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Characterization of Two Types of Endothelial Progenitor Cells and Their Different Contributions to Neovasculogenesis
Characterization of Two Types of Endothelial Progenitor Cells and Their Different Contributions to Neovasculogenesis
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Characterization of Two Types of Endothelial Progenitor Cells and Their Different Contributions to Neovasculogenesis

Hur, Jin ; Yoon, Chang-Hwan ; Kim, Hyo-Soo ; Choi, Jin-Ho ; Kang, Hyun-Jae ; Hwang, Kyung-Kook ; Oh, Byung-Hee ; Lee, Myoung-Mook ; Park, Young-Bae

Arteriosclerosis, thrombosis, and vascular biology, 2004-02, Vol.24 (2), p.288-293 [Periódico revisado por pares]

Philadelphia, PA: American Heart Association, Inc

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2
Delta-like 4 Notch Ligand Regulates Tumor Angiogenesis, Improves Tumor Vascular Function, and Promotes Tumor Growth In vivo
Delta-like 4 Notch Ligand Regulates Tumor Angiogenesis, Improves Tumor Vascular Function, and Promotes Tumor Growth In vivo
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Delta-like 4 Notch Ligand Regulates Tumor Angiogenesis, Improves Tumor Vascular Function, and Promotes Tumor Growth In vivo

LI, Ji-Liang ; SAINSON, Richard C. A ; HARRIS, Adrian L ; WEN SHI ; LEEK, Russell ; HARRINGTON, Laura S ; PREUSSER, Matthias ; BISWAS, Swethajit ; TURLEY, Helen ; HEIKAMP, Emily ; HAINFELLNER, Johannes A

Cancer research (Chicago, Ill.), 2007-12, Vol.67 (23), p.11244-11253 [Periódico revisado por pares]

Philadelphia, PA: American Association for Cancer Research

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3
Activation of AMP-Activated Protein Kinase Inhibits Oxidized LDL-Triggered Endoplasmic Reticulum Stress In Vivo
Activation of AMP-Activated Protein Kinase Inhibits Oxidized LDL-Triggered Endoplasmic Reticulum Stress In Vivo
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Activation of AMP-Activated Protein Kinase Inhibits Oxidized LDL-Triggered Endoplasmic Reticulum Stress In Vivo

YUNZHOU DONG ; MIAO ZHANG ; SHUANGXI WANG ; BIN LIANG ; ZHENGXING ZHAO ; CHAO LIU ; MINGYUAN WU ; HYOUNG CHUL CHOI ; LYONS, Timothy J ; ZOU, Ming-Hui

Diabetes (New York, N.Y.), 2010-06, Vol.59 (6), p.1386-1396 [Periódico revisado por pares]

Alexandria, VA: American Diabetes Association

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4
Selective Activation of Peroxisome Proliferator–Activated Receptor (PPAR)α and PPARγ Induces Neoangiogenesis Through a Vascular Endothelial Growth Factor–Dependent Mechanism
Selective Activation of Peroxisome Proliferator–Activated Receptor (PPAR)α and PPARγ Induces Neoangiogenesis Through a Vascular Endothelial Growth Factor–Dependent Mechanism
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Selective Activation of Peroxisome Proliferator–Activated Receptor (PPAR)α and PPARγ Induces Neoangiogenesis Through a Vascular Endothelial Growth Factor–Dependent Mechanism

BISCETTI, Federico ; GAETANI, Eleonora ; CASTELLOT, John J ; POLA, Roberto ; FLEX, Andrea ; APRAHAMIAN, Tamar ; HOPKINS, Teresa ; STRAFACE, Giuseppe ; PECORINI, Giovanni ; STIGLIANO, Egidio ; SMITH, Roy C ; ANGELINI, Flavia

Diabetes (New York, N.Y.), 2008-05, Vol.57 (5), p.1394-1404 [Periódico revisado por pares]

Alexandria, VA: American Diabetes Association

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5
Peroxisome Proliferator-Activated Receptor γ Ligands Increase Release of Nitric Oxide From Endothelial Cells
Peroxisome Proliferator-Activated Receptor γ Ligands Increase Release of Nitric Oxide From Endothelial Cells
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Peroxisome Proliferator-Activated Receptor γ Ligands Increase Release of Nitric Oxide From Endothelial Cells

