the International Standards for Neurological Classification of Spinal Cord Injury
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The Science and Practice of Pharmacy
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Encyclopedia of Pharmaceutical Technology
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Encyclopedia of Pharmaceutical Technology
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Peripheral myelin protein 22 is in complex with alpha6beta4 integrin, and its absence alters the Schwann cell basal lamina
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Developmental abnormalities in the nerves of peripheral myelin protein 22-deficient mice
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Proliferation of Schwann Cells and Regulation of Cyclin D1 Expression in an Animal Model of Charcot-Marie-Tooth Disease Type 1A
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Chlorpromazine inhibits the glucocorticoid receptor-mediated gene transcription in a calcium-dependent manner
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Muscarinic-receptor-mediated inhibition of insulin-like growth factor-1 receptor-stimulated phosphoinositide 3-kinase signalling in 1321N1 astrocytoma cells
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Cellular stresses differentially activate c-Jun N-terminal protein kinases and extracellular signal-regulated protein kinases in cultured ventricular myocytes
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Rho-dependent regulation of cell spreading by the tetraspan membrane protein Gas3/PMP22
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Cyclooxygenase-2 and Colorectal Cancer Chemoprevention: The β-Catenin Connection
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A mixed model approach for intent-to-treat analysis in longitudinal clinical trials with missing values
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Neurological recovery-promoting, anti-inflammatory, and anti-oxidative effects afforded by fenofibrate, a PPAR alpha agonist, in traumatic brain injury
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Alterations in the Arf6-regulated plasma membrane endosomal recycling pathway in cells overexpressing the tetraspan protein Gas3/PMP22
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DMSO induction of the leukotriene LTC4 by Lewis rat Schwann cells
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The Neurotrophin Receptor p75NTR as a Positive Modulator of Myelination
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Long term treatment with metformin in patients with type 2 diabetes and risk of vitamin B-12 deficiency: randomised placebo controlled trial
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Altered ion channels in an animal model of Charcot-Marie-Tooth disease type IA
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PPAR alpha activator fenofibrate inhibits myocardial inflammation and fibrosis in angiotensin II-infused rats
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Myelin-associated mRNA and protein expression deficits in the anterior cingulate cortex and hippocampus in elderly schizophrenia patients
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Peripheral myelin protein 22 and protein zero: a novel association in peripheral nervous system myelin
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Emerging role for autophagy in the removal of aggresomes in Schwann cells
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Impaired proteasome activity and accumulation of ubiquitinated substrates in a hereditary neuropathy model
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Alterations in degradative pathways and protein aggregation in a neuropathy model based on PMP22 overexpression
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The formation of peripheral myelin protein 22 aggregates is hindered by the enhancement of autophagy and expression of cytoplasmic chaperones
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Spinal cord contusion in the rat: behavioral analysis of functional neurologic impairment
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Aldose reductase induced by hyperosmotic stress mediates cardiomyocyte apoptosis: differential effects of sorbitol and mannitol
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A modified peripheral neuropathy scale: the Overall Neuropathy Limitations Scale
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Expression and functional state of the corticosteroid receptors and 11 beta-hydroxysteroid dehydrogenase type 2 in Schwann cells
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Focal loss of the glutamate transporter EAAT2 in a transgenic rat model of SOD1 mutant-mediated amyotrophic lateral sclerosis (ALS)
| [0238]
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GISP: a novel brain-specific protein that promotes surface expression and function of GABA(B) receptors
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The Journal of Spinal Cord Medicine
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Oral curcumin mitigates the clinical and neuropathologic phenotype of the Trembler-J mouse: a potential therapy for inherited neuropathy
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Evidence for Macrophage-Mediated Myelin Disruption in an Animal Model for Charcot-Marie-Tooth Neuropathy Type 1A
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Phosphorylation of human progesterone receptors at serine-294 by mitogen-activated protein kinase signals their degradation by the 26S proteasome
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Identifying blood biomarkers for mood disorders using convergent functional genomics
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Muscle Study Group. High-Dosage Ascorbic Acid Treatment in Charcot-Marie-Tooth Disease Type 1A: Results of a Randomized, Double-Masked, Controlled Trial
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Induction of type 3 iodothyronine deiodinase by nerve injury in the rat peripheral nervous system
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Statistical Analysis with Missing Data
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On O ' Brien ' s OLS and GLS tests for multiple endpoints
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Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A
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Conditions for the Effectiveness of a Preliminary Test of Variance
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Disease progression of human SOD1 (G93A) transgenic ALS model rats
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Role of immune cells in animal models for inherited neuropathies: facts and visions
