Cargando…

Analysis of matrisome expression patterns in murine and human dorsal root ganglia

The extracellular matrix (ECM) is a dynamic structure of molecules that can be divided into six different categories and are collectively called the matrisome. The ECM plays pivotal roles in physiological processes in many tissues, including the nervous system. Intriguingly, alterations in ECM molec...

Descripción completa

Detalles Bibliográficos
Autores principales:	Vroman, Robin, Hunter, Rahel S., Wood, Matthew J., Davis, Olivia C., Malfait, Zoë, George, Dale S., Ren, Dongjun, Tavares-Ferreira, Diana, Price, Theodore J., Miller, Richard J., Malfait, Anne-Marie, Malfait, Fransiska, Miller, Rachel E., Syx, Delfien
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2023
Materias:	Molecular Neuroscience
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10471487/ https://www.ncbi.nlm.nih.gov/pubmed/37664243 http://dx.doi.org/10.3389/fnmol.2023.1232447

Ejemplares similares

Animal Models of Ehlers–Danlos Syndromes: Phenotype, Pathogenesis, and Translational Potential
por: Vroman, Robin, et al.
Publicado: (2021)

The Ehlers–Danlos Syndromes against the Backdrop of Inborn Errors of Metabolism
por: Van Damme, Tim, et al.
Publicado: (2022)

Sensory profiling in classical Ehlers-Danlos syndrome: a case-control study revealing pain characteristics, somatosensory changes, and impaired pain modulation
por: Colman, Marlies, et al.
Publicado: (2023)

Loss of TANGO1 Leads to Absence of Bone Mineralization
por: Guillemyn, Brecht, et al.
Publicado: (2021)

Ehlers-Danlos Syndrome, Hypermobility Type, Is Linked to Chromosome 8p22-8p21.1 in an Extended Belgian Family
por: Syx, Delfien, et al.
Publicado: (2015)

A Novel Splice Variant in the N-propeptide of COL5A1 Causes an EDS Phenotype with Severe Kyphoscoliosis and Eye Involvement
por: Symoens, Sofie, et al.
Publicado: (2011)

Notch signaling is activated in knee-innervating dorsal root ganglia in experimental models of osteoarthritis joint pain
por: Wang, Lai, et al.
Publicado: (2023)

Glycosaminoglycan linkage region of urinary bikunin as a potentially useful biomarker for β3GalT6‐deficient spondylodysplastic Ehlers–Danlos syndrome
por: Nikpour, Mahnaz, et al.
Publicado: (2022)

The clinical and mutational spectrum of B3GAT3 linkeropathy: two case reports and literature review
por: Colman, Marlies, et al.
Publicado: (2019)

Four decades in the making: Collagen III and mechanisms of vascular Ehlers Danlos Syndrome
por: Omar, Ramla, et al.
Publicado: (2021)

Recommendations for anesthesia and perioperative management in patients with Ehlers-Danlos syndrome(s)
por: Wiesmann, Thomas, et al.
Publicado: (2014)

Vascular phenotypes in nonvascular subtypes of the Ehlers-Danlos syndrome: a systematic review
por: D'hondt, Sanne, et al.
Publicado: (2018)

Editorial: Molecular Mechanisms of Heritable Connective Tissue Disorders
por: Malfait, Fransiska, et al.
Publicado: (2022)

The first step to embrace patient participation in the intensive care unit is to drop the paternalistic thinking
por: Malfait, S.
Publicado: (2022)

Delineation of musculocontractural Ehlers–Danlos Syndrome caused by dermatan sulfate epimerase deficiency
por: Lautrup, Charlotte K., et al.
Publicado: (2020)

b3galt6 Knock-Out Zebrafish Recapitulate β3GalT6-Deficiency Disorders in Human and Reveal a Trisaccharide Proteoglycan Linkage Region
por: Delbaere, Sarah, et al.
Publicado: (2020)

