1.Increased phosphorylation of c-Jun NH (2)-terminal protein kinase in the sciatic nerves of Lewis rats with experimental autoimmune neuritis.
Journal of Veterinary Science 2006;7(1):13-17
The phosphorylation of c-Jun NH (2)-terminal protein kinase (JNK), one of the mitogen-activated protein kinases, was analyzed in the sciatic nerves of Lewis rats with experimental autoimmune neuritis (EAN). Western blot analysis showed that the expression levels of both phosphorylated JNK1 (p-JNK1, approximately 46 kDa) and phosphorylated JNK2 (p-JNK2, approximately 54 kDa) in the sciatic nerves of rats with EAN increased significantly (p < 0.05) at day 14 post-immunization (PI) and remained at this level at days 24 and 30 PI, with a slight decrease. In EANaffected sciatic nerves, there was intense immunostaining for p-JNK in the infiltrating inflammatory cells (especially ED1- positive macrophages) and Schwann cells on days 14-24 PI, compared with those of controls. Some macrophages with increased p-JNK immunoreactivity was shown to be apoptotic, while some Schwann cells remained survived in this rat EAN model, suggesting that JNK is differentially involved in the EAN-affected sciatic nerves. These findings suggest that JNK phosphorylation is closely associated with the clearance of inflammatory cells as well as the activation of Schwann cells in the EAN affected sciatic nerves.
Animals
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Apoptosis/physiology
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Blotting, Western
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Ectodysplasins
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Female
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Immunohistochemistry
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In Situ Nick-End Labeling
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JNK Mitogen-Activated Protein Kinases/*metabolism
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Membrane Proteins/metabolism
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Neuritis, Autoimmune, Experimental/*enzymology/metabolism/pathology
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Phosphorylation
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Rats
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Rats, Inbred Lew
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S100 Proteins/metabolism
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Schwann Cells/metabolism
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Sciatic Nerve/*enzymology/metabolism/pathology
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Tumor Necrosis Factors/metabolism
2.Immunohistochemical study of caveolin-1 and -2 in the rat retina.
Heechul KIM ; Taeki LEE ; Jeeyoung LEE ; Meejung AHN ; Changjong MOON ; Myung Bok WIE ; Taekyun SHIN
Journal of Veterinary Science 2006;7(2):101-104
The expression of caveolin-1 and -2 in the retina was examined; Western blot analysis showed that both were present. Immunohistochemistry indicated that caveolin-1 was expressed in the majority of retinal layers, including the ganglion cell layer, inner plexiform layer, outer plexiform layer, and in the vascular endothelial cells of the retina. Caveolin-2 was primarily immunostained in the vessels, but in a few other elements as well. This is the first demonstration of caveolin differential expression in the retina of rats, and suggests that caveolin plays an important role in signal transduction in glial cells and neuronal cells.
Animals
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Caveolin 1/*analysis/immunology
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Caveolin 2/*analysis/immunology
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Gene Expression Regulation
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Immunohistochemistry
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Male
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Rats
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Rats, Sprague-Dawley
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Retina/*chemistry
3.Factors Associated with the Timeliness of Electronic Nursing Documentation.
Meejung AHN ; Mona CHOI ; YoungAh KIM
Healthcare Informatics Research 2016;22(4):270-276
OBJECTIVES: To investigate the factors associated with the timeliness of electronic nursing documentation using the entry time on the Electronic Medical Record (EMR) system. METHODS: As a retrospective study, data were extracted from January 1 to February 28, 2014 from a hospital EMR system and a nurses’ personnel information system. The timeliness of instances of nursing documentation was categorized into ‘timely’ or ‘untimely’ according to whether the entry time was time-stamped within the working hours during each day, evening, or night shift. Factors associated with the timeliness of the electronic nursing documentation were included in the logistic regression models as nurse- and patient-associated factors. RESULTS: Among 1,700,247 instances of electronic nursing documentation, 79.3% (n = 1,347,711) were completed within the working hours. Years of nursing experience, nursing shift, days of the week, patients’ age, and medical department had a statistically significant associated with the timeliness of nursing records. Nurses with experience of more than 1 year entered nursing records over 2 times more during their working hours than did less experienced nurses. During the evening and night shifts, nurses were 1.49 times and 9.19 times more likely to enter nursing documents in a timely manner, respectively, as compared to those in the day shift. CONCLUSIONS: Nursing documentation was typically completed outside of working hours when a nurse had little experience, worked during the day shift or weekdays, and when tasks were unpredictable. This shows that new nurses need support to familiarize them with various tasks and the overall workflow.
