标题
Diet-induced loss of adipose hexokinase 2 correlates with hyperglycemia
作者
关键词
-
出版物
eLife
Volume 12, Issue -, Pages -
出版商
eLife Sciences Publications, Ltd
发表日期
2023-03-15
DOI
10.7554/elife.85103
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- The role of somatosensory innervation of adipose tissues
- (2022) Yu Wang et al. NATURE
- Adipose mTORC2 is essential for sensory innervation in white adipose tissue and whole-body energy homeostasis
- (2022) Irina C. Frei et al. Molecular Metabolism
- Sensory neurons expressing calcitonin gene-related peptide α regulate adaptive thermogenesis and diet-induced obesity
- (2021) Kuldeep Makwana et al. Molecular Metabolism
- The mutational constraint spectrum quantified from variation in 141,456 humans
- (2020) Konrad J. Karczewski et al. NATURE
- FOXK1 and FOXK2 regulate aerobic glycolysis
- (2019) Valentina Sukonina et al. NATURE
- Carbohydrate Sensing Through the Transcription Factor ChREBP
- (2019) Paula Ortega-Prieto et al. Frontiers in Genetics
- Neuropathy and neural plasticity in the subcutaneous white adipose depot
- (2019) Magdalena Blaszkiewicz et al. PLoS One
- The integrative biology of type 2 diabetes
- (2019) Michael Roden et al. NATURE
- The catalytic inactivation of the N-half of human hexokinase 2 and structural and biochemical characterization of its mitochondrial conformation
- (2018) Mir Hussain Nawaz et al. BIOSCIENCE REPORTS
- Insulin resistance causes inflammation in adipose tissue
- (2018) Mitsugu Shimobayashi et al. JOURNAL OF CLINICAL INVESTIGATION
- Hexokinase-2 depletion inhibits glycolysis and induces oxidative phosphorylation in hepatocellular carcinoma and sensitizes to metformin
- (2018) Dannielle DeWaal et al. Nature Communications
- Insulin resistance in cavefish as an adaptation to a nutrient-limited environment
- (2018) Misty R. Riddle et al. NATURE
- Calcium Channel CaV2.3 Subunits Regulate Hepatic Glucose Production by Modulating Leptin-Induced Excitation of Arcuate Pro-opiomelanocortin Neurons
- (2018) Mark A. Smith et al. Cell Reports
- Proline metabolism supports metastasis formation and could be inhibited to selectively target metastasizing cancer cells
- (2017) Ilaria Elia et al. Nature Communications
- Absence of Carbohydrate Response Element Binding Protein in Adipocytes Causes Systemic Insulin Resistance and Impairs Glucose Transport
- (2017) Archana Vijayakumar et al. Cell Reports
- Distinct Akt phosphorylation states are required for insulin regulated Glut4 and Glut1-mediated glucose uptake
- (2017) Muheeb Beg et al. eLife
- Direct Hepatocyte Insulin Signaling Is Required for Lipogenesis but Is Dispensable for the Suppression of Glucose Production
- (2016) Paul M. Titchenell et al. Cell Metabolism
- Disruption of Adipose Rab10-Dependent Insulin Signaling Causes Hepatic Insulin Resistance
- (2016) Reema P. Vazirani et al. DIABETES
- ChREBP regulates fructose-induced glucose production independently of insulin signaling
- (2016) Mi-Sung Kim et al. JOURNAL OF CLINICAL INVESTIGATION
- Evaluation and Improvement of Quantification Accuracy in Isobaric Mass Tag-Based Protein Quantification Experiments
- (2016) Erik Ahrné et al. JOURNAL OF PROTEOME RESEARCH
- Adipose tissue mTORC2 regulates ChREBP-driven de novo lipogenesis and hepatic glucose metabolism
- (2016) Yuefeng Tang et al. Nature Communications
- Lack of AKT in adipocytes causes severe lipodystrophy
- (2016) Abigail L. Shearin et al. Molecular Metabolism
- Hepatic Acetyl CoA Links Adipose Tissue Inflammation to Hepatic Insulin Resistance and Type 2 Diabetes
- (2015) Rachel J. Perry et al. CELL
- Selective Insulin Resistance in Adipocytes
- (2015) Shi-Xiong Tan et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- The regulation of glucose metabolism: implications and considerations for the assessment of glucose homeostasis in rodents
- (2014) Greg M. Kowalski et al. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM
- Hexokinase 2 Is Required for Tumor Initiation and Maintenance and Its Systemic Deletion Is Therapeutic in Mouse Models of Cancer
- (2013) Krushna C. Patra et al. CANCER CELL
- Protocol for effective differentiation of 3T3-L1 cells to adipocytes
- (2012) Katja Zebisch et al. ANALYTICAL BIOCHEMISTRY
- A novel ChREBP isoform in adipose tissue regulates systemic glucose metabolism
- (2012) Mark A. Herman et al. NATURE
- Glucose 6-phosphate, rather than xylulose 5-phosphate, is required for the activation of ChREBP in response to glucose in the liver
- (2011) Renaud Dentin et al. JOURNAL OF HEPATOLOGY
- Reversed-phase chromatography with multiple fraction concatenation strategy for proteome profiling of human MCF10A cells
- (2011) Yuexi Wang et al. PROTEOMICS
- Glucose-6-phosphate mediates activation of the carbohydrate responsive binding protein (ChREBP)
- (2010) Ming V. Li et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Fat Cell-Specific Ablation of Rictor in Mice Impairs Insulin-Regulated Fat Cell and Whole-Body Glucose and Lipid Metabolism
- (2010) A. Kumar et al. DIABETES
- Chronically increased glucose uptake by adipose tissue leads to lactate production and improved insulin sensitivity rather than obesity in the mouse
- (2010) S. Muñoz et al. DIABETOLOGIA
- Tamoxifen-inducible Cre-mediated recombination in adipocytes
- (2010) Antonia Sassmann et al. GENESIS
- mTOR complex 2 in adipose tissue negatively controls whole-body growth
- (2009) N. Cybulski et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Four grams of glucose
- (2008) David H. Wasserman AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM
- Anterograde transneuronal viral tract tracing reveals central sensory circuits from white adipose tissue
- (2008) C. Kay Song et al. AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY
- Selective versus Total Insulin Resistance: A Pathogenic Paradox
- (2008) Michael S. Brown et al. Cell Metabolism
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