Published in Lab Invest on January 01, 1972
Ultrastructural findings in idiopathic recurrent cholestasis. Gut (1972) 0.75
Association of multiple copies of the N-myc oncogene with rapid progression of neuroblastomas. N Engl J Med (1985) 7.79
Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour. Nature (1984) 3.37
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Surface markers and prognostic factors in acute lymphoblastic leukemia. N Engl J Med (1976) 1.64
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Monoclonal antibodies to the human insulin receptor block insulin binding and inhibit insulin action. Proc Natl Acad Sci U S A (1982) 1.57
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Bile secretory apparatus: evidence for a vesicular transport mechanism for proteins in the rat, using horseradish peroxidase and [125I]insulin. Gastroenterology (1980) 1.42
Binding of cholecystokinin to high affinity receptors on isolated rat pancreatic acini. J Biol Chem (1980) 1.41
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Liver transplantation for glycogen storage disease types I, III, and IV. Eur J Pediatr (1999) 1.30
Entry of insulin into human cultured lymphocytes: electron microscope autoradiographic analysis. Science (1978) 1.25
Elevated serum 1,25 dihydroxyvitamin D concentrations in rickets of very low-birth-weight infants. J Pediatr (1981) 1.22
Loss of cyclic 3'5'-AMP dependent kinase and reduction of phosphorylase kinase in skeletal muscle of a girl with deactivated phosphorylase and glycogenosis of liver and muscle. Biochem Biophys Res Commun (1970) 1.22
Cyclic AMP triggers glucagon-like peptide-1 secretion from the GLUTag enteroendocrine cell line. Diabetologia (2007) 1.21
Imbalance of liver phosphorylase and accumulation of hepatic glycogen in a girl with progressive disease of the brain. J Pediatr (1965) 1.20
Dynamic aspects of native DNA structure: kinetics of the formaldehyde reaction with calf thymus DNA. J Mol Biol (1971) 1.19
Variation of proliferative activity in leukemic cell populations of patients with acute leukemia. J Clin Invest (1967) 1.19
Drug effect in acute leukemia. J Clin Invest (1969) 1.18
Relation of arterial stiffness with gestational age and birth weight. Arch Dis Child (2004) 1.17
The hepatic lesion in Reye's syndrome. Gastroenterology (1975) 1.16
Genealogy of cancer in a family. JAMA (1979) 1.15
Phosphorylase kinase of the liver: deficiency in a girl with increased hepatic glycogen. Science (1966) 1.14
Long-term survivors of childhood cancer: evaluation and identification of sequelae of treatment. CA Cancer J Clin (1992) 1.14
Efficacy and tolerability of a Chinese herbal medicine concoction for treatment of atopic dermatitis: a randomized, double-blind, placebo-controlled study. Br J Dermatol (2007) 1.09
Megaloblastic anemia of infancy secondary to maternal pernicious anemia. N Engl J Med (1966) 1.09
Congenital dyserythropoietic anemia type II: ultrastructural and radioautographic studies of blood and bone marrow. Blood (1972) 1.08
Ankle joint synoviography in rheumatoid arthritis. Ann Rheum Dis (1977) 1.07
Prognostic importance of serum ferritin in patients with Stages III and IV neuroblastoma: the Childrens Cancer Study Group experience. Cancer Res (1985) 1.06
Deficient activity of dephosphophosphorylase kinase and accumulation of glycogen in the liver. J Clin Invest (1969) 1.05
Emergency management of dental trauma: knowledge of Hong Kong primary and secondary school teachers. Hong Kong Med J (2012) 1.02
Nutritional vitamin B12 deficiency in an infant. J Pediatr (1969) 1.02
The significance of LMO2 expression in the progression of prostate cancer. J Pathol (2007) 1.02
Sporadic hypoglycemia: abnormal epinephrine response to the ketogenic diet or to insulin. J Pediatr (1971) 1.02
Synthesis of inducible tyrosine aminotransferase in a cell-free extract from cultured hepatoma cells. Proc Natl Acad Sci U S A (1972) 1.02
Transiently reduced activity of carbamyl phosphate synthetase and ornithine transcarbamylase in liver of children with Reye's syndrome. N Engl J Med (1976) 1.01
Alterations of the p15, p16,and p18 genes in osteosarcoma. Cancer Genet Cytogenet (1996) 1.01
Increased serum hexosaminidase in a woman pregnant with fetus affected by mucolipidosis II (I-cell disease) N Engl J Med (1984) 1.01
Insulin receptor monoclonal antibodies that mimic insulin action without activating tyrosine kinase. J Biol Chem (1989) 1.01
Design of fast enzymes by optimizing interaction potential in active site. Proc Natl Acad Sci U S A (1997) 1.01
Alpha 1-antitrypsin phenotype: transient cathodal shift in serum of infant girl with urinary cytomegalovirus and fatty liver. Pediatr Res (1982) 1.00
An evidence base for International Health Regulations: quantitative measurement of the impacts of epidemic disease on international trade. Rev Sci Tech (2005) 1.00
Degradation of insulin by isolated mouse pancreatic acini. Evidence for cell surface protease activity. Diabetes (1984) 1.00
Autoradiographic evidence for hepatic lobular concentration gradient of bile acid derivative. Am J Physiol (1980) 1.00
Glycogen storage disease, types I to X: criteria for morphologic diagnosis. Hum Pathol (1974) 0.99
