Published in Biochem Biophys Res Commun on March 17, 1995
Methionine sulfoxide reductase A is important for lens cell viability and resistance to oxidative stress. Proc Natl Acad Sci U S A (2004) 1.48
Insights into the domains required for dimerization and assembly of human alphaB crystallin. Protein Sci (2005) 1.23
Methionine sulfoxide reductases B1, B2, and B3 are present in the human lens and confer oxidative stress resistance to lens cells. Invest Ophthalmol Vis Sci (2005) 1.15
In vivo carbamylation and acetylation of water-soluble human lens alphaB-crystallin lysine 92. Protein Sci (2001) 1.13
Effect of glycation on alpha-crystallin structure and chaperone-like function. Biochem J (2007) 1.05
Methionine sulfoxide reductase A (MsrA) restores alpha-crystallin chaperone activity lost upon methionine oxidation. Biochim Biophys Acta (2009) 1.05
alpha-Crystallin chaperone-like activity and membrane binding in age-related cataracts. Biochemistry (2002) 1.04
Effect of dicarbonyl-induced browning on alpha-crystallin chaperone-like activity: physiological significance and caveats of in vitro aggregation assays. Biochem J (2004) 0.99
Effects of modifications of alpha-crystallin on its chaperone and other properties. Biochem J (2002) 0.94
Effect of site-directed mutagenesis of methylglyoxal-modifiable arginine residues on the structure and chaperone function of human alphaA-crystallin. Biochemistry (2006) 0.93
Effect of aging on the chaperone-like function of human alpha-crystallin assessed by three methods. Biochem J (1997) 0.93
New focus on alpha-crystallins in retinal neurodegenerative diseases. Exp Eye Res (2010) 0.91
Chaperones come of age. Cell Stress Chaperones (2002) 0.90
Modulation of the chaperone-like activity of bovine alpha-crystallin. Proc Natl Acad Sci U S A (1996) 0.89
Hydroimidazolone modification of the conserved Arg12 in small heat shock proteins: studies on the structure and chaperone function using mutant mimics. PLoS One (2012) 0.88
Hydroimidazolone modification of human alphaA-crystallin: Effect on the chaperone function and protein refolding ability. Biochim Biophys Acta (2010) 0.82
COOH-terminal truncations and site-directed mutations enhance thermostability and chaperone-like activity of porcine alphaB-crystallin. Mol Vis (2009) 0.82
X-ray spectroscopic approaches to the investigation and characterization of photochemical processes. J Synchrotron Radiat (2009) 0.75
Determination of the glycosylated hemoglobins (HB AI) with a new microcolumn procedure. Suitability of the technique for assessing the clinical management of diabetes mellitus. Diabetes (1978) 1.51
Separation of human hemoglobins by DEAE-cellulose chromatography using glycine-KCN-NaC1 developers. Hemoglobin (1977) 1.32
Mutation of R116C results in highly oligomerized alpha A-crystallin with modified structure and defective chaperone-like function. Biochemistry (2000) 1.21
Minor hemoglobins in sickle cell anemia, beta-thalassemia, and related conditions: a study of red cell fractions isolated by density gradient centrifugation. Biochem Med (1975) 1.06
Influence of mouse age and erythrocyte age on glutathione metabolism. Biochem J (1978) 1.06
Lens protein composition, glycation and high molecular weight aggregation in aging rats. Invest Ophthalmol Vis Sci (1987) 0.94
Identification of hydrogen peroxide oxidation sites of alpha A- and alpha B-crystallins. Free Radic Res (1997) 0.93
Diabetes affects alpha-crystallin chaperone function. Biochem Biophys Res Commun (1995) 0.91
Inhibition of lens crystallin glycation and high molecular weight aggregate formation by aspirin in vitro and in vivo. Invest Ophthalmol Vis Sci (1989) 0.91
Minor (glycosylated) hemoglobins in cord blood of infants of normal and diabetic mothers. Am J Obstet Gynecol (1981) 0.90
On the chromatographic heterogeneity of human fetal hemoglobin. Biochim Biophys Acta (1979) 0.89
Progressive changes in lens crystallin glycation and high-molecular-weight aggregate formation leading to cataract development in streptozotocin-diabetic rats. Exp Eye Res (1987) 0.89
Advanced glycation end products in human senile and diabetic cataractous lenses. Mol Cell Biochem (2000) 0.88
Substituted hydrophobic and hydrophilic residues at methionine-68 influence the chaperone-like function of alphaB-crystallin. Mol Cell Biochem (2001) 0.88
