Vesicoureteral reflux and the extracellular matrix connection

No abstract is available for this paper.

• Publication year

  2017

• Venue

  Pediatric nephrology (Berlin, West)

• Publication date

  2017-04-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/s00467-016-3386-5PMID 27139901PMCID PMC5376290
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Cutis laxa

  2020cited by this paper
• Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux

  2016cited by this paper
• Vesicoureteral Reflux Index: 2-Institution Analysis and Validation.

  2016cited by this paper
• Vesicoureteric reflux in children.

  2015cited by this paper
• Giant Urinary Bladder Diverticula presenting as Epigastric Mass and Dyspepsia

  2014cited by this paper
• First Prize: Evaluation of the Tensile Strength of the Human Ureter—Preliminary Results

  2014cited by this paper
• Basic Science : First Prize Evaluation of the Tensile Strength of the Human Ureter — Preliminary Results

  2014cited by this paper
• Cellular and molecular mechanisms in kidney fibrosis.

  2014cited by this paper
• Vesicoureteric reflux and reflux nephropathy: from mouse models to childhood disease

  2014cited by this paper
• Vesicoureteral Refl ux

  2014cited by this paper
• Remodelling the extracellular matrix in development and disease

  2014cited by this paper
• Cutis Laxa.

  2014cited by this paper
• Lamina propria: The functional center of the bladder?

  2014cited by this paper
• Extracellular matrix assembly: a multiscale deconstruction

  2014cited by this paper
• Biaxial mechanical properties of human ureter under tension.

  2014cited by this paper
• Tenascin-X promotes epithelial-to-mesenchymal transition by activating latent TGF-β

  2014cited by this paper
• Relationship of generalized joint hypermobility with vesicoureteral reflux and urinary tract infection.

  2014cited by this paper
• Vesicourethral Reflux in Pediatrics With Hypermobility Syndrome

  2013cited by this paper
• TNXB mutations can cause vesicoureteral reflux.

  2013cited by this paper
• Radiologic Findings in Cutis Laxa Syndrome and Unusual Association with Hypertrophic Pyloric Stenosis

  2013cited by this paper
• Clinical heterogeneity in patients with the hypermobility type of Ehlers-Danlos syndrome.

  2013cited by this paper
• Multiaxial mechanical behaviour of the passive ureteral wall: experimental study and mathematical characterisation

  2012cited by this paper
• Is joint hypermobility associated with vesico‐ureteral reflux? An assessment of 50 patients

  2012cited by this paper
• The Ehlers–Danlos syndrome, a disorder with many faces

  2012cited by this paper
• Diverse Roles of TGF-β/Smads in Renal Fibrosis and Inflammation

  2011cited by this paper
• Cellular and molecular mechanisms of renal fibrosis

  2011cited by this paper
• Extracellular matrix degradation and remodeling in development and disease.

  2011cited by this paper
• The natural history of vesicoureteral reflux

  2011cited by this paper
• Defining protein expression in the urothelium: a problem of more than transitional interest.

  2011cited by this paper
• Mild Muscular Features in Tenascin-X Knockout Mice, A Model of Ehlers–Danlos Syndrome

  2011cited by this paper
• Role of TGF-β in chronic kidney disease: an integration of tubular, glomerular and vascular effects

  2011cited by this paper
• Clinical and genetic aspects of Ehlers-Danlos syndrome, classic type

  2010cited by this paper
• Williams-Beuren syndrome.

  2010cited by this paper
• Renal fibrosis

  2010cited by this paper
• Fibulin-4 Deficiency Results in Ascending Aortic Aneurysms: A Potential Link Between Abnormal Smooth Muscle Cell Phenotype and Aneurysm Progression

  2010cited by this paper
• Williams-Beuren syndrome.

  2010cited by this paper
• COL5A1 signal peptide mutations interfere with protein secretion and cause classic Ehlers‐Danlos syndrome

  2009cited by this paper
• Collagens

  2009cited by this paper
• Fibulin-5, an integrin-binding matricellular protein: its function in development and disease

  2009cited by this paper
• Tissue elasticity and the ageing elastic fibre

  2009cited by this paper
• Extracellular Matrix Molecules: Potential Targets in Pharmacotherapy

  2009cited by this paper
• Tenascin-X induces cell detachment through p38 mitogen-activated protein kinase activation.

  2009cited by this paper
• Autosomal recessive cutis laxa syndrome revisited

  2009cited by this paper
• The lack of clinical distinction between the hypermobility type of Ehlers–Danlos syndrome and the joint hypermobility syndrome (a.k.a. hypermobility syndrome)

  2009cited by this paper
• The bladder extracellular matrix. Part I: architecture, development and disease

  2009cited by this paper
• Embryology and anatomy of the vesicoureteric junction with special reference to the etiology of vesicoureteral reflux

  2009cited by this paper
• Uroplakins in urothelial biology, function, and disease.

