Published in Biophys J on May 01, 1999
Fundamental aspects of protein-protein association kinetics. Chem Rev (2009) 3.43
Anomalous diffusion of proteins due to molecular crowding. Biophys J (2005) 2.93
Multifrequency electron spin resonance study of the dynamics of spin labeled T4 lysozyme. J Phys Chem B (2010) 1.53
Proliferating cell nuclear antigen uses two distinct modes to move along DNA. J Biol Chem (2009) 1.53
A mathematical explanation of an increase in bacterial swimming speed with viscosity in linear-polymer solutions. Biophys J (2002) 1.35
Fast dynamics and stabilization of proteins: binary glasses of trehalose and glycerol. Biophys J (2004) 1.08
Effect of macromolecular crowding on protein folding dynamics at the secondary structure level. J Mol Biol (2009) 1.07
Proteins as micro viscosimeters: Brownian motion revisited. Eur Biophys J (2006) 1.03
Down to atomic-scale intracellular water dynamics. EMBO Rep (2008) 0.96
Direct observation of protein unfolded state compaction in the presence of macromolecular crowding. Biophys J (2013) 0.95
Anisotropy and temperature dependence of myoglobin translational diffusion in myocardium: implication for oxygen transport and cellular architecture. Biophys J (2007) 0.87
A direct coupling between global and internal motions in a single domain protein? MD investigation of extreme scenarios. Biophys J (2011) 0.85
15N relaxation study of the cold shock protein CspB at various solvent viscosities. J Biomol NMR (2003) 0.83
Trehalose-mediated inhibition of the plasma membrane H+-ATPase from Kluyveromyces lactis: dependence on viscosity and temperature. J Bacteriol (2002) 0.82
Transient anomalous subdiffusion: effects of specific and nonspecific probe binding with actin gels. J Phys Chem B (2010) 0.77
Protein brownian rotation at the glass transition temperature of a freeze-concentrated buffer probed by superparamagnetic nanoparticles. Biophys J (2013) 0.75
Effects of macromolecular crowding agents on protein folding in vitro and in silico. Biophys Rev (2013) 0.75
Solvent viscosity and protein dynamics. Biochemistry (1980) 4.35
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Myoglobin and hemoglobin rotational diffusion in the cell. Biophys J (1997) 1.06
The reassociation of Lumbricus terrestris hemoglobin dissociated at alkaline pH. J Biol Chem (1984) 1.04
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Evidence for rotational contribution to protein-facilitated proton transport. Proc Natl Acad Sci U S A (1984) 0.95
Possible coupling of chemical to structural dynamics in subtilisin BPN' catalyzed hydrolysis. Biophys Chem (1991) 0.94
Viscosity and transient solvent accessibility of Trp-63 in the native conformation of lysozyme. Biophys Chem (1988) 0.94
Comparison between internal microviscosity of low-density erythrocytes and the microviscosity of hemoglobin solutions: an electron paramagnetic resonance study. Biophys J (1996) 0.83
Diabetic control in 102 insulin-treated out-patients. Diabetologia (1980) 1.47
Towards a transgenic mouse model of sickle cell disease: hemoglobin SAD. EMBO J (1991) 1.40
Structural study of circulating thymic factor: a peptide isolated from pig serum. II. Amino acid sequence. J Biol Chem (1977) 1.34
Hemoglobin S Antilles: a variant with lower solubility than hemoglobin S and producing sickle cell disease in heterozygotes. Proc Natl Acad Sci U S A (1986) 1.23
