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1 content in biological tissues (i.e., porcine intervertebral disc).
2 yme regulating GAG synthesis in cells of the intervertebral disc.
3 uctures, such as the articular cartilage and intervertebral disc.
4 cornea, and successive lamellar rings in an intervertebral disc.
5 en a result of a degenerative process in the intervertebral disc.
6 agnosed with large calcifications within the intervertebral disc.
7 y neuron changes to a single affected lumbar intervertebral disc.
8 ogically hyperosmotic environment within the intervertebral disc.
9 adaptation to diurnal osmotic loading of the intervertebral disc.
10 ten the direct result of degeneration of the intervertebral disc.
11 TS activity in nucleus pulposus cells of the intervertebral disc.
12 lcium phosphate-like whitlockite crystals in intervertebral discs.
13 perichondrium, and mesenchymal cells of the intervertebral discs.
14 directly by forming the nucleus pulposus of intervertebral discs.
15 re necessary for the resorption of herniated intervertebral discs.
16 us fibrosus in 48 (60%) of the 80 samples of intervertebral discs.
17 ome, which later comprises the vertebrae and intervertebral discs.
18 nges in achieving functional regeneration of intervertebral discs.
19 ing rise to the cells that form and maintain intervertebral discs.
20 premature degeneration and calcification of intervertebral discs.
21 ignaling mechanisms control this response in intervertebral discs.
22 and water content in the nucleus pulposus of intervertebral discs.
23 g signaling is required for formation of the intervertebral discs.
24 cular mechanisms responsible for forming the intervertebral discs.
25 CCN3 was expressed in embryonic and adult intervertebral discs.
26 of alternating vertebral bodies (centra) and intervertebral discs.(1) Recent studies in zebrafish hav
27 worsening destruction of vertebral body and intervertebral disc, abnormal vertebral marrow signal ch
28 f this study was that Chd synthesized in the intervertebral disc accumulates in the vertebral body.
29 Sensory afferent nerve fiber growth into the intervertebral disc after injury-induced inflammation ma
30 y has correlated macroscopic and microscopic intervertebral disc alterations starting in the second d
31 how that the loss of residual strains in the intervertebral disc alters the microenvironment and inst
34 hich only revealed a protrusion of the L5-S1 intervertebral disc and no apparent cause for the patien
35 low back pain is degenerative disease of the intervertebral disc and other structures of the lumbar s
36 e a novel mechanism of NGF regulation in the intervertebral disc and potentially other pathogenic con
37 th circumferentially aligned fibers, such as intervertebral discs and arteries, are abundant in natur
38 ithin the developing annulus fibrosis of the intervertebral discs and increased apoptosis of chondroc
39 es were taken at lumbar vertebrae L1-L5 plus intervertebral discs and the thigh (midthigh, 10 cm dist
40 hat express substance P deep within diseased intervertebral discs and their association with pain sug
43 ading of the lower back with degeneration of intervertebral discs, and experiments on cadaver spines
44 tebrae, zygapophyseal and sacroiliac joints, intervertebral discs, and neurovascular structures) are
49 f a metameric series of vertebral bodies and intervertebral discs, as well as adjoining ribs and ster
51 pain is associated with degeneration of the intervertebral disc, but specific mechanisms of pain gen
53 n our study, we present a case of idiopathic intervertebral disc calcification within the cervical se
55 we investigated LPP action in rabbit primary intervertebral disc cells cultured ex vivo in a three-di
56 CHST3 mRNA was significantly reduced in the intervertebral disc cells of human subjects carrying the
63 wn, studies on the effects and mechanisms of intervertebral disc degeneration (IVDD) are still lackin
69 or for several chronic conditions, including intervertebral disc degeneration and associated back pai
70 ales, and thickening of the skin, as well as intervertebral disc degeneration and extensive synovial
71 e therapeutic strategy for the prevention of intervertebral disc degeneration and its associated morb
72 ative connective tissue pathologies, such as intervertebral disc degeneration and osteoarthritis.
73 ation (Col9a1(-/-)), osteoarthritis (OA) and intervertebral disc degeneration develop prematurely.
