James L. Boyer mainly investigates Internal medicine, Endocrinology, Cholestasis, Hepatocyte and Bile acid. As a part of the same scientific study, James L. Boyer usually deals with the Internal medicine, concentrating on Gastroenterology and frequently concerns with Asymptomatic. His research investigates the connection with Endocrinology and areas like Triphosphatase which intersect with concerns in Messenger RNA.
His Cholestasis research incorporates themes from Pathogenesis, Biliary tract, Liver injury, Organic anion transporter 1 and Multidrug resistance-associated protein 2. His study on Hepatocyte is covered under Biochemistry. His work deals with themes such as Taurine, Kidney and Downregulation and upregulation, which intersect with Bile acid.
James L. Boyer mainly focuses on Internal medicine, Biochemistry, Endocrinology, Cholestasis and Hepatocyte. His work focuses on many connections between Internal medicine and other disciplines, such as Gastroenterology, that overlap with his field of interest in Asymptomatic. The various areas that James L. Boyer examines in his Biochemistry study include Biophysics and Skate.
His Endocrinology study combines topics from a wide range of disciplines, such as Bile duct and Biliary tract. The concepts of his Cholestasis study are interwoven with issues in Liver injury and Pharmacology. James L. Boyer works mostly in the field of Hepatocyte, limiting it down to concerns involving Cell biology and, occasionally, Apical membrane.
His primary areas of study are Internal medicine, Cholestasis, Endocrinology, Liver injury and Bile acid. As part of his studies on Internal medicine, James L. Boyer frequently links adjacent subjects like Gastroenterology. James L. Boyer interconnects Pathogenesis, Ursodeoxycholic acid, Hepatocyte, Proinflammatory cytokine and Pharmacology in the investigation of issues within Cholestasis.
His studies deal with areas such as Innate immune system and Cell biology as well as Hepatocyte. The Bile acid study combines topics in areas such as Bilirubin, Farnesoid X receptor and Bile duct proliferation. As a member of one scientific family, James L. Boyer mostly works in the field of Gallbladder, focusing on Homeostasis and, on occasion, Biochemistry.
James L. Boyer spends much of his time researching Cholestasis, Internal medicine, Endocrinology, Bile acid and Liver injury. His Cholestasis research is multidisciplinary, incorporating perspectives in Homeostasis, Biochemistry, Molecular biology, Internalization and Pharmacology. His work carried out in the field of Internal medicine brings together such families of science as Gastroenterology and MEDLINE.
His study in the field of Insulin resistance is also linked to topics like Metabolic syndrome. His work investigates the relationship between Bile acid and topics such as Bilirubin that intersect with problems in Retinoic acid, Tretinoin, Cholesterol, Combination therapy and Alkaline phosphatase. He combines subjects such as Innate immune system, Bile duct proliferation, Hepatocyte and Cancer research with his study of Liver injury.
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The Liver: Biology and Pathobiology
Irwin M. Arias;J. L. Boyer.
(2001)
Bile Salt Transporters: Molecular Characterization, Function, and Regulation
Michael Trauner;James L. Boyer.
Physiological Reviews (2003)
Molecular Pathogenesis of Cholestasis
Michael Trauner;Peter J. Meier;James L. Boyer.
(2012)
The Prognostic Importance of Clinical and Histologic Features in Asymptomatic and Symptomatic Primary Biliary Cirrhosis
Joseph Roll;James L. Boyer;Daniel Barry;Gerald Klatskin.
The New England Journal of Medicine (1983)
The rat canalicular conjugate export pump (Mrp2) is down-regulated in intrahepatic and obstructive cholestasis
Michael Trauner;Marco Arrese;Carol J. Soroka;Meenakshisundaram Ananthanarayanan.
Gastroenterology (1997)
Mechanisms and regulation of bile secretion.
Michael H. Nathanson;James L. Boyer.
Hepatology (1991)
Bile formation and secretion.
James L. Boyer.
Comprehensive Physiology (2013)
Structural and functional polarity of canalicular and basolateral plasma membrane vesicles isolated in high yield from rat liver.
P J Meier;E S Sztul;A Reuben;J L Boyer.
Journal of Cell Biology (1984)
Drug‐induced cholestasis
Manmeet S. Padda;Mayra Sanchez;Abbasi J. Akhtar;James L. Boyer.
Hepatology (2011)
A randomized, double-blind, placebo-controlled trial of ursodeoxycholic acid in primary biliary cirrhosis
Burton Combes;Robert L. Carithers;Willis C. Maddrey;Willis C. Maddrey;Danyu Lin.
Hepatology (1993)
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