Published in J Med Genet on April 01, 1976
Urinary amylase/urinary creatinine ratio (uAm/uCr)--a less-invasive parameter for management of hyperamylasemia. BMC Pediatr (2013) 0.83
Low serum amylase and obesity, diabetes and metabolic syndrome: A novel interpretation. World J Diabetes (2016) 0.81
Amylase polymorphism. J Med Genet (1977) 0.75
DISC ELECTROPHORESIS. II. METHOD AND APPLICATION TO HUMAN SERUM PROTEINS. Ann N Y Acad Sci (1964) 127.96
Salivary and pancreatic amylase: electrophoretic characterizations and genetic studies. Am J Hum Genet (1973) 3.12
Amylase heterogeneity. Some genetik and clinical aspects. Humangenetik (1965) 1.78
Human amylase loci: genetic linkage with the Duffy blood group locus and assignment to linkage group I. Am J Hum Genet (1973) 1.38
Human salivary amylase: genetics of electrophoretic variants. Am J Hum Genet (1971) 1.33
Evidence for close linkage of human amylase loci. Nat New Biol (1972) 1.32
Further studies on the structural differences between the isoenzymes of human parotid -amylase. Biochemistry (1971) 1.10
Evidence for post-transcriptional modification of human salivary amylase (amyl) isozymes. Biochem Genet (1973) 1.06
[Development of salivary and pancreatic amylase in children during the 1st year of life]. Z Klin Chem Klin Biochem (1970) 1.00
Digestibility of starches in infants and children. J Pediatr (1975) 0.93
Human amniotic fluid isoamylases. Functional development of fetal pancreas and salivary glands. Obstet Gynecol (1973) 0.91
Antenatal development of amylase isoenzymes. J Med Genet (1972) 0.86
Linkage group I: the simultaneous estimation of recombination and interference. Birth Defects Orig Artic Ser (1976) 8.63
Salivary and pancreatic amylase: electrophoretic characterizations and genetic studies. Am J Hum Genet (1973) 3.12
Osteopetrosis. A clinical, genetic, metabolic, and morphologic study of the dominantly inherited, benign form. Medicine (Baltimore) (1968) 2.39
Hepatitis A outbreaks among illicit drug users and their contacts in Queensland, 1997. Med J Aust (1999) 2.05
Holoprosencephaly: birth data, benetic and demographic analyses of 30 families. Birth Defects Orig Artic Ser (1975) 1.40
Human amylase loci: genetic linkage with the Duffy blood group locus and assignment to linkage group I. Am J Hum Genet (1973) 1.38
Hyperamylasemia in diabetic ketoacidosis: sources and significance. Ann Intern Med (1979) 1.36
Human salivary amylase: genetics of electrophoretic variants. Am J Hum Genet (1971) 1.33
Evidence for close linkage of human amylase loci. Nat New Biol (1972) 1.32
Ring chromosome 18 in a patient with multiple anomalies. J Med Genet (1967) 1.30
Simplified method for collection of pure submandibular saliva in large volumes. J Dent Res (1968) 1.28
Two contiguous outbreaks of dengue type 2 in north Queensland. Med J Aust (1998) 1.26
Partial trisomy 1 due to a "shift" and probable location of the Duffy (Fy) locus. Am J Hum Genet (1977) 1.23
The hepatitis knowledge base (short form). Ann Intern Med (1980) 1.22
Genetic family history questionnaire. J Med Genet (1978) 1.21
Localization of the human salivary protein complex (SPC) to chromosome band 12p13.2. Cytogenet Cell Genet (1985) 1.19
Female preference for male saliva: implications for sexual isolation of Mus musculus subspecies. Evolution (2001) 1.12
A procedure for the electrophoretic analysis of phosphoenolpyruvate carboxylase. Biochim Biophys Acta (1973) 1.11
A syndrome of bizarre vertebral anomalies. J Pediatr (1966) 1.10
Evidence for post-transcriptional modification of human salivary amylase (amyl) isozymes. Biochem Genet (1973) 1.06
Genetic control of the eighth component of complement. J Clin Invest (1979) 1.03
Immunological relationships and post-translational modification of human salivary amylase (Amy) and pancreatic amylase (Amy) isozymes. Biochem Genet (1974) 1.03
