Published in Immunology on April 01, 1978
An extension of the 51Cr-release assay for the estimation of mouse cytotoxins. Transplantation (1968) 9.80
The dynamic state of the lymphocyte membrane. Factors affecting the distribution and turnover of surface immunoglobulins. Eur J Immunol (1972) 7.05
Antigenic modulation. Loss of TL antigen from cells exposed to TL antibody. Study of the phenomenon in vitro. J Exp Med (1968) 4.63
Immunoglobulin D as a lymphocyte receptor. J Exp Med (1973) 4.62
An approach to the mapping of antigens on the cell surface. Proc Natl Acad Sci U S A (1968) 3.46
Modification of the antigenic structure of the cell membrane by thymus-leukemia (TL) antibody. Proc Natl Acad Sci U S A (1967) 3.26
A new rapid method for genetic typing of human immunoglobulins. J Immunol (1968) 2.61
Immunoglobulin determinants on the lymphocytes of normal rabbits. 3. As4 and As6 determinants on individual lymphocytes and the concept of allelic exclusion. Immunology (1971) 1.54
Surface immunoglobulin on rabbit lymphoid cells. III. Double expression and separate endocytosis of surface immunoglobulin allotypes on heterozygous lymphocytes demonstrated by immunoelectron microscopic labeling. Cell Immunol (1976) 0.93
Modulation and regrowth of allotype on normal rabbit peripheral blood lymphocytes: allelic inclusion of b4 and b6 in single cells. Cell Immunol (1976) 0.88
Regulation of allotype expression in heterozygous rabbits. II. Concomitant suppression of b4 and b6 allotypes in the same cell. Immunology (1978) 0.82
On the origin and direction of replication of the Escherichia coli K12 chromosome. J Mol Biol (1968) 3.46
Biotinidase deficiency: the enzymatic defect in late-onset multiple carboxylase deficiency. Clin Chim Acta (1983) 2.17
Growth inhibition of human tumor cells in athymic mice by anti-epidermal growth factor receptor monoclonal antibodies. Cancer Res (1984) 2.17
A qualitative study of physicians' own wellness-promotion practices. West J Med (2001) 1.88
Monitoring of cellular behaviour by impedance measurements on interdigitated electrode structures. Biosens Bioelectron (1997) 1.83
Phenotypic variation in biotinidase deficiency. J Pediatr (1983) 1.74
Comparative West Nile virus detection in organs of naturally infected American Crows (Corvus brachyrhynchos). Emerg Infect Dis (2001) 1.73
Mutational hotspot in the human biotinidase gene causes profound biotinidase deficiency. Nat Genet (1995) 1.67
Structure of class I major histocompatibility antigens. Contemp Top Mol Immunol (1983) 1.64
Biotinylation of histones by human serum biotinidase: assessment of biotinyl-transferase activity in sera from normal individuals and children with biotinidase deficiency. Biochem Mol Med (1995) 1.64
Expression of multiple functional chemokine receptors and monocyte chemoattractant protein-1 in human neurons. Neuroscience (2000) 1.61
KRAS status and outcome of liver resection after neoadjuvant chemotherapy including bevacizumab. Br J Surg (2012) 1.60
Interleukin 1 activity in normal human urine. J Immunol (1984) 1.56
The characteristics and genetic map location of a temperature sensitive DNA mutant of E. coli K12. Genetics (1972) 1.55
Immunoglobulin determinants on the lymphocytes of normal rabbits. 3. As4 and As6 determinants on individual lymphocytes and the concept of allelic exclusion. Immunology (1971) 1.54
A screening method for biotinidase deficiency in newborns. Clin Chem (1984) 1.46
Relative abuse liability of different benzodiazepines in drug abusers. J Clin Psychopharmacol (1990) 1.45
Radiochemical sequence analysis of biosynthetically labeled proteins. Methods Enzymol (1983) 1.43
Structural transitions of deoxyribonucleic acid in aqueous electrolyte solutions. II. The role of hydration. Biochemistry (1975) 1.39
Ligament length patterns, strength, and rotational axes of the knee joint. Clin Orthop Relat Res (1976) 1.39
Biotinidase deficiency: initial clinical features and rapid diagnosis. Ann Neurol (1985) 1.26
On the origin and direction of replication of the E. coli chromosome. Cold Spring Harb Symp Quant Biol (1968) 1.26
Glycogen storage disease type III (glycogen debranching enzyme deficiency): correlation of biochemical defects with myopathy and cardiomyopathy. Ann Intern Med (1992) 1.25
Contralateral breast cancer: molecular differentiation between metastasis and second primary cancer. Breast Cancer Res Treat (2001) 1.25
Biochemical differences between mutant propionyl-CoA carboxylases from two complementation groups. Am J Hum Genet (1978) 1.25
