> top > projects > sentences > docs > PubMed:12002902 > annotations
sentences Home  

PubMed:12002902 JSONTXT 8 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-121 Sentence denotes Screening for mutations in exons encoding the ligand-binding domain of the LDL receptor gene using PCR-CFLP and PCR-SSCP.
T1 0-121 Sentence denotes Screening for mutations in exons encoding the ligand-binding domain of the LDL receptor gene using PCR-CFLP and PCR-SSCP.
TextSentencer_T2 122-210 Sentence denotes Primary hypercholesterolemia includes both monogenic disorders and polygenic conditions.
T2 122-210 Sentence denotes Primary hypercholesterolemia includes both monogenic disorders and polygenic conditions.
TextSentencer_T3 211-343 Sentence denotes Two well defined monogenic disorders are familial hypercholesterolemia (FH) and familial defective apolipoprotein (apo) B-100 (FDB).
T3 211-343 Sentence denotes Two well defined monogenic disorders are familial hypercholesterolemia (FH) and familial defective apolipoprotein (apo) B-100 (FDB).
TextSentencer_T4 344-413 Sentence denotes Both disorders convey high risk of premature coronary artery disease.
T4 344-413 Sentence denotes Both disorders convey high risk of premature coronary artery disease.
TextSentencer_T5 414-499 Sentence denotes FH and FDB are caused by mutations in LDL receptor and apo B-100 genes, respectively.
T5 414-499 Sentence denotes FH and FDB are caused by mutations in LDL receptor and apo B-100 genes, respectively.
TextSentencer_T6 500-611 Sentence denotes In the present study, mutations in both genes in Thai subjects with primary hypercholesterolemia were screened.
T6 500-611 Sentence denotes In the present study, mutations in both genes in Thai subjects with primary hypercholesterolemia were screened.
TextSentencer_T7 612-670 Sentence denotes For apo B-100 gene, a common mutation R3500Q was screened.
T7 612-670 Sentence denotes For apo B-100 gene, a common mutation R3500Q was screened.
TextSentencer_T8 671-727 Sentence denotes This mutation was not observed in the patients (n = 45).
T8 671-727 Sentence denotes This mutation was not observed in the patients (n = 45).
TextSentencer_T9 728-823 Sentence denotes For LDL receptor gene, mutations in the exons encoding the ligand-binding domain were screened.
T9 728-823 Sentence denotes For LDL receptor gene, mutations in the exons encoding the ligand-binding domain were screened.
TextSentencer_T10 824-941 Sentence denotes By PCR-CFLP analysis, 18 abnormal CFLP patterns in exon 4, the hot spot for mutations, were found in patients (n=45).
T10 824-941 Sentence denotes By PCR-CFLP analysis, 18 abnormal CFLP patterns in exon 4, the hot spot for mutations, were found in patients (n=45).
TextSentencer_T11 942-1085 Sentence denotes One of the DNA samples with abnormal CFLP patterns was previously identified and reported as a possible disease-causing mutation, namely D151Y.
T11 942-1085 Sentence denotes One of the DNA samples with abnormal CFLP patterns was previously identified and reported as a possible disease-causing mutation, namely D151Y.
TextSentencer_T12 1086-1144 Sentence denotes For the other exons, the screening technique was PCR-SSCP.
T12 1086-1144 Sentence denotes For the other exons, the screening technique was PCR-SSCP.
TextSentencer_T13 1145-1282 Sentence denotes Abnormal SSCP patterns in DNA samples from patients (n=20) were found as follows, two in exon 3, one in exon 5 and another one in exon 6.
T13 1145-1282 Sentence denotes Abnormal SSCP patterns in DNA samples from patients (n=20) were found as follows, two in exon 3, one in exon 5 and another one in exon 6.
TextSentencer_T14 1283-1386 Sentence denotes Further characterization by DNA sequencing and family studies for these abnormal patterns are underway.
T14 1283-1386 Sentence denotes Further characterization by DNA sequencing and family studies for these abnormal patterns are underway.