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1 alism, including an increase in the width of intervertebral articular facets from the upper to lower
2 , DAPS maintained their structure, prevented intervertebral bony fusion, and matched native disc mech
4 t the protein is required for maintenance of intervertebral, carpal and sternal joints, and the joint
6 r understanding of functional changes in the intervertebral disc (IVD) and interaction with endplate
8 l loads are important for homeostasis of the intervertebral disc (IVD) cell matrix, with physiologic
9 ithout pro-inflammatory cytokine IL-1beta in intervertebral disc (IVD) cells such as human annulus fi
10 dies have demonstrated biologic responses of intervertebral disc (IVD) cells to loading, although the
16 of significant socio-economic importance and intervertebral disc (IVD) degeneration has been implicat
17 ommon cause of low back pain, the cascade of intervertebral disc (IVD) degeneration is initiated by t
20 on of senescent cells is closely linked with intervertebral disc (IVD) degeneration, a prevalent age-
30 sues also require interactions for postnatal intervertebral disc (IVD) growth and maintenance is less
34 anical signals can either promote or disrupt intervertebral disc (IVD) homeostasis, the molecular mec
38 anabolic and anti-catabolic growth factor on intervertebral disc (IVD) matrix and cell homeostasis.
41 -derived shear stiffness measurements of the intervertebral disc (IVD) taken throughout the day and t
44 breakdown of the extracellular matrix of the intervertebral disc (IVD), disc height loss, and inflamm
45 commonly implicated in this condition is the intervertebral disc (IVD), which frequently herniates, r
48 atic activity elevated in degenerative human intervertebral disc (IVD). Here, we examined the discs i
50 f this study was that Chd synthesized in the intervertebral disc accumulates in the vertebral body.
51 Sensory afferent nerve fiber growth into the intervertebral disc after injury-induced inflammation ma
52 y has correlated macroscopic and microscopic intervertebral disc alterations starting in the second d
53 how that the loss of residual strains in the intervertebral disc alters the microenvironment and inst
56 hich only revealed a protrusion of the L5-S1 intervertebral disc and no apparent cause for the patien
57 low back pain is degenerative disease of the intervertebral disc and other structures of the lumbar s
58 e a novel mechanism of NGF regulation in the intervertebral disc and potentially other pathogenic con
62 n our study, we present a case of idiopathic intervertebral disc calcification within the cervical se
63 we investigated LPP action in rabbit primary intervertebral disc cells cultured ex vivo in a three-di
64 CHST3 mRNA was significantly reduced in the intervertebral disc cells of human subjects carrying the
71 wn, studies on the effects and mechanisms of intervertebral disc degeneration (IVDD) are still lackin
77 or for several chronic conditions, including intervertebral disc degeneration and associated back pai
78 ales, and thickening of the skin, as well as intervertebral disc degeneration and extensive synovial
79 e therapeutic strategy for the prevention of intervertebral disc degeneration and its associated morb
80 ative connective tissue pathologies, such as intervertebral disc degeneration and osteoarthritis.
81 ation (Col9a1(-/-)), osteoarthritis (OA) and intervertebral disc degeneration develop prematurely.
82 was to assess the prevalence and timeline of intervertebral disc degeneration in mice homozygous for
89 ioral phenotype in a rodent model of chronic intervertebral disc degeneration which provides a means
90 (12.5 mo old) showed increased incidence of intervertebral disc degeneration with a concomitant decr
91 a future therapeutic intervention to retard intervertebral disc degeneration, partial inhibition of
97 osis for several spinal disorders, including intervertebral disc degenerative changes in T1w and T2w
98 defects in caudal vertebrae due to abnormal intervertebral disc development, although with higher pe
100 arrow signal changes, and abnormal signal in intervertebral disc did not necessarily indicate worseni
101 thin a single breed (PBonferroni = 0.01) and intervertebral disc disease (IVDD) across breeds (PBonfe
104 nking sulfate homeostasis with back pain and intervertebral disc disorder, our study identifies SLC26
105 [1.01-1.06]), arthrosis (1.15 [1.09-1.21]), intervertebral disc disorders (1.13 [1.09-1.17]), and sp
109 sures in the central nucleus pulposus of the intervertebral disc generate prestrain in the outer annu
111 Conventional microdiscectomy treatment for intervertebral disc herniation alleviates pain but does
112 painful neuroinflammation that can accompany intervertebral disc herniation, is associated with local
113 likely to have low back pain or symptoms of intervertebral disc herniation, with secondary problems
115 g to increased susceptibility of spontaneous intervertebral disc herniations in a clinically relevant
117 an important role for nerve growth into the intervertebral disc in the pathogenesis of chronic low b
118 from the dorsal root ganglia in animals with intervertebral disc injury demonstrated altered TRPV1 ac
120 to hypoxia in nucleus pulposus cells of the intervertebral disc is regulated by the hypoxia-inducibl
121 hondrocytes in knee joint and in NP cells in intervertebral disc led to the decrease in CTGF expressi
123 study to assess the therapeutic benefits of intervertebral disc matrix repair and regeneration by ev
124 ned peptide therapy with LfcinB and BMP7 for intervertebral disc matrix repair and to understand cell
125 he alterations in the range of motion (ROM), intervertebral disc pressure (IDP), articular cartilage
126 patients: dyspnoea, headache, hypertension, intervertebral disc protrusion, and malignant lung neopl
130 h varying anatomic corridors to approach the intervertebral disc space and implanted materials have e
132 expression of Notch signaling components in intervertebral disc tissue from mature rats and from hum
134 anases other than ADAMTS-8 was identified in intervertebral disc tissue, as was mRNA for TIMP-3.
