Elegir campos a generar del autor Tania Del Mar

Datos personales Todos / Ninguno
Correo Electrónico
Artículos Todos / Ninguno
Positive allosteric γ‐aminobutyric acid type A receptor modulation prevents lipotoxicity‐induced injury in hepatocytes in vitro
DPP4 and ACE2 in Diabetes and COVID-19: Therapeutic Targets for Cardiovascular Complications?
DPP4 deletion in adipose tissue improves hepatic insulin sensitivity in diet-induced obesity
Visfatin/eNampt induces endothelial dysfunction in vivo: a role for Toll-Like Receptor 4 and NLRP3 inflammasome
Soluble dipeptidyl peptidase 4 triggers endothelial cell senescence: which role for thromboxane A2 (TXA2)?
The angiotensin-(1-7)/Mas receptor axis protects from endothelial cell senescence via klotho and Nrf2 activation
SOLUBLE DIPEPTIDYL PEPTIDASE 4 INDUCES SENESCENCE IN HUMAN ENDOTHELIAL CELLS
THE PHARMACOLOGICAL BLOCKADE OF INTERLEUKIN-1 beta PREVENTS ENDOTHELIAL SENESCENCE AND VASCULAR SMOOTH MUSCLE CELL INFLAMMATION
IS VISFATIN INVOLVED IN THE VASCULAR DYSFUNCTION ASSOCIATED WITH DIABESITY AND AGEING?
ANGIOTENSIN-(1-7) ATTENUATES ENDOTHELIAL CELL SENESCENCE VIA NRF2 ACTIVATION
THE ANGIOTENSIN-(1-7)/ MAS RECEPTOR AXIS COUNTERACT PRO-INFLAMMATORY SIGNALING IN HUMAN VASCULAR SMOOTH MUSCLE CELLS
DPP4 DELETION IN ADIPOSE TISSUE PROMOTES HEPATIC INSULIN SENSITIVITY VIA IGF1
IGF1 Links DPP-4 to Hepatic Insulin Sensitivity
Inflammation, glucose, and vascular cell damage: the role of the pentose phosphate pathway (vol 15, 82, 2016)
Protease-Activated Receptor 2 Promotes Pro-Atherogenic Effects through Transactivation of the VEGF Receptor 2 in Human Vascular Smooth Muscle Cells
Soluble Dipeptidyl Peptidase-4 Impairs Vasodilatation via Proteinase-Activated Receptor-2 and Thromboxane A2
The angiotensin-(1-7)/mas axis counteracts angiotensin II-dependent and -independent pro-inflammatory signaling in human vascular smooth muscle cells
Eicosapentaenoic acid and arachidonic acid differentially regulate adipogenesis, acquisition of a brite phenotype and mitochondrial function in primary human adipocytes
Inflammation, glucose, and vascular cell damage: the role of the pentose phosphate pathway
Soluble dipeptidyl peptidase-4 induces microvascular endothelial dysfunction through proteinase-activated receptor-2 and thromboxane A(2) release
ANGIOTENSIN-(1-7) MITIGATES VASCULAR INFLAMMATION AND SENESCENCE THROUGH MAS RECEPTOR
THE ADIPOKINE SOLUBLE DIPEPTIDYL PEPTIDASE-4 IMPAIRS MICROVASCULAR REACTIVITY THROUGH PROTEINASE-ACTIVATED RECEPTOR-2 AND THROMBOXANE A2 PRODUCTION
PAR2 is upregulated by adipocyte-derived factors and high fat diet in the vascular wall
Adipose-specific Dipeptidyl Peptidase 4 (DPP4) knockout mice display improved fasting insulin and smaller adipocytes on High Fat Diet (HFD)
Eicosapentaenoic Acid but Not Docosahexaenoic Acid Promotes a Brite Phenotype in Primary Human Adipocytes
Adipose-specific Dipeptidyl Peptidase-4 (DPP-4) Knockout Mice Display Improved Fasting Insulin and Cholesterol Levels Despite Increased Weight Gain on HFD
Adipose-Tissue Specific Deletion of Dipeptidyl Peptidase-4 (DPP-4) Enhances M2 Macrophage Markers and Results in Smaller Adipocytes Under HFD
Nutritional ingredients modulate adipokine secretion and inflammation in human primary adipocytes
The interleukin-1 receptor antagonist anakinra improves endothelial dysfunction in streptozotocin-induced diabetic rats
Soluble Dipeptidyl Peptidase-4 Induces Endothelial Dysfunction by the Release of Vasoconstrictor Prostanoids: Protective Effect of Dipeptidyl Peptidase Inhibitors
Effect of the n-3 LC-PUFA EPA on white-to-brown transition of primary human adipose-derived stem cells
Inflammatory stimulation transforms glucose into a deleterious agent in human vascular smooth muscle cells
Soluble dipeptidyl peptidase 4 induces inflammation and proliferation of human vascular smooth muscle cells via protease-activated receptor 2