Inhibition of cataracts in moderately diabetic rats by aminoguanidine. Exp Eye Res (1996) 0.87
Microchromatography of hemoglobins. IV. An improved procedure for the detection of hemoglobins S and C at birth. J Lab Clin Med (1975) 0.87
New less temperature-sensitive microchromatographic method for the separation and quantitation of glycosylated hemoglobins using a non-cyanide buffer system. J Chromatogr (1985) 0.85
Quantitative microchromatographic determination of hemoglobin F in patients with hemoglobins S and/or C. Am J Hematol (1976) 0.85
Reverse-phase HPLC analysis of human alpha crystallin. Curr Eye Res (1991) 0.84
Influence of protein-glutathione mixed disulfide on the chaperone-like function of alpha-crystallin. J Biol Chem (1997) 0.84
Application of affinity chromatography for separation and quantitation of glycosylated hemoglobins. J Lab Clin Med (1983) 0.83
Non-enzymatic glycosylation influences Hb S polymerization. Hemoglobin (1986) 0.82
Glycation mediated lens crystallin aggregation and cross-linking by various sugars and sugar phosphates in vitro. Exp Eye Res (1993) 0.82
In vitro glycation and acetylation (by aspirin) of rat crystallins. Life Sci (1993) 0.81
Evidence of a glycemic threshold for the development of cataracts in diabetic rats. Curr Eye Res (1999) 0.81
Role of glycine 1 and lysine 2 in the glycation of bovine gamma B-crystallin. Site-directed mutagenesis of lysine to threonine. J Biol Chem (1995) 0.81
Differential glycation of rat alpha-, beta- and gamma-crystallins. Exp Eye Res (1991) 0.81
A controlled investigation of propofol, thiopentone and methohexitone. Can J Anaesth (1987) 0.80
Glycation of human lens proteins: preferential glycation of alpha A subunits. Exp Eye Res (1992) 0.80
Minor hemoglobins in sickle-cell heterozygotes and homozygotes with and without diabetes. Biochim Biophys Acta (1980) 0.80
Glycation of human lens crystallins: effect of age and aspirin treatment. Ophthalmic Res (1993) 0.80
High-performance liquid chromatographic separation of lens crystallins and their subunits. J Chromatogr (1986) 0.80
Immunochemical evidence for increased formation of advanced glycation end products and inhibition by aminoguanidine in diabetic rat lenses. Biochem Biophys Res Commun (1997) 0.80
Sites of glycation of beta B2-crystallin by glucose and fructose. Biochem Biophys Res Commun (1996) 0.79
Differences in affinity of variant beta chains for alpha chains: a possible explanation for the variation in the percentages of beta chain variants in heterozygotes. Hemoglobin (1977) 0.79
Oxidation-reduction potentials of human fetal hemoglobin and gamma chains. Effects of blocking sulfhydryl groups. J Biol Chem (1975) 0.78
High-pressure liquid chromatographic separation of glycosylated and acetylated minor hemoglobins in newborn infants and in patients with sickle cell disease. J Lab Clin Med (1984) 0.78
The role of alpha- and epsilon-amino groups in the glycation-mediated cross-linking of gammaB-crystallin. Study of three site-directed mutants. J Biol Chem (1997) 0.78
Retracted Proteins of urea-soluble high molecular weight (HMW) aggregates from diabetic cataract: identification of in vivo glycation sites. Exp Eye Res (1991) 0.78
Non-enzymatic acetylation of human hemoglobins. Biochim Biophys Acta (1981) 0.78
Glycation of lens membrane intrinsic proteins. Curr Eye Res (1992) 0.77
Glycation of lens MIP26 affects the permeability in reconstituted liposomes. Biochem Biophys Res Commun (1992) 0.77
Age-dependent variation in the cytosol/membrane distribution of red cell protein kinase-C. Am J Hematol (1989) 0.76
Intrapolypeptide disulfides in human alphaA-crystallin and their effect on chaperone-like function. Mol Cell Biochem (1999) 0.76
Demonstration of a minor hemoglobin with modified alpha chains and additional modified hemoglobins in normal and diabetic adults. Biochim Biophys Acta (1983) 0.75
Glycosylated and acetylated hemoglobins in relation to gestational age and red cell age. Hemoglobin (1984) 0.75
Human fetal hemoglobin synthesis and its NH2-terminal acetylation in a rabbit reticulocyte lysate translational system. Biochim Biophys Acta (1986) 0.75
Hemoglobin F levels in patients with chronic renal failure. Hemoglobin (1977) 0.75
Modification of sickle hemoglobin by acetaldehyde and its effect on oxygenation, gelation and sickling. Biochim Biophys Acta (1982) 0.75
