Published in FEBS Lett on December 15, 1976
Alternative transcription and splicing of the human porphobilinogen deaminase gene result either in tissue-specific or in housekeeping expression. Proc Natl Acad Sci U S A (1988) 3.11
Reducing unnecessary laboratory use with new test request form: example of tumour markers. Lancet (1993) 2.08
Growth failure in pediatric inflammatory bowel disease. J Pediatr Gastroenterol Nutr (1993) 2.05
Long-term 6-mercaptopurine treatment in adolescents with Crohn's disease. Gastroenterology (1990) 2.00
A 5' splice-region G----C mutation in exon 1 of the human beta-globin gene inhibits pre-mRNA splicing: a mechanism for beta+-thalassemia. Proc Natl Acad Sci U S A (1989) 1.48
Diabetic control in 102 insulin-treated out-patients. Diabetologia (1980) 1.47
The prevalence of metabolic syndrome and its components in two main types of primary aldosteronism. J Hum Hypertens (2010) 1.40
Towards a transgenic mouse model of sickle cell disease: hemoglobin SAD. EMBO J (1991) 1.40
Prenatal diagnosis of sickle-cell anemia in the first trimester of pregnancy. N Engl J Med (1983) 1.35
Structural study of circulating thymic factor: a peptide isolated from pig serum. II. Amino acid sequence. J Biol Chem (1977) 1.34
Biochemical characterisation of a serum thymic factor. Nature (1977) 1.33
Isolation and identification of a cDNA clone coding for rat uroporphyrinogen decarboxylase. Proc Natl Acad Sci U S A (1984) 1.27
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 of a cDNA sequence complementary to porphobilinogen deaminase mRNA from rat. Proc Natl Acad Sci U S A (1984) 1.22
Home nocturnal supplemental nasogastric feedings in growth-retarded adolescents with Crohn's disease. Gastroenterology (1989) 1.20
Molecular cloning and sequencing of the human erythrocyte 2,3-bisphosphoglycerate mutase cDNA: revised amino acid sequence. EMBO J (1986) 1.17
Microscopic viscosity and rotational diffusion of proteins in a macromolecular environment. Biophys J (1999) 1.14
Beta-chain contact sites in the haemoglobin S polymer. Nature (1980) 1.13
Effect of thyroid hormones on the switch from larval to adult hemoglobin synthesis in the salamander Pleurodeles waltlii. Cell Differ (1982) 1.10
Cloning and sequencing of mRNAs coding for two adult alpha globin chains of the salamander Pleurodeles waltlii. Gene (1986) 1.07
Human erythrocyte band 3 polymorphism (band 3 Memphis): characterization of the structural modification (Lys 56----Glu) by protein chemistry methods. Blood (1991) 1.04
A study of membrane protein defects and alpha hemoglobin chains of red blood cells in human beta thalassemia. J Biol Chem (1989) 1.04
Cation- and peptide-binding properties of human centrin 2. FEBS Lett (2000) 1.04
Covalent binding of glutathione to hemoglobin. I. Inhibition of hemoglobin S polymerization. J Biol Chem (1986) 1.04
The peculiar spectrum of beta-thalassemia genes in Tunisia. Hum Genet (1988) 1.02
Diphosphoglycerate mutase and 2,3-diphosphoglycerate phosphatase activities of red cells: comparative electrophoretic study. Biochem Biophys Res Commun (1973) 1.01
Hb Fontainebleau [alpha 21(B2)Ala----pro], a new silent mutant hemoglobin. Hemoglobin (1989) 1.01
Two mild cystic fibrosis-associated mutations result in severe cystic fibrosis when combined in cis and reveal a residue important for cystic fibrosis transmembrane conductance regulator processing and function. J Biol Chem (2000) 1.00
Hemoglobin variants and activity of the (K+Cl-) cotransport system in human erythrocytes. Blood (1992) 0.99
Resveratrol, a natural dietary phytoalexin, possesses similar properties to hydroxyurea towards erythroid differentiation. Br J Haematol (2001) 0.98
Mouse alpha chains inhibit polymerization of hemoglobin induced by human beta S or beta S Antilles chains. Biochim Biophys Acta (1988) 0.98
Covalent binding of glutathione to hemoglobin. II. Functional consequences and structural changes reflected in NMR spectra. J Biol Chem (1986) 0.97