  2009cited by this paper
• Dextranomer/hyaluronic Acid copolymer implant for vesicoureteral reflux: role of myofibroblast differentiation.

  2009cited by this paper
• Ehlers-Danlos syndromes and Marfan syndrome.

  2008cited by this paper
• Endoscopic Treatment of Vesicoureteral Reflux with Dextranomer/Hyaluronic Acid in Children

  2008cited by this paper
• Laminin and transforming growth factor beta-1 in children with vesicoureteric reflux

  2008cited by this paper
• Reflux nephropathy.

  2008cited by this paper
• Vesicoureteral reflux.

  2008cited by this paper
• Urological radiographic manifestations of the Ehlers-Danlos syndrome.

  2007cited by this paper
• Extracellular microenvironment and cytokine profile of the ureterovesical junction in children with vesicoureteral reflux.

  2007cited by this paper
• Ehlers–Danlos syndrome due to tenascin‐X deficiency: Muscle weakness and contractures support overlap with collagen VI myopathies

  2007cited by this paper
• TGF-β in renal injury and disease

  2007cited by this paper
• Reduced quantitative muscle function in tenascin-X deficient Ehlers-Danlos patients.

  2007cited by this paper
• Histopathological changes associated with dextranomer/hyaluronic acid injection for pediatric vesicoureteral reflux.

  2007cited by this paper
• Are diagnostic criteria for general joint hypermobility and benign joint hypermobility syndrome based on reproducible and valid tests? A review of the literature.

  2007cited by this paper
• TGF-beta in renal injury and disease.

  2007cited by this paper
• Epidemiology of general joint hypermobility and basis for the proposed criteria for benign joint hypermobility syndrome: review of the literature.

  2007cited by this paper
• Dermal connective tissue development in mice: an essential role for tenascin-X

  2006cited by this paper
• Structural changes of the intravesical ureter in children with vesicoureteral reflux-does ischemia have a role?

  2006cited by this paper
• Elastic fibres in health and disease

  2006cited by this paper
• A model of tenascin‐X integration within the collagenous network

  2006cited by this paper
• Interactions of human tenascin-X domains with dermal extracellular matrix molecules

  2006cited by this paper
• Elastic fibres in health and disease

  2006cited by this paper
• Collagen XII Interacts with Avian Tenascin-X through Its NC3 Domain*

  2006cited by this paper
• Histological response to injected gluteraldehyde cross-linked bovine collagen based implant in a rat model

  2006cited by this paper
• The genetic basis of the joint hypermobility syndromes.

  2006cited by this paper
• Claudins: emerging targets for cancer therapy

  2006cited by this paper
• The Physiological Function of the Urothelium – More than a Simple Barrier

  2006cited by this paper
• Latent transforming growth factor-beta (TGF-beta) binding proteins: orchestrators of TGF-beta availability.

  2005cited by this paper
• Transplantation of reconstructed human skin on nude mice: a model system to study expression of human tenascin-X and elastic fiber components

  2005cited by this paper
• Association of transforming growth factor-beta1 gene polymorphism with reflux nephropathy.

  2005cited by this paper
• Tenascin‐X deficiency in autosomal recessive Ehlers–Danlos syndrome

  2005cited by this paper
• Joint hypermobility syndrome in childhood. A not so benign multisystem disorder?

  2005cited by this paper
• Fetal development of the vesico-ureteric junction, and immunohistochemistry of the ends of refluxing ureters.

  2005cited by this paper
• Tenascin‐X, collagen, elastin, and the Ehlers–Danlos syndrome

  2005cited by this paper
• Giant bladder diverticula causing bladder outlet obstruction in children.

  2004cited by this paper
• Elastic fiber homeostasis requires lysyl oxidase–like 1 protein

  2004cited by this paper
• Fibrillin-rich microfibrils: elastic biopolymers of the extracellular matrix

  2004cited by this paper
• The natural history, including orofacial features of three patients with Ehlers–Danlos syndrome, dermatosparaxis type (EDS type VIIC)

  2004cited by this paper
• Latent TGF-beta binding proteins: extracellular matrix association and roles in TGF-beta activation.

  2004cited by this paper
• Insights into the molecular mechanism of chronic fibrosis: the role of connective tissue growth factor in scleroderma.

  2004cited by this paper
• Induction of matrix metalloproteinase-2 by tenascin-X deficiency is mediated through the c-Jun N-terminal kinase and protein tyrosine kinase phosphorylation pathway.

