TY  - JOUR
  - Pereira-Fantini PM, Lapthorne S, Joyce SA, Dellios NL, Wilson G, Fouhy F, Thomas SL, Scurr M, Hill C, Gahan CG, Cotter PD, Fuller PJ, Hardikar W, Bines JE
  - 2014
  - July
  - Journal of hepatology
  - Altered FXR signaling is associated with bile acid dysmetabolism in short bowel syndrome-associated liver disease.
  - Validated
  - Altmetric: 1 ()
  - Despite the mortality associated with liver disease observed in patients with short bowel syndrome (SBS), mechanisms underlying the development of SBS-associated liver disease (SBS-ALD) are poorly understood. This study examines the impact of bacterially-mediated bile acid (BA) dysmetabolism on FXR signaling pathways and clinical outcome in a piglet model of SBS-ALD.
  - 10.1016/j.jhep.2014.06.025
DA  - 2014/07
ER  - 

@article{V268806212,
   = {Pereira-Fantini PM,  Lapthorne S and  Joyce SA,  Dellios NL and  Wilson G,  Fouhy F and  Thomas SL,  Scurr M and  Hill C,  Gahan CG and  Cotter PD,  Fuller PJ and  Hardikar W,  Bines JE },
   = {2014},
   = {July},
   = {Journal of hepatology},
   = {Altered FXR signaling is associated with bile acid dysmetabolism in short bowel syndrome-associated liver disease.},
   = {Validated},
   = {Altmetric: 1 ()},
   = {{Despite the mortality associated with liver disease observed in patients with short bowel syndrome (SBS), mechanisms underlying the development of SBS-associated liver disease (SBS-ALD) are poorly understood. This study examines the impact of bacterially-mediated bile acid (BA) dysmetabolism on FXR signaling pathways and clinical outcome in a piglet model of SBS-ALD.}},
   = {10.1016/j.jhep.2014.06.025},
  source = {IRIS}
}