scholarly article | Q13442814 |
P819 | ADS bibcode | 2015PLoSO..1025205D |
P356 | DOI | 10.1371/JOURNAL.PONE.0125205 |
P932 | PMC publication ID | 4407904 |
P698 | PubMed publication ID | 25905915 |
P5875 | ResearchGate publication ID | 275358726 |
P2093 | author name string | Janice E A Braun | |
Milen Velinov | |||
Eva Ahrendt | |||
Andrew P Braun | |||
Julien Donnelier | |||
Natalia Dolzhanskaya | |||
Samuel T Braun | |||
P2860 | cites work | Exome-sequencing confirms DNAJC5 mutations as cause of adult neuronal ceroid-lipofuscinosis | Q21090977 |
J protein mutations and resulting proteostasis collapse | Q21129474 | ||
Quercetin targets cysteine string protein (CSPalpha) and impairs synaptic transmission | Q21562195 | ||
Mutations in DNAJC5, encoding cysteine-string protein alpha, cause autosomal-dominant adult-onset neuronal ceroid lipofuscinosis | Q24319132 | ||
CSPα knockout causes neurodegeneration by impairing SNAP-25 function | Q26269887 | ||
Rab-alphaGDI activity is regulated by a Hsp90 chaperone complex | Q28578339 | ||
Oligomerization characteristics of cysteine string protein | Q28580744 | ||
Alpha-synuclein cooperates with CSPalpha in preventing neurodegeneration | Q28587785 | ||
The HSP70 chaperone machinery: J proteins as drivers of functional specificity | Q29616140 | ||
Caenorhabditis elegans dnj-14, the orthologue of the DNAJC5 gene mutated in adult onset neuronal ceroid lipofuscinosis, provides a new platform for neuroprotective drug screening and identifies a SIR-2.1-independent action of resveratrol. | Q30594778 | ||
The regulation of BK channel activity by pre- and post-translational modifications | Q34077885 | ||
Phosphorylation of cysteine string protein by protein kinase A. Implications for the modulation of exocytosis | Q34095436 | ||
Mutations in the gene DNAJC5 cause autosomal dominant Kufs disease in a proportion of cases: study of the Parry family and 8 other families | Q34123856 | ||
A charged prominence in the linker domain of the cysteine-string protein Cspα mediates its regulated interaction with the calcium sensor synaptotagmin 9 during exocytosis | Q34138424 | ||
Oligomerization of Cysteine String Protein alpha mutants causing adult neuronal ceroid lipofuscinosis | Q34302115 | ||
The synaptic vesicle protein CSP alpha prevents presynaptic degeneration. | Q34314406 | ||
Extensive lipidation of a Torpedo cysteine string protein. | Q34330430 | ||
Characterization of the G alpha(s) regulator cysteine string protein | Q34428333 | ||
Identification of CSPα clients reveals a role in dynamin 1 regulation. | Q35893528 | ||
Motorneurons require cysteine string protein-α to maintain the readily releasable vesicular pool and synaptic vesicle recycling. | Q50499095 | ||
Overexpression of cysteine-string proteins in Drosophila reveals interactions with syntaxin. | Q52574622 | ||
CSPα promotes SNARE-complex assembly by chaperoning SNAP-25 during synaptic activity. | Q54397791 | ||
Case 8-2011 | Q60800665 | ||
Interaction of cysteine string proteins with the alpha1A subunit of the P/Q-type calcium channel | Q74567363 | ||
Two distinct domains in hsc70 are essential for the interaction with the synaptic vesicle cysteine string protein | Q78074534 | ||
Palmitoylation-induced aggregation of cysteine-string protein mutants that cause neuronal ceroid lipofuscinosis | Q36347832 | ||
Biological roles of neural J proteins | Q37148343 | ||
DNAJ proteins and protein aggregation diseases. | Q38075883 | ||
CSPα-chaperoning presynaptic proteins | Q38210203 | ||
Cysteine string protein functions directly in regulated exocytosis | Q38612674 | ||
Cysteine string protein limits expression of the large conductance, calcium-activated K⁺ (BK) channel | Q39029381 | ||
Crosstalk between huntingtin and syntaxin 1A regulates N-type calcium channels. | Q40373593 | ||
Cysteine string protein regulates G protein modulation of N-type calcium channels | Q40841138 | ||
Phosphorylation-dependent interaction of the synaptic vesicle proteins cysteine string protein and synaptotagmin I. | Q42123208 | ||
Activation of the ATPase activity of heat-shock proteins Hsc70/Hsp70 by cysteine-string protein | Q42216617 | ||
The large conductance, calcium-activated K+ (BK) channel is regulated by cysteine string protein | Q42555501 | ||
Cysteine string protein-alpha prevents activity-dependent degeneration in GABAergic synapses. | Q43053624 | ||
Molecular determinants of cysteine string protein modulation of N-type calcium channels | Q44463991 | ||
The cysteine string secretory vesicle protein activates Hsc70 ATPase | Q46053336 | ||
Paralysis and early death in cysteine string protein mutants of Drosophila | Q46085105 | ||
Cysteine string protein, a DnaJ family member, is present on diverse secretory vesicles | Q48069405 | ||
Proteasome inhibition alleviates SNARE-dependent neurodegeneration | Q48407910 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | neuronal ceroid lipofuscinosis | Q4358039 |
P304 | page(s) | e0125205 | |
P577 | publication date | 2015-04-23 | |
P1433 | published in | PLOS One | Q564954 |
P1476 | title | Increased Expression of the Large Conductance, Calcium-Activated K+ (BK) Channel in Adult-Onset Neuronal Ceroid Lipofuscinosis | |
P478 | volume | 10 |
Q30356551 | BK Channels in the Central Nervous System. |
Q36321613 | Clinically early-stage CSPα mutation carrier exhibits remarkable terminal stage neuronal pathology with minimal evidence of synaptic loss |
Q51246997 | Early Alterations of Hippocampal Neuronal Firing Induced by Abeta42. |
Q42269174 | Neurons Export Extracellular Vesicles Enriched in Cysteine String Protein and Misfolded Protein Cargo |
Q42490346 | Presynaptic BK channels control transmitter release: physiological relevance and potential therapeutic implications. |
Q38663518 | Primary fibroblasts from CSPα mutation carriers recapitulate hallmarks of the adult onset neuronal ceroid lipofuscinosis |
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