Pages that link to "Q24299145"
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The following pages link to Dystonia-causing mutant torsinA inhibits cell adhesion and neurite extension through interference with cytoskeletal dynamics (Q24299145):
Displaying 50 items.
- Vimentin (Q411624) (← links)
- Torsin 1A interacting protein 1 (Q21117780) (← links)
- Torsin family 1 member A (Q21173891) (← links)
- Relative tissue expression of homologous torsinB correlates with the neuronal specific importance of DYT1 dystonia-associated torsinA (Q22001542) (← links)
- CSN complex controls the stability of selected synaptic proteins via a torsinA-dependent process (Q24307876) (← links)
- LULL1 retargets TorsinA to the nuclear envelope revealing an activity that is impaired by the DYT1 dystonia mutation (Q24311570) (← links)
- TorsinA binds the KASH domain of nesprins and participates in linkage between nuclear envelope and cytoskeleton (Q24317502) (← links)
- Printor, a novel torsinA-interacting protein implicated in dystonia pathogenesis (Q24338612) (← links)
- Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia (Q24605412) (← links)
- Cerebellothalamocortical connectivity regulates penetrance in dystonia (Q24652781) (← links)
- Torsins: not your typical AAA ATPases (Q28087663) (← links)
- Dystonia-associated mutations cause premature degradation of torsinA protein and cell-type-specific mislocalization to the nuclear envelope (Q28386148) (← links)
- Abnormal structure-function relationships in hereditary dystonia (Q33402008) (← links)
- The BiP molecular chaperone plays multiple roles during the biogenesis of torsinA, an AAA ATPase associated with the neurological disease early-onset torsion dystonia (Q33556224) (← links)
- Cell-autonomous alteration of dopaminergic transmission by wild type and mutant (DeltaE) TorsinA in transgenic mice. (Q33723034) (← links)
- Mutant torsinA interacts with tyrosine hydroxylase in cultured cells. (Q33750936) (← links)
- Lamin-binding Proteins (Q33752204) (← links)
- Altered dendritic morphology of Purkinje cells in Dyt1 ΔGAG knock-in and purkinje cell-specific Dyt1 conditional knockout mice. (Q33867544) (← links)
- Biochemical and cellular analysis of human variants of the DYT1 dystonia protein, TorsinA/TOR1A (Q34052884) (← links)
- The early-onset torsion dystonia-associated protein, torsinA, is a homeostatic regulator of endoplasmic reticulum stress response (Q34083670) (← links)
- Current Gaps in the Understanding of the Subcellular Distribution of Exogenous and Endogenous Protein TorsinA. (Q34245374) (← links)
- A unique redox-sensing sensor II motif in TorsinA plays a critical role in nucleotide and partner binding (Q34333556) (← links)
- The zebrafish homologue of the human DYT1 dystonia gene is widely expressed in CNS neurons but non-essential for early motor system development (Q34428283) (← links)
- 4-Phenylbutyrate attenuates the ER stress response and cyclic AMP accumulation in DYT1 dystonia cell models (Q34472800) (← links)
- Evaluation of TorsinA as a target for Parkinson disease therapy in mouse models (Q34490978) (← links)
- Mutant torsinA interferes with protein processing through the secretory pathway in DYT1 dystonia cells (Q34578567) (← links)
- Untethering the nuclear envelope and cytoskeleton: biologically distinct dystonias arising from a common cellular dysfunction (Q34638417) (← links)
- Increased cerebellar activation during sequence learning in DYT1 carriers: an equiperformance study (Q34703465) (← links)
- Genetic and clinical features of primary torsion dystonia (Q34777884) (← links)
- Torsin A Localization in the Mouse Cerebellar Synaptic Circuitry (Q34808401) (← links)
- Abnormal striatal and thalamic dopamine neurotransmission: Genotype-related features of dystonia (Q34986983) (← links)
- The pathogenic human Torsin A in Drosophila activates the unfolded protein response and increases susceptibility to oxidative stress (Q35555819) (← links)
- Motor deficits and hyperactivity in Dyt1 knockdown mice. (Q35629540) (← links)
- Functional imaging in hereditary dystonia (Q36276626) (← links)
- TorsinA participates in endoplasmic reticulum-associated degradation (Q36487761) (← links)
- Experimental therapeutics for dystonia (Q36569704) (← links)
- Lack of adrenomedullin in the mouse brain results in behavioral changes, anxiety, and lower survival under stress conditions. (Q36858688) (← links)
- Identifying the genetic components underlying the pathophysiology of movement disorders (Q36925207) (← links)
- The genetics of dystonias (Q36934972) (← links)
- Glial elements contribute to stress-induced torsinA expression in the CNS and peripheral nervous system (Q37001321) (← links)
- Genetics of dystonia: an overview (Q37082079) (← links)
- Subtle microstructural changes of the cerebellum in a knock-in mouse model of DYT1 dystonia (Q37424519) (← links)
- Dystonia as a network disorder: what is the role of the cerebellum? (Q37592345) (← links)
- Primary dystonia: molecules and mechanisms. (Q37614200) (← links)
- Early-onset primary dystonia (Q37865669) (← links)
- Milestones in dystonia (Q37882600) (← links)
- The genetics of dystonia: new twists in an old tale (Q38115272) (← links)
- Emerging common molecular pathways for primary dystonia. (Q38124786) (← links)
- TorsinA controls TAN line assembly and the retrograde flow of dorsal perinuclear actin cables during rearward nuclear movement. (Q38714582) (← links)
- Membrane defects and genetic redundancy: Are we at a turning point for DYT1 dystonia? (Q39026993) (← links)