138 n clock phase and amplitude in cartilage and intervertebral disc tissues in vivo and in tissue explan
143 worsening destruction of vertebral body and intervertebral disc, abnormal vertebral marrow signal ch
145 pain is associated with degeneration of the intervertebral disc, but specific mechanisms of pain gen
147 Interestingly, lubricin was prominent in the intervertebral disc, especially in the nucleus pulposus.
148 Nucleus pulposus, the central zone of the intervertebral disc, is gel-like and has a similar colla
149 proteins in articular cartilages, meniscus, intervertebral disc, rib, and tracheal cartilages on sam
150 n nucleus pulposus (NP) cells of the healthy intervertebral disc, the mechanisms that control express
151 (alpha1) XI protein both localize within the intervertebral disc-vertebral junction region encompassi
163 ures of nucleus pulposus (NP) cells from the intervertebral discs (IVD) of bovine tails were transfec
165 o-vanillin and RG-7112, remove SnCs in human intervertebral discs (IVDs) and reduce SASP release, but
166 uloskeletal (MSK) tissues like cartilage and intervertebral discs (IVDs) but require long acquisition
167 al bodies were only moderately affected, the intervertebral discs (IVDs) were either missing or incom
169 th circumferentially aligned fibers, such as intervertebral discs and arteries, are abundant in natur
170 ithin the developing annulus fibrosis of the intervertebral discs and increased apoptosis of chondroc
171 es were taken at lumbar vertebrae L1-L5 plus intervertebral discs and the thigh (midthigh, 10 cm dist
172 hat express substance P deep within diseased intervertebral discs and their association with pain sug
175 pression of Sca1 in mesenchymal cells of the intervertebral discs during development of the spinal co
179 orphometry and deformation of lumbar (L2-S1) intervertebral discs in 10 healthy participants while pe
182 ry responses associated with degeneration of intervertebral discs that cause chronic back pain, and w
184 a murine organ culture model in which intact intervertebral discs were cocultured with peritoneal mac
185 of the spine and hips, and deterioration of intervertebral discs with characteristic radiographic ch
187 ading of the lower back with degeneration of intervertebral discs, and experiments on cadaver spines
188 tebrae, zygapophyseal and sacroiliac joints, intervertebral discs, and neurovascular structures) are
189 f a metameric series of vertebral bodies and intervertebral discs, as well as adjoining ribs and ster
192 ures including cortical and cancellous bone, intervertebral discs, ligaments, and cartilage directly
194 sforming growth factor can be transferred to intervertebral discs, resulting in increased proteogylca
209 of alternating vertebral bodies (centra) and intervertebral discs.(1) Recent studies in zebrafish hav
210 spine alters the osmotic environment in the intervertebral disk (IVD) as interstitial water is expre
219 had ligamentous injuries, three patients had intervertebral disk edema, and one patient had a cord co
220 rs; 42% women) with imaging-confirmed lumbar intervertebral disk herniation and persistent signs and
221 cal candidates with imaging-confirmed lumbar intervertebral disk herniation who were treated at 13 sp
222 ctures, vertebral body and facet contusions, intervertebral disk herniations, ligamentum nuchae strai
223 Magnetic resonance (MR) images of a lumbar intervertebral disk in a healthy volunteer were obtained
230 n 10-week-old dKO mice showed replacement of intervertebral disk structures (annulus fibrosus and nuc
232 Thin-section spin-echo images of an excised intervertebral disk were obtained with a horizontal fiel
233 ium (from the occiput to the second cervical intervertebral disk) may be radiographically obscure due
234 The results suggest that MR imaging of the intervertebral disk, using sodium imaging and T2 mapping
235 n the literature this year include herniated intervertebral disk-associated radiculopathy, facet join
237 ation of facet joints, sacroiliac joints, or intervertebral disks (combination trial, 202 participant
238 rtilage, muscle, bone, connective tissue and intervertebral disks (IVDs) as drivers of AIS susceptibi
240 onal procedures involving bone, soft tissue, intervertebral disks, and joints are safe and sufficient
241 ation of facet joints, sacroiliac joints, or intervertebral disks, radiofrequency denervation combine
244 r this retrospective study, 41 patients (243 intervertebral disks; overall mean age, 68 years; 24 wom
247 The method involves the installation of an intervertebral fusion mount to reduce spinal movement, a
250 aset, we traced the evolution of the amniote intervertebral joint through ancestral character state r
253 nal adipose tissue compartments at the L2-L3 intervertebral level by MRI is an acceptably reliable an
255 onance imaging (MRI) slices taken at various intervertebral levels from the 12th thoracic to 1st sacr
259 bnormal collagen fibrillogenesis in skin and intervertebral ligaments and ectopic bone formation on t
261 ponsive to hypoxia, we speculate that in the intervertebral niche, notch proteins participate in the
264 al development, Smad1 phosphorylation in the intervertebral region was decreased in the Cv2 mutant, e
267 iote tree revealed preservation of different intervertebral soft tissue types (cartilage, probable no
268 sensitivity included decreased height of the intervertebral space (n = 23, 52.3% sensitivity) and dis
269 bra in 85% of subjects and crossed the L2-L3 intervertebral space or the L2 vertebra for 15% of subje
271 ents are sometimes offered fusion surgery if intervertebral translation, measured from static, end of