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Decorin prevents the development of juvenile communicating hydrocephalus
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ddrr.94openalex-snapshot
Neuropathology and structural changes in hydrocephalus
inferredcites →https://doi.org/10.1002/glia.20207openalex-snapshot
Astrocyte activation and reactive gliosis
inferredcites →https://doi.org/10.1006/exnr.1999.7180openalex-snapshot
Decorin Attenuates Gliotic Scar Formation in the Rat Cerebral Hemisphere
inferredcites →https://doi.org/10.1007/978-88-470-2121-1_4openalex-snapshot
Pathophysiology of Hydrocephalus
inferredcites →https://doi.org/10.1007/bf00573851openalex-snapshot
Neurodevelopmental outcome of hydrocephalus following intra-/periventricular hemorrhage in preterm infants: short- and long-term results
inferredcites →https://doi.org/10.1007/bf01405236openalex-snapshot
Changes in the subarachnoid space after experimental subarachnoid haemorrhage in the dog: Scanning electron microscopic observation
inferredcites →https://doi.org/10.1007/bf01411441openalex-snapshot
Subarachnoid haemorrhage induced proliferation of leptomeningeal cells and deposition of extracellular matrices in the arachnoid granulations and subarachnoid space
inferredcites →https://doi.org/10.1007/bf03656638openalex-snapshot
Current methods in the treatment of posthemorrhagic hydrocephalus in infants
inferredcites →https://doi.org/10.1007/s00381-011-1552-4openalex-snapshot
Reactive astrocytosis in feline neonatal hydrocephalus: acute, chronic, and shunt-induced changes
inferredcites →https://doi.org/10.1007/s00401-009-0624-yopenalex-snapshot
Ependymal cells: biology and pathology
inferredcites →https://doi.org/10.1007/s007010170036openalex-snapshot
Rapid Induction of Meningeal Collagen Synthesis in the Cerebral Cisternal and Ventricular Compartments after Subarachnoid Hemorrhage
inferredcites →https://doi.org/10.1007/s11910-008-0058-2openalex-snapshot
Normal pressure hydrocephalus: Diagnosis and treatment
inferredcites →https://doi.org/10.1016/0006-8993(92)91000-5openalex-snapshot
Enhanced expression of transforming growth factor β1 in the rat brain after a localized cerebral injury
inferredcites →https://doi.org/10.1016/0165-5728(94)90041-8openalex-snapshot
Induction of communicating hydrocephalus in mice by intrathecal injection of human recombinant transforming growth factor-β1
inferredcites →https://doi.org/10.1016/0167-5699(89)90136-9openalex-snapshot
Inflammatory and immunomodulatory roles of TGF-β
inferredcites →https://doi.org/10.1016/0304-3940(95)11686-qopenalex-snapshot
Transforming growth factor-β1 levels are elevated in the striatum and in ventricular cerebrospinal fluid in Parkinson's disease
inferredcites →https://doi.org/10.1016/0306-4522(91)90082-yopenalex-snapshot
Transforming growth factor beta isoforms in the adult rat central and peripheral nervous system
inferredcites →https://doi.org/10.1016/0387-7604(95)00103-4openalex-snapshot
Glial reaction in periventricular areas of the brainstem in fetal and neonatal posthemorrhagic hydrocephalus and congenital hydrocephalus
inferredcites →https://doi.org/10.1016/0387-7604(95)00107-7openalex-snapshot
Maturational changes of VEPs in normal premature neonates: a longitudinal study
inferredcites →https://doi.org/10.1016/j.expneurol.2006.02.113openalex-snapshot
Brain damage in neonatal rats following kaolin induction of hydrocephalus
inferredcites →https://doi.org/10.1016/j.expneurol.2007.12.030openalex-snapshot
Communicating hydrocephalus in adult rats with kaolin obstruction of the basal cisterns or the cortical subarachnoid space
inferredcites →https://doi.org/10.1016/j.expneurol.2009.03.034openalex-snapshot
Ventricular dilation and elevated aqueductal pulsations in a new experimental model of communicating hydrocephalus
inferredcites →https://doi.org/10.1016/j.expneurol.2010.08.010openalex-snapshot
Reactive astrocytosis, microgliosis and inflammation in rats with neonatal hydrocephalus
inferredcites →https://doi.org/10.1016/j.matbio.2013.04.004openalex-snapshot
Effects of decorin proteoglycan on fibrillogenesis, ultrastructure, and mechanics of type I collagen gels
inferredcites →https://doi.org/10.1016/j.neuroscience.2012.05.004openalex-snapshot
Reactive gliosis and neuroinflammation in rats with communicating hydrocephalus
inferredcites →https://doi.org/10.1016/j.siny.2012.06.004openalex-snapshot
Pathophysiology of congenital and neonatal hydrocephalus
inferredcites →https://doi.org/10.1016/s0021-9258(18)31681-8openalex-snapshot
Bone matrix decorin binds transforming growth factor-beta and enhances its bioactivity.
