Published in Isr J Med Sci on March 01, 1977
Calcineurin is a common target of cyclophilin-cyclosporin A and FKBP-FK506 complexes. Cell (1991) 15.76
Weight-reducing effects of the plasma protein encoded by the obese gene. Science (1995) 13.05
A genetic map of the mouse suitable for typing intraspecific crosses. Genetics (1992) 8.53
Nucleotide sequence of a bovine clone encoding the angiogenic protein, basic fibroblast growth factor. Science (1986) 5.12
Compensation to a department of medicine and its faculty members for the teaching of medical students and house staff. N Engl J Med (1996) 4.49
A preliminary classification of the healing potential of medicinal plants, based on a rational analysis of an ethnopharmacological field survey among Bedouins in the Negev desert, Israel. J Ethnopharmacol (1986) 4.03
Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8. Genomics (1991) 3.93
Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1. Nat Genet (1996) 3.58
Validity and reliability of a rating scale for the primary torsion dystonias. Neurology (1985) 3.56
Incremental prognostic value of myocardial perfusion single photon emission computed tomography for the prediction of cardiac death: differential stratification for risk of cardiac death and myocardial infarction. Circulation (1998) 3.43
Human basic fibroblast growth factor: nucleotide sequence and genomic organization. EMBO J (1986) 3.35
Capillary endothelial cells express basic fibroblast growth factor, a mitogen that promotes their own growth. Nature (1987) 3.27
Exercise myocardial perfusion SPECT in patients without known coronary artery disease: incremental prognostic value and use in risk stratification. Circulation (1996) 2.86
Endotoxin and cytokines induce expression of leptin, the ob gene product, in hamsters. J Clin Invest (1996) 2.68
Mental stress and the induction of silent myocardial ischemia in patients with coronary artery disease. N Engl J Med (1988) 2.61
DNA methylation and its possible biological roles. Prog Nucleic Acid Res Mol Biol (1981) 2.55
Characterization of a halobacterial gene affecting bacterio-opsin gene expression. Nucleic Acids Res (1984) 2.37
BRCA1 and BRCA2 mutation analysis of 208 Ashkenazi Jewish women with ovarian cancer. Am J Hum Genet (2000) 2.31
Mouse hematopoietic stem cells. Blood (1991) 2.07
Qualitative study of pregnancy and childbirth experiences in Somalian women resident in Sweden. BJOG (2000) 2.06
Isolation of mutants of Staphylococcus aureus lacking extracellular nuclease activity. J Bacteriol (1970) 2.06
Thyrocalcitonin: inhibitor of bone resorption in tissue culture. Science (1965) 2.03
Torticollis due to cervical epidural abscess and osteomyelitis. Neurology (1992) 2.02
Association among rheumatoid arthritis, oral hygiene, and periodontitis. J Periodontol (2008) 1.99
Family size and children's education in Vietnam. Demography (1998) 1.95
Persistent hyperinsulinemic hypoglycemia of infancy: long-term octreotide treatment without pancreatectomy. J Pediatr (1993) 1.94
Bacterio-opsin mutants of Halobacterium halobium. Proc Natl Acad Sci U S A (1983) 1.91
A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism. Diabetes (1997) 1.86
Lymphocyte development from stem cells. Annu Rev Immunol (1992) 1.82
Dexamethasone and salbutamol in the treatment of acute wheezing in infants. Pediatrics (1983) 1.80
Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews. Hum Mol Genet (1996) 1.76
The cervical aortic arch. Am J Roentgenol Radium Ther Nucl Med (1975) 1.68
Genetic, biochemical, and crystallographic characterization of Fhit-substrate complexes as the active signaling form of Fhit. Proc Natl Acad Sci U S A (1998) 1.68
Effect of arginine on serum-levels of human growth-hormone. Lancet (1965) 1.65
Genetic aspects of clinical endocrinology. Recent Prog Horm Res (1968) 1.64
Beta-lactamase and the resistance of Pseudomonas aeruginosa to various penicillins and cephalosporins. J Gen Microbiol (1970) 1.62
Renal ultrasound findings and vesicoureteral reflux in children hospitalised with urinary tract infection. Arch Dis Child (2002) 1.62
