نتایج جستجو برای: dyt1 dystonia

تعداد نتایج: 6648  

Journal: :Annals of neurology 2001
E M Valente A R Bentivoglio E Cassetta P H Dixon M B Davis A Ferraris T Ialongo M Frontali N W Wood A Albanese

Primary torsion dystonia (PTD) is a clinically and genetically heterogeneous group of movement disorders, usually inherited in an autosomal dominant fashion with reduced penetrance. The DYT1 gene on chromosome 9q34 is responsible for most cases of early limb-onset PTD. Two other PTD loci have been mapped to date. The DYT6 locus on chromosome 8 is associated with a mixed phenotype, whereas the D...

2014
Brian A Sosa F Esra Demircioglu James Z Chen Jessica Ingram Hidde L Ploegh Thomas U Schwartz

Lamina-associated polypeptide 1 (LAP1) resides at the nuclear envelope and interacts with Torsins, poorly understood endoplasmic reticulum (ER)-localized AAA+ ATPases, through a conserved, perinuclear domain. We determined the crystal structure of the perinuclear domain of human LAP1. LAP1 possesses an atypical AAA+ fold. While LAP1 lacks canonical nucleotide binding motifs, its strictly conser...

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