inferredcites →https://doi.org/10.1016/s0021-9258(18)32345-7openalex-snapshot
Transforming growth factor-beta in human platelets. Identification of a major storage site, purification, and characterization.
inferredcites →https://doi.org/10.1016/s0925-4439(99)00016-2openalex-snapshot
Increase of collagen synthesis and deposition in the arachnoid and the dura following subarachnoid hemorrhage in the rat
inferredcites →https://doi.org/10.1016/s0945-053x(98)90070-1openalex-snapshot
Leucine-rich repeat glycoproteins of the extracellular matrix
inferredcites →https://doi.org/10.1016/s0967-5868(97)90011-4openalex-snapshot
A murine model of communicating hydrocephalus: Role of TGF-β1
inferredcites →https://doi.org/10.1038/346281a0openalex-snapshot
Negative regulation of transforming growth factor-β by the proteoglycan decorin
inferredcites →https://doi.org/10.1038/360361a0openalex-snapshot
Natural inhibitor of transforming growth factor-β protects against scarring in experimental kidney disease
inferredcites →https://doi.org/10.1038/cr.2008.328openalex-snapshot
Non-Smad pathways in TGF-β signaling
inferredcites →https://doi.org/10.1038/jcbfm.1990.140openalex-snapshot
The Time Course of Intracranial Pathophysiological Changes following Experimental Subarachnoid Haemorrhage in the Rat
inferredcites →https://doi.org/10.1038/jcbfm.2011.130openalex-snapshot
Neocortical Capillary Flow Pulsatility is Not Elevated in Experimental Communicating Hydrocephalus
inferredcites →https://doi.org/10.1046/j.0305-1846.2003.00524.xopenalex-snapshot
Disappearance of the post‐lesional laminin immunopositivity of brain vessels is parallel with the formation of gliovascular junctions and common basal lamina. A double‐labelling immunohistochemical study
inferredcites →https://doi.org/10.1046/j.1460-9568.1999.00654.xopenalex-snapshot
Inhibition of glial scarring in the injured rat brain by a recombinant human monoclonal antibody to transforming growth factor‐β2
inferredcites →https://doi.org/10.1046/j.1523-1747.2002.01641.xopenalex-snapshot
Transforming Growth Factor-β Signaling Through the Smad Pathway: Role in Extracellular Matrix Gene Expression and Regulation
inferredcites →https://doi.org/10.1074/jbc.m005609200openalex-snapshot
Sustained Down-regulation of the Epidermal Growth Factor Receptor by Decorin
inferredcites →https://doi.org/10.1074/jbc.m111.283499openalex-snapshot
Decorin Antagonizes the Angiogenic Network
inferredcites →https://doi.org/10.1083/jcb.118.6.1523openalex-snapshot
Regulation of cell substrate adhesion: effects of small galactosaminoglycan-containing proteoglycans.
inferredcites →https://doi.org/10.1093/brain/awq304openalex-snapshot
Decorin, erythroblastic leukaemia viral oncogene homologue B4 and signal transducer and activator of transcription 3 regulation of semaphorin 3A in central nervous system scar tissue
inferredcites →https://doi.org/10.1097/00004647-200102000-00007openalex-snapshot
Transforming Growth Factor-β1 in the Cerebrospinal Fluid of Patients with Subarachnoid Hemorrhage: Titers Derived from Exogenous and Endogenous Sources
inferredcites →https://doi.org/10.1097/00005072-199505000-00007openalex-snapshot
Overexpression of TGF-β1 in the Central Nervous System of Transgenic Mice Results in Hydrocephalus
inferredcites →https://doi.org/10.1111/j.1365-2990.2004.00588.xopenalex-snapshot
Transforming growth factor‐βs in a rat model of neonatal posthaemorrhagic hydrocephalus
inferredcites →https://doi.org/10.1111/j.1460-9568.2004.03184.xopenalex-snapshot
Decorin suppresses neurocan, brevican, phosphacan and NG2 expression and promotes axon growth across adult rat spinal cord injuries
inferredcites →https://doi.org/10.1111/j.1651-2227.2008.00903.xopenalex-snapshot
Do drugs that block transforming growth factor beta reduce posthaemorrhagic ventricular dilatation in a neonatal rat model?
