Serena Carra
Carra, Serena
VIAF ID: 3026152502925110800008 (Personal)
Permalink: http://viaf.org/viaf/3026152502925110800008
Preferred Forms
- 100 1 _ ‡a Carra, Serena
- 100 0 _ ‡a Serena Carra
4xx's: Alternate Name Forms (3)
5xx's: Related Names (1)
Works
Title | Sources |
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Aberrant Compartment Formation by HSPB2 Mislocalizes Lamin A and Compromises Nuclear Integrity and Function. | |
An aberrant phase transition of stress granules triggered by misfolded protein and prevented by chaperone function | |
Abnormal interaction of motor neuropathy-associated mutant HspB8 (Hsp22) forms with the RNA helicase Ddx20 (gemin3). | |
Alteration of protein folding and degradation in motor neuron diseases: Implications and protective functions of small heat shock proteins. | |
Autophagy researchers | |
BAG3 and BAG6 differentially affect the dynamics of stress granules by targeting distinct subsets of defective polypeptides released from ribosomes | |
BAG3 directly interacts with mutated alphaB-crystallin to suppress its aggregation and toxicity | |
BAG3 induces the sequestration of proteasomal clients into cytoplasmic puncta: implications for a proteasome-to-autophagy switch. | |
Barcoding heat shock proteins to human diseases: looking beyond the heat shock response | |
The chaperone HSPB8 reduces the accumulation of truncated TDP-43 species in cells and protects against TDP-43-mediated toxicity. | |
Chronic treatment with desipramine and fluoxetine modulate BDNF, CaMKKalpha and CaMKKbeta mRNA levels in the hippocampus of transgenic mice expressing antisense RNA against the glucocorticoid receptor | |
Clearance of the mutant androgen receptor in motoneuronal models of spinal and bulbar muscular atrophy. | |
Cloning of mouse Ca2+/calmodulin-dependent protein kinase kinase beta (CaMKKbeta) and characterization of CaMKKbeta and CaMKKalpha distribution in the adult mouse brain | |
Defective ribosomal products challenge nuclear function by impairing nuclear condensate dynamics and immobilizing ubiquitin | |
Different anti-aggregation and pro-degradative functions of the members of the mammalian sHSP family in neurological disorders. | |
Differential autophagy power in the spinal cord and muscle of transgenic ALS mice. | |
Emerging roles of molecular chaperones and co-chaperones in selective autophagy: focus on BAG proteins. | |
The growing world of small heat shock proteins: from structure to functions | |
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) | |
Hsp90-mediated regulation of DYRK3 couples stress granule disassembly and growth via mTORC1 signaling | |
HspB8, a small heat shock protein mutated in human neuromuscular disorders, has in vivo chaperone activity in cultured cells. | |
The HSPB8-BAG3 chaperone complex is upregulated in astrocytes in the human brain affected by protein aggregation diseases. | |
HspB8 chaperone activity toward poly(Q)-containing proteins depends on its association with Bag3, a stimulator of macroautophagy. | |
HspB8 participates in protein quality control by a non-chaperone-like mechanism that requires eIF2{alpha} phosphorylation | |
Identification of the Drosophila ortholog of HSPB8: implication of HSPB8 loss of function in protein folding diseases. | |
Inhibition of autophagy, lysosome and VCP function impairs stress granule assembly | |
An interaction study in mammalian cells demonstrates weak binding of HSPB2 to BAG3, which is regulated by HSPB3 and abrogated by HSPB8. | |
The landscape of molecular chaperones across human tissues reveals a layered architecture of core and variable chaperones | |
Modulation of glutamate receptors in response to the novel antipsychotic olanzapine in rats | |
Nucleoli and Promyelocytic Leukemia Protein (PML) bodies are phase separated nuclear protein quality control compartments for misfolded proteins | |
The regulation of the autophagic network and its implications for human disease | |
The Role of the Protein Quality Control System in SBMA. | |
en scientific article | |
The small heat shock protein B8 (HSPB8) efficiently removes aggregating species of dipeptides produced in C9ORF72-related neurodegenerative diseases. | |
The small heat shock protein B8 (HSPB8) modulates proliferation and migration of breast cancer cells | |
The small heat shock protein B8 (HspB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS). | |
Small heat shock proteins: multifaceted proteins with important implications for life | |
The stress-inducible HspB8-Bag3 complex induces the eIF2alpha kinase pathway: implications for protein quality control and viral factory degradation? | |
Structural and functional diversities between members of the human HSPB, HSPH, HSPA, and DNAJ chaperone families. | |
A Surveillance Function of the HSPB8-BAG3-HSP70 Chaperone Complex Ensures Stress Granule Integrity and Dynamism. | |
Tabibi Sabbu | |
Transcriptional induction of the heat shock protein B8 mediates the clearance of misfolded proteins responsible for motor neuron diseases |