SOCS1 and SHP1 hypermethylation in mantle cell lymphoma and follicular lymphoma: implications for epigenetic activation of the Jak/STAT pathway. Leukemia (2004) 0.99
Prenatal diagnosis of type-II glycogenosis. Lancet (1970) 0.98
Red-cell-membrane polypeptide aggregates in glucose-6-phosphate dehydrogenase mutants with chronic hemolytic disease. A clue to the mechanism of hemolysis. N Engl J Med (1979) 0.98
Transmission of in-vitro radioresistance in a cancer-prone family. Lancet (1981) 0.97
Congenital and neonatal leukemia. Semin Perinatol (1999) 0.97
Insulin receptors in isolated mouse pancreatic acini. Biochem Biophys Res Commun (1978) 0.97
Coinfection of multiple strains of Epstein-Barr virus in immunocompetent normal individuals: reassessment of the viral carrier state. Blood (2000) 0.96
Prevalence of six types of human papillomavirus in inverted papilloma and papillary transitional cell carcinoma of the bladder: an evaluation by polymerase chain reaction. J Clin Pathol (1997) 0.95
Interactions of a monoclonal antibody to the insulin receptor with receptors for insulin-like growth factors. Endocrinology (1983) 0.95
Idiopathic cardiomyopathy. Mitochondrial and cytoplasmic alterations in heart and liver. Lab Invest (1970) 0.95
Arylsulfatase A in the urine and metachromatic leukodystrophy. J Pediatr (1967) 0.94
Sequence and analysis of promoter region of human insulin-receptor gene. Diabetes (1988) 0.94
Regulating insulin-receptor-gene expression by differentiation and hormones. Diabetes Care (1990) 0.94
Infective endocarditis in childhood: a seven-year experience. Singapore Med J (2004) 0.93
Synchronization and recruitment in acute leukemia. J Clin Invest (1971) 0.93
Comparative analysis of Epstein-Barr virus gene polymorphisms in nasal T/NK-cell lymphomas and normal nasal tissues: implications on virus strain selection in malignancy. Int J Cancer (1999) 0.93
Comparison of the in vitro effect of biguanides and sulfonylureas on insulin binding of its receptors in target cells. J Clin Endocrinol Metab (1982) 0.93
The nuclear envelope. The major site of insulin binding in rat liver nuclei. J Biol Chem (1978) 0.92
Improvement in outcome for children with acute nonlymphocytic leukemia. A report from the Childrens Cancer Study Group. Cancer (1989) 0.92
Congenital pernicious anemia with coexistent transitory intestinal malabsorption of vitamin B12. Blood (1967) 0.92
Glycogen storage diseases. Birth Defects Orig Artic Ser (1976) 0.92
Biochemical and functional abnormalities in lymphocytes from an adenosine deaminase-deficient patient during enzyme replacement therapy. J Clin Invest (1981) 0.91
Statistical mechanics of image restoration and error-correcting codes. Phys Rev E Stat Phys Plasmas Fluids Relat Interdiscip Topics (1999) 0.91
Regulation of insulin-receptor mRNA levels by glucocorticoids. Diabetes (1987) 0.91
Profound carnitine palmitoyltransferase II deficiency. J Pediatr (1994) 0.91
Muscle cell differentiation is associated with increased insulin receptor biosynthesis and messenger RNA levels. J Clin Invest (1989) 0.91
Effects of parenteral L-carnitine supplementation on fat metabolism and nutrition in premature neonates. J Pediatr (1995) 0.90
Chemosensitisation by manganese superoxide dismutase inhibition is caspase-9 dependent and involves extracellular signal-regulated kinase 1/2. Br J Cancer (2008) 0.90
Instrumented PVP-augmented antiglobulin tests. II. Evaluation of acquired hemolytic anemia. Vox Sang (1974) 0.90
Pre- and postnatal pathology, enzyme treatment, and unresolved issues in five lysosomal disorders. Pharmacol Rev (1978) 0.90
Chronic lactic acidosis of infancy. J Pediatr (1970) 0.90
The newborn infant with leukemia. J Pediatr (1997) 0.89
Type VI glycogenosis: biochemical demonstration of liver phosphorylase deficiency. Biochem Biophys Res Commun (1970) 0.89
Frequent epigenetic inactivation of Rb1 in addition to p15 and p16 in mantle cell and follicular lymphoma. Hum Pathol (2007) 0.89
Emergency splenectomy for idiopathic thrombocytopenic purpura in children. J Pediatr Surg (1978) 0.89
Impact of high-dose cytarabine and asparaginase intensification on childhood acute myeloid leukemia: a report from the Childrens Cancer Group. J Clin Oncol (1993) 0.89
Determination of interfacial fracture toughness of bone-cement interface using sandwich Brazilian disks. Eng Fract Mech (2007) 0.88
Evolution of the haemagglutinin gene of the influenza A(H1N1)2009 virus isolated in Hong Kong, 2009-2011. Euro Surveill (2011) 0.88
Rapid prenatal diagnosis of glycogen-storage disease type II by electron microscopy of uncultured amniotic-fluid cells. N Engl J Med (1984) 0.88
Immunological and biochemical profiles in response to transfusion therapy in an adenosine deaminase-deficient patient with severe combined immunodeficiency disease. Clin Immunol Immunopathol (1979) 0.88
Electron microscope autoradiographic analysis of [125I]iodoinsulin entry into adult rat hepatocytes in vivo: evidence for multiple sites of hormone localization. Endocrinology (1981) 0.88
Glycogen storage disease type IX: benign glycogenosis of liver and hepatic phosphorylase kinase deficiency. J Pediatr (1973) 0.87
Myotonia, shortness of stature, and hip dysplasia. Schwartz-Jampel syndrome. Am J Dis Child (1969) 0.87