inferredcites →https://doi.org/10.1111/j.1742-4658.2010.07797.xopenalex-snapshot
Proteoglycans in health and disease: novel regulatory signaling mechanisms evoked by the small leucine‐rich proteoglycans
inferredcites →https://doi.org/10.1136/jnnp.2008.155671openalex-snapshot
High CSF transforming growth factor levels after subarachnoid haemorrhage: association with chronic communicating hydrocephalus
inferredcites →https://doi.org/10.1136/jnnp.67.2.185openalex-snapshot
Detection of meningeal fibrosis after subarachnoid haemorrhage by assaying procollagen propeptides in cerebrospinal fluid
inferredcites →https://doi.org/10.1152/ajpgi.2000.279.5.g845openalex-snapshot
V. TGF-β signaling pathways
inferredcites →https://doi.org/10.1159/000327842openalex-snapshot
Decorin and Colchicine as Potential Treatments for Post-Haemorrhagic Ventricular Dilatation in a Neonatal Rat Model
inferredcites →https://doi.org/10.1161/01.str.25.7.1400openalex-snapshot
Elevation of transforming growth factor-beta 1 level in cerebrospinal fluid of patients with communicating hydrocephalus after subarachnoid hemorrhage.
inferredcites →https://doi.org/10.1161/01.str.27.5.852openalex-snapshot
Increased Expression of TGF-β1 in Brain Tissue After Ischemic Stroke in Humans
inferredcites →https://doi.org/10.1164/ajrccm.163.3.2006084openalex-snapshot
Transient Transgene Expression of Decorin in the Lung Reduces the Fibrotic Response to Bleomycin
inferredcites →https://doi.org/10.1172/jci846openalex-snapshot
Decorin suppresses tumor cell growth by activating the epidermal growth factor receptor.
inferredcites →https://doi.org/10.1182/blood.v98.7.2124openalex-snapshot
Decorin inhibits macrophage colony-stimulating factor proliferation of macrophages and enhances cell survival through induction of p27Kip1 and p21Waf1
inferredcites →https://doi.org/10.1186/1743-8454-4-5openalex-snapshot
Reduction of astrogliosis and microgliosis by cerebrospinal fluid shunting in experimental hydrocephalus
inferredcites →https://doi.org/10.1186/1743-8454-4-9openalex-snapshot
Protein and synthetic polymer injection for induction of obstructive hydrocephalus in rats
inferredcites →https://doi.org/10.1186/1743-8454-6-1openalex-snapshot
A review of the current treatment methods for posthaemorrhagic hydrocephalus of infants
inferredcites →https://doi.org/10.1186/1743-8454-7-4openalex-snapshot
Elevated CSF outflow resistance associated with impaired lymphatic CSF absorption in a rat model of kaolin-induced communicating hydrocephalus
inferredcites →https://doi.org/10.1203/00006450-199911000-00014openalex-snapshot
Transforming Growth Factor-β1: A Possible Signal Molecule for Posthemorrhagic Hydrocephalus?
inferredcites →https://doi.org/10.1212/wnl.55.3.359openalex-snapshot
Transient increase in procollagen propeptides in the CSF after subarachnoid hemorrhage
inferredcites →https://doi.org/10.1227/01.neu.0000068863.37133.9eopenalex-snapshot
Cerebral Vasospasm after Subarachnoid Hemorrhage: Putative Role of Inflammation
inferredcites →https://doi.org/10.2174/1874312901206010156openalex-snapshot
The Role of TGF-β Receptors in Fibrosis
inferredcites →https://doi.org/10.3171/jns.1992.76.5.0856openalex-snapshot
Reconstitution of shunted mantle in experimental hydrocephalus
inferredcites →https://doi.org/10.3171/ped.2006.104.4.251openalex-snapshot
Heavy water inhibiting the expression of transforming growth factor–β1and the development of kaolin-induced hydrocephalus in mice
inferredcites →https://doi.org/10.4049/jimmunol.149.11.3695openalex-snapshot
The proteoglycan decorin binds C1q and inhibits the activity of the C1 complex
inferredcites →https://doi.org/10.4049/jimmunol.170.9.4450openalex-snapshot
Decorin Reverses the Repressive Effect of Autocrine-Produced TGF-β on Mouse Macrophage Activation
inferredcites →https://doi.org/10.4161/cc.20316openalex-snapshot
Small leucine-rich proteoglycans orchestrate receptor crosstalk during inflammation
inferredcites →https://doi.org/10.7150/ijbs.7.1056openalex-snapshot
Diverse Roles of TGF-β/Smads in Renal Fibrosis and Inflammation
