Role of kinesin-1 in the pathogenesis of SPG10, a rare form of hereditary spastic paraplegia.

Role of kinesin-1 in the pathogenesis of SPG10, a rare form of hereditary spastic paraplegia.

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http://www.wikidata.org/entity/Q38025542
Kinesin-5 allosteric inhibitors uncouple the dynamics of nucleotide, microtubule, and neck-linker binding sites.Whole exome sequencing and the clinician: we need clinical skills and functional validation in variant filtering.Forces and Disease: Electrostatic force differences caused by mutations in kinesin motor domains can distinguish between disease-causing and non-disease-causing mutations.KIF5A mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunction.Unique function of Kinesin Kif5A in localization of mitochondria in axonsOverexpression of Kinesin Superfamily Motor Proteins in Alzheimer's Disease.Axonal motor protein KIF5A and associated cargo deficits in multiple sclerosis lesional and normal-appearing white matter.Progressive ataxia of Charolais cattle highlights a role of KIF1C in sustainable myelination
P2860

Role of kinesin-1 in the pathogenesis of SPG10, a rare form of hereditary spastic paraplegia.

Item
http://www.wikidata.org/entity/Q38025542
description
article científic
@ca
article scientifique
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articol științific
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articolo scientifico
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artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
@id
artikull shkencor
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artículo científico
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name
Role of kinesin-1 in the patho ...... hereditary spastic paraplegia.
@en
type
label
Role of kinesin-1 in the patho ...... hereditary spastic paraplegia.
@en
prefLabel
Role of kinesin-1 in the patho ...... hereditary spastic paraplegia.
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P433
P478
P577
P698
P356
P1433
P1476
Role of kinesin-1 in the patho ...... hereditary spastic paraplegia.
@en
P2093
P2860
P304
P31
P356
P433
P478
P577
P698