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Action of mefloquine/amitriptyline THN101 combination on neuropathic mechanical hypersensitivity in mice.
Enhanced analgesic cholinergic tone in the spinal cord in a mouse model of neuropathic pain.
Platelet-rich plasma and cytokines in neuropathic pain: A narrative review and a clinical perspective.
Time Course of Homeostatic Structural Plasticity in Response to Optogenetic Stimulation in Mouse Anterior Cingulate Cortex.
beta(2)-adrenoceptors are critical for antidepressant treatment of neuropathic pain.
Tissue-specific expression of tryptophan hydroxylase mRNAs in the rat midbrain: anatomical evidence and daily profiles.
The Role of Skeletal Muscle in Amyotrophic Lateral Sclerosis.
Serotonin 2B receptor slows disease progression and prevents degeneration of spinal cord mononuclear phagocytes in amyotrophic lateral sclerosis.
Alterations in the hypothalamic melanocortin pathway in amyotrophic lateral sclerosis.
Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy.
Toxic gain of function from mutant FUS protein is crucial to trigger cell autonomous motor neuron loss.
APP-dependent glial cell line-derived neurotrophic factor gene expression drives neuromuscular junction formation.
Motor neuron intrinsic and extrinsic mechanisms contribute to the pathogenesis of FUS-associated amyotrophic lateral sclerosis.
Loss of C9ORF72 impairs autophagy and synergizes with polyQ Ataxin-2 to induce motor neuron dysfunction and cell death.
A transgenic mouse expressing CHMP2Bintron5 mutant in neurons develops histological and behavioural features of amyotrophic lateral sclerosis and frontotemporal dementia.
The most prevalent genetic cause of ALS-FTD, C9orf72 synergizes the toxicity of ATXN2 intermediate polyglutamine repeats through the autophagy pathway.
Body fat distribution in Parkinson's disease: An MRI-based body fat quantification study.
Evaluating Behavior in Mouse Models of the Behavioral Variant of Frontotemporal Dementia: Which Test for Which Symptom?

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