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4624554openalex-extracted
Intraventricular Dimethyl Sulfoxide (Dmso) Induces Hydrocephalus in Mice
inferred← citeshttps://doi.org/10.1002/iid3.70268openalex-snapshot
Neutrophil Extracellular Traps Activate Meningeal Fibroblast to Aggravate Subarachnoid Fibrosis in Kaolin‐Induced Hydrocephalus in Rats
inferred← citeshttps://doi.org/10.1007/978-3-319-27250-4_35openalex-snapshot
Experimental Hydrocephalus
inferred← citeshttps://doi.org/10.1007/978-3-319-31512-6_24-1openalex-snapshot
Medical Treatment of Hydrocephalus
inferred← citeshttps://doi.org/10.1007/978-3-319-31889-9_35-1openalex-snapshot
Experimental Hydrocephalus
inferred← citeshttps://doi.org/10.1007/978-3-319-72168-2_24openalex-snapshot
Medical Treatment of Hydrocephalus
inferred← citeshttps://doi.org/10.1007/s00381-016-3313-xopenalex-snapshot
Edaravone reduces astrogliosis and apoptosis in young rats with kaolin-induced hydrocephalus
inferred← citeshttps://doi.org/10.1007/s00441-014-1978-6openalex-snapshot
VEGF: A potential target for hydrocephalus
inferred← citeshttps://doi.org/10.1007/s10072-016-2589-7openalex-snapshot
New concept of the pathogenesis and therapeutic orientation of acquired communicating hydrocephalus
inferred← citeshttps://doi.org/10.1007/s10143-025-03889-0openalex-snapshot
Elevated TNF-α in cerebrospinal fluid as a potential inflammatory marker in post-hemorrhagic hydrocephalus: a prospective study
inferred← citeshttps://doi.org/10.1007/s11060-026-05746-6openalex-snapshot
Anatomical and surgical factors associated with postoperative hydrocephalus after central neurocytoma resection: a large single-center cohort study
inferred← citeshttps://doi.org/10.1007/s12035-025-04823-7openalex-snapshot
The Role of Choroid Plexus in Hydrocephalus from the Perspective of Structure and Function: a Therapeutic Target
inferred← citeshttps://doi.org/10.1007/s12311-016-0778-9openalex-snapshot
Effects of Melatonin on the Cerebellum of Infant Rat Following Kaolin-Induced Hydrocephalus: a Histochemical and Immunohistochemical Study
inferred← citeshttps://doi.org/10.1007/s12975-016-0480-8openalex-snapshot
Intraventricular Hemorrhage: the Role of Blood Components in Secondary Injury and Hydrocephalus
inferred← citeshttps://doi.org/10.1007/s12975-022-01026-3openalex-snapshot
Metformin Alleviates Delayed Hydrocephalus after Intraventricular Hemorrhage by Inhibiting Inflammation and Fibrosis
inferred← citeshttps://doi.org/10.1016/b978-0-12-819507-9.00028-4openalex-snapshot
Post-hemorrhagic hydrocephalus in preterm infants
inferred← citeshttps://doi.org/10.1016/b978-0-323-43140-8.00008-1openalex-snapshot
Hydrocephalus in Children
inferred← citeshttps://doi.org/10.1016/j.actbio.2025.08.039openalex-snapshot
Structuring of gellan hydrogel enables the production of inherently antifibrotic, lubricating eye drops
inferred← citeshttps://doi.org/10.1016/j.bbi.2021.01.028openalex-snapshot
Meningeal immunity: Structure, function and a potential therapeutic target of neurodegenerative diseases
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2019.04.013openalex-snapshot
A self-healing hydrogel eye drop for the sustained delivery of decorin to prevent corneal scarring
inferred← citeshttps://doi.org/10.1016/j.brainres.2015.11.004openalex-snapshot
Decorin alleviated chronic hydrocephalus via inhibiting TGF-β1/Smad/CTGF pathway after subarachnoid hemorrhage in rats
inferred← citeshttps://doi.org/10.1016/j.brainres.2016.10.016openalex-snapshot
Cannabinoid receptor 2 activation restricts fibrosis and alleviates hydrocephalus after intraventricular hemorrhage
inferred← citeshttps://doi.org/10.1016/j.expneurol.2020.113523openalex-snapshot
Genes causing congenital hydrocephalus: Their chromosomal characteristics of telomere proximity and DNA compositions
inferred← citeshttps://doi.org/10.1016/j.expneurol.2025.115608openalex-snapshot
Suppression of microglial activation with anti-inflammatory drug bindarit enhances neural development in the shunt-treated neonatal hydrocephalus model rat