Consensus guidelines for the conduct and reporting of clinical trials in systemic light-chain amyloidosis. Leukemia (2012) 1.60
Characterization of insertions affecting the expression of the bacterio-opsin gene in Halobacterium halobium. Nucleic Acids Res (1984) 1.59
Timing of voiding cystourethrogram in the investigation of urinary tract infections in children. J Pediatr (2001) 1.55
A principal-components approach based on heritability for combining phenotype information. Hum Hered (1999) 1.53
Quantification of rotational thallium-201 myocardial tomography. J Nucl Med (1985) 1.52
The binding of the circumsporozoite protein to cell surface heparan sulfate proteoglycans is required for plasmodium sporozoite attachment to target cells. J Biol Chem (2001) 1.52
Quantitative single photon emission computed thallium-201 tomography for detection and localization of coronary artery disease: optimization and prospective validation of a new technique. J Am Coll Cardiol (1989) 1.51
Familial clustering of seizure types within the idiopathic generalized epilepsies. Neurology (2005) 1.51
Contemporaneous and longitudinal prediction of children's social functioning from regulation and emotionality. Child Dev (1997) 1.47
Spontaneous intracranial hypotension resulting in stupor caused by diencephalic compression. Neurology (1998) 1.46
Hexose uptake and transport in polymorphonuclear leukocytes from patients with glycogen storage disease Ib. Pediatr Res (1990) 1.45
Identification of a cell protein (FIP-3) as a modulator of NF-kappaB activity and as a target of an adenovirus inhibitor of tumor necrosis factor alpha-induced apoptosis. Proc Natl Acad Sci U S A (1999) 1.42
Antibiotic use and risk of ischemic stroke in the elderly. Am J Med (2001) 1.41
The effect of carbenoxolone on the peripheral metabolism of cortisol in human patients. J Lab Clin Med (1993) 1.39
Some endocrine and metabolic aspects of obesity. Annu Rev Med (1970) 1.37
The effect of marker heterozygosity on the power to detect linkage disequilibrium. Genetics (1997) 1.33
Studies on the biological role of DNA methylation. II. Role of phiX174 DNA methylation in the process of viral progeny DNA synthesis. Nucleic Acids Res (1976) 1.33
Localization of the sites mediating desensitization of the beta(2)-adrenergic receptor by the GRK pathway. Mol Pharmacol (2000) 1.32
Patterns of hormonal release after glucose, protein, and glucose plus protein. Lancet (1966) 1.31
Inactivation of the glucose 6-phosphate transporter causes glycogen storage disease type 1b. J Biol Chem (1999) 1.31
Chemokines in the cerebrospinal fluid of patients with meningitis. Clin Immunol Immunopathol (1996) 1.31
Regulation, emotionality, and preschoolers' socially competent peer interactions. Child Dev (1999) 1.30
Hyperglycemia per se (insulin and glucagon withdrawn) can inhibit hepatic glucose production in man. J Clin Endocrinol Metab (1979) 1.28
Secondary biosynthetic defects in women with late-onset congenital adrenal hyperplasia. N Engl J Med (1990) 1.28
Growth hormone and insulin release after arginine: indifference to hyperglycemia and epinephrine. J Clin Endocrinol Metab (1966) 1.27
Hyperinsulinemic hypoglycemia of infancy (nesidioblastosis) in clinical remission: high incidence of diabetes mellitus and persistent beta-cell dysfunction at long-term follow-up. J Clin Endocrinol Metab (1995) 1.27
DNA sequence analysis of a mouse pro alpha 1 (I) procollagen gene: evidence for a mouse B1 element within the gene. Mol Cell Biol (1982) 1.27
Comparison of predicted and experimentally determined secondary structure of adenyl kinase. Nature (1974) 1.21
Thyrocalcitonin and bone resorption. Studies employing a tissue culture bioassay. Am J Med (1967) 1.20
Testosterone deficiency and apathy in Parkinson's disease: a pilot study. J Neurol Neurosurg Psychiatry (2004) 1.20
Identification of a specific site required for rapid heterologous desensitization of the beta-adrenergic receptor by cAMP-dependent protein kinase. Mol Pharmacol (1989) 1.20
A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan origin. J Clin Invest (1991) 1.20