74 was to assess the prevalence and timeline of intervertebral disc degeneration in mice homozygous for
81 ioral phenotype in a rodent model of chronic intervertebral disc degeneration which provides a means
82 (12.5 mo old) showed increased incidence of intervertebral disc degeneration with a concomitant decr
83 a future therapeutic intervention to retard intervertebral disc degeneration, partial inhibition of
89 osis for several spinal disorders, including intervertebral disc degenerative changes in T1w and T2w
90 defects in caudal vertebrae due to abnormal intervertebral disc development, although with higher pe
92 arrow signal changes, and abnormal signal in intervertebral disc did not necessarily indicate worseni
93 thin a single breed (PBonferroni = 0.01) and intervertebral disc disease (IVDD) across breeds (PBonfe
96 nking sulfate homeostasis with back pain and intervertebral disc disorder, our study identifies SLC26
97 [1.01-1.06]), arthrosis (1.15 [1.09-1.21]), intervertebral disc disorders (1.13 [1.09-1.17]), and sp
99 pression of Sca1 in mesenchymal cells of the intervertebral discs during development of the spinal co
101 Interestingly, lubricin was prominent in the intervertebral disc, especially in the nucleus pulposus.
106 sures in the central nucleus pulposus of the intervertebral disc generate prestrain in the outer annu
109 Conventional microdiscectomy treatment for intervertebral disc herniation alleviates pain but does
110 painful neuroinflammation that can accompany intervertebral disc herniation, is associated with local
111 likely to have low back pain or symptoms of intervertebral disc herniation, with secondary problems
113 g to increased susceptibility of spontaneous intervertebral disc herniations in a clinically relevant
115 an important role for nerve growth into the intervertebral disc in the pathogenesis of chronic low b
116 orphometry and deformation of lumbar (L2-S1) intervertebral discs in 10 healthy participants while pe
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 Nucleus pulposus, the central zone of the intervertebral disc, is gel-like and has a similar colla
122 r understanding of functional changes in the intervertebral disc (IVD) and interaction with endplate
124 l loads are important for homeostasis of the intervertebral disc (IVD) cell matrix, with physiologic
125 ithout pro-inflammatory cytokine IL-1beta in intervertebral disc (IVD) cells such as human annulus fi
126 dies have demonstrated biologic responses of intervertebral disc (IVD) cells to loading, although the
130 Cellular senescence is a contributor to intervertebral disc (IVD) degeneration and low back pain
132 of significant socio-economic importance and intervertebral disc (IVD) degeneration has been implicat
133 ommon cause of low back pain, the cascade of intervertebral disc (IVD) degeneration is initiated by t
136 on of senescent cells is closely linked with intervertebral disc (IVD) degeneration, a prevalent age-
146 sues also require interactions for postnatal intervertebral disc (IVD) growth and maintenance is less
150 anical signals can either promote or disrupt intervertebral disc (IVD) homeostasis, the molecular mec
154 anabolic and anti-catabolic growth factor on intervertebral disc (IVD) matrix and cell homeostasis.
157 -derived shear stiffness measurements of the intervertebral disc (IVD) taken throughout the day and t
160 breakdown of the extracellular matrix of the intervertebral disc (IVD), disc height loss, and inflamm
161 commonly implicated in this condition is the intervertebral disc (IVD), which frequently herniates, r
164 atic activity elevated in degenerative human intervertebral disc (IVD). Here, we examined the discs i
166 ures of nucleus pulposus (NP) cells from the intervertebral discs (IVD) of bovine tails were transfec
168 o-vanillin and RG-7112, remove SnCs in human intervertebral discs (IVDs) and reduce SASP release, but
169 uloskeletal (MSK) tissues like cartilage and intervertebral discs (IVDs) but require long acquisition
170 al bodies were only moderately affected, the intervertebral discs (IVDs) were either missing or incom
172 hondrocytes in knee joint and in NP cells in intervertebral disc led to the decrease in CTGF expressi
173 ures including cortical and cancellous bone, intervertebral discs, ligaments, and cartilage directly
175 study to assess the therapeutic benefits of intervertebral disc matrix repair and regeneration by ev
176 ned peptide therapy with LfcinB and BMP7 for intervertebral disc matrix repair and to understand cell
181 he alterations in the range of motion (ROM), intervertebral disc pressure (IDP), articular cartilage
182 patients: dyspnoea, headache, hypertension, intervertebral disc protrusion, and malignant lung neopl
184 sforming growth factor can be transferred to intervertebral discs, resulting in increased proteogylca
186 proteins in articular cartilages, meniscus, intervertebral disc, rib, and tracheal cartilages on sam
188 h varying anatomic corridors to approach the intervertebral disc space and implanted materials have e
190 ry responses associated with degeneration of intervertebral discs that cause chronic back pain, and w
191 n nucleus pulposus (NP) cells of the healthy intervertebral disc, the mechanisms that control express
192 expression of Notch signaling components in intervertebral disc tissue from mature rats and from hum
194 anases other than ADAMTS-8 was identified in intervertebral disc tissue, as was mRNA for TIMP-3.
198 n clock phase and amplitude in cartilage and intervertebral disc tissues in vivo and in tissue explan
202 (alpha1) XI protein both localize within the intervertebral disc-vertebral junction region encompassi
204 a murine organ culture model in which intact intervertebral discs were cocultured with peritoneal mac
205 of the spine and hips, and deterioration of intervertebral discs with characteristic radiographic ch