Electronic Health Records
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Information Systems
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Logistic Models
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Nursing Informatics
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Nursing Process
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Nursing Records
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Nursing*
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Retrospective Studies
4.Melatonin ameliorates autoimmune encephalomyelitis through suppression of intercellular adhesion molecule-1.
Jong Chul KANG ; Meejung AHN ; Yong Sik KIM ; Changjong MOON ; Yongduk LEE ; Myung Bok WIE ; Young Jae LEE ; Taekyun SHIN
Journal of Veterinary Science 2001;2(2):85-89
Melatonin (N-acetyl-5-methoxytryptamine), a pineal neurohormone, is a hydroxyl radical scavenger and antioxidant, and plays an important role in the immune system. We studied the effect of exogenous melatonin on the pathogenesis of experimental autoimmune encephalomyelitis (EAE). EAE was induced in Lewis rats by immunization with rat spinal cord homogenates. Subsequent oral administration of melatonin at 5 mg/kg significantly reduced the clinical severity of EAE paralysis compared with administration of the vehicle alone (p<0.01). Infiltration of ED1 macrophages and CD4 T cells into spinal cords occurred both in the absence and presence of melatonin treatment, but melatonin-treated rats had less spinal cord infiltration of inflammatory cells than did the control group. ICAM-1 immunoreactivity in the blood vessels of EAE lesions was decreased in melatonin-treated rats compared to vehicle-treated rats. These findings suggest that exogenous melatonin ameliorates EAE via a mechanism involving reduced expression of ICAM-1 and lymphocyte function associated antigen-1a in autoimmune target organs.
Animals
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Encephalomyelitis, Autoimmune, Experimental/*immunology/prevention & control
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Female
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Immunohistochemistry
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Intercellular Adhesion Molecule-1/analysis/*immunology
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Male
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Melatonin/administration & dosage/*physiology
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Rats
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Rats, Inbred Lew
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Spinal Cord/chemistry/pathology
5.Expression of nitric oxide synthase isoforms in the porcine ovary during follicular development.
Heechul KIM ; Changjong MOON ; Meejung AHN ; Yongduk LEE ; Hwanglyong KIM ; Seungjoon KIM ; Taeyoung HA ; Youngheun JEE ; Taekyun SHIN
Journal of Veterinary Science 2005;6(2):97-101
The expression of nitric oxide synthase (NOS) isoforms in the ovaries of pigs was examined to study the involvement of nitric oxide, a product of NOS activity, in the function of the ovary. Western blot analysis detected three types of NOS in the ovary, including constitutive neuronal NOS (nNOS), endothelial NOS (eNOS) and inducible NOS (iNOS); eNOS immunoreactivity was more intense compared with that of iNOS or nNOS. Immunohistochemical studies demonstrated the presence of nNOS and eNOS in the surface epithelium, stroma, oocytes, thecal cells, and endothelial cells of blood vessels. Positive immunoreactions for nNOS and iNOS were detected in the granulosa cells from multilaminar and antral follicles, but not in those of unilaminar follicles. iNOS was detected in the surface epithelium, oocytes, and theca of multilaminar and antral follicles. Taking all of the findings into consideration, the observed differential expression of the three NOS isoforms in the ovary suggests a role for nitric oxide in modulating reproduction in pigs.
