Tenascin-X deficiency mimics Ehlers-Danlos syndrome in mice through alteration of collagen deposition

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Items 101–200 of 231

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2. Muscle characteristics and altered myofascial force transmission in tenascin-X-deficient mice, a mouse model of Ehlers-Danlos syndrome
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4. Noticeable Decreased Expression of Tenascin-X in Calcific Aortic Valves
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5. Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population
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6. Mutation in TNXB gene causes moderate to severe Ehlers-Danlos syndrome
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7. The Effects of Tenascin C Knockdown on Trabecular Meshwork Outflow Resistance
   Kate E. Keller, Janice A. Vranka, Ramez I. Haddadin, Min-Hyung Kang, Dong‐Jin Oh, Douglas J. Rhee, Yong-Feng Yang, Ying Ying Sun, Mary J. Kelley, Ted S. Acott · 2013 · Investigative Ophthalmology & Visual Science
8. Vesicoureteral reflux and the extracellular matrix connection
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10. Biomechanical and molecular characteristics of hereditary equine regional dermal asthenia in Quarter Horses.
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11. Avian tenascin‐W: Expression in smooth muscle and bone, and effects on calvarial cell spreading and adhesion in vitro
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12. Induction of matrix metalloproteinase-2 by tenascin-X deficiency is mediated through the c-Jun N-terminal kinase and protein tyrosine kinase phosphorylation pathway.
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13. High-Throughput Screening for CYP21A1P-TNXA/TNXB Chimeric Genes Responsible for Ehlers Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia.
    Lao, Qizong, Brookner, Brittany, Merke, Deborah P. · 2019 · The Journal of Molecular Diagnostics
14. Matricellular proteins in cutaneous wound healing
    Claudia Griselda Cárdenas‐León, Kristina Mäemets‐Allas, Mariliis Klaas, Heli Lagus, Esko M Kankuri, Viljar Jaks · 2022 · Frontiers in Cell and Developmental Biology
15. Ehlers-Danlos Syndrome in the Field of Psychiatry: A Review
    Hiroki Ishiguro, Hideaki Yagasaki, Yasue Horiuchi · 2022 · Frontiers in Psychiatry
16. Global Proteome Profiling of Dental Cementum under Experimentally-Induced Apposition
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17. Joint Hypermobility and Headache: Understanding the Glue That Binds the Two Together – Part 1
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18. Well-defined clinical presentation of Ehlers–Danlos syndrome in patients with tenascin-X deficiency: a report of four cases
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19. Mild Muscular Features in Tenascin-X Knockout Mice, A Model of Ehlers–Danlos Syndrome
    N. Voermans, K. Verrijp, L. Eshuis, M. Balemans, D. Egging, E. Sterrenburg, I. V. van Rooij, J. A. van der Laak, J. Schalkwijk, S. M. van der Maarel et al. · 2011 · Connective Tissue Research
20. Analysis of obstetric complications and uterine connective tissue in tenascin-X-deficient humans and mice
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21. Tenascin-X—Discovery and Early Research
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22. Revisiting the Tenascins: Exploitable as Cancer Targets?
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23. A novel role for the extracellular matrix glycoprotein‐Tenascin‐X in gastric function
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24. Impairment of corneal epithelial wound healing is association with increased neutrophil infiltration and reactive oxygen species activation in tenascin X-deficient mice
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25. DNA Methylation in Babies Born to Nonsmoking Mothers Exposed to Secondhand Smoke during Pregnancy: An Epigenome-Wide Association Study
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26. Clinical and Molecular Characterization of Classical-Like Ehlers-Danlos Syndrome Due to a Novel TNXB Variant
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27. Distribution of extracellular matrix tenascin-X in sciatic nerves
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28. Behavioral Alterations in Mice Lacking the Gene for Tenascin-X
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29. Structural extracellular matrix-mediated molecular signaling in wound repair and tissue regeneration
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30. Abdominal Aortic Aneurysm Is Associated With High Serum Levels of Tenascin-X and Decreased Aneurysmal Tissue Tenascin-X
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31. Multiple Roles of Tenascins in Homeostasis and Pathophysiology of Aorta
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32. Genetic effects of a titanium surface on osteoblasts: a meta-analysis.
