2025年1月16日 · Adipocyte is a fully open access, multi-disciplinary journal that publishes research on all aspects of adipose tissue physiology and pathophysiology.

2024年12月7日 · Journal Suggester; Open access publishing; We’re here to help. Find guidance on Author Services. Home All Journals Adipocyte List of Issues Volume 14, Issue 1 ... Adipocyte, Volume 14, Issue 1 (2025) See all volumes and issues. Share.

Adipocyte is a fully open access, multi-disciplinary journal that publishes research on all aspects of adipose tissue physiology and pathophysiology. The journal accepts the following types of articles; Research Papers/Reports, Brief Reports, Reviews, Mini-reviews, Technical Reports, Commentaries, Meeting Reports, Methods & Protocols.

Articles from Adipocyte are provided here courtesy of Taylor & Francis.

2012年1月1日 · Thus, it is with great pleasure that we launch Adipocyte, the first international peer-reviewed multi-disciplinary journal to focus exclusively on research covering all aspects of adipose tissue physiology and pathology.

2019年3月11日 · A peer-reviewed, open access journal in cell biology, adipose tissue, physiology, pathophysiology, metabolism & adipogenesis.

Adipocyte recognizes that the adipose tissue is the largest endocrine organ in the body, and explores the link between dysfunctional adipose tissue and the growing number of chronic diseases including diabetes, hypertension, cardiovascular disease and cancer.

We focus on those genetic events that link effectors to induction of adipocyte gene expression. J. Nutr. 130: 3122S-3126S, 2000. The study of adipocyte development has become an area of intense research in recent years. First, adipocyte differentiation has …

2018年2月5日 · This study shows that OvCa cells co-cultured with primary human omental adipocytes express high levels of the FA receptor, CD36, in the plasma membrane, thereby facilitating exogenous FA uptake.

Adipocyte-specific deletion of Noggin in mice affects heat production, respiratory exchange ratio and oxygen consumption. Female and male mice with adipocyte-specific deletion of Noggin (Nog fl/fl;Adipoq Cre or KO) and control mice (Nog fl/fl or F/F) aged 2 months were examined in metabolic cages.