inferred← citeshttps://doi.org/10.1016/j.expneurol.2026.115941openalex-snapshot
ADAM10-dependent disruption of N-cadherin and ventricular zone in post-hemorrhagic hydrocephalus
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e27295openalex-snapshot
Intraventricular dimethyl sulfoxide (DMSO) induces hydrocephalus in a dose-dependent pattern
inferred← citeshttps://doi.org/10.1016/j.ijdevneu.2014.02.002openalex-snapshot
Kaolin‐induced ventriculomegaly at weaning produces long‐term learning, memory, and motor deficits in rats
inferred← citeshttps://doi.org/10.1016/j.intimp.2021.108486openalex-snapshot
Pharmacological Inhibition of TLR4-NF-κB Signaling by TAK-242 Attenuates Hydrocephalus after Intraventricular Hemorrhage
inferred← citeshttps://doi.org/10.1016/j.jchemneu.2021.102059openalex-snapshot
The association of Edaravone with shunt surgery improves behavioral performance, reduces astrocyte reaction and apoptosis, and promotes neuroprotection in young hydrocephalic rats
inferred← citeshttps://doi.org/10.1016/j.jchemneu.2022.102165openalex-snapshot
Memantine associated with ventricular-subcutaneous shunt promotes behavioral improvement, reduces reactive astrogliosis and cell death in juvenile hydrocephalic rats
inferred← citeshttps://doi.org/10.1016/j.msec.2020.111446openalex-snapshot
Promotion of collagen deposition during skin healing through Smad3/mTOR pathway by parathyroid hormone-loaded microneedle
inferred← citeshttps://doi.org/10.1016/j.neulet.2020.135011openalex-snapshot
uPA alleviates kaolin-induced hydrocephalus by promoting the release and activation of hepatocyte growth factor in rats
inferred← citeshttps://doi.org/10.1016/j.placenta.2014.12.021openalex-snapshot
Vitamin D promotes human extravillous trophoblast invasion in vitro
inferred← citeshttps://doi.org/10.1016/j.trsl.2016.08.004openalex-snapshot
Intraventricular administration of urokinase as a novel therapeutic approach for communicating hydrocephalus
inferred← citeshttps://doi.org/10.1016/j.wneu.2019.06.070openalex-snapshot
Efficacy and Safety of Lumboperitoneal Shunt in the Treatment of All-Cause Communicating Hydrocephalus: Analysis of Risk Factors of Shunt Failure
inferred← citeshttps://doi.org/10.1016/j.wneu.2021.12.100openalex-snapshot
Hydrocephalus Study Design: Testing New Hypotheses in Clinical Studies and Bench-to-Bedside Research
inferred← citeshttps://doi.org/10.1038/s41390-024-03733-zopenalex-snapshot
Neuroinflammatory pathways and potential therapeutic targets in neonatal post-hemorrhagic hydrocephalus
inferred← citeshttps://doi.org/10.1038/s41392-024-01764-wopenalex-snapshot
TGF-β signaling in health, disease and therapeutics
inferred← citeshttps://doi.org/10.1038/s41433-019-0751-1openalex-snapshot
Guide to preclinical models used to study the pathophysiology of idiopathic intracranial hypertension
inferred← citeshttps://doi.org/10.1038/s41536-018-0061-4openalex-snapshot
Sustained release of decorin to the surface of the eye enables scarless corneal regeneration
inferred← citeshttps://doi.org/10.1038/s41536-020-00110-2openalex-snapshot
ILB® resolves inflammatory scarring and promotes functional tissue repair
inferred← citeshttps://doi.org/10.1038/srep26794openalex-snapshot
Excess HB-EGF, which promotes VEGF signaling, leads to hydrocephalus
inferred← citeshttps://doi.org/10.1038/srep42436openalex-snapshot
Comprehensive Proteomic Characterization of the Human Colorectal Carcinoma Reveals Signature Proteins and Perturbed Pathways
inferred← citeshttps://doi.org/10.1055/s-0042-1758559openalex-snapshot
Cerebrospinal fluid levels of sortilin-1, lipocalin-2, autotaxin, decorin and interleukin-33 in patients with idiopathic intracranial hypertension
inferred← citeshttps://doi.org/10.1080/14728222.2017.1397628openalex-snapshot
Challenges for intraventricular hemorrhage research and emerging therapeutic targets
inferred← citeshttps://doi.org/10.1093/brain/awae155openalex-snapshot
Biomechanical instability of the brain–CSF interface in hydrocephalus
inferred← citeshttps://doi.org/10.1093/neuros/nyx150openalex-snapshot
