scholarly article | Q13442814 |
P356 | DOI | 10.1371/JOURNAL.PGEN.1006531 |
P8608 | Fatcat ID | release_e3ezilygpzctbeotdx3e6ruio4 |
P932 | PMC publication ID | 5201269 |
P698 | PubMed publication ID | 28036392 |
P50 | author | Anat Peres Ben-Zvi | Q73579663 |
Esti Yeger-Lotem | Q39383798 | ||
P2093 | author name string | Rivka Ofir | |
Netta Shemesh | |||
Yael Bar-Lavan | |||
Shiran Dror | |||
P2860 | cites work | A quantitative chaperone interaction network reveals the architecture of cellular protein homeostasis pathways | Q24300926 |
Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy | Q24306218 | ||
A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathy | Q24311671 | ||
Collapse of proteostasis represents an early molecular event in Caenorhabditis elegans aging | Q24643933 | ||
The J-domain protein Rme-8 interacts with Hsc70 to control clathrin-dependent endocytosis in Drosophila | Q24677964 | ||
JASPAR 2016: a major expansion and update of the open-access database of transcription factor binding profiles | Q24700982 | ||
Destabilizing protein polymorphisms in the genetic background direct phenotypic expression of mutant SOD1 toxicity | Q27312600 | ||
Modulation of the maladaptive stress response to manage diseases of protein folding | Q27313626 | ||
Identification of a tissue-selective heat shock response regulatory network | Q27322992 | ||
Genome-wide identification of binding sites defines distinct functions for Caenorhabditis elegans PHA-4/FOXA in development and environmental response | Q27348311 | ||
A widespread distribution of genomic CeMyoD binding sites revealed and cross validated by ChIP-Chip and ChIP-Seq techniques | Q27438090 | ||
The Myosin Chaperone UNC-45 Is Organized in Tandem Modules to Support Myofilament Formation in C. elegans | Q27675937 | ||
Systems analyses reveal two chaperone networks with distinct functions in eukaryotic cells | Q27932599 | ||
The ephrin VAB-2/EFN-1 functions in neuronal signaling to regulate epidermal morphogenesis in C. elegans | Q28141789 | ||
A chaperome subnetwork safeguards proteostasis in aging and neurodegenerative disease | Q28252463 | ||
The embryonic cell lineage of the nematode Caenorhabditis elegans | Q28271877 | ||
Integrative analysis of the Caenorhabditis elegans genome by the modENCODE project | Q28301622 | ||
The HSP70 chaperone machinery: J proteins as drivers of functional specificity | Q29616140 | ||
HSP90 at the hub of protein homeostasis: emerging mechanistic insights | Q29616824 | ||
Neuronal circuitry regulates the response of Caenorhabditis elegans to misfolded proteins | Q30503728 | ||
Developmental milestones punctuate gene expression in the Caenorhabditis embryo. | Q51786897 | ||
The myogenic potency of HLH-1 reveals wide-spread developmental plasticity in early C. elegans embryos. | Q52054945 | ||
Ultra-structural time-course study in the C. elegans model for Duchenne muscular dystrophy highlights a crucial role for sarcomere-anchoring structures and sarcolemma integrity in the earliest steps of the muscle degeneration process. | Q52663455 | ||
Stress chaperone mortalin contributes to epithelial-mesenchymal transition and cancer metastasis. | Q53205003 | ||
The p.G154S mutation of the alpha-B crystallin gene (CRYAB) causes late-onset distal myopathy | Q57390077 | ||
Less is more: how protein degradation regulates muscle development | Q58414130 | ||
Polyglutamine protein aggregates are dynamic | Q78315034 | ||
Regulation of organismal proteostasis by transcellular chaperone signaling | Q37638939 | ||
Caenorhabditis elegans muscle: a genetic and molecular model for protein interactions in the heart | Q37945585 | ||
The small heat shock proteins family: the long forgotten chaperones | Q37997166 | ||
HSPBs: small proteins with big implications in human disease | Q38020613 | ||
The chaperone Hsp90: changing partners for demanding clients | Q38090850 | ||
Motoneuronal and muscle-selective removal of ALS-related misfolded proteins. | Q38164394 | ||
Body-wall muscle formation in Caenorhabditis elegans embryos that lack the MyoD homolog hlh-1. | Q38329468 | ||
Heat shock proteins as potential targets for protective strategies in neurodegeneration | Q38815318 | ||
Chaperone families and interactions in metazoa. | Q38981682 | ||
SKN-1 links C. elegans mesendodermal specification to a conserved oxidative stress response | Q39896060 | ||
Actin mutations in hypertrophic and dilated cardiomyopathy cause inefficient protein folding and perturbed filament formation | Q40437046 | ||
Role of the myosin assembly protein UNC-45 as a molecular chaperone for myosin | Q40754906 | ||
FOXO4 is necessary for neural differentiation of human embryonic stem cells. | Q41409424 | ||
The consequences of expressing hsp70 in Drosophila cells at normal temperatures | Q41609447 | ||
Regional deficiencies in chaperone-mediated autophagy underlie α-synuclein aggregation and neurodegeneration | Q42078692 | ||
HSP43, a small heat-shock protein localized to specific cells of the vulva and spermatheca in the nematode Caenorhabditis elegans | Q42158356 | ||
Genetic suppression of phenotypes arising from mutations in dystrophin-related genes in Caenorhabditis elegans. | Q42634221 | ||
Autophagy is essential for cardiac morphogenesis during vertebrate development | Q42729290 | ||
