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Volumn 170, Issue 1, 2017, Pages 199-212.e20

Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms

(148)  Rusu, Victor a,b,l   Hoch, Eitan b   Mercader, Josep M b,c,d,k   Gymrek, Melissa b,c,m   von Grotthuss, Marcin b   Fontanillas, Pierre b,n   Spooner, Alexandra b   Altshuler, David M a,b,c,j,k,o   Florez, Jose C a,b,c,k   Jacobs, Suzanne B R b,c   Clish, Clary B b   Tenen, Danielle E b,e   Hartigan, Christina R b   DeRan, Michael b   Guzman, Gaelen b   Deik, Amy A b   Pierce, Kerry A b   Dennis, Courtney b   Carr, Steven A b   Wagner, Bridget K b   more..


Author keywords

disease mechanism; fatty acid metabolism; genetics; lipid metabolism; MCT11; monocarboxylates; precision medicine; SLC16A11; solute carrier (SLC); type 2 diabetes (T2D)

Indexed keywords

MONOCARBOXYLATE TRANSPORTER; PROATEIN SLC16A11; PROTEIN; UNCLASSIFIED DRUG; BSG PROTEIN, HUMAN; CD147 ANTIGEN; SLC16A11 PROTEIN, HUMAN;

EID: 85021628341     PISSN: 00928674     EISSN: 10974172     Source Type: Journal    
DOI: 10.1016/j.cell.2017.06.011     Document Type: Article
Times cited : (117)

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