Red cell age-related changes of minor fetal hemoglobin components. Hemoglobin (1981) 0.75
The fate of gamma L crystallins in rat lens during diabetic cataractogenesis as determined by a monoclonal antibody. Curr Eye Res (1989) 0.75
Synthesis of hemoglobin chains in adult and newborn goats: possible influence of the beta c synthesis on the production of alpha chains. Hemoglobin (1982) 0.75
Human red cell acetyltransferase. Life Sci (1988) 0.75
Glycosylated hemoglobin and plasma protein in newborns of normal and diabetic women. Pediatr Res (1984) 0.75
Post-translational control of human hemoglobin synthesis; the number of alpha chain genes and the synthesis of HB S. Prog Clin Biol Res (1978) 0.75
Minor fetal hemoglobins in relation to gestational age. Am J Obstet Gynecol (1981) 0.75
Synthesis of the minor fetal hemoglobin Fic in colonies of erythropoietic precursors isolated from human umbilical cord blood. Am J Hematol (1982) 0.75
Glycosylated minor components of human fetal hemoglobin. Chromatographic separation, identification, and functional characterization. Biochim Biophys Acta (1981) 0.75
Effect of germanium-132 on galactose cataracts and glycation in rats. Exp Eye Res (1995) 0.75
Proteins of urea-soluble high molecular weight (HMW) aggregates from diabetic cataract: identification of in vivo glycation sites. Exp Eye Res (1992) 0.75
High-performance liquid chromatographic separation and quantitation of glycosylated hemoglobin A2 as an alternate index of glycemic control. J Chromatogr (1986) 0.75
Microchromatographic quantitation of minor fetal hemoglobin components. Hemoglobin (1981) 0.75
Microchromatographic quantitation of fetal hemoglobin in patients with sickle cell disease. Hemoglobin (1979) 0.75
Glycosylated hemoglobins in heterozygotes and homozygotes for hemoglobin C with or without diabetes. J Lab Clin Med (1984) 0.75
Scheimpflug densitometric analysis of cataracts in diabetic rats: correlation with glycation. Ophthalmic Res (1996) 0.75
A preliminary report on periodic or chronic dialysis. J Assoc Physicians India (1965) 0.75
Influence of gamma-chain amino-terminal acetylation on subunit assembly of human fetal hemoglobin. Biochim Biophys Acta (1987) 0.75
Affinity chromatographic quantitation of glycosylated hemoglobin in newborn infants. Hemoglobin (1983) 0.75
The relationship between fetal hemoglobin level and glycosylation in sickle cell disease. Am J Hematol (1984) 0.75
Changes in glycosylated hemoglobins with red cell aging in normal and diabetic subjects and in newborn infants of normal and diabetic mothers. J Lab Clin Med (1983) 0.75
High pressure liquid chromatographic separation of the labile aldimine (pre-hemoglobin AIc) and the stable Hb AIc. Hemoglobin (1984) 0.75
Variability in the interaction of beta-thalassemia with the alpha-chain variants Hb G-Philadelphia and Hb Rampa. J Lab Clin Med (1978) 0.75
Is the trimodality of Hb Leslie (alpha 2 beta 2 131 Gln---O) in heterozygotes the result of a variable number of active alpha-chain genes? Evidence for posttranslational control of hemoglobin synthesis. Am J Hematol (1978) 0.75
Glycosylated hemoglobin and protein levels in normal and diabetic pregnancies: relation to birth weight. Obstet Gynecol (1986) 0.75
The cat hemoglobin polymorphism: Southern blot analysis of the beta-globin gene region from cats of various Hb A/Hb B phenotypes. Biochem Genet (1988) 0.75
Hemoglobin Athens-Georgia, or alpha 2 beta 2 40(C6)Arg replaced by Lys, a hemoglobin variant with an increased oxygen affinity. Biochim Biophys Acta (1976) 0.75
Heterogeneity in the globin chain composition of a human minor fetal hemoglobin component. Biochim Biophys Acta (1985) 0.75
Identification of the glycation site of lens gamma B-crystallin by fast atom bombardment tandem mass spectrometry. Anal Biochem (1996) 0.75
An improved chromatographic procedure for quantitation of human fetal hemoglobin. Hemoglobin (1977) 0.75
Increased membrane-associated phorbol-12,13 dibutyrate (PDBu) receptor function in sickle red cells. Biochem Biophys Res Commun (1987) 0.75
Evidence for posttranslational control of fetal hemoglobin synthesis. Am J Hematol (1988) 0.75
Stimulation of minor fetal hemoglobin synthesis in cord blood reticulocytes by butyrate. Biochem Biophys Res Commun (1981) 0.75