
- Polymorphism of the uteroglobin gene in systemic lupus erythematosus and IgA nephropathy
- Prednisone-induced sustained remission in a patient with familial fibronectin glomerulopathy (GFND)
- Renal diseases with organized deposits: an algorithmic approach to classification and clinicopathologic diagnosis
- Renal lesions of paraproteinemias and fibrillary glomerulopathies
- The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster
- Ultrastructural immunohistochemical localization of polyclonal IgG, C3, and amyloid P component on the congo red-negative amyloid-like fibrils of fibrillary glomerulopathy
- Uteroglobin: physiological role in normal glomerular function uncovered by targeted disruption of the uteroglobin gene in mice