Pages that link to "Q79733723"
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The following pages link to Early electrophysiological abnormalities in lumbar motoneurons in a transgenic mouse model of amyotrophic lateral sclerosis (Q79733723):
Displaying 50 items.
- Inhibitory synaptic regulation of motoneurons: a new target of disease mechanisms in amyotrophic lateral sclerosis (Q27687333) (← links)
- Monoaminergic control of spinal locomotor networks in SOD1G93A newborn mice (Q33845902) (← links)
- Effect of fluoxetine on disease progression in a mouse model of ALS. (Q33900692) (← links)
- Optimised and rapid pre-clinical screening in the SOD1(G93A) transgenic mouse model of amyotrophic lateral sclerosis (ALS). (Q34005426) (← links)
- Persistent inward currents in spinal motoneurons: important for normal function but potentially harmful after spinal cord injury and in amyotrophic lateral sclerosis (Q34399203) (← links)
- Progressive changes in synaptic inputs to motoneurons in adult sacral spinal cord of a mouse model of amyotrophic lateral sclerosis (Q34399344) (← links)
- Soma size and Cav1.3 channel expression in vulnerable and resistant motoneuron populations of the SOD1G93A mouse model of ALS. (Q34582367) (← links)
- Glycine Receptor Channels in Spinal Motoneurons Are Abnormal in a Transgenic Mouse Model of Amyotrophic Lateral Sclerosis (Q34847712) (← links)
- The Effect of Training on Motoneuron Survival in Amyotrophic Lateral Sclerosis: Which Motoneuron Type is Saved? (Q34875134) (← links)
- Human iPSC-derived motoneurons harbouring TARDBP or C9ORF72 ALS mutations are dysfunctional despite maintaining viability (Q35114316) (← links)
- Comparison of dendritic calcium transients in juvenile wild type and SOD1(G93A) mouse lumbar motoneurons (Q35357235) (← links)
- Reactive oxygen species trigger motoneuron death in non-cell-autonomous models of ALS through activation of c-Abl signaling (Q35701794) (← links)
- Persistent inward currents in spinal motoneurons and their influence on human motoneuron firing patterns (Q35889120) (← links)
- Effect of prolonged riluzole exposure on cultured motoneurons in a mouse model of ALS. (Q35951394) (← links)
- Developing electrical properties of postnatal mouse lumbar motoneurons (Q36018256) (← links)
- Evidence from computer simulations for alterations in the membrane biophysical properties and dendritic processing of synaptic inputs in mutant superoxide dismutase-1 motoneurons (Q36351201) (← links)
- Mutant SOD1-expressing astrocytes release toxic factors that trigger motoneuron death by inducing hyperexcitability (Q36924065) (← links)
- Active properties of motoneurone dendrites: diffuse descending neuromodulation, focused local inhibition (Q36975543) (← links)
- Mutant SOD1 protein increases Nav1.3 channel excitability (Q37088701) (← links)
- Fast kinetics, high-frequency oscillations, and subprimary firing range in adult mouse spinal motoneurons (Q37447133) (← links)
- Motoneuron excitability: the importance of neuromodulatory inputs (Q37603971) (← links)
- Respiratory motoneurons and pathological conditions: Lessons from hypoglossal motoneurons challenged by excitotoxic or oxidative stress (Q37858680) (← links)
- Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis (Q37952528) (← links)
- The changing scene of amyotrophic lateral sclerosis (Q38086771) (← links)
- Motor unit (Q38110501) (← links)
- ER Dysfunction and Protein Folding Stress in ALS. (Q38170112) (← links)
- Fishing for causes and cures of motor neuron disorders (Q38224042) (← links)
- New perspectives on amyotrophic lateral sclerosis: the role of glial cells at the neuromuscular junction (Q38955746) (← links)
- Selective mitochondrial Ca2+ uptake deficit in disease endstage vulnerable motoneurons of the SOD1G93A mouse model of amyotrophic lateral sclerosis (Q39468775) (← links)
- Directed differentiation of human-induced pluripotent stem cells generates active motor neurons (Q39863440) (← links)
- Rebound from Inhibition: Self-Correction against Neurodegeneration? (Q40095203) (← links)
- Is hyperexcitability really guilty in amyotrophic lateral sclerosis? (Q41817857) (← links)
- Voltage-gated calcium channels are abnormal in cultured spinal motoneurons in the G93A-SOD1 transgenic mouse model of ALS. (Q41842390) (← links)
- Early pathogenesis in the adult-onset neurodegenerative disease amyotrophic lateral sclerosis (Q41862808) (← links)
- A Stem Cell Model of the Motor Circuit Uncouples Motor Neuron Death from Hyperexcitability Induced by SMN Deficiency. (Q41885598) (← links)
- Early intrinsic hyperexcitability does not contribute to motoneuron degeneration in amyotrophic lateral sclerosis. (Q41957945) (← links)
- Direct Lineage Reprogramming Reveals Disease-Specific Phenotypes of Motor Neurons from Human ALS Patients (Q43098018) (← links)
- Homeostatic dysregulation in membrane properties of masticatory motoneurons compared with oculomotor neurons in a mouse model for amyotrophic lateral sclerosis. (Q43104922) (← links)
- Links between electrophysiological and molecular pathology of amyotrophic lateral sclerosis (Q43577107) (← links)
- Calcium channel agonists protect against neuromuscular dysfunction in a genetic model of TDP-43 mutation in ALS. (Q45929410) (← links)
- Increased anxiety-like behavior and selective learning impairments are concomitant to loss of hippocampal interneurons in the presymptomatic SOD1(G93A) ALS mouse model. (Q47744597) (← links)
- Opposite Synaptic Alterations at the Neuromuscular Junction in an ALS Mouse Model: When Motor Units Matter. (Q47933159) (← links)
- Chronic electromyograms in treadmill running SOD1 mice reveal early changes in muscle activation (Q48099230) (← links)
- Sigma-1 Receptor in Motoneuron Disease (Q48258033) (← links)
- Altered postnatal maturation of electrical properties in spinal motoneurons in a mouse model of amyotrophic lateral sclerosis. (Q51871496) (← links)
- Morphological differences between wild-type and transgenic superoxide dismutase 1 lumbar motoneurons in postnatal mice. (Q51949007) (← links)
- Hypoexcitability precedes denervation in the large fast-contracting motor units in two unrelated mouse models of ALS. (Q55215170) (← links)
- Synaptic Failure: Focus in an Integrative View of ALS. (Q55233896) (← links)
- Neuromuscular Plasticity in a Mouse Neurotoxic Model of Spinal Motoneuronal Loss (Q64119448) (← links)
- Motoneuron afterhyperpolarisation duration in amyotrophic lateral sclerosis (Q83842225) (← links)