Aberrant binding of mutant HSP47 affects posttranslational modification of type I collagen and leads to osteogenesis imperfecta
por: Syx, Delfien, et al.
Publicado: (2021)

The role of intra-articular neuronal CCR2 receptors in knee joint pain associated with experimental osteoarthritis in mice
por: Ishihara, Shingo, et al.
Publicado: (2021)

Hearing impairment in Stickler syndrome: a systematic review
por: Acke, Frederic R E, et al.
Publicado: (2012)

Neuroimmune interactions and osteoarthritis pain: focus on macrophages
por: Geraghty, Terese, et al.
Publicado: (2021)

Piezo2 expressing nociceptors mediate mechanical sensitization in experimental osteoarthritis
por: Obeidat, Alia M., et al.
Publicado: (2023)

CCL2 and CCR2 regulate pain-related behaviour and early gene expression in post-traumatic murine osteoarthritis but contribute little to chondropathy
por: Miotla Zarebska, J., et al.
Publicado: (2017)

On the predictive utility of animal models of osteoarthritis
por: Malfait, Anne-Marie, et al.
Publicado: (2015)

Muscle Strength, Muscle Mass and Physical Impairment in Women with hypermobile Ehlers-Danlos syndrome and Hypermobility Spectrum Disorder
por: Coussens, Marie, et al.
Publicado: (2022)

The Role of Motor Learning in Spatial Adaptation near a Tool
por: Brown, Liana E., et al.
Publicado: (2011)

Mitochondrial calcium uniporter deletion prevents painful diabetic neuropathy by restoring mitochondrial morphology and dynamics
por: George, Dale S., et al.
Publicado: (2022)

Nanoparticles for Improved Local Retention after Intra-Articular Injection into the Knee Joint
por: Morgen, Michael, et al.
Publicado: (2012)

A Systematic Study on Bio-Based Hybrid Aerogels Made of Tannin and Silica
por: Koopmann, Ann-Kathrin, et al.
Publicado: (2021)

Societal participation in ehlers-danlos syndromes and hypermobility spectrum disorder, compared to fibromyalgia and healthy controls
por: De Baets, Stijn, et al.
Publicado: (2022)

Acute Type A Aortic Dissection Complicated by COVID-19 Infection
por: Martens, Thomas, et al.
Publicado: (2020)

EMQN best practice guidelines for the laboratory diagnosis of osteogenesis imperfecta
por: van Dijk, Fleur S, et al.
Publicado: (2012)

Is privacy a problem during bedside handovers? A practice-oriented discussion paper
por: Malfait, Simon, et al.
Publicado: (2018)

Silica–Resorcinol–Melamine–Formaldehyde Composite Aerogels as High-Performance Thermal Insulators
por: Civioc, Romain, et al.
Publicado: (2022)

The Impact of Hypermobile “Ehlers-Danlos Syndrome” and Hypermobile Spectrum Disorder on Interpersonal Interactions and Relationships
por: De Baets, Stijn, et al.
Publicado: (2022)

Deficiency for the ER-stress transducer OASIS causes severe recessive osteogenesis imperfecta in humans
por: Symoens, Sofie, et al.
Publicado: (2013)

Genetic analysis of osteogenesis imperfecta in the Palestinian population: molecular screening of 49 affected families
por: Essawi, Osama, et al.
Publicado: (2017)

Recommendations For a Standardized Approach to Histopathologic Evaluation of Synovial Membrane in Murine Models of Experimental Osteoarthritis
por: Obeidat, Alia M, et al.
Publicado: (2023)

Microgravity Effects on the Matrisome
por: Buravkova, Ludmila, et al.
Publicado: (2021)

Reporting of “dialysis adequacy” as an outcome in randomised trials conducted in adults on haemodialysis
por: Steyaert, Sanne, et al.
Publicado: (2019)

Is there an Intrinsic Relationship between LFP Beta Oscillation Amplitude and Firing Rate of Individual Neurons in Macaque Motor Cortex?
por: Confais, Joachim, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_u77sj89n311rhl5ha83dtn6e7k