Search Results - "Killoy, Kelby M"
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Evaluation of the NAD+ biosynthetic pathway in ALS patients and effect of modulating NAD+ levels in hSOD1-linked ALS mouse models
Published in Experimental neurology (01-05-2020)“…Amyotrophic lateral sclerosis (ALS) is characterized by progressive degeneration of motor neurons. Astrocytes from diverse ALS models induce motor neuron death…”
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FABP7 upregulation induces a neurotoxic phenotype in astrocytes
Published in Glia (01-12-2020)“…Fatty acid binding proteins (FABPs) are key regulators of lipid metabolism, energy homeostasis, and inflammation. They participate in fatty acid metabolism by…”
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3
Role and Therapeutic Potential of Astrocytes in Amyotrophic Lateral Sclerosis
Published in Current pharmaceutical design (01-01-2017)“…Amyotrophic lateral sclerosis (ALS) is characterized by the progressive degeneration of motor neurons in the spinal cord, brain stem, and motor cortex. The…”
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4
Effects of RAGE inhibition on the progression of the disease in hSOD1G93A ALS mice
Published in Pharmacology research & perspectives (01-08-2020)“…Astrocytes play a key role in the progression of amyotrophic lateral sclerosis (ALS) by actively inducing the degeneration of motor neurons. Motor neurons…”
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5
Nicotinamide Adenine Dinucleotide Metabolism and Neurodegeneration
Published in Antioxidants & redox signaling (20-06-2018)“…Nicotinamide adenine dinucleotide (NAD ) participates in redox reactions and NAD -dependent signaling processes, which involve the cleavage of NAD coupled to…”
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Enhanced SIRT6 activity abrogates the neurotoxic phenotype of astrocytes expressing ALS‐linked mutant SOD1
Published in The FASEB journal (01-06-2019)“…ABSTRACT Sirtuins (SIRTs) are NAD+‐dependent deacylases that play a key role in transcription, DNA repair, metabolism, and oxidative stress resistance…”
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NR1D1 downregulation in astrocytes induces a phenotype that is detrimental to cocultured motor neurons
Published in The FASEB journal (01-04-2022)“…Nuclear receptor subfamily 1 group D member 1 (NR1D1, also known as Rev‐erbα) is a nuclear transcription factor that is part of the molecular clock encoding…”
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Altered expression of clock and clock‐controlled genes in a hSOD1‐linked amyotrophic lateral sclerosis mouse model
Published in The FASEB journal (01-02-2021)“…Most physiological processes in mammals are subjected to daily oscillations that are governed by a circadian system. The circadian rhythm orchestrates…”
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Decreased glutathione levels cause overt motor neuron degeneration in hSOD1WT over-expressing mice
Published in Experimental neurology (01-04-2018)“…Mutations in Cu/Zn-superoxide dismutase (SOD1) cause familial forms of amyotrophic lateral sclerosis (ALS), a fatal disorder characterized by the progressive…”
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10
Nitration and Glycation Turn Mature NGF into a Toxic Factor for Motor Neurons: A Role for p75 NTR and RAGE Signaling in ALS
Published in Antioxidants & redox signaling (20-06-2018)“…Glycating stress can occur together with oxidative stress during neurodegeneration and contribute to the pathogenic mechanism. Nerve growth factor (NGF)…”
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11
Effects of RAGE inhibition on the progression of the disease in hSOD1 G93A ALS mice
Published in Pharmacology research & perspectives (01-08-2020)“…Astrocytes play a key role in the progression of amyotrophic lateral sclerosis (ALS) by actively inducing the degeneration of motor neurons. Motor neurons…”
Get full text
Journal Article -
12
FABP7 up-regulation induces a neurotoxic phenotype in astrocytes
Published in Glia (03-07-2020)“…Fatty acid binding proteins (FABPs) are key regulators of lipid metabolism, energy homeostasis and inflammation. They participate in fatty acid metabolism by…”
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Journal Article -
13
Decreased glutathione levels cause overt motor neuron degeneration in hSOD1WT overexpressing mice
Published in Experimental neurology (04-01-2018)“…Mutations in Cu/Zn-superoxide dismutase (SOD1) cause familial forms of amyotrophic lateral sclerosis (ALS), a fatal disorder characterized by the progressive…”
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Journal Article -
14
Decreased glutathione levels cause overt motor neuron degeneration in hSOD1 WT over-expressing mice
Published in Experimental neurology (01-04-2018)“…Mutations in Cu/Zn-superoxide dismutase (SOD1) cause familial forms of amyotrophic lateral sclerosis (ALS), a fatal disorder characterized by the progressive…”
Get full text
Journal Article