Clinical heterogeneity in 80 home-reared children with cri du chat syndrome. J Pediatr (1983) 1.24
Structure of the human biotinidase gene. Mamm Genome (1998) 1.23
Purification of human interleukin 1 from human monocyte culture supernatants and identity of thymocyte comitogenic factor, fibroblast-proliferation factor, acute-phase protein-inducing factor, and endogenous pyrogen. Cell Immunol (1985) 1.23
Spondylocostal dysostosis associated with anal and urogenital anomalies in a Mennonite sibship. Am J Med Genet (1981) 1.21
Mutations in the human biotinidase gene that cause profound biotinidase deficiency in symptomatic children: molecular, biochemical, and clinical analysis. Pediatr Res (1997) 1.20
Expression pattern of heme oxygenase isoenzymes 1 and 2 in normal and stress-exposed rat liver. Hepatology (1998) 1.20
The biotin-dependent carboxylase deficiencies. Am J Hum Genet (1982) 1.19
Heterozygote expression in propionyl coenzyme A carboxylase deficiency. Differences between major complementation groups. J Clin Invest (1978) 1.18
New low resolution model for 50S subunit of Escherichia coli ribosomes. Proc Natl Acad Sci U S A (1976) 1.18
Impact of particle size distribution on rheological and textural properties of chocolate models with reduced fat content. J Food Sci (2007) 1.18
Structural transitions of deoxyribonucleic acid in aqueous electrolyte solutions. I. Reference spectra of conformational limits. Biochemistry (1975) 1.17
Mutations in BTD causing biotinidase deficiency. Hum Mutat (2001) 1.16
Effect of a high loading dose of clopidogrel on platelet function in patients undergoing coronary stent placement. Heart (2001) 1.16
Modulation of gastrointestinal function by MuDelta, a mixed µ opioid receptor agonist/ µ opioid receptor antagonist. Br J Pharmacol (2012) 1.16
Expression of the c-erbB-2 gene product (p185) at different stages of neoplastic progression in the colon. Oncogene (1989) 1.15
Human serum biotinidase. cDNA cloning, sequence, and characterization. J Biol Chem (1994) 1.12
Mixed conformations of deoxyribonucleic acid in chromatin: a preliminary report. Proc Natl Acad Sci U S A (1972) 1.12
Deficient biotinidase activity in late-onset multiple carboxylase deficiency. N Engl J Med (1983) 1.12
Biotinidase and its roles in biotin metabolism. Clin Chim Acta (1996) 1.12
Low-dose caffeine discrimination in humans. J Pharmacol Exp Ther (1990) 1.11
Preparation of polymeric protein markers and an investigation of their behavior in sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Biochim Biophys Acta (1970) 1.09
Workshop on inborn errors of metabolism. Prog Clin Biol Res (1982) 1.09
Biotinidase deficiency: accumulation of lactate in the brain and response to physiologic doses of biotin. Neurology (1986) 1.07
Phospholipid hydroperoxide glutathione peroxidase is a selenoenzyme distinct from the classical glutathione peroxidase as evident from cDNA and amino acid sequencing. Free Radic Res Commun (1991) 1.07
The spectrum of neurologic disorder from vitamin E deficiency. Neurology (1986) 1.06
Psychomotor development in 65 home-reared children with cri-du-chat syndrome. J Pediatr (1980) 1.05
Adverse drug reactions. An epidemiological study at psychiatric hospitals. Acta Psychiatr Scand (1984) 1.05
Pulmonary manifestations in HIV seropositivity and malnutrition in Zimbabwe. Arch Dis Child (1997) 1.05
Low-dose caffeine physical dependence in humans. J Pharmacol Exp Ther (1990) 1.04
Clinical findings in four children with biotinidase deficiency detected through a statewide neonatal screening program. N Engl J Med (1985) 1.03
Neurologic symptoms of biotinidase deficiency: possible explanation. Neurology (1985) 1.03
Mutations causing profound biotinidase deficiency in children ascertained by newborn screening in the United States occur at different frequencies than in symptomatic children. Pediatr Res (1999) 1.01
Evidence for three carbohydrate prosthetic groups on mouse histocompatibility antigens H-2Kd and H-2Db. Mol Immunol (1981) 0.99
An unusual case of splenic abscess and sepsis in an immunocompromised host. Am J Clin Pathol (1987) 0.99
Stain intensity of human nucleolus organizer region reflects incorporation of uridine into mature ribosomal RNA. Exp Cell Res (1983) 0.99
Glycogen debranching enzyme deficiency: long-term study of serum enzyme activities and clinical features. J Inherit Metab Dis (1992) 0.98
Nonketotic hyperglycinemia in two retarded adults: a mild form of infantile nonketotic hyperglycinemia. Neurology (1983) 0.97
Partial biotinidase deficiency is usually due to the D444H mutation in the biotinidase gene. Hum Genet (1998) 0.97
