Leveraging cross-species transcription factor binding site patterns: From diabetes risk loci to disease mechanisms

Cell

Volumn 156, Issue 1-2, 2014, Pages 343-358

  Claussnitzer, Melina ^a,b,c,d   Dankel, Simon N ^e,f   Klocke, Bernward ^g   Grallert, Harald ^b,c   Glunk, Viktoria ^a,b,c   Berulava, Tea ^h   Lee, Heekyoung ^a,b,c   Oskolkov, Nikolay ⁱ   Fadista, Joao ⁱ   Ehlers, Kerstin ^a,b,c   Wahl, Simone ^b,c   Hoffmann, Christoph ^a   Qian, Kun ^a,b,c   Rönn, Tina ⁱ   Riess, Helene ^c,j   Müller Nurasyid, Martina ^c,k,l   Bretschneider, Nancy ^g   Schroeder, Timm ^c,m   Skurk, Thomas ^a,n   Horsthemke, Bernhard ^h   Spieler, Derek ^c,n   Klingenspor, Martin ^a   Seifert, Martin ^g   Kern, Michael J ^o   Mejhert, Niklas ^p   Dahlman, Ingrid ^p   Hansson, Ola ⁱ   Hauck, Stefanie M ^b,c   Blüher, Matthias ^q   Arner, Peter ^p   Groop, Leif ⁱ   Illig, Thomas ^c,r   Suhre, Karsten ^c,s   Hsu, Yi Hsiang ^d,t   Mellgren, Gunnar ^e,f   Hauner, Hans ^a,b,c,n   Laumen, Helmut ^a,b,c   more..

^a TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^b GERMAN CENTER FOR DIABETES RESEARCH DZD   (Germany)

^c INSTITUTE OF EPIDEMIOLOGY   (Germany)

^d HARVARD MEDICAL SCHOOL   (United States)

^e UNIVERSITY OF BERGEN   (Norway)

^f HAUKELAND UNIVERSITY HOSPITAL   (Norway)

^g Genomatix GmbH   (Germany)

^h UNIVERSITY HOSPITAL ESSEN   (Germany)

ⁱ LUND UNIVERSITY   (Sweden)

^j UNIVERSITY HOSPITAL ULM   (Germany)

^k LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

^l UNIVERSITY OF MUNICH   (Germany)

^m ETH ZURICH   (Switzerland)

ⁿ TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^o MEDICAL UNIVERSITY OF SOUTH CAROLINA   (United States)

^p KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^q UNIVERSITY OF LEIPZIG   (Germany)

^r HANNOVER MEDICAL SCHOOL   (Germany)

^s QATAR FOUNDATION   (Qatar)

^t HARVARD SCHOOL OF PUBLIC HEALTH   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR GAMMA; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR GAMMA 2; TRANSCRIPTION FACTOR; FATTY ACID;

ALLELE; ARTICLE; BINDING SITE; CODING; EXON; GENE EXPRESSION; GENE LOCUS; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; HOMEOBOX; HOMEOSTASIS; HUMAN; HUMAN CELL; HUMAN TISSUE; INSULIN RELEASE; INSULIN SENSITIVITY; INTRON; LIPID METABOLISM; MOLECULAR MECHANICS; NON INSULIN DEPENDENT DIABETES MELLITUS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SPECIES CONSERVATION; TRANSCRIPTION INITIATION SITE; ADIPOSE TISSUE CELL; DNA FLANKING REGION; GEL MOBILITY SHIFT ASSAY; GENE REPRESSION; GENETIC RISK; GENETIC VARIABILITY; GLUCOSE HOMEOSTASIS; HUMAN GENOME; PHYLOGENY; SINGLE NUCLEOTIDE POLYMORPHISM;

ANIMALS; CELL LINE; CELLS, CULTURED; CONSERVED SEQUENCE; DIABETES MELLITUS, TYPE 2; GENE EXPRESSION REGULATION; GENOME-WIDE ASSOCIATION STUDY; HOMEODOMAIN PROTEINS; HUMANS; INSULIN RESISTANCE; POLYMORPHISM, SINGLE NUCLEOTIDE; PPAR GAMMA; REGULATORY SEQUENCES, NUCLEIC ACID; TRANSCRIPTION FACTORS;

EID: 84892689100     PISSN: 00928674     EISSN: 10974172     Source Type: Journal    
DOI: 10.1016/j.cell.2013.10.058     Document Type: Article

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