Molecular cloning and sequencing of the human erythrocyte 2,3-bisphosphoglycerate mutase cDNA: revised amino acid sequence. EMBO J (1986) 1.17
Human erythrocyte band 3 polymorphism (band 3 Memphis): characterization of the structural modification (Lys 56----Glu) by protein chemistry methods. Blood (1991) 1.04
Cation- and peptide-binding properties of human centrin 2. FEBS Lett (2000) 1.04
Hb Fontainebleau [alpha 21(B2)Ala----pro], a new silent mutant hemoglobin. Hemoglobin (1989) 1.01
Hemoglobin variants and activity of the (K+Cl-) cotransport system in human erythrocytes. Blood (1992) 0.99
Structural study of hemoglobin Hazebrouck, beta 38(C4)Thr----Pro. A new abnormal hemoglobin with instability and low oxygen affinity. FEBS Lett (1984) 0.92
Self-association of haemoglobin Olympia (alpha 2 beta 2 20 (B2) Val----Met). A human haemoglobin bearing a substitution at the surface of the molecule. J Mol Biol (1986) 0.90
L-arginine restores endothelium-dependent relaxation in pulmonary circulation of chronically hypoxic rats. Am J Physiol (1992) 0.90
The human alpha-globin gene. The protein products of the duplicated genes are identical. Eur J Biochem (1980) 0.89
Insulin injections enhance cholesterol gallstone incidence by changing the biliary cholesterol saturation index and apo A-I concentration in hamsters fed a lithogenic diet. J Hepatol (2001) 0.89
Hemoglobin J Iran alpha 2 beta 2 77 (EF1) his----Asp in a Russian-Armenian family. Hemoglobin (1986) 0.88
Hemoglobin Saint Mandé beta 102 (G4) asn replaced by tyr: a new low oxygen affinity variant. FEBS Lett (1981) 0.88
A new silent hemoglobin variant in a black family from French West Indies, hemoglobin Le Lamentin alpha 20 His replaced by Gln. FEBS Lett (1982) 0.87
Structural study of hemoglobin Knossos, beta 27 (B9) Ala leads to Ser. A new abnormal hemoglobin present as a silent beta-thalassemia. FEBS Lett (1982) 0.87
Isolation and characterization of the gene encoding the muscle-specific isozyme of human phosphoglycerate mutase. Gene (1990) 0.86
Structure of the EF corner favors deamidation of asparaginyl residues in hemoglobin: the example of Hb La Roche-sur-Yon [beta 81 (EF5) Leu----His]. Biochim Biophys Acta (1992) 0.85
Hemoglobin Phnom Penh [alpha117Phe(H1)-Ile-alpha118Thr(H2)]; evidence for a hotspot for insertion of residues in the third exon of the alpha1-globin gene. Hum Mutat (1998) 0.84
Hb Henri Mondor: beta26 (B8) Glu leads to Val: a variant with a substitution localized at the same position as that of HbE beta26 Glu leads to Lys. FEBS Lett (1976) 0.84
The surface-exposed, trypsin-accessible segments of apolipoprotein B in the low-density lipoprotein of human serum. Fractionation and characterisation of the liberated peptides. Eur J Biochem (1982) 0.84
Loss of endothelium-dependent relaxation in proximal pulmonary arteries from rats exposed to chronic hypoxia: effects of in vivo and in vitro supplementation with L-arginine. J Cardiovasc Pharmacol (1993) 0.83
Hb Marseille [alpha 2 beta 2 N methionyl-2 (NA2) His----Pro]: a new beta chain variant having an extended N-terminus. FEBS Lett (1984) 0.82
Hemoglobin M Saskatoon (alpha 2 beta 2 63(E7) His----Tyr) in an Algerian family. Hemoglobin (1985) 0.82
