Published in Ann Hum Genet on January 01, 1983
Identification of thymidine nucleotidase and deoxyribonucleotidase activities among normal isozymes of 5'-nucleotidase in human erythrocytes. Proc Natl Acad Sci U S A (1984) 1.02
5'-Nucleotidase activities in human erythrocytes. Identification of a purine 5'-nucleotidase stimulated by ATP and glycerate 2,3-bisphosphate. Biochem J (1988) 0.94
Homogeneous pyrimidine nucleotidase from human erythrocytes: enzymic and molecular properties. Biochem J (1994) 0.75
Why dentists don't use rubber dam during endodontics and how to promote its usage? BMC Oral Health (2016) 0.75
Average heterozygosity per locus in man: an estimate based on the incidence of enzyme polymorphisms. Ann Hum Genet (1972) 4.29
Esterase D: a new human polymorphism. Ann Hum Genet (1973) 3.85
An endothelial receptor for oxidized low-density lipoprotein. Nature (1997) 3.76
Further data on the adenosine deaminase (ADA) polymprphism and a report of a new phenotype. Ann Hum Genet (1969) 3.60
Lactase haplotype diversity in the Old World. Am J Hum Genet (2000) 3.19
Rare phosphoglucomutase phenotypes. Ann Hum Genet (1966) 2.96
Demonstration of a sex difference in recombination fraction in the loose linkage, Rh and PGM. Ann Hum Genet (1972) 2.56
A third phosphoglucomutase locus in man. Ann Hum Genet (1968) 2.37
Inherited variations in human phosphohexose isomerase. Ann Hum Genet (1968) 2.16
Studies on the "insoluble" glycoprotein complex from human colon. Identification of reduction-insensitive MUC2 oligomers and C-terminal cleavage. J Biol Chem (1999) 2.11
The causal element for the lactase persistence/non-persistence polymorphism is located in a 1 Mb region of linkage disequilibrium in Europeans. Ann Hum Genet (2003) 1.96
Nuclear inclusions of the androgen receptor protein in spinal and bulbar muscular atrophy. Ann Neurol (1998) 1.93
Two genetic markers closely linked to adult polycystic kidney disease on chromosome 16. Br Med J (Clin Res Ed) (1986) 1.93
Beta2-adrenoceptor polymorphism and bronchoprotective sensitivity with regular short- and long-acting beta2-agonist therapy. Clin Sci (Lond) (1999) 1.92
The human tumour-associated epithelial mucins are coded by an expressed hypervariable gene locus PUM. Nature (1987) 1.88
Molecular cloning of cDNAs derived from a novel human intestinal mucin gene. Biochem Biophys Res Commun (1990) 1.88
The human glutathione S-transferases: studies on the tissue distribution and genetic variation of the GST1, GST2 and GST3 isozymes. Ann Hum Genet (1984) 1.85
The incidence of rare alleles determining electrophoretic variants: data on 43 enzyme loci in man. Ann Hum Genet (1974) 1.85
Investigation and management of chronic cough using a probability-based algorithm. Eur Respir J (2005) 1.82
Developmental changes and polymorphism in human alcohol dehydrogenase. Ann Hum Genet (1971) 1.79
Rapid formation of secondary structure framework in protein folding studied by stopped-flow circular dichroism. FEBS Lett (1987) 1.70
Effect of different methods of internal thoracic artery harvest on pulmonary function. Ann Thorac Surg (1997) 1.65
Firearm injuries. Br J Surg (1967) 1.59
Inherited variants of human nucleoside phosphorylase. Ann Hum Genet (1971) 1.55
Characterisation of human cell lines and differentiation from HeLa by enzyme typing. Nature (1976) 1.53
Polymorphism and the subunit structure of enzymes: a contribution to the neutralist-selectionist controversy. Proc Natl Acad Sci U S A (1977) 1.53
Adenosine deaminase isozymes in human tissues. Ann Hum Genet (1971) 1.50
Human mucin genes assigned to 11p15.5: identification and organization of a cluster of genes. Genomics (1996) 1.48
Usefulness of serum procalcitonin levels in pulmonary tuberculosis. Eur Respir J (2010) 1.48
Molecular study of eight Japanese cases of glucose-6-phosphate dehydrogenase deficiency by nonradioisotopic single-strand conformation polymorphism analysis. Blood (1994) 1.46
Chromosome assignment of some human enzyme loci: mitochondrial malate dehydrogenase to 7, mannosephosphate isomerase and pyruvate kinase to 15 and probably, esterase D to 13. Ann Hum Genet (1975) 1.45
Human gene mapping using an X/autosome translocation. Somatic Cell Genet (1976) 1.44