Letter: A Novel Experimental Animal Model of Adult Chronic Hydrocephalus
inferred← citeshttps://doi.org/10.1097/wnr.0000000000000904openalex-snapshot
Characterization of spontaneous hydrocephalus development in the young atherosclerosis-prone mice
inferred← citeshttps://doi.org/10.1101/2022.09.28.509923openalex-snapshot
Treatment of Hydrocephalus by Decreasing Inflammatory Cytokine Response Using GIT 27
inferred← citeshttps://doi.org/10.1111/cns.13526openalex-snapshot
Pathogenesis and pathophysiology of idiopathic normal pressure hydrocephalus
inferred← citeshttps://doi.org/10.1111/cns.13695openalex-snapshot
Novel therapeutics for hydrocephalus: Insights from animal models
inferred← citeshttps://doi.org/10.11606/t.17.2016.tde-27072016-162552openalex-snapshot
Análise dos efeitos clínico-radiológicos, histopatológicos e bioquímicos da derivação ventrículo-subcutânea na hidrocefalia induzida por caulim em ratos
inferred← citeshttps://doi.org/10.1161/jaha.124.037890openalex-snapshot
Systematic Review of the Differential Effects of TGF‐β1 in Ischemic and Hemorrhagic Preclinical Stroke Models
inferred← citeshttps://doi.org/10.1167/iovs.14-15622openalex-snapshot
Decorin Reduces Intraocular Pressure and Retinal Ganglion Cell Loss in Rodents Through Fibrolysis of the Scarred Trabecular Meshwork
inferred← citeshttps://doi.org/10.1167/iovs.18-24299openalex-snapshot
Altered Decorin Biology in Proliferative Vitreoretinopathy: A Mechanistic and Cohort Study
inferred← citeshttps://doi.org/10.1177/1457496918812210openalex-snapshot
Risk Factors Associated with the Outcome of Post-Traumatic Hydrocephalus
inferred← citeshttps://doi.org/10.1177/1747493017706187openalex-snapshot
Biomarkers in adult posthemorrhagic hydrocephalus
inferred← citeshttps://doi.org/10.1186/2045-8118-11-23openalex-snapshot
Oral antioxidant therapy for juvenile rats with kaolin-induced hydrocephalus
inferred← citeshttps://doi.org/10.1186/2045-8118-12-s1-o59openalex-snapshot
Decorin reduces white matter pathology in experimental hydrocephalus: a diffusion tensor imaging and immunohistochemical study
inferred← citeshttps://doi.org/10.1186/s12014-021-09335-9openalex-snapshot
Proteomics and functional study reveal kallikrein-6 enhances communicating hydrocephalus
inferred← citeshttps://doi.org/10.1186/s12987-016-0025-2openalex-snapshot
Nonsurgical therapy for hydrocephalus: a comprehensive and critical review
inferred← citeshttps://doi.org/10.1186/s12987-016-0031-4openalex-snapshot
Magnesium sulfate treatment for juvenile ferrets following induction of hydrocephalus with kaolin
inferred← citeshttps://doi.org/10.1186/s12987-016-0033-2openalex-snapshot
Diffusion tensor imaging with direct cytopathological validation: characterisation of decorin treatment in experimental juvenile communicating hydrocephalus
inferred← citeshttps://doi.org/10.1186/s12987-017-0083-0openalex-snapshot
Chemokine and cytokine levels in the lumbar cerebrospinal fluid of preterm infants with post-hemorrhagic hydrocephalus
inferred← citeshttps://doi.org/10.1186/s12987-018-0096-3openalex-snapshot
Opportunities in posthemorrhagic hydrocephalus research: outcomes of the Hydrocephalus Association Posthemorrhagic Hydrocephalus Workshop
inferred← citeshttps://doi.org/10.1186/s12987-022-00393-1openalex-snapshot
Modulation of striatal glutamatergic, dopaminergic and cholinergic neurotransmission pathways concomitant with motor disturbance in rats with kaolin-induced hydrocephalus
inferred← citeshttps://doi.org/10.1186/s12987-023-00433-4openalex-snapshot
Early postnatal microglial ablation in the Ccdc39 mouse model reveals adverse effects on brain development and in neonatal hydrocephalus
inferred← citeshttps://doi.org/10.1186/s12987-023-00503-7openalex-snapshot
Postnatal meningeal CSF transport is primarily mediated by the arachnoid and pia maters and is not altered after intraventricular hemorrhage-posthemorrhagic hydrocephalus
inferred← citeshttps://doi.org/10.1186/s12987-026-00779-5openalex-snapshot
Exploring and translating novel approaches targeting the choroid plexus for the treatment of hydrocephalus: a literature review
