Con: Use of Hepatitis C Virus–Positive Donors Should Be Restricted to Research Protocols
Grace S. Lee, Judith A. Anesi, Behdad D. Besharatian, Therese Bittermann, Stephanie Hamel, David S. Goldberg – 6 November 2018
Grace S. Lee, Judith A. Anesi, Behdad D. Besharatian, Therese Bittermann, Stephanie Hamel, David S. Goldberg – 6 November 2018
Christopher Moore, Adam C. Stein – 6 November 2018
Zurabi Lominadze, Eric R. Kallwitz – 6 November 2018
William A. Werbel, Christine M. Durand – 6 November 2018
Magdalena Meszaros, Jose Ursic‐Bedoya, Stéphanie Faure, Georges‐Philippe Pageaux – 5 November 2018
Divya P. Kumar, Prasanna K. Santhekadur, Mulugeta Seneshaw, Faridoddin Mirshahi, Cora Uram‐Tuculescu, Arun J. Sanyal – 5 November 2018 – Hepatocellular carcinoma (HCC) is increasing as a cause of liver‐related mortality largely because of the growing burden of nonalcoholic steatohepatitis (NASH). The mechanisms of HCC development in nonalcoholic fatty liver disease (NAFLD) are incompletely understood. We initially identified apoptosis antagonizing transcription factor (AATF) to be associated with HCC in a mouse model of NASH that develops HCC without the addition of specific carcinogens.
Xinwen Yan, Ziyuan Zou, Xun Li, Xiaolong Qi – 4 November 2018
Chris Davis, George S. Mgomella, Ana da Silva Filipe, Eric H. Frost, Genevieve Giroux, Joseph Hughes, Catherine Hogan, Pontiano Kaleebu, Gershim Asiki, John McLauchlan, Marc Niebel, Ponsiano Ocama, Cristina Pomila, Oliver G. Pybus, Jacques Pépin, Peter Simmonds, Joshua B. Singer, Vattipally B. Sreenu, Clara Wekesa, Elizabeth H. Young, Donald G. Murphy, Manj Sandhu, Emma C.
Christopher J. Danford, Margery A. Connelly, Irina Shalaurova, Misung Kim, Mark A. Herman, Imad Nasser, James D. Otvos, Nezam H. Afdhal, Z. Gordon Jiang, Michelle Lai – 1 November 2018 – Nonalcoholic fatty liver disease (NAFLD) is a complex disease dictated by both genetic and environmental factors. While insulin resistance (IR) is a key pathogenic driver, two common genetic variants in patatin‐like phospholipase domain containing 3 (PNPLA3) and transmembrane 6 superfamily member 2 (TM6SF2) also impart significant risk for disease progression.