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Andreas L. Birkenfeld
Researcher at King's College London
Publications - 203
Citations - 8539
Andreas L. Birkenfeld is an academic researcher from King's College London. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 36, co-authored 113 publications receiving 6362 citations. Previous affiliations of Andreas L. Birkenfeld include Max Delbrück Center for Molecular Medicine & University of Cambridge.
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Journal ArticleDOI
Consequences of the COVID-19 pandemic for patients with metabolic diseases.
Stefan R Bornstein,Francesco Rubino,Francesco Rubino,Barbara Ludwig,Hannes Rietzsch,Peter Schwarz,Roman N. Rodionov,Kamlesh Khunti,David L. Hopkins,Andreas L. Birkenfeld,Bernhard O. Boehm,Bernhard O. Boehm,Stephanie A. Amiel,Richard I. G. Holt,Jay S. Skyler,J. Hans DeVries,Eric Renard,Robert H. Eckel,Paul Zimmet,K. G. M. M. Alberti,Bruno Geloneze,Juliana C.N. Chan,Jean Claude Mbanya,Henry Chijioke Onyegbutulem,Ambady Ramachandran,Abdul Basit,Mohamed Hassanein,Giatgen A. Spinas,Felix Beuschlein,Geltrude Mingrone,Geltrude Mingrone,Geltrude Mingrone +31 more
TL;DR: In this article, the authors encourage clinicians and patient interest groups in the field of diabetes and metabolism to raise their voices to ensure adequate care and admission of patients during the COVID-19 pandemic.
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The Role of INDY in Metabolic Regulation
TL;DR: The role of mINDY (SLCl3A5) is highlighted as a putative therapeutic target for the treatment of obesity, non-alcoholic fatty liver disease and type 2 diabetes.
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Retinol saturase coordinates liver metabolism by regulating ChREBP activity
Steffi Heidenreich,Nicole Witte,Pamela Weber,Isabel Goehring,Alexander Tolkachov,Christian von Loeffelholz,S Döcke,Michael Bauer,Martin Stockmann,Andreas Pfeiffer,Andreas L. Birkenfeld,Andreas L. Birkenfeld,Matthias Pietzke,Stefan Kempa,Matthias Muenzner,Michael Schupp +15 more
TL;DR: It is shown that retinol saturase is implicated in hepatic lipid metabolism by regulating the activity of the transcription factor ChREBP, and pharmacological inhibition of liver RetSat may represent a therapeutic approach for steatosis.
The Role of Non-exercise Activity Thermogenesis in Human Obesity
TL;DR: Data support the hypothesis that targeting NEAT with an intervention could be an essential tool for body weight control and suggest practical approaches, relevant implications, and limitations to integrating NEAT into daily life.
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Knockdown of the gene encoding Drosophila tribbles homologue 3 (Trib3) improves insulin sensitivity through peroxisome proliferator-activated receptor-γ (PPAR-γ) activation in a rat model of insulin resistance
Dirk Weismann,Derek M. Erion,I. Ignatova-Todorava,Yoshio Nagai,Romana Stark,Jennifer J. Hsiao,Clare A. Flannery,Andreas L. Birkenfeld,T. May,Mario Kahn,Dongyan Zhang,Xing-Xian Yu,Sue Murray,Sanjay Bhanot,Brett P. Monia,Gary W. Cline,Gerald I. Shulman,Varman T. Samuel,Varman T. Samuel +18 more
TL;DR: Data suggest that TRIB3 inhibition improves insulin sensitivity in vivo primarily in a PPAR-γ-dependent manner and without any change in AKT2 activity.