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PubMed:23182699 JSONTXT 18 Projects

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Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-75 Sentence denotes Mutation of keratin 4 gene causing white sponge nevus in a Japanese family.
T1 0-75 Sentence denotes Mutation of keratin 4 gene causing white sponge nevus in a Japanese family.
TextSentencer_T2 76-237 Sentence denotes White sponge nevus (WSN) is a rare autosomal dominant disorder characterized by white plaques of oral mucosa; it is benign condition with no effective treatment.
T2 76-237 Sentence denotes White sponge nevus (WSN) is a rare autosomal dominant disorder characterized by white plaques of oral mucosa; it is benign condition with no effective treatment.
TextSentencer_T3 238-307 Sentence denotes The disorder usually manifests during early childhood or adolescence.
T3 238-307 Sentence denotes The disorder usually manifests during early childhood or adolescence.
TextSentencer_T4 308-378 Sentence denotes Mutations of keratin 4 or 13 gene have been identified as causing WSN.
T4 308-378 Sentence denotes Mutations of keratin 4 or 13 gene have been identified as causing WSN.
TextSentencer_T5 379-507 Sentence denotes The aim of this study is to determine whether keratin 4 or 13 gene mutation was the molecular basis of WSN in a Japanese family.
T5 379-507 Sentence denotes The aim of this study is to determine whether keratin 4 or 13 gene mutation was the molecular basis of WSN in a Japanese family.
TextSentencer_T6 508-599 Sentence denotes The proband in this family was an 11-year-old boy, with three other people affected by WSN.
T6 508-599 Sentence denotes The proband in this family was an 11-year-old boy, with three other people affected by WSN.
TextSentencer_T7 600-677 Sentence denotes Genomic DNA was extracted from two affected members and an unaffected member.
T7 600-677 Sentence denotes Genomic DNA was extracted from two affected members and an unaffected member.
TextSentencer_T8 678-778 Sentence denotes Segments of keratin 4 and 13 genes were amplified by PCR, and direct DNA sequencing was carried out.
T8 678-778 Sentence denotes Segments of keratin 4 and 13 genes were amplified by PCR, and direct DNA sequencing was carried out.
TextSentencer_T9 779-968 Sentence denotes Sequence analysis revealed a heterozygous 3bp deletion (N160Del) localized in the helix-initiation motif at the beginning of alpha-helical domain 1A of keratin 4 gene from affected members.
T9 779-968 Sentence denotes Sequence analysis revealed a heterozygous 3bp deletion (N160Del) localized in the helix-initiation motif at the beginning of alpha-helical domain 1A of keratin 4 gene from affected members.
TextSentencer_T10 969-1032 Sentence denotes One member lacking the phenotype was genetically tested normal.
T10 969-1032 Sentence denotes One member lacking the phenotype was genetically tested normal.
TextSentencer_T11 1033-1127 Sentence denotes The authors identified a mutation of the keratin 4 gene recurrent in a family affected by WSN.
T11 1033-1127 Sentence denotes The authors identified a mutation of the keratin 4 gene recurrent in a family affected by WSN.
TextSentencer_T12 1128-1337 Sentence denotes Further investigation of the multifunctional role of keratin genes is warranted in the group of inherited epithelial disorders that may result in identification of effective treatment for this genetic disease.
T12 1128-1337 Sentence denotes Further investigation of the multifunctional role of keratin genes is warranted in the group of inherited epithelial disorders that may result in identification of effective treatment for this genetic disease.