Sturcture and expression of the human XPBC/ERCC-3 gene involved in DNA repair disorders xeroderma pigmentosum and cockayne's syndrome

Keyphrases

• 3′-untranslated Region (3′-UTR) 50%
• Actinomycin D 50%
• AU-rich Elements 50%
• CAAT Box 50%
• Cockayne Syndrome 100%
• Complementation Group 50%
• CpG Island 50%
• Dinucleotide 50%
• DNA Repair Disorders 100%
• DNA Repair Genes 50%
• Donor Splice Site 50%
• ERCC1 100%
• Excision Repair 100%
• Exon 100%
• Failed Repair 50%
• First Exons 50%
• First Intron 50%
• GC Box 50%
• Genetic Architecture 50%
• Human Cancer 50%
• MRNA Half-life 50%
• Nucleotide Sequence 50%
• Polypyrimidine 50%
• Promoter Elements 50%
• Promoter Region 50%
• Rodents 50%
• Sequence Elements 50%
• Southern Blot Analysis 50%
• Sturcture 100%
• TATA Box 50%
• Xeroderma pigmentosum 100%

Biochemistry, Genetics and Molecular Biology

• AU-rich Element 33%
• Base Excision Repair 66%
• CAAT Box 33%
• Cockayne Syndrome 100%
• CpG Island 33%
• Dactinomycin 33%
• DNA Repair 100%
• Exon 100%
• GC Box 33%
• Genomics 33%
• Half-Life 33%
• Intron 33%
• Messenger RNA 66%
• Nucleotide Sequence 33%
• Pribnow Box 33%
• Promoter Region 100%
• Repair Gene 33%
• Southern Blotting 33%
• TATA Box 33%
• Transcription Initiation Site 33%
• Untranslated Region 33%
• Xeroderma pigmentosum 100%