EEG complexity and performance measures of creative thinking. Psychophysiology (1999) 0.97
A canine febrile disorder associated with elevated interleukin-6. Clin Immunol Immunopathol (1992) 0.96
Biotinidase deficiency: a novel vitamin recycling defect. J Inherit Metab Dis (1985) 0.96
Kinetic analysis of genetic complementation in heterokaryons of propionyl CoA carboxylase-deficient human fibroblasts. Am J Hum Genet (1980) 0.95
Ophthalmologic findings in biotinidase deficiency. Ophthalmologica (1993) 0.95
Partial biotinidase deficiency: clinical and biochemical features. J Pediatr (1990) 0.95
Mutation (Q456H) is the most common cause of profound biotinidase deficiency in children ascertained by newborn screening in the United States. Biochem Mol Med (1997) 0.95
A mechanism of the irreversible inactivation of bovine pancreatic ribonuclease by diethylpyrocarbonate. A general reaction of diethylpyrocarbonate . A general reaction of diethylpyrocarbonate with proteins. Eur J Biochem (1970) 0.95
Identification of an abundant S-thiolated rat liver protein as carbonic anhydrase III; characterization of S-thiolation and dethiolation reactions. Arch Biochem Biophys (1991) 0.94
Propionic acidemia: a clinical update. J Pediatr (1981) 0.94
Deficient acetyl CoA carboxylase activity in multiple carboxylase deficiency. Clin Chim Acta (1981) 0.94
Microvascular phenomena during pancreatic islet graft rejection. Langenbecks Arch Chir (1991) 0.93
Immunological studies of propionyl CoA carboxylase in livers and fibroblasts of patients with propionic acidemia. Clin Chim Acta (1980) 0.93
Multiple carboxylase deficiency: clinical and biochemical improvement following neonatal biotin treatment. Pediatrics (1981) 0.92
Immunoglobulin determinants on the lymphocytes of normal rabbits. II. Difficulty in demonstrating the a locus determinants As1, 2 and 3 by the mixed antiglobulin reaction. Immunology (1970) 0.92
Nonallelic inheritance of VH region alpha group allotypes: cell surface and serum studies in double and triple expressing rabbits. J Immunol (1979) 0.91
Structural studies on H-2Db and H-2Kd molecules indicate that murine major histocompatibility b and d haplotype alloantigens share structural features. Mol Immunol (1980) 0.91
Dynamics of biomolecules: assignment of local motions by fluorescence anisotropy decay. Biophys J (1998) 0.91
Amino acid sequence of residues 1-98 of the K-2Kb murine major histocompatibility alloantigen: comparison with H-2Kb and H-2db reveals extensive localized differences. Biochemistry (1981) 0.91
Determination of second messengers and protein kinase C in bone marrow derived macrophages stimulated with a bacterial lipopeptide. Mol Immunol (1990) 0.91
Equine leukocyte antigens: relationships with sarcoid tumors and laminitis in two pure breeds. Immunogenetics (1986) 0.91
Human biotinidase isn't just for recycling biotin. J Nutr (1999) 0.91
Double mutation (A171T and D444H) is a common cause of profound biotinidase deficiency in children ascertained by newborn screening the the United States. Mutations in brief no. 128. Online. Hum Mutat (1998) 0.91
Cross-sectional study discloses a positive family history for Parkinson's disease and male gender as epidemiological risk factors for substantia nigra hyperechogenicity. J Neural Transm (Vienna) (2007) 0.91
Characterisation of chocolate eating behaviour. Physiol Behav (2011) 0.90
Immunohistochemical localization of human immunodeficiency virus p24 antigen in placental tissue. Hum Pathol (1992) 0.90
Antibody synthesis in vitro by the rabbit vagina against diphtheria toxoid. Nature (1967) 0.90
Asymptomatic adults and older siblings with biotinidase deficiency ascertained by family studies of index cases. J Inherit Metab Dis (2005) 0.90
Low biotinidase activities in the sera of patients with impaired liver function: evidence that the liver is the source of serum biotinidase. Clin Chim Acta (1990) 0.90
Asymptomatic propionyl CoA carboxylase deficiency in a 13-year-old girl. J Pediatr (1979) 0.89
Theophylline suppresses human alveolar macrophage respiratory burst through phosphodiesterase inhibition. Am J Respir Cell Mol Biol (1994) 0.89
Structural transitions of calf thymus DNA in concentrated LiCl solutions. Biochemistry (1977) 0.89
Distinct high-performance liquid chromatography pattern of transforming growth factor activity in urine of cancer patients as compared with that of normal individuals. Cancer Res (1984) 0.89
Synthesis and evaluation of fluorine-18 labeled glyburide analogs as beta-cell imaging agents. Nucl Med Biol (2004) 0.89