Haemoglobin Lyon (beta17-18 (A 14-15) Lys-Val leads to O). Determination by sequenator analysis. Biochim Biophys Acta (1974) 0.81
Hemoglobin Hotel-Dieu beta 99 Asp replaced by Gly (g1). A new abnormal hemoglobin with high oxygen affinity. Hemoglobin (1981) 0.81
Structural and functional studies of hemoglobin Poissy alpha 2 beta 2(56) (D7) Gly----Arg and 86 (F2) Ala----Pro. Eur J Biochem (1985) 0.81
Lipoprotein(a) and apolipoprotein(a) in a New World monkey, the common marmoset (Callithrix jacchus). Association of variable plasma lipoprotein(a) levels with a single apolipoprotein(a) isoform. Arterioscler Thromb (1991) 0.81
Dynamics of carbon monoxide binding with neuronal nitric oxide synthase. Biochemistry (1999) 0.81
Hemoglobin Dakar = Hb Grady: demonstration by a new approach to the analysis of the tryptic core region of the alpha chain and oxygen equilibrium properties. Biochim Biophys Acta (1976) 0.81
A method for isolation of abnormal haemoglobins with high oxygen affinity due to a frozen quaternary r-structure: application to Hb Creteil alpha 2 A beta 2 (F5) 89 ASN. FEBS Lett (1974) 0.80
Hemoglobin Saint Mandé [beta 102 (G4) Asn----Tyr]. Functional studies and structural modeling reveal an altered T state. Eur J Biochem (1990) 0.80
A new case of hemoglobin Providence (alpha 2 beta 2 82 (EF6) Lys----Asn or Asp) discovered in a French Caucasian family. Structural and functional studies. Hemoglobin (1985) 0.80
Haemoglobin Strasbourg alpha2beta2 23 (B5) Val replaced by Asp: revised structure anf functional properties. FEBS Lett (1978) 0.80
Hemoglobin Roanne [alpha 94(G1) Asp-->Glu]: a variant of the alpha 1 beta 2 interface with an unexpected high oxygen affinity. Biochim Biophys Acta (1995) 0.79
Structure of the human adult hemoglobin minor fraction A1b by electrospray and secondary ion mass spectrometry. Pyruvic acid as amino-terminal blocking group. J Biol Chem (1991) 0.79
Use of combined mass spectrometry methods for the characterization of a new variant of human hemoglobin: The double mutant hemoglobin villeparisis β77(EF1) His → Tyr, β 80 (EF4) Asn → Ser. J Am Soc Mass Spectrom (1996) 0.79
[Localization of binding sites in the hemoglobin-haptoglobin complex]. C R Seances Soc Biol Fil (1979) 0.79
Hemoglobin Hekinan [alpha (2)27(B8)Glu----Asp beta 2] detected in Guyana. Hemoglobin (1989) 0.78
Effects of the alpha 20 mutation on the polymerization of Hb S. Biochim Biophys Acta (1984) 0.78
Conformational relaxation in hemoproteins: the cytochrome P-450cam case. Biochemistry (2000) 0.78
Hemoglobin variants in North Africa. Hemoglobin (1994) 0.78
Two new human hemoglobin variants caused by unusual mutational events: Hb Zaïre contains a five residue repetition within the alpha-chain and Hb Duino has two residues substituted in the beta-chain. Hum Genet (1992) 0.78
Sickle cell hemoglobin fiber formation strongly inhibited by the Stanleyville II mutation (alpha 78 Asn leads to Lys). Biochem Biophys Res Commun (1983) 0.78
New results of hemoglobin variant structure determinations by fast atom bombardment mass spectrometry. Hemoglobin (1990) 0.78
Hemoglobin La Desirade alpha A2 beta 2 129 (H7) Ala----Val: a new unstable hemoglobin. Hemoglobin (1986) 0.78
Human bisphosphoglycerate mutase expressed in E coli: purification, characterization and structure studies. Biochimie (1990) 0.78