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Peripheral nerves: a target for the action of neuroactive steroids
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Rapid effects of triiodothyronine on immediate-early gene expression in Schwann cells
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Animal models of inherited neuropathies
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Antiprogesterone therapy uncouples axonal loss from demyelination in a transgenic rat model of CMT1A neuropathy
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Pathway interactions between MAPKs, mTOR, PKA, and the glucocorticoid receptor in lymphoid cells
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Identification and functional characterization of thromboxane A2 receptors in Schwann cells
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In vivo Regulation of Extracellular Signal-Regulated Protein Kinase (ERK) and Protein Kinase B (Akt) Phosphorylation by Acute and Chronic Morphine
| [0238]
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Attenuation of aldose reductase gene suppresses high-glucose-induced apoptosis and oxidative stress in rat lens epithelial cells
| [0238]
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Mechanisms of disease: inherited demyelinating neuropathies-from basic to clinical research
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CMT rat'': peripheral neuropathy and dysmyelination caused by transgenic overexpression of PMP22
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Upregulation of the endosomal-lysosomal pathway in the trembler-J neuropathy
| [0238]
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Procedures for Comparing Samples with Multiple Endpoints
| [0238]
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GABAB receptor-mediated inhibition of GABAA receptor calcium elevations in developing hypothalamic neurons
| [0238]
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Opposing extracellular signal-regulated kinase and Akt pathways control Schwann cell myelination
| [0238]
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Peripheral myelin protein 22 is expressed in human central nervous system
| [0238]
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Randomized, double-blind, placebo-controlled phase II study of single-agent oral talactoferrin in patients with locally advanced or metastatic non-small-cell lung cancer that progressed after chemotherapy
| [0238]
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Ascorbic acid treatment corrects the phenotype of a mouse model of Charcot-Marie-Tooth disease
| [0238]
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Induced myelination and demyelination in a conditional mouse model of Charcot-Marie-Tooth disease type 1A
| [0238]
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Pharmacological induction of the heat shock response improves myelination in a neuropathic model
| [0238]
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Charcot-Marie-Tooth disease type 1A. Association with a spontaneous point mutation in the PMP22 gene
| [0238]
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PMP22 overexpression causes dysmyelination in mice
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Synthesis of progesterone in Schwann cells: regulation by sensory neurons
| [0238]
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The temporospatial expression of peripheral myelin protein 22 at the developing blood-nerve and blood-brain barriers
| [0238]
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Regulation of Schwann cell proliferation and apoptosis in PMP22-deficient mice and mouse models of Charcot-Marie-Tooth disease type 1A
| [0238]
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A more realistic look at the robustness and Type II error properties of the t test to departures from population normality
| [0238]
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Progesterone synthesis and myelin formation in peripheral nerves
| [0238]
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Therapeutic administration of progesterone antagonist in a model of Charcot-Marie-Tooth disease (CMT-1A)
| [0238]
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Animal models of Charcot-Marie-Tooth disease type 1A (CMT1A)
| [0238]
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Reliability and validity of the CMT neuropathy score as a measure of disability
| [0238]
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Muscarinic M2 receptors mediate transactivation of EGF receptor through Fyn kinase and without matrix metalloproteases
| [0238]
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Disease mechanisms in inherited neuropathies
| [0238]
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Trembler mouse carries a point mutation in a myelin gene
| [0238]
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Identification of early disease progression in an ALS rat model
| [0238]
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The phenotypic manifestations of chromosome 17p 11.2 duplication
| [0238]
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Differential aggregation of the Trembler and Trembler J mutants of peripheral myelin protein 22
| [0238]
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Dominant role of GABAB2 and Gbetagamma for GABAB receptor-mediated-ERK1/2/CREB pathway in cerebellar neurons
| [0238]
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Transcriptional activities of estrogen and glucocorticoid receptors are functionally integrated at the AP-1 response element
| [0238]
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Altered expression of ion channel isoforms at the node of Ranvier in P0-deficient myelin mutants
| [0238]
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Ultrastructural PMP22 expression in inherited demyelinating neuropathies
| [0238]
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Parametric versus non-parametric statistics in the analysis of randomized trials with non-normally distributed data. BMC Med
| [0238]
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Nuclear triiodothyronine receptor expression is regulated by axon-Schwann cell contact
| [0238]
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Differential expression of triiodothyronine receptors in schwannoma and neurofibroma: role of Schwann cell-axon interaction
| [0238]
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Influence of molecular and chemical chaperones on protein folding
| [0238]
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Localisation and modulation of prostanoid receptors EP1 and EP4 in the rat chronic constriction injury model of neuropathic pain
| [0238]
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