Studies on the biological role of DNA methylation: inhibition of methylation and maturation of the bacteriophage phichi174 by nicotinamide. Nucleic Acids Res (1975) 1.20
Evidence for an important role of glucagon in the regulation of hepatic glucose production in normal man. J Clin Invest (1977) 1.19
Novel mutation in the TOR1A (DYT1) gene in atypical early onset dystonia and polymorphisms in dystonia and early onset parkinsonism. Neurogenetics (2001) 1.18
Familial hyperinsulinism maps to chromosome 11p14-15.1, 30 cM centromeric to the insulin gene. Nat Genet (1994) 1.18
Chromatin-positive Klinefelter's syndrome with undetectable peripheral FSH levels. Am J Med (1975) 1.16
Fc gamma RII/III and CD2 expression mark distinct subpopulations of immature CD4-CD8- murine thymocytes: in vivo developmental kinetics and T cell receptor beta chain rearrangement status. J Exp Med (1993) 1.16
Diazepam in the treatment of strychnine poisoning. Case report. Br J Anaesth (1972) 1.16
Magnesium-induced reversal of vitamin-D resistance in hypoparathyroidism. Lancet (1973) 1.16
Mutations in DYT1: extension of the phenotypic and mutational spectrum. Neurology (2004) 1.15
Multicenter trial validation for quantitative analysis of same-day rest-stress technetium-99m-sestamibi myocardial tomograms. J Nucl Med (1994) 1.14
Plants used for the treatment of diabetes in Israel. J Ethnopharmacol (1987) 1.13
Frequent HHV-6 reactivation in multiple sclerosis (MS) and chronic fatigue syndrome (CFS) patients. J Clin Virol (2000) 1.13
The convergence of neuropsychological testing and clinical ratings of cognitive impairment in patients with schizophrenia. Compr Psychiatry (2001) 1.13
Kinetic, structural, and spectroscopic identification of geminate states of myoglobin: a ligand binding site on the reaction pathway. Biochemistry (1987) 1.13
Networks of coactive neurons in developing layer 1. Neuron (1998) 1.12
A syndrome of apparent mineralocorticoid excess associated with defects in the peripheral metabolism of cortisol. J Clin Endocrinol Metab (1979) 1.12
Plasma growth hormone after arginine infusion. Clinical experiences. N Engl J Med (1967) 1.11
Peripheral subresponsiveness to human growth hormone in the African pygmies. N Engl J Med (1969) 1.11
Activation of cAMP-dependent protein kinase is required for heterologous desensitization of adenylyl cyclase in S49 wild-type lymphoma cells. Proc Natl Acad Sci U S A (1988) 1.11
Incremental prognostic value of adenosine stress myocardial perfusion single-photon emission computed tomography and impact on subsequent management in patients with or suspected of having myocardial ischemia. Am J Cardiol (1997) 1.11
Nephrogenic diabetes insipidus, cystinosis, and vitamin D. Arch Dis Child (1988) 1.10
Social correlates of fetal mortality. Milbank Mem Fund Q (1966) 1.10
Mutations in the human CYP11B2 (aldosterone synthase) gene causing corticosterone methyloxidase II deficiency. Proc Natl Acad Sci U S A (1992) 1.09
Comparative feasibility of separate or simultaneous rest thallium-201/stress technetium-99m-sestamibi dual-isotope myocardial perfusion SPECT. J Nucl Med (1994) 1.09
[Medicine in old age and in the elderly. Educational concepts in area Q7 of the accreditation requirements and its first evaluation by students]. Z Gerontol Geriatr (2005) 1.08
Late reversibility of tomographic myocardial thallium-201 defects: an accurate marker of myocardial viability. J Am Coll Cardiol (1988) 1.07
Selective speech motor, syntax and cognitive deficits associated with bilateral damage to the putamen and the head of the caudate nucleus: a case study. Neuropsychologia (1998) 1.07
Predictors of survival in patients with systemic light-chain amyloidosis and cardiac involvement initially ineligible for stem cell transplantation and treated with oral melphalan and dexamethasone. Br J Haematol (2008) 1.06
Agonist-induced desensitization, internalization, and phosphorylation of the sst2A somatostatin receptor. J Biol Chem (1997) 1.06
Idiopathic inflammatory pseudotumor of the orbit and Tolosa-Hunt syndrome--are they the same disease? J Neurol (2002) 1.05