MICROVASCULAR ENDOTHELIAL DYSFUNCTION BY SOLUBLE DIPEPTIDYL PEPTIDASE-4: RELEASE OF THROMBOXANE-A(2)
Inflammation Converts Glucose Into A Deleterious Agent In Human Aortic Smooth Muscle Cells
Soluble DPP4 induces inflammation and proliferation of human smooth muscle cells via protease-activated receptor 2
THE ANGIOTENSIN (1-7)/MAS RECEPTOR AXIS AND VASCULAR CELL INFLAMMATION
THE ADIPOKINE VISFATIN/NAMPT INDUCES PREMATURE SENESCENCE AND TELOMERE DAMAGE IN HUMAN ENDOTHELIAL CELLS
Visfatin/Nampt induces telomere damage and senescence in human endothelial cells
THE ADIPOKINE VISFATIN/NAMPT PROMOTES TELOMERE DAMAGE AND PREMATURE SENESCENCE IN HUMAN ENDOTHELIAL CELLS
THE ACTIVATION OF THE ANGIOTENSIN (1-7)/MAS RECEPTOR AXIS PROTECTS AGAINST VASCULAR CELL INFLAMMATION
SOLUBLE DIPEPTIDYL PEPTIDASE-4 IMPAIRS MICROVASCULAR ENDOTHELIUM-DEPENDENT RELAXATION: A ROLE FOR VASOCONSTRICTOR PROSTANOIDS
DPP-4 Is a Novel Adipokine Contributing to Endothelial Dysfunction Through Its Enzymatic Activity and the Release of Thromboxane A2
Adipose tissue and its role in organ crosstalk
BMP4 and BMP7 induce the white-to-brown transition of primary human adipose stem cells
Visfatin/Nampt: An Adipokine with Cardiovascular Impact
Evidence against a beneficial effect of irisin in humans.
Visfatin as a Novel Mediator Released by Inflamed Human Endothelial Cells
THE ADIPOKINE VISFATIN INDUCES TELOMERE DAMAGE AND CELL SENESCENCE IN HUMAN ENDOTHELIAL CELLS
The novel adipokines BMP4 and BMP7 promote browning of primary human adipose-derived stem cells
Endothelial dysfunction induced by dipeptidyl peptidase-4 in isolated mice mesenteric microvessels
Evidence against a beneficial effect of irisin in humans
Evidence against a Beneficial Effect of Irisin in Humans
Dipeptidyl Peptidase-4 Impairs Microvascular Endothelial-Dependent Relaxation: The Role of Cyclooxygenase
The Novel Adipokines BMP4 and BMP7 Induce Browning in Primary Human Adipose Stem Cells
Inflammation enhances visfatin synthesis in the vascular wall
Evidence against a beneficial effect of irisin in humans
Pathways responsible for apoptosis resulting from Amadori-induced oxidative and nitrosative stress in human mesothelial cells
VISFATIN IMPAIRS ENDOTHELIUM-DEPENDENT RELAXATION IN HUMAN PENILE RESISTANCE ARTERIES THROUGH NICOTINAMIDE PHOPHORIBOSYL TRANSFERASE (NAMPT) ACTIVITY
Visfatin Impairs Endothelium-Dependent Relaxation in Rat and Human Mesenteric Microvessels through Nicotinamide Phosphoribosyltransferase Activity
VISFATIN IMPAIRS ENDOTHELIUM-DEPENDENT RELAXATION IN MICROVESSELS: ROLE OF NAMPT AND NAD
THE ANGIOTENSIN-(1-7)/MAS AXIS EXHIBITS ANTI-INFLAMMATORY PROPERTIES IN VASCULAR HUMAN SMOOTH MUSCLE CELLS
Inhibition of vascular endothelial growth factor (VEGF)-induced endothelial proliferation, arterial relaxation, vascular permeability and angiogenesis by dobesilate
Visfatin/PBEF/Nannpt: a new cardiovascular target?
Inflammation Determines the Pro-Adhesive Properties of High Extracellular D-Glucose in Human Endothelial Cells In Vitro and Rat Microvessels In Vivo
Extracellular PBEF/NAMPT/visfatin activates pro-inflammatory signalling in human vascular smooth muscle cells through nicotinamide phosphoribosyltransferase activity
VISFATIN/NAMPT/PBEF: ROLE IN VASCULAR WALL INFLAMMATION
THE ADIPOKINE VISFATIN IS SYNTHESIZED BY HUMAN ENDOTHELIAL CELLS AND EXERTS A DIRECT INFLAMMATORY EFFECT ON HUMAN SMOOTH MUSCLE CELLS.
Insulin Resistance, Endothelial Dysfunction and Inflammation: A Role for Adipokines
The adipokine visfatin is synthesized by human endothelial cells and promotes inflammation in human smooth muscle cells
In vitro and In vivo induction of adhesion molecules and leukocyte recruitment: interaction between high glucose and inflammation
The deleterious effect of high concentrations of D-glucose requires pro-inflammatory preconditioning
Libros, capítulos, tesis Todos / Ninguno
Adipose Tissue Dysfunction and Inflammation in Cardiovascular Disease
Métricas del autor Todos / Ninguno
Indice H