scholarly article | Q13442814 |
P50 | author | Vivek Malhotra | Q39199774 |
David Cruz-García | Q59688805 | ||
Gabriel Mora | Q81113543 | ||
P2093 | author name string | Nathalie Brouwers | |
Juan M Duran | |||
Amy J Curwin | |||
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Superoxide dismutase multigene family: a comparison of the CuZn-SOD (SOD1), Mn-SOD (SOD2), and EC-SOD (SOD3) gene structures, evolution, and expression | Q28215218 | ||
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Evidence of calcium- and SNARE-dependent release of CuZn superoxide dismutase from rat pituitary GH3 cells and synaptosomes in response to depolarization | Q28566100 | ||
Impaired extracellular secretion of mutant superoxide dismutase 1 associates with neurotoxicity in familial amyotrophic lateral sclerosis | Q28592161 | ||
Autophagy-based unconventional secretory pathway for extracellular delivery of IL-1β | Q29030555 | ||
Presenting your structures: the CCP4mg molecular-graphics software | Q29547443 | ||
Rapid and reliable protein extraction from yeast | Q29617781 | ||
Activities at the Universal Protein Resource (UniProt) | Q29617787 | ||
Protein degradation and protection against misfolded or damaged proteins | Q29618400 | ||
Unraveling the mechanisms involved in motor neuron degeneration in ALS | Q29619073 | ||
Intermolecular transmission of superoxide dismutase 1 misfolding in living cells | Q30155471 | ||
Unconventional secretion of Pichia pastoris Acb1 is dependent on GRASP protein, peroxisomal functions, and autophagosome formation. | Q33689637 | ||
A novel secretory pathway for interleukin-1 beta, a protein lacking a signal sequence | Q33919640 | ||
Signals for COPII-dependent export from the ER: what's the ticket out? | Q35147357 | ||
Biogenesis of a novel compartment for autophagosome-mediated unconventional protein secretion | Q35621009 | ||
Translocation of interleukin-1β into a vesicle intermediate in autophagy-mediated secretion | Q36506015 | ||
Insulin-degrading enzyme secretion from astrocytes is mediated by an autophagy-based unconventional secretory pathway in Alzheimer disease. | Q36862693 | ||
Mutant copper-zinc superoxide dismutase (SOD1) induces protein secretion pathway alterations and exosome release in astrocytes: implications for disease spreading and motor neuron pathology in amyotrophic lateral sclerosis | Q36890607 | ||
ESCRT-III drives the final stages of CUPS maturation for unconventional protein secretion. | Q36905226 | ||
Extracellular mutant SOD1 induces microglial-mediated motoneuron injury | Q37442209 | ||
Intercellular propagated misfolding of wild-type Cu/Zn superoxide dismutase occurs via exosome-dependent and -independent mechanisms | Q37628107 | ||
Diversity in unconventional protein secretion | Q38078812 | ||
The changing scene of amyotrophic lateral sclerosis | Q38086771 | ||
Unconventional protein secretion: an evolving mechanism | Q38105910 | ||
New links between SOD1 and metabolic dysfunction from a yeast model of amyotrophic lateral sclerosis | Q39363902 | ||
Evidence for secretion of Cu,Zn superoxide dismutase via exosomes from a cell model of amyotrophic lateral sclerosis | Q40066703 | ||
CuZn-superoxide dismutase in human thymus: immunocytochemical localisation and secretion in thymus-derived epithelial and fibroblast cell lines | Q40709559 | ||
Remodeling of secretory compartments creates CUPS during nutrient starvation | Q41883607 | ||
The Golgi-associated protein GRASP is required for unconventional protein secretion during development. | Q46828620 | ||
Secretion and increase of intracellular CuZn superoxide dismutase content in human neuroblastoma SK-N-BE cells subjected to oxidative stress | Q48478877 | ||
Variation in the biochemical/biophysical properties of mutant superoxide dismutase 1 enzymes and the rate of disease progression in familial amyotrophic lateral sclerosis kindreds. | Q54089001 | ||
Evidence for secretion of cytosolic CuZn superoxide dismutase by Hep G2 cells and human fibroblasts | Q71169525 | ||
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 9 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | amyotrophic lateral sclerosis | Q206901 |
P304 | page(s) | 2691-2700 | |
P577 | publication date | 2017-08-09 | |
P1433 | published in | Journal of Cell Biology | Q1524550 |
P1476 | title | A diacidic motif determines unconventional secretion of wild-type and ALS-linked mutant SOD1. | |
P478 | volume | 216 |
Q64273759 | A Potential Lock-Type Mechanism for Unconventional Secretion in Fungi |
Q98564428 | Does wild-type Cu/Zn-superoxide dismutase have pathogenic roles in amyotrophic lateral sclerosis? |
Q58779209 | Evaluation of Unconventional Protein Secretion by Saccharomyces cerevisiae and other Fungi |
Q64923502 | Exploring the context of diacidic motif DE as a signal for unconventional protein secretion in eukaryotic proteins. |
Q55515366 | Unconventional Secretion and Intercellular Transfer of Mutant Huntingtin. |
Q46207582 | Unconventional secretion of FABP4 by endosomes and secretory lysosomes. |
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