Haptoglobin therapy for acute favism: a Japanese boy with glucose-6-phosphate dehydrogenase Guadalajara. Br J Haematol (1995) 1.42
Identical point mutations of the R-type pyruvate kinase (PK) cDNA found in unrelated PK variants associated with hereditary hemolytic anemia. Blood (1992) 1.39
Genetics and mode of expression of temperature-sensitive mutations arresting embryonic development in Caenorhabditis elegans. Dev Biol (1980) 1.39
The genetically programmed down-regulation of lactase in children. Gastroenterology (1998) 1.37
Upregulated EMMPRIN/CD147 might contribute to growth and angiogenesis of gastric carcinoma: a good marker for local invasion and prognosis. Br J Cancer (2006) 1.36
Cholesterol oxidation switches the internalization pathway of endothelin receptor type A from caveolae to clathrin-coated pits in Chinese hamster ovary cells. J Biol Chem (2000) 1.36
Genetic polymorphism of human phosphoglycolate phosphatase (PGP). Ann Hum Genet (1978) 1.31
Alcohol dehydrogenase isozymes in adult human stomach and liver: evidence for activity of the ADH 3 locus. Ann Hum Genet (1972) 1.31
Characterization of a mucin cDNA clone isolated from HT-29 mucus-secreting cells. The 3' end of MUC5AC? J Biol Chem (1995) 1.29
The detection and differentiation of the products of the human carbonic anhydrase loci, CAI and CAII using fluorogenic substrates. Ann Hum Genet (1974) 1.28
Human adenylate kinase deficiency associated with hemolytic anemia. A single base substitution affecting solubility and catalytic activity of the cytosolic adenylate kinase. J Biol Chem (1989) 1.27
A single nucleotide base transition is the basis of the common human glucose-6-phosphate dehydrogenase variant A (+). Genomics (1987) 1.27
The distributions of subunit numbers and subunit sizes of enzymes: a study of the products of 100 human gene loci. Ann Hum Genet (1976) 1.27
Immunochemical analysis of the N-acetyl hexosaminidases in human-mouse hybrids made using a double selective system. Cytogenet Cell Genet (1977) 1.26
Assignment of the human locus determining phosphoglycolate phosphatase (PGP) to chromosome 16. Ann Hum Genet (1980) 1.26
Involvement of a gene on chromosome 9 in human fibroblast interferon production. Nature (1979) 1.26
The lactase persistence/non-persistence polymorphism is controlled by a cis-acting element. Hum Mol Genet (1995) 1.24
The human glutathione S-transferases: developmental aspects of the GST1, GST2, and GST3 loci. Biochem Genet (1985) 1.23
Evidence for a second "structural" locus determining human phosphoglucomutase. Nature (1965) 1.23
Variable number tandem repeat polymorphism of the mucin genes located in the complex on 11p15.5. Hum Genet (1998) 1.20
Studies on the properties of the human alcohol dehydrogenase isozymes determined by the different loci ADH1, ADH2, ADH3. Ann Hum Genet (1973) 1.20
Distribution of glucose-6-phosphate dehydrogenase mutations in Southeast Asia. Hum Genet (2001) 1.20
Thyroid hormone induces metamorphosis of flounder larvae. Gen Comp Endocrinol (1985) 1.19
Expression of ErbB receptors and mucins in the airways of long term current smokers. Thorax (2004) 1.18
Determinants of survival after inferior vena cava trauma. Am Surg (1999) 1.18
Deletion mapping: further evidence for the location of acid phosphatase (ACP1) within 2p23. Am J Med Genet (1979) 1.16
Genetic analysis of the 15;17 chromosome translocation associated with acute promyelocytic leukemia. Proc Natl Acad Sci U S A (1983) 1.16
Disease recurrence patterns after R0 resection of hilar cholangiocarcinoma. Br J Surg (2010) 1.15
Genetic regulation of MUC1 alternative splicing in human tissues. Br J Cancer (2008) 1.14
The human homolog T of the mouse T(Brachyury) gene; gene structure, cDNA sequence, and assignment to chromosome 6q27. Genome Res (1996) 1.13
Acid alpha-glucosidase: a new polymorphism in man demonstrable by 'affinity' electrophoresis. Ann Hum Genet (1975) 1.12
Dihydropyridine type calcium channel blocker-induced turbid dialysate in patients undergoing peritoneal dialysis. Clin Nephrol (1998) 1.11
DNA test for hypolactasia premature. Gut (2006) 1.10
Differences between the N-acetyl hexosaminidase isozymes in serum and tissues. Ann Hum Genet (1974) 1.09
