Pages that link to "Q37198800"
Jump to navigation
Jump to search
The following pages link to Mutation R120G in alphaB-crystallin, which is linked to a desmin-related myopathy, results in an irregular structure and defective chaperone-like function (Q37198800):
Displaying 50 items.
- Detection of protein-protein interactions among lens crystallins in a mammalian two-hybrid system assay (Q24291887) (← links)
- Temperature-dependent structural and functional properties of a mutant (F71L) αA-crystallin: molecular basis for early onset of age-related cataract (Q24297386) (← links)
- Human alphaA- and alphaB-crystallins bind to Bax and Bcl-X(S) to sequester their translocation during staurosporine-induced apoptosis (Q24306784) (← links)
- Phosphorylation of αB-crystallin: Role in stress, aging and patho-physiological conditions (Q26785450) (← links)
- Crystal Structure of R120G Disease Mutant of Human αB-Crystallin Domain Dimer Shows Closure of a Groove (Q27666994) (← links)
- Multiple molecular architectures of the eye lens chaperone B-crystallin elucidated by a triple hybrid approach (Q27675996) (← links)
- Changes in the quaternary structure and function of MjHSP16.5 attributable to deletion of the IXI motif and introduction of the substitution, R107G, in the -crystallin domain (Q27677069) (← links)
- Crystal Structure of an Activated Variant of Small Heat Shock Protein Hsp16.5 (Q27679512) (← links)
- Increased monomerization of mutant HSPB1 leads to protein hyperactivity in Charcot-Marie-Tooth neuropathy (Q28115297) (← links)
- Effects of modifications of alpha-crystallin on its chaperone and other properties (Q28193145) (← links)
- Conformational change and destabilization of cataract gammaC-crystallin T5P mutant (Q28208192) (← links)
- Myofibrillar myopathies (Q28303812) (← links)
- Substitution of conserved methionines by leucines in chloroplast small heat shock protein results in loss of redox-response but retained chaperone-like activity (Q28346488) (← links)
- αB-crystallin/sHSP protects cytochrome c and mitochondrial function against oxidative stress in lens and retinal cells (Q28384995) (← links)
- Hydroimidazolone modification of the conserved Arg12 in small heat shock proteins: studies on the structure and chaperone function using mutant mimics (Q28478922) (← links)
- Phe71 is essential for chaperone-like function in alpha A-crystallin (Q28579431) (← links)
- Acute effects of desmin mutations on cytoskeletal and cellular integrity in cardiac myocytes (Q28579684) (← links)
- Role of the C-terminal extensions of alpha-crystallins. Swapping the C-terminal extension of alpha-crystallin to alphaB-crystallin results in enhanced chaperone activity (Q28910389) (← links)
- The cardiomyopathy and lens cataract mutation in alphaB-crystallin alters its protein structure, chaperone activity, and interaction with intermediate filaments in vitro. (Q30323290) (← links)
- Behavioral defects in chaperone-deficient Alzheimer's disease model mice (Q30476539) (← links)
- Protein aggregates and novel presenilin gene variants in idiopathic dilated cardiomyopathy (Q30493863) (← links)
- The R116C mutation in alpha A-crystallin diminishes its protective ability against stress-induced lens epithelial cell apoptosis (Q30784416) (← links)
- Phosphorylation-induced change of the oligomerization state of alpha B-crystallin (Q31629257) (← links)
- Chaperone function of mutant versions of alpha A- and alpha B-crystallin prepared to pinpoint chaperone binding sites (Q31897258) (← links)
- Deamidation affects structural and functional properties of human alphaA-crystallin and its oligomerization with alphaB-crystallin (Q33205334) (← links)
- Site-directed mutations in the C-terminal extension of human alphaB-crystallin affect chaperone function and block amyloid fibril formation (Q33302904) (← links)
- Anti-chaperone betaA3/A1(102-117) peptide interacting sites in human alphaB-crystallin (Q33327497) (← links)
- AlphaA-crystallin R49Cneo mutation influences the architecture of lens fiber cell membranes and causes posterior and nuclear cataracts in mice (Q33484430) (← links)
- Desmin aggregate formation by R120G alphaB-crystallin is caused by altered filament interactions and is dependent upon network status in cells (Q33693023) (← links)
- Small heat-shock proteins and their potential role in human disease (Q33840764) (← links)
- BAG3 directly interacts with mutated alphaB-crystallin to suppress its aggregation and toxicity (Q33851451) (← links)
- Alpha-crystallin-type heat shock proteins: socializing minichaperones in the context of a multichaperone network. (Q33969470) (← links)
- Structural and functional changes in the alpha A-crystallin R116C mutant in hereditary cataracts (Q33989123) (← links)
- Gene duplication and separation of functions in alphaB-crystallin from zebrafish (Danio rerio). (Q34013579) (← links)
- Structural and functional roles of deamidation of N146 and/or truncation of NH2- or COOH-termini in human αB-crystallin. (Q34041520) (← links)
- Surplus protein myopathies (Q34134421) (← links)
- Sequence and spatial expression of zebrafish (Danio rerio) alphaA-crystallin (Q34214967) (← links)
- Human alpha B-crystallin mutation causes oxido-reductive stress and protein aggregation cardiomyopathy in mice (Q34231667) (← links)
- Evidence for an essential function of the N terminus of a small heat shock protein in vivo, independent of in vitro chaperone activity (Q34244942) (← links)
- Constitutively active calcineurin induces cardiac endoplasmic reticulum stress and protects against apoptosis that is mediated by α-crystallin-B (Q34276711) (← links)
- Selective degradation of aggregate-prone CryAB mutants by HSPB1 is mediated by ubiquitin-proteasome pathways (Q34288280) (← links)
- Withaferin A induces proteasome inhibition, endoplasmic reticulum stress, the heat shock response and acquisition of thermotolerance (Q34316709) (← links)
- The interaction of unfolding α-lactalbumin and malate dehydrogenase with the molecular chaperone αB-crystallin: a light and X-ray scattering investigation (Q34389165) (← links)
- Mechanism of cataract formation in alphaA-crystallin Y118D mutation (Q34402815) (← links)
- Conformational changes resulting from pseudophosphorylation of mammalian small heat shock proteins--a two-hybrid study (Q34451159) (← links)
- The novel αB-crystallin (CRYAB) mutation p.D109G causes restrictive cardiomyopathy (Q34556520) (← links)
- Tubulin hyperacetylation is adaptive in cardiac proteotoxicity by promoting autophagy (Q34661083) (← links)
- A knock-in mouse model for the R120G mutation of αB-crystallin recapitulates human hereditary myopathy and cataracts. (Q34699001) (← links)
- The NADPH metabolic network regulates human αB-crystallin cardiomyopathy and reductive stress in Drosophila melanogaster (Q34789370) (← links)
- Muscle giants: molecular scaffolds in sarcomerogenesis (Q34793699) (← links)