Pages that link to "Q34323307"
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The following pages link to Molecular genetic basis of the histo-blood group ABO system. (Q34323307):
Displaying 50 items.
- Population genetics of malaria resistance in humans (Q21032506) (← links)
- Ancient human genome sequence of an extinct Palaeo-Eskimo (Q21972850) (← links)
- A beta-1,3-N-acetylglucosaminyltransferase with poly-N-acetyllactosamine synthase activity is structurally related to beta-1,3-galactosyltransferases (Q22008686) (← links)
- Red cell genotyping and the future of pretransfusion testing (Q22241774) (← links)
- Large-scale blood group genotyping - clinical implications (Q22242632) (← links)
- Cloning and expression of the histo-blood group Pk UDP-galactose: Ga1beta-4G1cbeta1-cer alpha1, 4-galactosyltransferase. Molecular genetic basis of the p phenotype (Q22253436) (← links)
- Sequence and expression of a candidate for the human Secretor blood group alpha(1,2)fucosyltransferase gene (FUT2). Homozygosity for an enzyme-inactivating nonsense mutation commonly correlates with the non-secretor phenotype (Q24315968) (← links)
- The human UDP-N-acetylglucosamine: alpha-6-D-mannoside-beta-1,2- N-acetylglucosaminyltransferase II gene (MGAT2). Cloning of genomic DNA, localization to chromosome 14q21, expression in insect cells and purification of the recombinant protein (Q24321959) (← links)
- Porcine, mouse and human galactose 3-O-sulphotransferase-2 enzymes have different substrate specificities; the porcine enzyme requires basic compounds for its catalytic activity (Q24536237) (← links)
- Expression cloning of cDNA encoding a seven-helix receptor from human placenta with affinity for opioid ligands (Q24561648) (← links)
- Molecular basis for H blood group deficiency in Bombay (Oh) and para-Bombay individuals (Q24562744) (← links)
- Cloning of glycoprotein D cDNA, which encodes the major subunit of the Duffy blood group system and the receptor for the Plasmodium vivax malaria parasite (Q24564153) (← links)
- Expression cloning of Forssman glycolipid synthetase: a novel member of the histo-blood group ABO gene family (Q24601244) (← links)
- Human red cell aquaporin CHIP. I. Molecular characterization of ABH and Colton blood group antigens (Q24633828) (← links)
- Molecular basis for secretor type alpha(1,2)-fucosyltransferase gene deficiency in a Japanese population: a fusion gene generated by unequal crossover responsible for the enzyme deficiency (Q24675940) (← links)
- ABO exon and intron analysis in individuals with the AweakB phenotype reveals a novel O1v-A2 hybrid allele that causes four missense mutations in the A transferase (Q24802111) (← links)
- The role of galectin-4 in physiology and diseases (Q26750700) (← links)
- The prognostic value of ABO blood group in cancer patients (Q26775411) (← links)
- Trans-species polymorphism in humans and the great apes is generally maintained by balancing selection that modulates the host immune response (Q26785914) (← links)
- Bovine alpha1,3-galactosyltransferase catalytic domain structure and its relationship with ABO histo-blood group and glycosphingolipid glycosyltransferases (Q27629621) (← links)
- Structure of UDP complex of UDP-galactose:beta-galactoside-alpha -1,3-galactosyltransferase at 1.53-A resolution reveals a conformational change in the catalytically important C terminus (Q27635303) (← links)
- Structural basis of ordered binding of donor and acceptor substrates to the retaining glycosyltransferase, alpha-1,3-galactosyltransferase (Q27638986) (← links)
- The influence of an intramolecular hydrogen bond in differential recognition of inhibitory acceptor analogs by human ABO(H) blood group A and B glycosyltransferases (Q27642029) (← links)
- Structural effects of naturally occurring human blood group B galactosyltransferase mutations adjacent to the DXD motif (Q27643682) (← links)
- Bacterial glycosidases for the production of universal red blood cells (Q27644317) (← links)
- Structural basis for red cell phenotypic changes in newly identified, naturally occurring subgroup mutants of the human blood group B glycosyltransferase (Q27644623) (← links)
- ABO(H) blood group A and B glycosyltransferases recognize substrate via specific conformational changes (Q27649533) (← links)
- Molecular mechanism of elongation factor 1A inhibition by a Legionella pneumophila glycosyltransferase (Q27658750) (← links)
- Cysteine-to-Serine Mutants Dramatically Reorder the Active Site of Human ABO(H) Blood Group B Glycosyltransferase without Affecting Activity: Structural Insights into Cooperative Substrate Binding (Q27663591) (← links)
- Sequence-dependent effects of cryoprotectants on the active sites of the human ABO(H) blood group A and B glycosyltransferases (Q27677373) (← links)
- Human histo-blood group A2 transferase coded by A2 allele, one of the A subtypes, is characterized by a single base deletion in the coding sequence, which results in an additional domain at the carboxyl terminal (Q28115513) (← links)
- Humans lack iGb3 due to the absence of functional iGb3-synthase: implications for NKT cell development and transplantation (Q28119060) (← links)
- Polymorphism of the h allele and the population frequency of sporadic nonfunctional alleles (Q28236328) (← links)
- Molecular genetic basis of the human Rhesus blood group system (Q28255437) (← links)
- Molecular basis of evolutionary loss of the alpha 1,3-galactosyltransferase gene in higher primates (Q28344377) (← links)
- Genomic cloning and expression of three murine UDP-galactose: beta-N-acetylglucosamine beta1,3-galactosyltransferase genes (Q28507395) (← links)
- Murine equivalent of the human histo-blood group ABO gene is a cis-AB gene and encodes a glycosyltransferase with both A and B transferase activity (Q28511961) (← links)
- Blood group A glycosyltransferase occurring as alleles with high sequence difference is transiently induced during a Nippostrongylus brasiliensis parasite infection (Q28581142) (← links)
- Functional assignment of motifs conserved in beta 1,3-glycosyltransferases (Q28584953) (← links)
- Reappraisal of known malaria resistance loci in a large multicenter study (Q28608567) (← links)
- Genetic basis for the lack of N-glycolylneuraminic acid expression in human tissues and its implication to human evolution (Q28650148) (← links)
- PP13, maternal ABO blood groups and the risk assessment of pregnancy complications (Q28742192) (← links)
- Amino-acid substitution in the disordered loop of blood group B-glycosyltransferase enzyme causes weak B phenotype (Q28910440) (← links)
- A genome-wide association study identifies two susceptibility loci for duodenal ulcer in the Japanese population (Q28943441) (← links)
- Norovirus drug candidates that inhibit viral capsid attachment to human histo-blood group antigens (Q30248992) (← links)
- Report of a critical recombination further narrowing the TSC1 region (Q30443033) (← links)
- Innate immune lectins kill bacteria expressing blood group antigen (Q30494049) (← links)
- O-glycan variability of egg-jelly mucins from Xenopus laevis: characterization of four phenotypes that differ by the terminal glycosylation of their mucins (Q30620011) (← links)
- Comparative analysis of glycoside hydrolases activities from phylogenetically diverse marine bacteria of the genus Arenibacter (Q30644735) (← links)
- A genetic linkage map of human chromosome 9q (Q30741023) (← links)