Animals
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Blotting, Western/veterinary
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Female
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Immunohistochemistry/veterinary
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Nerve Tissue Proteins/*biosynthesis
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Nitric Oxide/metabolism
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Nitric Oxide Synthase/*biosynthesis
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Nitric Oxide Synthase Type I
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Nitric Oxide Synthase Type II
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Nitric Oxide Synthase Type III
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Ovarian Follicle/*enzymology/growth&development
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Swine/*physiology
6.Blood-retina barrier dysfunction in experimental autoimmune uveitis: the pathogenesis and therapeutic targets
Jeongtae KIM ; Jiyoon CHUN ; Meejung AHN ; Kyungsook JUNG ; Changjong MOON ; Taekyun SHIN
Anatomy & Cell Biology 2022;55(1):20-27
Experimental autoimmune uveitis (EAU), an animal model of human uveitis, is characterized by infiltration of autoimmune T cells in the uvea as well as in the retina of susceptible animals. EAU is induced by the immunization of uveitogenic antigens, including either retinal soluble-antigen or interphotoreceptor retinoid-binding proteins, in Lewis rats. The pathogenesis of EAU in rats involves the proliferation of autoimmune T cells in peripheral lymphoid tissues and breakdown of the blood-retinal barrier, primarily in the uvea and retina, finally inducing visual dysfunction. In this review, we describe recent EAU studies to facilitate the design of a therapeutic strategy through the interruption of uveitogenic factors during the course of EAU, which will be helpful for controlling human uveitis.
7.A study of animal bones excavated from the shell mound of Jeju Jongdali 1819 archaeological site.
Yoonhyoung KANG ; Jihwan MOON ; Meejung AHN ; Moon Bae BANG ; Taekyun SHIN
Korean Journal of Veterinary Research 2014;54(1):13-19
Animal bones excavated with earthenware from the shell mound at the Jeju Jongdali 1819 archeological site, where three consecutive chronological layers covering the Neolithic (B.C. 15C-B.C. 10C), early Tamra, and late Tamra periods have been identified, were morphologically classified. The majority of the bones from all three periods were broken or split. The major fauna of the mammalian bones in all periods were Cervus spp., Sus scrofa, and Bos taurus. In the early and late Tamra periods, bones of small animals including Mustela sibirica coreana, Meles meles, Rodentia, and Aves were also found in small number. The excavated bones were from all parts of the animal bodies, including head, trunk, forelimb, and hindlimb. Collectively, these findings suggest that the major fauna from the Neolithic to late Tamra periods consisted of Cervus spp., Sus scrofa, and Bos taurus and that the fauna was dissected and carried to the shell mound site after hunting. Information from the bone remains in the shell mound are useful data for study of the wildlife and domestic animals living during the prehistoric period of Jeju Island.
Animals*
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Animals, Domestic
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Birds
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Cattle
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Forelimb
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Head
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Hindlimb
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Rodentia
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Sus scrofa
8.Inducible nitric oxide synthase is involved in neuronal death induced by trimethyltin in the rat hippocampus.
Sukwon JANG ; Sungyoung CHOI ; Changnam PARK ; Meejung AHN ; Taekyun SHIN ; Seungjoon KIM
Korean Journal of Veterinary Research 2011;51(3):185-191
Trimethyltin chloride (TMT) has been used as a neurotoxin for inducing brain dysfunction and neuronal death. Neuronal death in the hippocampus by TMT may generate excessive nitric oxide, but there are few studies about nitric oxide synthase enzyme involved in the synthesis of nitric oxide. The purpose of present study is to analyze the TMT toxicity in each region of rat hippocampus. To evaluate the involvement of nitric oxide, we analyzed the effects of aminoguanidine known as a selective inhibitor for inducible nitric oxide synthase on behavioral changes and the hippocampus of rat by TMT toxicity. 6-week-old male Sprague-Dawley rats were administered with a single dose of TMT (8 mg/kg b.w., i.p.) and the control group was similarly administered with distilled water. TMT + aminoguanidine-treated groups were administered with aminoguanidine (10 mg/kg or 100 mg/kg b.w., i.p.) for 3 days prior to TMT injection. The rats were sacrificed 2 days after TMT administration. In the TMT-treated group, a number of cell losses were seen in CA1, CA3 and the dentate gyrus. In the TMT + aminoguanidine-treated group, neuronal death was seen in CA1 and CA3, but reduced in the dentate gyrus compared to the TMT-treated group. Western blot analysis showed that cleaved caspase-3 expression was increased in the TMT-treated group compared to the control group. However, the expression significantly declined in the TMT + aminoguanidine-treated group. The present findings suggest that inducible nitric oxide synthase is involved in neuronal death induced by TMT.
