> top > projects > sentences > docs > PubMed:2104828 > annotations
sentences Home  

PubMed:2104828 JSONTXT 40 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T1 0-70 Sentence denotes Cloning and characterization of DNA complementary to human UDP-GalNAc:
T1 0-70 Sentence denotes Cloning and characterization of DNA complementary to human UDP-GalNAc:
T2 71-161 Sentence denotes Fuc alpha 1----2Gal alpha 1----3GalNAc transferase (histo-blood group A transferase) mRNA.
T2 71-161 Sentence denotes Fuc alpha 1----2Gal alpha 1----3GalNAc transferase (histo-blood group A transferase) mRNA.
T3 162-389 Sentence denotes Based on the partial amino acid sequence, the cDNA encoding UDP-GalNAc:Fuc alpha 1----2Gal alpha 1----3GalNAc transferase, the specific primary gene product of histo-blood group A gene (A transferase), was cloned and sequenced.
T3 162-389 Sentence denotes Based on the partial amino acid sequence, the cDNA encoding UDP-GalNAc:Fuc alpha 1----2Gal alpha 1----3GalNAc transferase, the specific primary gene product of histo-blood group A gene (A transferase), was cloned and sequenced.
T4 390-539 Sentence denotes Poly(A)+ RNA from human stomach cancer cell line MKN45, expressing high levels of A antigen, was used for construction of a lambda gt10 cDNA library.
T4 390-539 Sentence denotes Poly(A)+ RNA from human stomach cancer cell line MKN45, expressing high levels of A antigen, was used for construction of a lambda gt10 cDNA library.
T5 540-849 Sentence denotes Degenerate synthetic oligodeoxynucleotides were used for polymerase chain reactions to detect the presence of the sequence of interest in cDNA (presence test) and to identify the correct clones (identification test) after screening the library with a radiolabeled polymerase chain reaction amplified fragment.
T5 540-849 Sentence denotes Degenerate synthetic oligodeoxynucleotides were used for polymerase chain reactions to detect the presence of the sequence of interest in cDNA (presence test) and to identify the correct clones (identification test) after screening the library with a radiolabeled polymerase chain reaction amplified fragment.
T6 850-952 Sentence denotes Nucleotide sequence analysis revealed a coding region of 1062 base pairs encoding a protein of 41 kDa.
T6 850-952 Sentence denotes Nucleotide sequence analysis revealed a coding region of 1062 base pairs encoding a protein of 41 kDa.
T7 953-1172 Sentence denotes Hydrophobicity plot analysis shows the existence of three domains: N-terminal short stretch, transmembranous hydrophobic region, and a long C-terminal domain (a feature common to all glycosyltransferases cloned so far).
T7 953-1172 Sentence denotes Hydrophobicity plot analysis shows the existence of three domains: N-terminal short stretch, transmembranous hydrophobic region, and a long C-terminal domain (a feature common to all glycosyltransferases cloned so far).
T8 1173-1267 Sentence denotes Southern hybridization analysis has shown that this DNA does not represent a multigene family.
T8 1173-1267 Sentence denotes Southern hybridization analysis has shown that this DNA does not represent a multigene family.
T9 1268-1361 Sentence denotes No restriction fragment length polymorphism was found to correlate with ABO blood group type.
T9 1268-1361 Sentence denotes No restriction fragment length polymorphism was found to correlate with ABO blood group type.
T10 1362-1468 Sentence denotes Bands were detected in Northern hybridization of mRNAs from cell lines expressing A, B, AB, or H antigens.
T10 1362-1468 Sentence denotes Bands were detected in Northern hybridization of mRNAs from cell lines expressing A, B, AB, or H antigens.
T11 1469-1730 Sentence denotes These results suggest that sequences of ABO genes are essentially very similar (with minimal differences), and the inability of the O gene to encode A or B transferases is probably due to structural differences rather than A or B transferase expression failure.
T11 1469-1730 Sentence denotes These results suggest that sequences of ABO genes are essentially very similar (with minimal differences), and the inability of the O gene to encode A or B transferases is probably due to structural differences rather than A or B transferase expression failure.