New monoclonal antibodies to non-glycosylated domains of the secreted mucins MUC5B and MUC7. Hybrid Hybridomics (2003) 1.09
Multiple transcripts of MUC3: evidence for two genes, MUC3A and MUC3B. Biochem Biophys Res Commun (2000) 1.09
Phosphoglucomutase 1: complete human and rabbit mRNA sequences and direct mapping of this highly polymorphic marker on human chromosome 1. Proc Natl Acad Sci U S A (1992) 1.08
Activity of the "red cell" acid phosphatase locus in other tissues. Ann Hum Genet (1973) 1.08
MUC3 human intestinal mucin. Analysis of gene structure, the carboxyl terminus, and a novel upstream repetitive region. J Biol Chem (1997) 1.08
Allergic bronchopulmonary aspergillosis in cystic fibrosis. Eur Respir J (2001) 1.08
Concomitant caudate lobe resection as an option for donor hepatectomy in adult living related liver transplantation. Transplantation (1998) 1.08
Palmitoylation of human endothelinB. Its critical role in G protein coupling and a differential requirement for the cytoplasmic tail by G protein subtypes. J Biol Chem (1997) 1.06
Polymorphism of human mucin genes in chest disease: possible significance of MUC2. Am J Respir Cell Mol Biol (2000) 1.06
Characterization of human carbonic anhydrase III from skeletal muscle. Biochem Genet (1979) 1.05
Human FAD-dependent NAD(P)H diaphorase. Biochem J (1980) 1.05
Lactate dehydrogenase A-subunit and B-subunit deficiencies: comparison of the physiological roles of LDH isozymes. Isozymes Curr Top Biol Med Res (1983) 1.05
The investigation of reactive sulphydryls in enzymes and their variants by starch gel electrophoresis. Studies on red cell adenosine deaminase. Ann Hum Genet (1969) 1.04
Mycotic aneurysm of the left coronary artery. Ann Thorac Surg (1998) 1.04
MUC1 gene polymorphism in the gastric carcinogenesis pathway. Eur J Hum Genet (2001) 1.04
Hereditary triosephosphate isomerase (TPI) deficiency: two severely affected brothers one with and one without neurological symptoms. Hum Genet (1993) 1.03
Studies on the subunit structure and molecular size of the human alcohol dehydrogenase isozymes determined by the different loci, ADH1, ADH2, and ADH3. Ann Hum Genet (1973) 1.03
Linkage data on Rh, PGM1, PGD, Peptidase C and Fy from family studies. Ann Hum Genet (1973) 1.03
Allelic association and recombination hotspots in the mucin gene (MUC) complex on chromosome 11p15.5. Ann Hum Genet (2007) 1.03
Contribution of functional variation in the IL13 gene to allergy, hay fever and asthma in the NSHD longitudinal 1946 birth cohort. Allergy (2009) 1.02
Abnormal oesophageal motility in patients with chronic cough. Thorax (2003) 1.02
A phylogenetic approach to the identification of phosphoglucomutase genes. Mol Biol Evol (1998) 1.02
Binding of N-acetyl-chitotriose to human lysozyme. J Biochem (1975) 1.02
Genetic polymorphism of MUC7: allele frequencies and association with asthma. Eur J Hum Genet (2001) 1.02
Lactase haplotype frequencies in Caucasians: association with the lactase persistence/non-persistence polymorphism. Ann Hum Genet (1998) 0.99
Activation of two types of Ca2+-permeable nonselective cation channel by endothelin-1 in A7r5 cells. Br J Pharmacol (1998) 0.99
Regulation of expression of liver-specific enzymes. III. Further analysis of a series of rat hepatoma X human somatic cell hybrids. Ann Hum Genet (1982) 0.99
A high dose of albuterol does not overcome bronchoprotective subsensitivity in asthmatic subjects receiving regular salmeterol or formoterol. J Allergy Clin Immunol (1999) 0.98
Activation of three types of voltage-independent Ca2+ channel in A7r5 cells by endothelin-1 as revealed by a novel Ca2+ channel blocker LOE 908. Br J Pharmacol (1999) 0.98
Mapping recombination hotspots in human phosphoglucomutase (PGM1). Hum Mol Genet (1999) 0.98
Human M2-type pyruvate kinase: cDNA cloning, chromosomal assignment and expression in hepatoma. Gene (1988) 0.98
Suppression of mixed lymphocyte reaction by cells of human first trimester pregnancy endometrium. J Reprod Immunol (1985) 0.98
Initial effects of the left ventricular repair by plication may not last long in a rat ischemic cardiomyopathy model. Circulation (2001) 0.98
Mapping of the gene coding for the human GM2 activator protein to chromosome 5. Ann Hum Genet (1985) 0.98