PHA-4/Foxa mediates diet-restriction-induced longevity of C. elegans | Q44731575 | ||
A neuronal GPCR is critical for the induction of the heat shock response in the nematode C. elegans. | Q46962604 | ||
Regulation of the myosin-directed chaperone UNC-45 by a novel E3/E4-multiubiquitylation complex in C. elegans | Q47068938 | ||
The Caenorhabditis elegans MYOD homologue HLH-1 is essential for proper muscle function and complete morphogenesis | Q47069135 | ||
Differential localization of two myosins within nematode thick filaments | Q47069424 | ||
HSP25, a small heat shock protein associated with dense bodies and M-lines of body wall muscle in Caenorhabditis elegans | Q47069548 | ||
MyoD and the specification of muscle and non-muscle fates during postembryonic development of the C. elegans mesoderm. | Q47909297 | ||
Germline stem cell arrest inhibits the collapse of somatic proteostasis early in Caenorhabditis elegans adulthood. | Q48623757 | ||
Loss of the proteostasis factor AIRAPL causes myeloid transformation by deregulating IGF-1 signaling. | Q50236752 | ||
CLICK and EXPANDER: a system for clustering and visualizing gene expression data | Q30881196 | ||
BioVenn - a web application for the comparison and visualization of biological lists using area-proportional Venn diagrams | Q33377261 | ||
Hierarchical functional specificity of cytosolic heat shock protein 70 (Hsp70) nucleotide exchange factors in yeast | Q33676604 | ||
Determining the sub-cellular localization of proteins within Caenorhabditis elegans body wall muscle | Q33911164 | ||
RME-8, a conserved J-domain protein, is required for endocytosis in Caenorhabditis elegans. | Q33937385 | ||
Using Caenorhabditis elegans as a model system to study protein homeostasis in a multicellular organism | Q33950581 | ||
Molecular chaperones are nanomachines that catalytically unfold misfolded and alternatively folded proteins | Q34038270 | ||
Downregulation of the Hsp90 system causes defects in muscle cells of Caenorhabditis elegans | Q34043288 | ||
The balanced regulation of Hsc70 by DNJ-13 and UNC-23 is required for muscle functionality. | Q34139157 | ||
Chromosomal clustering of muscle-expressed genes in Caenorhabditis elegans | Q34148035 | ||
The heat shock response: systems biology of proteotoxic stress in aging and disease | Q34257283 | ||
Caenorhabditis elegans chaperonin CCT/TRiC is required for actin and tubulin biogenesis and microvillus formation in intestinal epithelial cells | Q34337954 | ||
Molecular chaperone functions in protein folding and proteostasis | Q34349321 | ||
The biological and chemical basis for tissue-selective amyloid disease | Q34410187 | ||
Protein aggregation can inhibit clathrin-mediated endocytosis by chaperone competition | Q34413909 | ||
The biology of proteostasis in aging and disease | Q34467650 | ||
Widespread Proteome Remodeling and Aggregation in Aging C. elegans | Q34475749 | ||
Progressive disruption of cellular protein folding in models of polyglutamine diseases. | Q34493281 | ||
FIMO: scanning for occurrences of a given motif | Q34729603 | ||
The Atg6/Vps30/Beclin 1 ortholog BEC-1 mediates endocytic retrograde transport in addition to autophagy in C. elegans | Q35024395 | ||
Spatiotemporal transcriptomics reveals the evolutionary history of the endoderm germ layer | Q35178248 | ||
Comparative analysis of human tissue interactomes reveals factors leading to tissue-specific manifestation of hereditary diseases | Q35186314 | ||
Defining the transcriptional redundancy of early bodywall muscle development in C. elegans: evidence for a unified theory of animal muscle development | Q35221163 | ||
Challenging muscle homeostasis uncovers novel chaperone interactions in Caenorhabditis elegans | Q35596765 | ||
Protein homeostasis in models of aging and age-related conformational disease | Q36109387 | ||
The UNC-45 chaperone mediates sarcomere assembly through myosin degradation in Caenorhabditis elegans | Q36118132 | ||
Assembly of body wall muscle and muscle cell attachment structures in Caenorhabditis elegans | Q36233664 | ||
Transcription factor redundancy and tissue-specific regulation: evidence from functional and physical network connectivity | Q36285399 | ||
The embryonic muscle transcriptome of Caenorhabditis elegans | Q36643272 | ||
The myosin-binding UCS domain but not the Hsp90-binding TPR domain of the UNC-45 chaperone is essential for function in Caenorhabditis elegans | Q36995989 | ||
Protein quality control gets muscle into shape | Q37169974 | ||
Accelerated neurodegeneration through chaperone-mediated oligomerization of tau. | Q37200867 | ||
Build it up-Tear it down: protein quality control in the cardiac sarcomere | Q37313697 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 12 | |
P921 | main subject | Caenorhabditis elegans | Q91703 |
P304 | page(s) | e1006531 | |
P577 | publication date | 2016-12-30 | |
P1433 | published in | PLOS Genetics | Q1893441 |
P1476 | title | A Differentiation Transcription Factor Establishes Muscle-Specific Proteostasis in Caenorhabditis elegans | |
P478 | volume | 12 |
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Q64056478 | HSP-4/BiP expression in secretory cells is regulated by a developmental program and not by the unfolded protein response |
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