The enzymes of the glycolytic pathway in erythrocytes infected with Plasmodium falciparum malaria parasites. Blood (1988) 0.96
Highly destructive perianal disease in children with Crohn's disease. J Pediatr Gastroenterol Nutr (1995) 0.95
Chromosomal assignment of the human 2,3-bisphosphoglycerate mutase gene (BPGM) to region 7q34----7q22. Hum Genet (1987) 0.94
Is DNA ploidy and proliferative activity of prognostic value in advanced gastric carcinoma? Hum Pathol (1991) 0.94
Short chain fatty acids are effective in short-term treatment of chronic radiation proctitis: randomized, double-blind, controlled trial. Dis Colon Rectum (1999) 0.94
Molecular cloning and nucleotide sequence of murine 2,3-bisphosphoglycerate mutase cDNA. Biochem Biophys Res Commun (1988) 0.92
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
The first case of a complete deficiency of diphosphoglycerate mutase in human erythrocytes. J Clin Invest (1978) 0.91
Haemoglobin Saint Louis beta28 (B10) leucine leads to glutamine. A new unstable haemoglobin only present in a ferri form. FEBS Lett (1973) 0.91
Modification of the electronic structure of ferrous iron in hemoglobin by ligandation and by alterations of the protein structure inferred from Mössbauer measurements. J Chem Phys (1970) 0.90
Functional and physicochemical studies of hemoglobin St. Louis beta 28 (B10) Leu replaced by Gln: a variant with ferric beta heme iron. J Clin Invest (1976) 0.90
L-arginine restores endothelium-dependent relaxation in pulmonary circulation of chronically hypoxic rats. Am J Physiol (1992) 0.90
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
Enhanced cardiac function in transgenic mice expressing a Ca(2+)-stimulated adenylyl cyclase. Circ Res (2000) 0.90
[An acquired S hemoglobin in the adult]. Nouv Presse Med (1974) 0.89
The human alpha-globin gene. The protein products of the duplicated genes are identical. Eur J Biochem (1980) 0.89
Hemoglobin expression in clones of K562 cell line. Eur J Biochem (1982) 0.89
Globin-chain affinity chromatography on Sepharose-haptoglobin: a new method of study of hemoglobin synthesis in reticulocytes, in bone marrow and in colonies of erythroid precursors. 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
Inhibition of erythrocyte sickling by thiol reagents. Mol Pharmacol (1984) 0.87
Disulfide scrambling of interleukin-2: HPLC resolution of the three possible isomers. Anal Biochem (1986) 0.87
Latent membrane protein 1 suppresses RASSF1A expression, disrupts microtubule structures and induces chromosomal aberrations in human epithelial cells. Oncogene (2006) 0.86
Isolation and characterization of the gene encoding the muscle-specific isozyme of human phosphoglycerate mutase. Gene (1990) 0.86
Genetic regulation of gamma gene expression: study of the interaction of beta-thalassemia with heterocellular HPFH. Hum Genet (1981) 0.85
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
Evidence for three enzymatic activities in one electrophoretic band of 3-phosphoglycerate mutase from red cells. Biochimie (1975) 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
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
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
Amino acid residues involved in the catalytic site of human erythrocyte bisphosphoglycerate mutase. Functional consequences of substitutions of His10, His187 and Arg89. Eur J Biochem (1993) 0.83
Beta-thalassemia and sickle cell disease in culture of early erythroid precursors: hemoglobin synthesis and ultrastructural study. Blood Cells (1981) 0.83
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
Adrenocorticotropin-independent bilateral macronodular adrenal hyperplasia: an unusual cause of Cushing's syndrome. J Clin Endocrinol Metab (1989) 0.83
Hemoglobin C Ziguinchor alphaA2 beta62 (A3) Glu leads to Val beta58 (E2) Pro leads to Arg: the second sickling variant with amino acid substitutions in 2 residues of the beta polypeptide chain. FEBS Lett (1975) 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