H. Lin

发表

Butyrate and Propionate Protect against Diet-Induced Obesity and Regulate Gut Hormones via Free Fatty Acid Receptor 3-Independent Mechanisms

Hua V. Lin, D. Marsh, A. Frassetto, 2012, PloS one.

Hormonal regulation of hepatic glucose production in health and disease.

D. Accili, H. Lin, H. Lin, 2011, Cell metabolism.

Proatherogenic abnormalities of lipid metabolism in SirT1 transgenic mice are mediated through Creb deacetylation.

D. Accili, W. Gu, L. Qiang, 2011, Cell metabolism.

Reconstitution of Insulin Action in Muscle, White Adipose Tissue, and Brain of Insulin Receptor Knock-out Mice Fails to Rescue Diabetes*

Hua V. Lin, D. Accili, H. Lin, 2011, The Journal of Biological Chemistry.

Hepatic GALE Regulates Whole-Body Glucose Homeostasis by Modulating Tff3 Expression

Hua V. Lin, P. Scherer, P. Xu, 2017, Diabetes.

Connexin 43 Mediates White Adipose Tissue Beiging by Facilitating the Propagation of Sympathetic Neuronal Signals.

Hua V. Lin, D. Spray, J. Elmquist, 2016, Cell metabolism.

Pancreatic β Cell Dedifferentiation as a Mechanism of Diabetic β Cell Failure

C. Talchai, S. Xuan, Hua V. Lin, 2012, Cell.

Adiponectin Resistance Exacerbates Insulin Resistance in Insulin Receptor Transgenic/Knockout Mice

Hua V. Lin, D. Accili, L. Shapiro, 2007, Diabetes.

Role of the forkhead protein FoxO1 in beta cell compensation to insulin resistance.

Hua V. Lin, D. Accili, H. Okamoto, 2006, The Journal of clinical investigation.

Diabetes in Mice With Selective Impairment of Insulin Action in Glut4-Expressing Tissues

G. Shulman, D. Accili, Hui-Young Lee, 2011, Diabetes.

Divergent Regulation of Energy Expenditure and Hepatic Glucose Production by Insulin Receptor in Agouti-Related Protein and POMC Neurons

T. Horvath, D. Accili, E. Borók, 2009, Diabetes.

InsR/FoxO1 Signaling Curtails Hypothalamic POMC Neuron Number

Hua V. Lin, D. Accili, L. Plum, 2012, PloS one.

Normal bone density obtained in the absence of insulin receptor expression in bone.

L. McCabe, Regina Irwin, Hua V Lin, 2006, Endocrinology.

Identification and Characterization of Sebaceous Gland Atrophy-Sparing DGAT1 Inhibitors

Guanghui Hu, Hua V. Lin, Shirly Pinto, 2014, PloS one.

The Obesity Susceptibility Gene Carboxypeptidase E Links FoxO1 Signaling in Hypothalamic Pro–opiomelanocortin Neurons with Regulation of Food Intake

R. DePinho, D. Accili, Y. Loh, 2009, Nature Medicine.

A FOXO1-dependent transcription network is a targetable vulnerability of mantle cell lymphomas

O. Elemento, Jun Yao, L. Marchionni, 2021, The Journal of clinical investigation.

Increased Atherosclerosis and Endothelial Dysfunction in Mice Bearing Constitutively Deacetylated Alleles of Foxo1 Gene*

Hua V. Lin, D. Accili, K. Tsuchiya, 2012, The Journal of Biological Chemistry.

Chemical induction of gut β-like-cells by combined FoxO1/Notch inhibition as a glucose-lowering treatment for diabetes

Hua V. Lin, D. Accili, Wendy M. McKimpson, 2021, bioRxiv.

GPR142 Controls Tryptophan-Induced Insulin and Incretin Hormone Secretion to Improve Glucose Metabolism

Hua V. Lin, L. Beavers, A. Efanov, 2016, PloS one.

GPR142 Agonists Stimulate Glucose-Dependent Insulin Secretion via Gq-Dependent Signaling

Hua V. Lin, J. J. Carrillo, Jingru Wang, 2016, PloS one.

Diacylglycerol Acyltransferase-1 (DGAT1) Inhibition Perturbs Postprandial Gut Hormone Release

Hua V. Lin, Shirly Pinto, M. Garcia-Calvo, 2013, PloS one.

GPR142 prompts glucagon-like Peptide-1 release from islets to improve β cell function

Hua V. Lin, Melissa K Thomas, A. Efanov, 2018, Molecular metabolism.

FOXO1 inhibition synergizes with FGF21 to normalize glucose control in diabetic mice

D. Accili, Samuel X. Lee, Yun-Kyoung Lee, 2021, Molecular metabolism.