  2004cited by this paper
• Deficiency of tenascin-X causes abnormalities in dermal elastic fiber morphology.

  2004cited by this paper
• Modulation of collagen fibrillogenesis by tenascin-X and type VI collagen.

  2004cited by this paper
• Extracellular matrix degradation and reduced nerve supply in refluxing ureteral endings.

  2004cited by this paper
• Reduced type I collagen utilization: A pathogenic mechanism in COL5A1 haplo‐insufficient Ehlers–Danlos syndrome

  2004cited by this paper
• Type V Collagen Controls the Initiation of Collagen Fibril Assembly*

  2004cited by this paper
• Latent TGF-β Binding Proteins: Extracellular Matrix Association and Roles in TGF-β Activation

  2004cited by this paper
• Spontaneous resolution of high grade infantile vesicoureteral reflux.

  2004cited by this paper
• Renal and urinary findings in 20 patients with Williams-Beuren syndrome diagnosed by fluorescence in situ hybridization (FISH).

  2004cited by this paper
• Joint hypermobility syndromes: the pathophysiologic role of tenascin-X gene defects.

  2004cited by this paper
• Bilateral popliteal aneurysms complicating adult polycystic kidney disease in a patient with a marfanoid habitus

  2003cited by this paper
• TGF-β signal transduction and mesangial cell fibrogenesis

  2003cited by this paper
• Medical versus surgical treatment in children with severe bilateral vesicoureteric reflux and bilateral nephropathy: a randomised trial.

  2003cited by this paper
• Collagens--structure, function, and biosynthesis.

  2003cited by this paper

• Robotic-assisted sacrocolpopexy (RASC) in a renal transplant patient with Ehlers-Danlos syndrome (EDS), case report and literature review of perioperative considerations

  2025cites this paper
• Bilateral ureteral obstruction after open ureteral reimplantation in a 3-year-old patient with Williams Beuren syndrome

  2024cites this paper
• Lower urinary tract involvement in Ehlers Danlos and Joint Hypermobility Syndromes: Review of the literature.

  2024cites this paper
• Is Ultrasound Adding Values to Voiding Cystourethrogram In Pediatric Vesico Ureteric Reflux?

  2023cites this paper
• Disease mechanisms of monogenic congenital anomalies of the kidney and urinary tract American Journal of Medical Genetics Part C

  2022cites this paper
• Tenascin-X—Discovery and Early Research

  2021cites this paper
• Experimental study on the repair of ureteral functional regeneration with highly bioactive extracellular matrix stent.

  2020cites this paper
• Intérêt de l'échographie rénale et des voies urinaires dans la prise en charge de l'orchi-épididymite chez l'enfant de moins de 16 ans

  2020cites this paper
• ECMPride: prediction of human extracellular matrix proteins based on the ideal dataset using hybrid features with domain evidence

  2020cites this paper
• Генетические факторы наследственных фенотипов пузырно-мочеточникового рефлюкса и рефлюкс-нефропатии

  2020cites this paper
• URINARY EXCRETION OF TGF-Β1 AND VEGF IN CHILDREN WITH VESICOURETERAL REFLUX.

  2020cites this paper
• Genetic factors of hereditary phenotypes of vesicoureteral reflux and reflux nephropathy

  2020influential citation
• Congenital Anomalies of the Kidney and Urinary Tract: a Clinical Review

  2019cites this paper
• Comparative Transcriptome Analysis of Unusual Localized Skin Laxity in Sika Deer (Cervus nippon)

  2019cites this paper
• Children with vesico-ureteric reflux have joint hypermobility and occasional TNXB sequence variants.

  2019cites this paper
• Detection of Extended - Spectrum Beta - Lactamases in Escherichia coli Isolates and it’s Correlation with Vesicoureteral Reflux Nephropathy

  2018cites this paper
• Tenascin-X, Congenital Adrenal Hyperplasia, and the CAH-X Syndrome

  2018cites this paper
• Endoscopic treatment of vesicoureteral refluks in children

  2017cites this paper
• Physiopathology of vesico-ureteral reflux

  2016cites this paper
• Reflux-Related Renal Injury (Reflux Nephropathy): Do Nonsteroidal AntiInflammatory Drugs (Ibuprofen) Increases’ the Risks?

  2016cites this paper
• Vesicoureteral Reflux Index: 2-Institution Analysis and Validation.

  2016cites this paper
• Еволюція поглядів на функціональну анатомію міхурово-сечовідного сегмента та етіопатогенетичні особливості міхурово-сечовідного рефлюксу в дітей

  year unknowncites this paper