Familial myocardial disease with and without obstruction to left ventricular outflow. Clinical, hemodynamic, and angiographic findings. Circulation (1967) 1.03
Cystic fibrosis: population genetics. Tex Rep Biol Med (1973) 1.02
A complementary DNA sequence that predicts a human pancreatic amylase primary structure consistent with the electrophoretic mobility of the common isozyme, Amy2 A. Mol Biol Med (1984) 1.01
The comparative biochemistry, physiology, and genetics of animal alpha-amylases. Adv Comp Physiol Biochem (1978) 1.00
Linkage relationships and multipoint mapping of the human parotid salivary proteins (Pr, Pa, Db). Am J Hum Genet (1980) 1.00
Partial purification and characterization of a polymorphic protein (Pa) in human parotid saliva. Am J Hum Genet (1975) 0.99
Linkage group I: a statistically significant locus order from family studies. Cytogenet Cell Genet (1978) 0.99
Genetic studies of human acidic salivary protein (Pa). Am J Hum Genet (1975) 0.97
The tissue source and cellular control of the apparent size of androgen binding protein (Abp), a mouse salivary protein whose electrophoretic mobility is under the control of sex-limited saliva pattern (Ssp). Biochem Genet (1983) 0.95
The genes for mouse salivary androgen-binding protein (ABP) subunits alpha and gamma are located on chromosome 7. Genetics (1987) 0.93
Confirmation of genetic heterogeneity in autosomal dominant forms of congenital cataracts from linkage studies. Cytogenet Cell Genet (1978) 0.93
Production of an antibody to mouse salivary androgen binding protein (ABP) and its use in identifying a prostate protein produced by a gene distinct from Abp. Biochem Genet (1986) 0.92
Characterization of the amino termini of mouse salivary and pancreatic amylases. FEBS Lett (1981) 0.91
Autosomal dominant "spheroid body myopathy". Muscle Nerve (1979) 0.91
Human parotid proline-rich proteins: correlation of genetic polymorphisms to dental caries. Genet Epidemiol (1986) 0.90
An evaluation of the usefulness of amylase isozyme differentiation in patients with hyperamylasemia. Am J Clin Pathol (1976) 0.90
Multiple gene action determining a mouse salivary protein phenotype: identification of the structural gene for androgen binding protein (Abp). Biochem Genet (1984) 0.89
The microevolution of mouse salivary androgen-binding protein (ABP) paralleled subspeciation of Mus musculus. J Hered (1997) 0.88
Linkage relationships of 1qh to Amy, Fy, PGM1, and Rh. Birth Defects Orig Artic Ser (1975) 0.88
Identification of a human salivary amylase gene. Partial sequence of genomic DNA suggests a mode of regulation different from that of mouse, Amy1. Mol Biol Med (1987) 0.87
Urinary pepsinogen isozymes: a highly polymorphic locus in man. Hum Genet (1979) 0.85
Hyperammonemia after transurethral resection of the prostate: a report of 2 cases. J Urol (1984) 0.85
The human salivary protein complex (SPC): a large block of related genes. Am J Hum Genet (1985) 0.84
Linkage group I: the simultaneous estimation of recombination and interference. Cytogenet Cell Genet (1976) 0.84
The tissue origins of serum and urinary alpha-amylase. Arch Biochem Biophys (1976) 0.84
Linkage relationships of the proline-rich salivary proteins (Pr, Pa, Db). Cytogenet Cell Genet (1978) 0.83
Human salivary proline-rich (Pr) proteins: a posttranslational derivation of the phenotypes. Biochem Genet (1979) 0.81
A rapid spectrophotometric method for the determination of esterase activity. J Biochem Biophys Methods (1980) 0.81
Immunological relationships and a genetic interpretation of major and minor acidic proteins in human parotid saliva. Biochem Genet (1977) 0.81