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33. Biomarkers for Ehlers-Danlos Syndromes: There Is a Role?
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34. A Hidden Structural Vulnerability in the Thrombospondin-2 Deficient Aorta Increases the Propensity to Intramural Delamination
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35. An overlapping phenotype of Osteogenesis imperfecta and Ehlers–Danlos syndrome due to a heterozygous mutation in COL1A1 and biallelic missense variants in TNXB identified by whole exome sequencing
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37. Transforming growth factor-β (TGF-β) pathway abnormalities in tenascin-X deficiency associated with CAH-X syndrome
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38. Mechanical allodynia in mice with tenascin-X deficiency associated with Ehlers-Danlos syndrome
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39. Wound healing-related properties detected in an experimental model with a collagen gel contraction assay are affected in the absence of tenascin-X
    Kei Hashimoto, Naoyo Kajitani, Yasunori Miyamoto, Kenichi Matsumoto · 2017 · Experimental Cell Research
40. Animal Models of Ehlers–Danlos Syndromes: Phenotype, Pathogenesis, and Translational Potential
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41. Pivotal Role of Tenascin-W (-N) in Postnatal Incisor Growth and Periodontal Ligament Remodeling
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42. Combining segmental bulk- and single-cell RNA-sequencing to define the chondrocyte gene expression signature in the murine knee joint
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43. A 3-gene panel improves the prediction of left ventricular dysfunction after acute myocardial infarction.
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45. Regulation of Myocardial Extracellular Matrix Dynamic Changes in Myocardial Infarction and Postinfarct Remodeling
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46. Evaluation of artificial selection in Standard Poodles using whole-genome sequencing
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47. Invasion of Melanoma in Double Knockout Mice Lacking Tenascin‐X and Tenascin‐C
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48. Molecular basis and genetic testing strategies for diagnosing 21-hydroxylase deficiency, including CAH-X syndrome
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51. Abnormal oral mucosal light reflectance: a new clinical sign of Ehlers-Danlos syndrome.
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52. Le syndrome d’Ehlers-Danlos : l’architecture matricielle en question
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53. Heterozygous THBS2 pathogenic variant causes Ehlers–Danlos syndrome with prominent vascular features in humans and mice
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54. Tenascin-X as a causal gene for classical-like Ehlers-Danlos syndrome
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55. Vocal Fold Fibroblasts in Reinke’s Edema Show Alterations Involved in Extracellular Matrix Production, Cytokine Response and Cell Cycle Control
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56. Pathogenic mechanisms in genetically defined Ehlers–Danlos syndromes
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57. Compound heterozygosity for TNXB genetic variants in a mixed-breed dog with Ehlers-Danlos syndrome.
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58. Analysis of the cartilage proteome from three different mouse models of genetic skeletal diseases reveals common and discrete disease signatures
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59. Transplantation of reconstructed human skin on nude mice: a model system to study expression of human tenascin-X and elastic fiber components
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60. Adhesive Defect in Extracellular Matrix Tenascin-X-Null Fibroblasts: A Possible Mechanism of Tumor Invasion.
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61. Les collagènes du derme : au-delà de leurs propriétés structurales
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62. Micromechanics and constitutive modeling of connective soft tissues.
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63. Mmp14-dependent remodeling of the pericellular–dermal collagen interface governs fibroblast survival
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67. Ehlers-Danlos syndrome-molecular genetics beyond the collagens.
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68. Localization and Analysis of the Principal Promoter for Human Tenascin-X
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71. Novel localization of tenascin-X in adult mouse leptomeninges and choroid plexus.
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73. A COL5A2 In-Frame Deletion in a Chihuahua with Ehlers-Danlos Syndrome
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