Published in Genomics on May 01, 1988
Genomic organization of the selectin family of leukocyte adhesion molecules on human and mouse chromosome 1. J Exp Med (1990) 1.06
Coagulation factor V(A2440G) causes east Texas bleeding disorder via TFPIα. J Clin Invest (2013) 0.92
Comparative map for mice and humans. Mamm Genome (1991) 0.81
Increased risk of venous thrombosis by AB alleles of the ABO blood group and Factor V Leiden in a Brazilian population. Genet Mol Biol (2009) 0.81
A PstI polymorphism in the human coagulation factor V (F5) gene. Nucleic Acids Res (1990) 0.75
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy. Nature (1986) 4.13
A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities. Clin Genet (1975) 3.81
Characterization of the complementary deoxyribonucleic acid and gene coding for human prothrombin. Biochemistry (1983) 2.49
Down syndrome and recent demographic trends in Manitoba. J Med Genet (1978) 2.34
Human genes encoding prothrombin and ceruloplasmin map to 11p11-q12 and 3q21-24, respectively. Somat Cell Mol Genet (1987) 2.21
Characterization of an almost full-length cDNA coding for human blood coagulation factor X. Proc Natl Acad Sci U S A (1985) 2.08
Prenatal diagnosis of genetic disease in Canada: report of a collaborative study. Can Med Assoc J (1976) 2.07
Chorionic villus sampling and amniocentesis for prenatal diagnosis. Lancet (1997) 2.04
Aceruloplasminemia: molecular characterization of this disorder of iron metabolism. Proc Natl Acad Sci U S A (1995) 2.01
The primary structure of human serum transferrin. The structures of seven cyanogen bromide fragments and the assembly of the complete structure. J Biol Chem (1983) 1.83
Robertsonian translocations in man: evidence for prezygotic selection. Cytogenetics (1968) 1.82
Rational engineering of activity and specificity in a serine protease. Nat Biotechnol (1997) 1.79
The Na+ binding site of thrombin. J Biol Chem (1995) 1.77
Polysome immunoprecipitation of phenylalanine hydroxylase mRNA from rat liver and cloning of its cDNA. Proc Natl Acad Sci U S A (1982) 1.69
Familial mental retardation in a family with an inherited chromosome rearrangement. J Med Genet (1974) 1.57
Regional localization of 18 human X-linked DNA sequences. Cytogenet Cell Genet (1986) 1.48
Cloning and sequencing of liver cDNA coding for bovine protein C. Proc Natl Acad Sci U S A (1984) 1.45
Chromosome studies in a neonatal population. Can Med Assoc J (1972) 1.42
The characteristics of a population of Canadian women offered maternal serum alphafetoprotein screening during pregnancy. Can J Public Health (1986) 1.39
Chromosomal mosaicism in diagnostic amniotic fluid cell cultures. Pediatr Res (1974) 1.34
Isolation and characterization of an alpha-satellite repeated sequence from human chromosome 22. Chromosoma (1986) 1.33
Ligand-induced conformational change in transferrins: crystal structure of the open form of the N-terminal half-molecule of human transferrin. Biochemistry (1998) 1.31
Cloning and analysis of a cDNA coding for bovine prothrombin. Proc Natl Acad Sci U S A (1980) 1.28
Characterization of human blood coagulation factor XII cDNA. Prediction of the primary structure of factor XII and the tertiary structure of beta-factor XIIa. J Biol Chem (1985) 1.28
Expression of the amino-terminal half-molecule of human serum transferrin in cultured cells and characterization of the recombinant protein. Biochemistry (1990) 1.28
Dual role of Lys206-Lys296 interaction in human transferrin N-lobe: iron-release trigger and anion-binding site. Biochemistry (1999) 1.27
Transmutation of a heme protein. Proc Natl Acad Sci U S A (1993) 1.25
Chromosomal assignment of human sequences encoding arginine vasopressin-neurophysin II and growth hormone releasing factor. Somat Cell Mol Genet (1985) 1.24
Blood coagulation factor X mRNA encodes a single polypeptide chain containing a prepro leader sequence. Nucleic Acids Res (1984) 1.20