inferred← citeshttps://doi.org/10.1186/s12987-026-00838-xopenalex-snapshot
Hydrocephalus-associated persistent pain: a preclinical investigation correlating brain fluid imbalance and sensory alterations
inferred← citeshttps://doi.org/10.1186/s40478-022-01345-4openalex-snapshot
AQP4 labels a subpopulation of white matter-dependent glial radial cells affected by pediatric hydrocephalus, and its expression increased in glial microvesicles released to the cerebrospinal fluid in obstructive hydrocephalus
inferred← citeshttps://doi.org/10.1242/dmm.040972openalex-snapshot
Impaired neural differentiation and glymphatic CSF flow in the Ccdc39 rat model of neonatal hydrocephalus: genetic interaction with L1cam
inferred← citeshttps://doi.org/10.1371/journal.pone.0336346openalex-snapshot
Inhibition of NF-κB pathways alleviates hydrocephalus via modulation of choroid plexus epithelium inflammation in a rat intraventricular hemorrhage model
inferred← citeshttps://doi.org/10.1515/tnsci-2016-0015openalex-snapshot
High fibrosis indices in cerebrospinal fluid of patients with shunt-dependent post-traumatic chronic hydrocephalus
inferred← citeshttps://doi.org/10.1523/jneurosci.1160-21.2021openalex-snapshot
The Anti-Inflammatory Agent Bindarit Attenuates the Impairment of Neural Development through Suppression of Microglial Activation in a Neonatal Hydrocephalus Mouse Model
inferred← citeshttps://doi.org/10.1542/neo.20-11-e636openalex-snapshot
Intraventricular Hemorrhage and White Matter Injury in Preclinical and Clinical Studies
inferred← citeshttps://doi.org/10.1542/pir.2015-0134openalex-snapshot
Pediatric Hydrocephalus: Current State of Diagnosis and Treatment
inferred← citeshttps://doi.org/10.1586/14737175.2014.972945openalex-snapshot
Should losartan be administered following brain injury?
inferred← citeshttps://doi.org/10.17340/jkna.2024.0030openalex-snapshot
Pathophysiology of Normal Pressure Hydrocephalus
inferred← citeshttps://doi.org/10.21203/rs.2.17044/v1openalex-snapshot
Inhibition of PAR1 attenuates meningeal macrophage activation and vascular inflammation in a rat model of thrombin-induced hydrocephalus
inferred← citeshttps://doi.org/10.21203/rs.2.19125/v1openalex-snapshot
Inhibition of PAR1 attenuates meningeal macrophage activation and vascular inflammation in a rat model of thrombin-induced hydrocephalus
inferred← citeshttps://doi.org/10.21203/rs.2.19125/v2openalex-snapshot
Inhibition of PAR1 attenuates meningeal macrophage activation and vascular inflammation in a rat model of thrombin-induced hydrocephalus
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3762291/v1openalex-snapshot
Calpeptin mitigates ventriculomegaly and microvascular impairment in a novel LPS- dependent mouse model of acquired hydrocephalus
inferred← citeshttps://doi.org/10.21203/rs.3.rs-403838/v1openalex-snapshot
Proteomic and Functional Analyses Reveal That Kallikrein 6 Enhances Communicating Hydrocephalus by Injuring Neuronal Synapses
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4687466/v1openalex-snapshot
The double-edged sword of transforming growth factor β 1: a systematic review of pre-clinical stroke models
inferred← citeshttps://doi.org/10.2174/1389450120666190214121342openalex-snapshot
Recent Advances in Rational Diagnosis and Treatment of Normal Pressure Hydrocephalus: A Critical Appraisal on Novel Diagnostic, Therapy Monitoring and Treatment Modalities
inferred← citeshttps://doi.org/10.22514/sv.2021.021openalex-snapshot
Hydrocephalus after aneurysmal subarachnoid hemorrhage: Epidemiology, Pathogenesis, Diagnosis, and Management
inferred← citeshttps://doi.org/10.3171/2014.12.jns132352openalex-snapshot
An update on research priorities in hydrocephalus: overview of the third National Institutes of Health-sponsored symposium “Opportunities for Hydrocephalus Research: Pathways to Better Outcomes”
inferred← citeshttps://doi.org/10.3389/fmicb.2019.00576openalex-snapshot
The Role of Microglia in Bacterial Meningitis: Inflammatory Response, Experimental Models and New Neuroprotective Therapeutic Strategies