Animals
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Blotting, Western
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Brain
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Caspase 3
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Dentate Gyrus
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Guanidines
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Hippocampus
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Humans
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Male
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Neurons
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Nitric Oxide
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Nitric Oxide Synthase
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Nitric Oxide Synthase Type II
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Rats
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Rats, Sprague-Dawley
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Trimethyltin Compounds
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Water
9.SMART Careplan System for Continuum of Care.
Young Ah KIM ; Seon Young JANG ; Meejung AHN ; Kyung Duck KIM ; Sung Soo KIM
Healthcare Informatics Research 2015;21(1):56-60
OBJECTIVES: This paper describes the integrated Careplan system, designed to manage and utilize the existing Electronic Medical Record (EMR) system; the system also defines key items for interdisciplinary communication and continuity of patient care. METHODS: We structured the Careplan system to provide effective interdisciplinary communication for healthcare services. The design of the Careplan system architecture proceeded in four steps-defining target datasets; construction of conceptual framework and architecture; screen layout and storyboard creation; screen user interface (UI) design and development, and pilot test and step-by-step deployment. This Careplan system architecture consists of two parts, a server-side and client-side area. On the server-side, it performs the roles of data retrieval and storage from target EMRs. Furthermore, it performs the role of sending push notifications to the client depending on the careplan series. Also, the Careplan system provides various convenient modules to easily enter an individual careplan. RESULTS: Currently, Severance Hospital operates the Careplan system and provides a stable service dealing with dynamic changes (e.g., domestic medical certification, the Joint Commission International guideline) of EMR. CONCLUSIONS: The Careplan system should go hand in hand with key items for strengthening interdisciplinary communication and information sharing within the EMR environment. A well-designed Careplan system can enhance user satisfaction and completed performance.
Certification
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Continuity of Patient Care*
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Dataset
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Delivery of Health Care
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Electronic Health Records
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Hand
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Information Dissemination
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Information Storage and Retrieval
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Interdisciplinary Communication
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Joints
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Patient Care
10.Lithium ameliorates rat spinal cord injury by suppressing glycogen synthase kinase-3β and activating heme oxygenase-1.
Yonghoon KIM ; Jeongtae KIM ; Meejung AHN ; Taekyun SHIN
Anatomy & Cell Biology 2017;50(3):207-213
Glycogen synthase kinase (GSK)-3β and related enzymes are associated with various forms of neuroinflammation, including spinal cord injury (SCI). Our aim was to evaluate whether lithium, a non-selective inhibitor of GSK-3β, ameliorated SCI progression, and also to analyze whether lithium affected the expression levels of two representative GSK-3β–associated molecules, nuclear factor erythroid 2-related factor-2 (Nrf-2) and heme oxygenase-1 (HO-1) (a target gene of Nrf-2). Intraperitoneal lithium chloride (80 mg/kg/day for 3 days) significantly improved locomotor function at 8 days post-injury (DPI); this was maintained until 14 DPI (P<0.05). Western blotting showed significantly increased phosphorylation of GSK-3β (Ser9), Nrf-2, and the Nrf-2 target HO-1 in the spinal cords of lithium-treated animals. Fewer neuropathological changes (e.g., hemorrhage, inflammatory cell infiltration, and tissue loss) were observed in the spinal cords of the lithium-treated group compared with the vehicle-treated group. Microglial activation (evaluated by measuring the immunoreactivity of ionized calcium-binding protein-1) was also significantly reduced in the lithium-treated group. These findings suggest that GSK-3β becomes activated after SCI, and that a non-specific enzyme inhibitor, lithium, ameliorates rat SCI by increasing phosphorylation of GSK-3β and the associated molecules Nrf-2 and HO-1.
Animals
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Blotting, Western
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Glycogen Synthase Kinases
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Glycogen Synthase*
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Glycogen*
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Heme Oxygenase-1*
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Heme*
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Hemorrhage
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Lithium Chloride
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Lithium*
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Phosphorylation
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Rats*
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Spinal Cord Injuries*
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Spinal Cord*