Characterization of bovine prothrombin mRNA and its translation product. Biochemistry (1984) 1.19
Characterization of a cDNA clone coding for the beta chain of bovine fibrinogen. Proc Natl Acad Sci U S A (1981) 1.19
Report of the committee on the genetic constitution of chromosome 1. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping. Cytogenet Cell Genet (1982) 1.16
Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR. Am J Med Genet (1990) 1.16
Complete cDNA sequence of human preceruloplasmin. Proc Natl Acad Sci U S A (1986) 1.13
A cytogenetic survey of 14,069 newborn infants. III. an analysis of the significance and cytologic behavior of the Robertsonian and reciprocal translocations. Cytogenet Cell Genet (1978) 1.11
Expression of glycosylated and nonglycosylated human transferrin in mammalian cells. Characterization of the recombinant proteins with comparison to three commercially available transferrins. Biochemistry (1993) 1.10
Genetic intersexuality in goats. J Reprod Fertil Suppl (1969) 1.10
Expression, purification, and characterization of recombinant nonglycosylated human serum transferrin containing a C-terminal hexahistidine tag. Protein Expr Purif (2001) 1.09
Efficient production and isolation of recombinant amino-terminal half-molecule of human serum transferrin from baby hamster kidney cells. Protein Expr Purif (1992) 1.09
Effects of mutations of aspartic acid 63 on the metal-binding properties of the recombinant N-lobe of human serum transferrin. Biochemistry (1997) 1.08
The complete amino acid sequence of human serum transferrin. Proc Natl Acad Sci U S A (1982) 1.08
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21. Am J Hum Genet (1987) 1.08
A DNA marker for human chromosome 8 that detects alleles of differing sizes. Cytogenet Cell Genet (1986) 1.08
Associations between genetic polymorphisms of Phase I and II metabolizing enzymes, p53 and susceptibility to esophageal adenocarcinoma. Cancer Detect Prev (2003) 1.08
Loss of prothrombin and of factor Xa-factor Va interactions upon inactivation of factor Va by activated protein C. J Biol Chem (1984) 1.08
A gene family in Drosophila melanogaster coding for trypsin-like enzymes. Nucleic Acids Res (1985) 1.08
Mutations in NPC1 highlight a conserved NPC1-specific cysteine-rich domain. Am J Hum Genet (1999) 1.08
Human population cytogenetics: dilemmas and problems. Am J Hum Genet (1976) 1.07
Thrombin Glu-39 restricts the P'3 specificity to nonacidic residues. J Biol Chem (1991) 1.04
Expression and initial characterization of five site-directed mutants of the N-terminal half-molecule of human transferrin. Biochemistry (1991) 1.04
Use of a BamHI polymorphism in the factor IX gene for the determination of hemophilia B carrier status. Blood (1986) 1.04
"Founder" effect in different families with haemophilia B mutation. Lancet (1990) 1.04
Receptor recognition sites reside in both lobes of human serum transferrin. Biochem J (1997) 1.04
The Nova Scotia (type D) form of Niemann-Pick disease is caused by a G3097-->T transversion in NPC1. Am J Hum Genet (1998) 1.02
Structural analysis of the three vitellogenin genes in Drosophila melanogaster. Nucleic Acids Res (1981) 1.02
Mutagenic, electrochemical, and crystallographic investigation of the cytochrome b5 oxidation-reduction equilibrium: involvement of asparagine-57, serine-64, and heme propionate-7. Biochemistry (1990) 1.01
Characterization of the human blood coagulation factor XII gene. Intron/exon gene organization and analysis of the 5'-flanking region. J Biol Chem (1987) 1.01
Inequivalence of the two tyrosine ligands in the N-lobe of human serum transferrin. Biochemistry (1997) 1.01
Interlobe communication in 13C-methionine-labeled human transferrin. Biochemistry (1996) 0.98
A summary of the human gene map, 1973-1977. Cytogenet Cell Genet (1978) 0.96
Apolipoprotein E genotyping using the polymerase chain reaction and allele-specific oligonucleotide primers. J Lipid Res (1991) 0.96