[Metabolic control in 107 maturity onset diabetic out patients (author's transl)]. Nouv Presse Med (1980) 0.78
Hemoglobin Castilla beta 32 (B14) Leu leads to Arg; a new unstable variant producing severe hemolytic disease. FEBS Lett (1975) 0.78
Hemoglobin Ty GARD (alphaA2beta2 124 (H2) Pro replaced by Gln). A stable high O2 affinity variant at the alpha1beta1 contact. FEBS Lett (1978) 0.77
Hemoglobin Thionville. An alpha-chain variant with a substitution of a glutamate for valine at NA-1 and having an acetylated methionine NH2 terminus. J Biol Chem (1992) 0.77
Isolation, characterization, and structure of a mutant 89 Arg----Cys bisphosphoglycerate mutase. Implication of the active site in the mutation. J Biol Chem (1989) 0.77
Oxidative dimerization of proteins: role of tyrosine accessibility. Arch Biochem Biophys (2000) 0.77
Two new cases of heterozygosity for hemoglobin Knossos alpha 2 beta 2 27 Ala----Ser detected in the French West Indies and Algeria. Hemoglobin (1984) 0.77
Hemoglobin Redondo [beta 92(F8) His----Asn]: an unstable hemoglobin variant associated with heme loss which occurs in two forms. Am J Hematol (1991) 0.77
Hemoglobin Saverne: a new variant with elongated beta chains: structural and functional properties. Hemoglobin (1988) 0.77
Hemoglobin Pontoise alpha63 Ala replaced by Asp(E12). A new fast moving variant. Biochim Biophys Acta (1977) 0.77
[Biological study of spontaneous amyloidosis in PS mice]. Pathol Biol (Paris) (1984) 0.77
Hb N-Timone [alpha 2 beta 2(8)(A5)Lys----Glu]: a new fast-moving variant with normal stability and oxygen affinity. Hemoglobin (1989) 0.76
[Hemoglobin Boumerdès alpha 2(37) (C2) Pro----Arg beta 2: a new variant of the alpha chain associated with hemoglobin S in an Algerian family]. Nouv Rev Fr Hematol (1987) 0.76
A new case of Hb Dagestan [alpha 60(E9)Lys----Glu]. Hemoglobin (1987) 0.76
Hb J-Cordoba [alpha 2A beta 2(95)(FG2)Lys----Met]. A new Hb variant found in Argentina. Hemoglobin (1988) 0.76
Key interactions in the immunoglobulin-like structure of apo-neocarzinostatin: evidence from nuclear magnetic resonance relaxation data and molecular dynamics simulations. Protein Sci (2001) 0.75
[Hemoglobin J. Broussais alpha-2 90 Lys leads to Asn beta-2A (FG2) discovered in a Martinique family. Comparison of several analytical technics]. Nouv Rev Fr Hematol (1976) 0.75
Hemoglobin Beirut [alpha 2 beta 2(126)(H4)Val----Ala] in an Algerian family. Hemoglobin (1986) 0.75
[Clinical and biochemical studies of a new case of Hb J Baltimore (alpha 2A beta2 16 Gly yields Asp) isolated in France (author's transl)]. Nouv Rev Fr Hematol (1975) 0.75
Prenatal diagnosis of haemoglobinopathies by ion exchange HPLC of haemoglobins. Prenat Diagn (1989) 0.75
Proton NMR studies of human hemoglobin variants modified in the proximal side of beta heme pocket. Implications for the affinity control and cooperative mechanism. J Biol Chem (1988) 0.75
[Evaluation of three commercial kits for the estimation of total glycolysed hemoglobin: Hb Al (author's transl)]. Ann Biol Clin (Paris) (1980) 0.75
Functional studies of Hb Malmö beta97 (FG4) His leads to Gln. FEBS Lett (1977) 0.75
Use of the sequenator for the study of abnormal haemoglobins. Application to haemoglobins Saint Louis [beta28 (B10) Leu yields Gln] and Lyon [beta17-18 (A14-15) Lys yields Val deleted]. Haematologia (Budap) (1974) 0.75
