Published in Endocrinology on October 01, 1976
An investigation of sites that bind human somatotropin (growth hormone) in the liver of the pregnant rabbit. Biochem J (1981) 1.10
Characterization of human somatotropin binding to detergent-solubilized lactogenic receptors from rat liver. Biochem J (1981) 0.87
Purification of a prolactin receptor. Proc Natl Acad Sci U S A (1982) 0.85
Heterogeneity of growth-hormone receptors detected with monoclonal antibodies to human growth hormone. Biochem J (1987) 0.83
Characterization of prolactin binding by membrane preparations from rat liver. Biochem J (1979) 0.81
Lactogenic and somatogenic binding sites in intact and detergent-solubilized membrane preparations of female rat liver. Biochem J (1988) 0.79
Bovine growth hormone induces oscillations in cytosolic free Ca2+ in single rat hepatocytes. Biochem J (1996) 0.78
Human somatotropin binding to rabbit kidney microsomal fraction. Biochem J (1981) 0.77
Role of the hypothalamo-pituitary-liver axis in sex differences in susceptibility of the liver to toxic agents. Environ Health Perspect (1981) 0.77
Formation of complexes between 125I-labelled human or bovine somatotropins and binding proteins in vivo in rat liver and kidney. Biochem J (1983) 0.77
Characterization of hepatic lactogen receptor. Subcellular distribution and characterization of N-linked carbohydrate chains. Biochem J (1989) 0.75
Binding in vitro to rat liver receptors does not correlate with activities in vivo of bovine somatotropin. Use of chemically modified derivatives as probes. Biochem J (1984) 0.75
Ligand: a versatile computerized approach for characterization of ligand-binding systems. Anal Biochem (1980) 28.03
Simultaneous analysis of families of sigmoidal curves: application to bioassay, radioligand assay, and physiological dose-response curves. Am J Physiol (1978) 13.02
Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome. Nat Genet (1997) 4.95
Incidence of diabetes mellitus and impaired glucose tolerance in children and adolescents receiving growth-hormone treatment. Lancet (2000) 4.34
Estimation of molecular radius, free mobility, and valence using polyacylamide gel electrophoresis. Anal Biochem (1971) 3.98
Statistical quality control and routine data processing for radioimmunoassays and immunoradiometric assays. Clin Chem (1974) 3.97
Rapid calculation of radioimmunoassay results. J Lab Clin Med (1969) 2.93
Polyacrylamide gel electrophoresis in sodium dodecyl sulfate-containing buffers using multiphasic buffer systems: properties of the stack, valid Rf- measurement, and optimized procedure. Anal Biochem (1977) 2.63
Familial hyperinsulinism caused by an activating glucokinase mutation. N Engl J Med (1998) 2.57
Polyacrylamide gel electrophoresis. Science (1971) 2.43
Statistical quality control of radioimmunoassays. J Clin Endocrinol Metab (1968) 2.41
Computer analysis of radioligand assay and radioimmunoassay data. Acta Endocrinol Suppl (Copenh) (1970) 2.36
Familial hyperinsulinism with apparent autosomal dominant inheritance: clinical and genetic differences from the autosomal recessive variant. J Pediatr (1998) 2.33
A syndrome of congenital hyperinsulinism and hyperammonemia. J Pediatr (1997) 2.15
Transport of steroid hormones: binding of 21 endogenous steroids to both testosterone-binding globulin and corticosteroid-binding globulin in human plasma. J Clin Endocrinol Metab (1981) 2.07
Horizontal stomach: a new sonographic clue to the antenatal diagnosis of right-sided congenital diaphragmatic hernia. Ultrasound Obstet Gynecol (2013) 2.00
A versatile method for simultaneous analysis of families of curves. FASEB J (1988) 1.97
Characterization of the human growth hormone receptor gene and demonstration of a partial gene deletion in two patients with Laron-type dwarfism. Proc Natl Acad Sci U S A (1989) 1.95
Unified theory for gel electrophoresis and gel filtration. Proc Natl Acad Sci U S A (1970) 1.92
Statistical analysis of radioligand assay data. Methods Enzymol (1975) 1.91
Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levels. Pediatr Res (1983) 1.91
A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism. Diabetes (1997) 1.86
Mathematical analysis of kinetics of radioligand assays: improved sensitivity obtained by delayed addition of labeled ligand. J Clin Endocrinol Metab (1971) 1.86
Recommendations for the diagnosis and management of Turner syndrome. J Clin Endocrinol Metab (2001) 1.84
Pituitary and gonadal hormones in women during spontaneous and induced ovulatory cycles. Recent Prog Horm Res (1970) 1.82
Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews. Hum Mol Genet (1996) 1.76
Genetic deficiency of medium-chain acyl coenzyme A dehydrogenase: studies in cultured skin fibroblasts and peripheral mononuclear leukocytes. Pediatr Res (1985) 1.75
Inhibition of coronary artery atherosclerosis by 17-beta estradiol in ovariectomized monkeys. Lack of an effect of added progesterone. Arteriosclerosis (1990) 1.73
The causes of neonatal hypoglycemia. N Engl J Med (1999) 1.68
Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. Am J Gastroenterol (1996) 1.66
Short- and long-term use of octreotide in the treatment of congenital hyperinsulinism. J Pediatr (1993) 1.65
Pelvic ultrasonography: early differentiation between isolated premature thelarche and central precocious puberty. Eur J Pediatr (1995) 1.61
Growth and symptoms in Silver-Russell syndrome: review on the basis of 386 patients. Eur J Pediatr (1995) 1.59
Regulation of gal messenger ribonucleic acid synthesis in Escherichia coli by 3',5'-cyclic adenosine monophosphate. J Biol Chem (1971) 1.58
Insulin-like growth factor binding protein-1 levels in the diagnosis of hypoglycemia caused by hyperinsulinism. J Pediatr (1997) 1.58
Cortical bone density is normal in prepubertal children with growth hormone (GH) deficiency, but initially decreases during GH replacement due to early bone remodeling. J Clin Endocrinol Metab (2003) 1.57
Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemia. Pediatr Res (1985) 1.56
Integrin-mediated action of insulin-like growth factor binding protein-2 in tumor cells. J Mol Endocrinol (2004) 1.55
The plasma growth hormone response to insulin-induced hypoglycemia in children with retardation of growth. Pediatrics (1967) 1.53
Optic nerve hypoplasia: absence of posterior pituitary bright signal on magnetic resonance imaging correlates with diabetes insipidus. Am J Ophthalmol (1996) 1.53
Linkage-disequilibrium mapping without genotyping. Nat Genet (1998) 1.52
Mutations in PROP1 cause familial combined pituitary hormone deficiency. Nat Genet (1998) 1.51
Intellectual outcome at 12 years of age in congenital hypothyroidism. Eur J Endocrinol (1999) 1.50
Enhanced inhibition of thymidylate synthase by methotrexate polyglutamates. J Biol Chem (1985) 1.49
Genotype and phenotype correlations in 417 children with congenital hyperinsulinism. J Clin Endocrinol Metab (2012) 1.49
Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine. N Engl J Med (1988) 1.49
Double vagina, cardiac, pulmonary, and other genital malformations with 46,XY karyotype. Am J Med Genet (1991) 1.49
Lipophilic thiamine treatment in long-standing insulin-dependent diabetes mellitus. Acta Diabetol (1999) 1.48
An IgG-Fc binding protein in seminal fluid. Am J Reprod Immunol (1983) 1.48
Dual regulation of insulin-like growth factor binding protein-1 levels by insulin and cortisol during fasting. J Clin Endocrinol Metab (1998) 1.48
Turner syndrome: spontaneous growth in 150 cases and review of the literature. Eur J Pediatr (1983) 1.48
Isolation of the gal repressor. Proc Natl Acad Sci U S A (1971) 1.47
Growth hormone responses to propranolol-glucagon stimulation: a comparison with other tests of growth hormone reserve. J Clin Endocrinol Metab (1973) 1.46
Mutation of the POU-specific domain of Pit-1 and hypopituitarism without pituitary hypoplasia. Science (1992) 1.45
Decreased oxygenation and hyperlipemia during intravenous fat infusions in premature infants. Pediatrics (1980) 1.45
Incidence of IDDM in German children aged 0-14 years. A 6-year population-based study (1987-1993) Diabetes Care (1997) 1.44
Sudden neonatal death in carnitine transporter deficiency. J Pediatr (1997) 1.43
Growth hormone insufficiency in a girl with the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy. J Endocrinol Invest (1999) 1.43
Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndrome. J Pediatr (2001) 1.42
Hyperinsulinism/hyperammonemia syndrome in children with regulatory mutations in the inhibitory guanosine triphosphate-binding domain of glutamate dehydrogenase. J Clin Endocrinol Metab (2001) 1.42
Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. Hepatology (1994) 1.41
Thrombocytosis in congenital adrenal hyperplasia at diagnosis. Clin Pediatr (Phila) (1996) 1.40
Spontaneous growth and bone age development in a patient with 17alpha-hydroxylase deficiency: evidence of the role of sexual steroids in prepubertal bone maturation. J Pediatr (1999) 1.39
Massive hepatomegaly, steatosis, and secondary plasma carnitine deficiency in an infant with cystic fibrosis. Pediatrics (1989) 1.39