Chromosome 6: linkage of the eighth component of complement (C8) to the histocompatibility region (HLA). Cytogenet Cell Genet (1976) 0.80
Heritable salivary proteins and dental disease. Hum Hered (1980) 0.80
Pancreatic and salivary amylase activity in undernourished Colombian children. Am J Clin Nutr (1977) 0.79
Sex-limited effects of the expression of the db gene in mice during puberty. Biochem Genet (1981) 0.79
Genetic analysis of urinary pepsinogen isozymes. Cytogenet Cell Genet (1978) 0.79
Genetic linkage studies in Huntington disease. Cytogenet Cell Genet (1978) 0.79
Description of a genetic polymorphism of a human proline-rich salivary protein, Pc, and its relationship to other proteins in the salivary protein complex (SPC). Biochem Genet (1985) 0.79
The linkage and mapping relationships of 1 qh. Cytogenet Cell Genet (1976) 0.78
The human alpha-amylases. Adv Hum Genet (1977) 0.78
Chromosome 6: linkage of the eighth component of complement (C8) to the histocompatibility region (HLA). Birth Defects Orig Artic Ser (1976) 0.78
Human parotid size polymorphism (Ps): characterization of two allelic products, Ps 1 and 2, by limited proteolysis. Biochem Genet (1983) 0.78
Intraocular pressure after intracapsular cataract extraction. Ophthalmic Surg (1984) 0.78
Characterization of phosphohydrolase activity in bovine spleen extracts: identification of a bis(p-nitrophenyl)phosphate-hydrolyzing activity (phosphodiesterase IV) which also acts on adenosine triphosphate. Anal Biochem (1985) 0.78
Sex-limited genetic variation in a mouse salivary protein. Biochem Genet (1982) 0.76
Genetic studies of tooth size factors in Pima Indian families. Am J Hum Genet (1968) 0.75
Human pancreatic alpha-amylase: phenotypic codominance and new electrophoretic variants. Am J Hum Genet (1978) 0.75
The linkage and mapping relationships of 1qh. Birth Defects Orig Artic Ser (1976) 0.75
A perspective from the Knowledge Base Research Program (KBRP). J Clin Comput (1983) 0.75
Immunohistochemical demonstration of the loss of immunoreactive amylase from neoplastic human salivary gland. Experientia (1981) 0.75
Linkage relationships of 1qh to Amy, Fy, PGM1, and Rh. Cytogenet Cell Genet (1975) 0.75
Nonfatal amniotic pulmonary embolism. Am J Roentgenol Radium Ther Nucl Med (1966) 0.75
A system for the retrieval of family structured information. Comput Biol Med (1977) 0.75
Electrophoretic analysis of serum proteins in cystic fibrosis. Pediatr Res (1977) 0.75
A photorepressible isozyme of malic enzyme in Euglena gracilis strain Z. J Protozool (1973) 0.75
Dominantly inherited periodic bone pain. Birth Defects Orig Artic Ser (1974) 0.75
An amylase-producing serous cystadenocarcinoma of the ovary. Oncology (1985) 0.75
Linkage group I: multipoint mapping. Birth Defects Orig Artic Ser (1975) 0.75
Immunological and chemical comparison on heterogeneous basic glycoproteins in human parotid saliva. Biochim Biophys Acta (1971) 0.75
An evaluation of differential methylation of ribonucleic acid in cystic fibrosis. Pediatr Res (1974) 0.75
Population genetics and hemophilia--implications of mutation and carrier recognition. Ann N Y Acad Sci (1975) 0.75
Semiautomatic digital printing caliper for tooth measurements. J Dent Res (1968) 0.75
Austin John Brogan, M.D. 1905-1972. Radiology (1973) 0.75
The utilization of a written family history questionnaire in genetic counseling. Birth Defects Orig Artic Ser (1978) 0.75
Genetic counseling at the Indiana University Medical Center. J Indiana State Med Assoc (1974) 0.75
Do brine shrimp diagnose cystic fibrosis? Pediatr Res (1975) 0.75
Linkage group I: multipoint mapping. Cytogenet Cell Genet (1975) 0.75
Genetic variants of thyroxine-binding globulin (TBG). Birth Defects Orig Artic Ser (1971) 0.75
Electrophoretic analysis of serum proteins in cystic fibrosis. Pediatr Res (1977) 0.75