inferred← citeshttps://doi.org/10.3390/ijms22105132openalex-snapshot
When the Blood Hits Your Brain: The Neurotoxicity of Extravasated Blood
inferred← citeshttps://doi.org/10.3390/ijms23042306openalex-snapshot
Delayed Minocycline Treatment Ameliorates Hydrocephalus Development and Choroid Plexus Inflammation in Spontaneously Hypertensive Rats
inferred← citeshttps://doi.org/10.3390/ijms231810438openalex-snapshot
AQP4, Astrogenesis, and Hydrocephalus: A New Neurological Perspective
inferred← citeshttps://doi.org/10.3390/ijms24065640openalex-snapshot
Generation of Periventricular Reactive Astrocytes Overexpressing Aquaporin 4 Is Stimulated by Mesenchymal Stem Cell Therapy
inferred← citeshttps://doi.org/10.3390/jcm10092026openalex-snapshot
Reappraisal of Pediatric Normal-Pressure Hydrocephalus
inferred← citeshttps://doi.org/10.37349/en.2026.1006126openalex-snapshot
Innovations in hydrocephalus modeling: bridging animal models, bioengineering platforms, and precision therapies
inferred← citeshttps://doi.org/10.3892/etm.2016.3640openalex-snapshot
LSKL peptide alleviates subarachnoid fibrosis and hydrocephalus by inhibiting TSP1-mediated TGF-β1 signaling activity following subarachnoid hemorrhage in rats
inferred← citeshttps://doi.org/10.4103/1673-5374.184489openalex-snapshot
Decorin treatment for reversing trabecular meshwork fibrosis in open-angle glaucoma
inferred← citeshttps://doi.org/10.5114/pjr.2019.87806openalex-snapshot
Evaluation of subarachnoid space and subarachnoid cisterns in children and teenagers based on computed tomography studies
inferred← citeshttps://doi.org/10.6084/m9.figshare.17254404openalex-snapshot
Additional file 1 of Proteomics and functional study reveal kallikrein-6 enhances communicating hydrocephalus
inferred← citeshttps://doi.org/10.6084/m9.figshare.17254410openalex-snapshot
Additional file 2 of Proteomics and functional study reveal kallikrein-6 enhances communicating hydrocephalus
inferred← citeshttps://doi.org/10.6084/m9.figshare.17254416openalex-snapshot
Additional file 3 of Proteomics and functional study reveal kallikrein-6 enhances communicating hydrocephalus
inferred← citeshttps://doi.org/10.6084/m9.figshare.17254419openalex-snapshot
Additional file 4 of Proteomics and functional study reveal kallikrein-6 enhances communicating hydrocephalus
inferred← citeshttps://doi.org/10.6084/m9.figshare.17254428openalex-snapshot
Additional file 5 of Proteomics and functional study reveal kallikrein-6 enhances communicating hydrocephalus
inferred← citeshttps://doi.org/10.6084/m9.figshare.17254434openalex-snapshot
Additional file 6 of Proteomics and functional study reveal kallikrein-6 enhances communicating hydrocephalus
inferred← citeshttps://doi.org/10.6084/m9.figshare.17254437openalex-snapshot
Additional file 7 of Proteomics and functional study reveal kallikrein-6 enhances communicating hydrocephalus
inferred← citeshttps://doi.org/10.6084/m9.figshare.17254440openalex-snapshot
Additional file 8 of Proteomics and functional study reveal kallikrein-6 enhances communicating hydrocephalus
inferred← citeshttps://doi.org/10.6084/m9.figshare.17254443openalex-snapshot
Additional file 9 of Proteomics and functional study reveal kallikrein-6 enhances communicating hydrocephalus
inferred← citeshttps://doi.org/10.6084/m9.figshare.26596106openalex-snapshot
Additional file 1 of Early postnatal microglial ablation in the Ccdc39 mouse model reveals adverse effects on brain development and in neonatal hydrocephalus
inferred← citeshttps://doi.org/10.6084/m9.figshare.26665084openalex-snapshot
Additional file 1 of Postnatal meningeal CSF transport is primarily mediated by the arachnoid and pia maters and is not altered after intraventricular hemorrhage-posthemorrhagic hydrocephalus
inferred← citeshttps://doi.org/10.64898/2026.09.07.749813openalex-snapshot
Cross-omics profiling reveals cortical neuronal dysfunction following neonatal intraventricular haemorrhage that is attenuated by decorin treatment
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