Danny M. Hatters
Hatters, Danny M.
VIAF ID: 305261489 (Personal)
Permalink: http://viaf.org/viaf/305261489
Preferred Forms
- 100 0 _ ‡a Danny M. Hatters
-
- 100 1 _ ‡a Hatters, Danny M.
- 100 1 _ ‡a Hatters, Danny M.
- 100 1 _ ‡a Hatters, Danny M.
- 100 1 _ ‡a Hatters, Danny M.
4xx's: Alternate Name Forms (2)
Works
Title | Sources |
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The allosteric mechanism induced by protein kinase A (PKA) phosphorylation of dematin (band 4.9). | |
Amino-terminal domain stability mediates apolipoprotein E aggregation into neurotoxic fibrils | |
AMP-activated protein kinase β-subunit requires internal motion for optimal carbohydrate binding | |
The anti-cancer IgM monoclonal antibody PAT-SM6 binds with high avidity to the unfolded protein response regulator GRP78. | |
Apolipoprotein E4 forms a molten globule. A potential basis for its association with disease. | |
Arginine in C9ORF72 Dipolypeptides Mediates Promiscuous Proteome Binding and Multiple Modes of Toxicity | |
The Asian Biophysics Association-supporting biophysics in the greater Asia region. | |
A biosensor-based framework to measure latent proteostasis capacity. | |
A biosensor of SRC family kinase conformation by exposable tetracysteine useful for cell-based screening. | |
The circularization of amyloid fibrils formed by apolipoprotein C-II. | |
Conformational detection of prion protein with biarsenical labeling and FlAsH fluorescence | |
Conformational dynamics and self-association of intrinsically disordered Huntingtin exon 1 in cells | |
Diagnostics for amyloid fibril formation: where to begin? | |
Distinct partitioning of ALS associated TDP-43, FUS and SOD1 mutants into cellular inclusions | |
Engineering conformational destabilization into mouse apolipoprotein E. A model for a unique property of human apolipoprotein E4. | |
Fibrillar amyloid protein present in atheroma activates CD36 signal transduction. | |
Hidden information on protein function in censuses of proteome foldedness | |
High-throughput quantitation of intracellular trafficking and organelle disruption by flow cytometry. | |
Human apolipoprotein C-II forms twisted amyloid ribbons and closed loops. | |
Huntingtin Inclusions Trigger Cellular Quiescence, Deactivate Apoptosis, and Lead to Delayed Necrosis | |
Identifying polyglutamine protein species in situ that best predict neurodegeneration | |
Immiscible inclusion bodies formed by polyglutamine and poly(glycine-alanine) are enriched with distinct proteomes but converge in proteins that are risk factors for disease and involved in protein degradation | |
Insight on the molecular envelope of lipid-bound apolipoprotein E from electron paramagnetic resonance spectroscopy. | |
Misfolded polyglutamine, polyalanine, and superoxide dismutase 1 aggregate via distinct pathways in the cell | |
Model of biologically active apolipoprotein E bound to dipalmitoylphosphatidylcholine | |
Modest Declines in Proteome Quality Impair Hematopoietic Stem Cell Self-Renewal | |
Modulation of apolipoprotein E structure by domain interaction: differences in lipid-bound and lipid-free forms | |
Nascent mutant Huntingtin exon 1 chains do not stall on ribosomes during translation but aggregates do recruit machinery involved in ribosome quality control and RNA | |
Phospholipid complexation and association with apolipoprotein C-II: insights from mass spectrometry. | |
A platform to view huntingtin exon 1 aggregation flux in the cell reveals divergent influences from chaperones hsp40 and hsp70. | |
Polyalanine expansions drive a shift into α-helical clusters without amyloid-fibril formation. | |
Polyglutamine aggregation in Huntington and related diseases. | |
Protein aggregation in cell biology: An aggregomics perspective of health and disease | |
Protein folding: Illuminating chaperone activity. | |
Putting huntingtin "aggregation" in view with windows into the cellular milieu. | |
Sedimentation analysis of novel DNA structures formed by homo-oligonucleotides. | |
SerpinB2 (PAI-2) Modulates Proteostasis via Binding Misfolded Proteins and Promotion of Cytoprotective Inclusion Formation | |
SOD1 protein aggregates stimulate macropinocytosis in neurons to facilitate their propagation | |
Structural and Functional Analysis of a Plant Resistance Protein TIR Domain Reveals Interfaces for Self-Association, Signaling, and Autoregulation | |
Structural insights into the multifunctionality of rabies virus P3 protein | |
Tadpole-like Conformations of Huntingtin Exon 1 Are Characterized by Conformational Heterogeneity that Persists regardless of Polyglutamine Length | |
Tandem repeats in genes, proteins, and disease, c2013: | |
A thiol probe for measuring unfolded protein load and proteostasis in cells. | |
Tracking mutant huntingtin aggregation kinetics in cells reveals three major populations that include an invariant oligomer pool. | |
Tracking protein aggregation and mislocalization in cells with flow cytometry | |
Transcriptional profiles for distinct aggregation states of mutant Huntingtin exon 1 protein unmask new Huntington's disease pathways | |
Tyrosine 416 is phosphorylated in the closed, repressed conformation of c-Src | |
VLDL lipolysis products increase VLDL fluidity and convert apolipoprotein E4 into a more expanded conformation. | |
Walking the tightrope: proteostasis and neurodegenerative disease | |
Widespread remodeling of proteome solubility in response to different protein homeostasis stresses |