Report of the committee on the genetic constitution of chromosome 1. Cytogenet Cell Genet (1979) 0.96
Characterization of a stable form of human meizothrombin derived from recombinant prothrombin (R155A, R271A, and R284A). J Biol Chem (1994) 0.95
A kinetically active site in the C-lobe of human transferrin. Biochemistry (1997) 0.95
A 48, XXXX female. J Med Genet (1974) 0.94
A moderate form of hemophilia B is caused by a novel mutation in the protease domain of factor IXVancouver. J Biol Chem (1989) 0.94
Partial characterization of vertebrate prothrombin cDNAs: amplification and sequence analysis of the B chain of thrombin from nine different species. Proc Natl Acad Sci U S A (1992) 0.93
The role of thrombin's Tyr-Pro-Pro-Trp motif in the interaction with fibrinogen, thrombomodulin, protein C, antithrombin III, and the Kunitz inhibitors. J Biol Chem (1993) 0.93
Canadian multicentre randomized clinical trial of chorion villus sampling and amniocentesis. Final report. Prenat Diagn (1992) 0.93
Three-dimensional structure of lactoferrin. Implications for function, including comparisons with transferrin. Adv Exp Med Biol (1998) 0.93
Chromosome findings in chronic psychotic patients. Br J Psychiatry (1968) 0.93
Spectral and metal-binding properties of three single-point tryptophan mutants of the human transferrin N-lobe. Biochem J (2001) 0.92
Significance of sex chromosome derived heterochromatin in mammals. Nature (1968) 0.92
Proceedings: Report of the Committee on the Genetic Constitution of Chromosome 1. Cytogenet Cell Genet (1974) 0.92
Report of the committee on the genetic constitution of chromosomes 1 and 2. Birth Defects Orig Artic Ser (1976) 0.91
Kinetic studies on the removal of iron and aluminum from recombinant and site-directed mutant N-lobe half transferrins. Biochemistry (1998) 0.91
Non-random X chromosome expression in female mules and hinnies. Nature (1971) 0.91
Non-random inactivation of the X chromosome in the female mule. Nature (1970) 0.91
Interaction of thrombin des-ETW with antithrombin III, the Kunitz inhibitors, thrombomodulin and protein C. Structural link between the autolysis loop and the Tyr-Pro-Pro-Trp insertion of thrombin. J Biol Chem (1992) 0.91
Localization of human gene loci using spontaneous chromosome rearrangements in human-Chinese hamster somatic cell hybrids. Am J Hum Genet (1975) 0.91
Transferrin: internal homology in the amino acid sequence. Science (1975) 0.90
Mutations at nonliganding residues Tyr-85 and Glu-83 in the N-lobe of human serum transferrin. Functional second shell effects. J Biol Chem (1998) 0.90
Cytogenetic disorders. N Engl J Med (1984) 0.89
Characterization of wild-type and an active-site mutant in Escherichia coli of short-chain acyl-CoA dehydrogenase from Megasphaera elsdenii. Biochemistry (1993) 0.88
Nucleotide sequence of the phosphotransacetylase gene of Escherichia coli strain K12. Biochim Biophys Acta (1994) 0.88
The association of glucose phasphate isomerase expression with human chromosome 19 using somatic cell hybrids. Cytogenet Cell Genet (1973) 0.88
Identification of thrombin residues that modulate its interactions with antithrombin III and alpha 1-antitrypsin. Biochemistry (1995) 0.87
Cloning, mutagenesis, and structural analysis of human pancreatic alpha-amylase expressed in Pichia pastoris. Protein Sci (1999) 0.87
Mapping the human 5S RNA genes on chromosome 1 using translocations. Cytogenet Cell Genet (1975) 0.86
Non-random x-inactivation in the female mule. Nature (1969) 0.86
Vectors for expressing proteins at the amino-terminus of an activation domain for use in the yeast two-hybrid system. Anal Biochem (1997) 0.86
Correlation between electroretinogram findings and molecular analysis in the Duchenne muscular dystrophy phenotype. Br J Ophthalmol (1994) 0.86
The nucleotide sequence of rabbit liver transferrin cDNA. Biochim Biophys Acta (1991) 0.86