A global map for dissecting phenotypic variants in human lincRNAs

European Journal of Human Genetics

Volumn 21, Issue 10, 2013, Pages 1128-1133

  Ning, Shangwei ^a   Wang, Peng ^a   Ye, Jingrun ^a   Li, Xiang ^a   Li, Ronghong ^a   Zhao, Zuxianglan ^a   Huo, Xiao ^a   Wang, Li ^a   Li, Feng ^a   Li, Xa ^a  

^a HARBIN MEDICAL UNIVERSITY   (China)

Author keywords

disease pathogenesis; evolutionarily conserved region (ECR); large intergenic noncoding RNA (lincRNA); RNA secondary structure; single nucleotide polymorphism (SNP)

Indexed keywords

LONG UNTRANSLATED RNA;

ARTICLE; ATTENTION DEFICIT DISORDER; BIOSYNTHESIS; BIPOLAR DISORDER; CHROMOSOME 1; CHROMOSOME 12; CHROMOSOME 3; CHROMOSOME 4; CHROMOSOME 5; DEVELOPMENT; DISEASE ASSOCIATION; DNA FLANKING REGION; EXON; GENE EXPRESSION; HEART ATRIUM FIBRILLATION; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; METABOLIC REGULATION; NON INSULIN DEPENDENT DIABETES MELLITUS; PHENOTYPE; PHENOTYPIC VARIATION; PRIORITY JOURNAL; PROSTATE CANCER; PROTEIN SECONDARY STRUCTURE; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM; TRANSCRIPTION REGULATION;

ARTHRITIS, RHEUMATOID; CONSERVED SEQUENCE; CORONARY ARTERY DISEASE; CROHN DISEASE; DATABASES, NUCLEIC ACID; DIABETES MELLITUS; GENOME, HUMAN; HUMANS; MULTIPLE SCLEROSIS; NEOPLASMS; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; RNA, LONG NONCODING; SEQUENCE ANALYSIS, DNA;

EID: 84884594782     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2013.7     Document Type: Article

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