Hemoglobin San Diego/beta zero thalassemia in a Greek adult. Hemoglobin (1986) 0.75
[The control of diabetes in 209 cases regularly followed by outpatient consultation]. Journ Annu Diabetol Hotel Dieu (1980) 0.75
Hb Knossos, beta 27 Ala leads to Ser (B 9): a new hemoglobinopathy presenting as a silent beta-thalassemia. Prog Clin Biol Res (1983) 0.75
Hb Kokura alpha 2 47 (CE5) Asp----Gly beta 2 in a French Jewish family. Nouv Rev Fr Hematol (1986) 0.75
Glycerated hemoglobin alpha 2 beta 2(82) (EF6) N-epsilon-glyceryllysine: a new post-translational modification occurring in erythrocyte bisphosphoglyceromutase deficiency. Biomed Biochim Acta (1987) 0.75
Hemoglobin kenitra alpha 2 beta 2 69 (E13) Gly----Arg. A new beta variant of elevated expression associated with alpha-thalassemia, found in a Moroccan woman. Hemoglobin (1985) 0.75
Structural and functional studies of hemoglobin J Cala-bria: beta64 (E8) Gly leads to Asp. Biochim Biophys Acta (1977) 0.75
Glycerated hemoglobin, alpha 2A beta 2(82) (EF6) N epsilon-glyceryllysine. A new post-translational modification occurring in erythrocyte bisphosphoglyceromutase deficiency. J Biol Chem (1986) 0.75
Ligand migration and escape pathways in haem proteins. Biochem Soc Trans (2006) 0.75
Hb Potomac [beta 101(G3)Glu----Asp] in a Polish family living in France. Hemoglobin (1987) 0.75
Hemoglobin Pitie-Salpetriere beta 34 (B16) Val replaced by Phe. A new high oxygen affinity variant associated with familial erythrocytosis. Biochim Biophys Acta (1980) 0.75
Hb I-High Wycombe [beta 59(E3)Lys----Glu] in a woman of Malian origin. Hemoglobin (1987) 0.75
Reaction products formed after strong acid treatment of alpha-amino-delta-hydroxyvaleric acid. Anal Biochem (1985) 0.75
Hb Strasbourg alpha2beta2 20 (B2) Val leads to Asp: a variant at the same locus as Hb Olympia beta 20 Val leads to Met. FEBS Lett (1976) 0.75
[Automation of peptide chromatography]. Biochimie (1975) 0.75
Hemoglobin Bougardirey-Mali beta 119 (GH2) Gly replaced by Val. An electrophoretically silent variant migrating in isoelectrofocusing as Hb F. Hemoglobin (1979) 0.75
Hb A1c: a review on its structure, biosynthesis, clinical significance and methods of assay. Biomedicine (1979) 0.75
Seven new cases of hemoglobin Camperdown alpha 2 beta 2 104(G6)Arg----Ser found in Malta, Sicily and Tunisia. Hemoglobin (1984) 0.75
[Different primary structure of 2 variants of Friend virus p 30 polypeptide separated by isoelectric focusing]. C R Seances Acad Sci D (1979) 0.75
An automatic method for determination of glycosylated hemoglobins using low-pressure liquid chromatography. J Chromatogr (1983) 0.75
New techniques for the prenatal diagnosis of hemoglobinopathies. Prog Clin Biol Res (1981) 0.75
Identification of some abnormal haemoglobins by fast atom bombardment mass spectrometry and fast atom bombardment tandem mass spectrometry. Biomed Environ Mass Spectrom (1988) 0.75
Hb Tunis [alpha 2 beta 2 124 (H2)Pro----Ser], a new beta chain variant identified by HPLC. Hemoglobin (1988) 0.75
Further characterization of Hb Henri Mondor or alpha 2 beta 2(26)(B8)Glu----Val. Hemoglobin (1987) 0.75
Purification of human erythrocyte phosphoglycerate kinase by dye ligand affinity chromatography. J Chromatogr (1983) 0.75
Antenatal diagnosis of haemoglobinopathies by Biorex chromatography of haemoglobin. Br J Haematol (1982) 0.75