Fractionation and characterization of an oligomeric series of bovine keratohyalin by polyacrylamide gel electrophoresis. Anal Biochem (1971) 1.39
Regulation of galactokinase synthesis by cyclic adenosine 3',5'-monophosphate in cell-free extracts of Escherichia coli. J Biol Chem (1971) 1.38
Mathematical theory of cross-reactive radioimmunoassay and ligand-binding systems of equilibrium. Anal Biochem (1972) 1.37
Genetic analysis of familial isolated growth hormone deficiency type I. J Clin Invest (1982) 1.36
Hyperinsulinism in infancy: diagnosis by demonstration of abnormal response to fasting hypoglycemia. Pediatrics (1976) 1.35
A specific radioimmunoassay for the growth hormone (GH)-dependent somatomedin-binding protein: its use for diagnosis of GH deficiency. J Clin Endocrinol Metab (1990) 1.35
Glycemic response to glucagon during fasting hypoglycemia: an aid in the diagnosis of hyperinsulinism. J Pediatr (1980) 1.34
Guidelines for immunoassay data processing. Clin Chem (1985) 1.33
Mitochondrial carnitine-acylcarnitine translocase deficiency presenting as sudden neonatal death. J Pediatr (1997) 1.32
Familial and sporadic hyperinsulinism: histopathologic findings and segregation analysis support a single autosomal recessive disorder. J Pediatr (1991) 1.30
Structures of bovine glutamate dehydrogenase complexes elucidate the mechanism of purine regulation. J Mol Biol (2001) 1.29
Number of receptor sites from Scatchard and Klotz graphs: a constructive critique. Science (1983) 1.27
Instability of pH gradients formed by isoelectric focusing in polyacrylamide gel. Ann N Y Acad Sci (1973) 1.27
Detection and characterization of peaks and estimation of instantaneous secretory rate for episodic pulsatile hormone secretion. Comput Biomed Res (1986) 1.26
Chromosomal assignment of human sequences encoding arginine vasopressin-neurophysin II and growth hormone releasing factor. Somat Cell Mol Genet (1985) 1.24
Serum levels of insulin-like growth factor I (IGF-I) and IGF binding protein 3 reflect spontaneous growth hormone secretion. J Clin Endocrinol Metab (1993) 1.24
Compared with dietary monounsaturated and saturated fat, polyunsaturated fat protects African green monkeys from coronary artery atherosclerosis. Arterioscler Thromb Vasc Biol (1995) 1.23
Insulin-like growth factor binding protein-2 binding to extracellular matrix plays a critical role in neuroblastoma cell proliferation, migration, and invasion. Endocrinology (2005) 1.22
An exact correction to the "Cheng-Prusoff" correction. J Recept Res (1988) 1.22
Serpentine fibula--polycystic kidney syndrome and Melnick-Needles syndrome are different disorders. Eur J Pediatr (1993) 1.22
Randomised, double-blind, placebo-controlled trial of human recombinant growth hormone in patients with chronic heart failure due to dilated cardiomyopathy. Lancet (1998) 1.22
Automated computer analysis for enzyme-multiplied immunological techniques. Clin Chem (1977) 1.20
Statistical characterization of the random errors in the radioimmunoassay dose--response variable. Clin Chem (1976) 1.20
Reference intervals from birth to adulthood for serum thyroxine (T4), triiodothyronine (T3), free T3, free T4, thyroxine binding globulin (TBG) and thyrotropin (TSH). Clin Chem Lab Med (2001) 1.20
Primary carnitine deficiency due to a failure of carnitine transport in kidney, muscle, and fibroblasts. N Engl J Med (1988) 1.19
Computer simulation of plasma insulin and glucose dynamics after subcutaneous insulin injection. Diabetes Care (1990) 1.19
Statistical estimation of the minimal detectable concentration ("sensitivity") for radioligand assays. Anal Biochem (1978) 1.19
Dimeric tetrapeptide enkephalins display extraordinary selectivity for the delta opiate receptor. Nature (1982) 1.18
Familial hyperinsulinism maps to chromosome 11p14-15.1, 30 cM centromeric to the insulin gene. Nat Genet (1994) 1.18
Drug efficacy at guanine nucleotide-binding regulatory protein-linked receptors: thermodynamic interpretation of negative antagonism and of receptor activity in the absence of ligand. Mol Pharmacol (1992) 1.18
Theory of protein-ligand interaction. Methods Enzymol (1975) 1.18
Longitudinal gonadal function after bone marrow transplantation for acute lymphoblastic leukemia during childhood. Pediatr Transplant (1999) 1.18
Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy. Hum Genet (1997) 1.18
The ratio between serum levels of insulin-like growth factor (IGF)-I and the IGF binding proteins (IGFBP-1, 2 and 3) decreases with age in healthy adults and is increased in acromegalic patients. Clin Endocrinol (Oxf) (1994) 1.17