Calnek, David S ; Mazzella, Louis ; Roser, Susanne ; Roman, Jesse ; Hart, C Michael

Arteriosclerosis, thrombosis, and vascular biology, 2003-01, Vol.23 (1), p.52-57 [Periódico revisado por pares]

Philadelphia, PA: American Heart Association, Inc

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6
AMG 706, an oral, multikinase inhibitor that selectively targets vascular endothelial growth factor, platelet-derived growth factor, and kit receptors, potently inhibits angiogenesis and induces regression in tumor xenografts
AMG 706, an oral, multikinase inhibitor that selectively targets vascular endothelial growth factor, platelet-derived growth factor, and kit receptors, potently inhibits angiogenesis and induces regression in tumor xenografts
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AMG 706, an oral, multikinase inhibitor that selectively targets vascular endothelial growth factor, platelet-derived growth factor, and kit receptors, potently inhibits angiogenesis and induces regression in tumor xenografts

POLVERINO, Anthony ; COXON, Angela ; DANLIN CHEN ; YONGMEI GAN ; KUMAR, Gondi ; MEYER, James ; NEERVANNAN, Sesha ; ALVA, Gonzalo ; TALVENHEIMO, Jane ; MONTESTRUQUE, Silvia ; TASKER, Andrew ; PATEL, Vinod ; STARNES, Charlie ; RADINSKY, Robert ; KENDALL, Richard ; DIAZ, Zobedia ; DEMELFI, Thomas ; LING WANG ; BREADY, James ; ESTRADA, Juan ; CATTLEY, Russell ; KAUFMAN, Stephen

Cancer research (Chicago, Ill.), 2006-09, Vol.66 (17), p.8715-8721 [Periódico revisado por pares]

Philadelphia, PA: American Association for Cancer Research

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7
In Vivo Activation of AMP-Activated Protein Kinase Attenuates Diabetes-Enhanced Degradation of GTP Cyclohydrolase I
In Vivo Activation of AMP-Activated Protein Kinase Attenuates Diabetes-Enhanced Degradation of GTP Cyclohydrolase I
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In Vivo Activation of AMP-Activated Protein Kinase Attenuates Diabetes-Enhanced Degradation of GTP Cyclohydrolase I

Wang, Shuangxi ; Xu, Jian ; Song, Ping ; Viollet, Benoit ; Zou, Ming-Hui

Diabetes (New York, N.Y.), 2009-08, Vol.58 (8), p.1893-1901 [Periódico revisado por pares]

Alexandria, VA: American Diabetes Association

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8
Intermittent high glucose enhances apoptosis related to oxidative stress in human umbilical vein endothelial cells: The role of protein kinase C and NAD(P)H-oxidase activation
Intermittent high glucose enhances apoptosis related to oxidative stress in human umbilical vein endothelial cells: The role of protein kinase C and NAD(P)H-oxidase activation
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Intermittent high glucose enhances apoptosis related to oxidative stress in human umbilical vein endothelial cells: The role of protein kinase C and NAD(P)H-oxidase activation

QUAGLIARO, Lisa ; PICONI, Ludovica ; ASSALONI, Roberta ; MARTINELLI, Lucia ; MOTZ, Enrico ; CERIELLO, Antonio

Diabetes (New York, N.Y.), 2003-11, Vol.52 (11), p.2795-2804 [Periódico revisado por pares]

Alexandria, VA: American Diabetes Association

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9
Kisspeptins Are Novel Potent Vasoconstrictors in Humans, with a Discrete Localization of Their Receptor, G Protein-Coupled Receptor 54, to Atherosclerosis-Prone Vessels
Kisspeptins Are Novel Potent Vasoconstrictors in Humans, with a Discrete Localization of Their Receptor, G Protein-Coupled Receptor 54, to Atherosclerosis-Prone Vessels
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Kisspeptins Are Novel Potent Vasoconstrictors in Humans, with a Discrete Localization of Their Receptor, G Protein-Coupled Receptor 54, to Atherosclerosis-Prone Vessels

Mead, Emma J ; Maguire, Janet J ; Kuc, Rhoda E ; Davenport, Anthony P

Endocrinology (Philadelphia), 2007-01, Vol.148 (1), p.140-147 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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10
Fetal cardiac output, distribution to the placenta and impact of placental compromise
Fetal cardiac output, distribution to the placenta and impact of placental compromise
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Fetal cardiac output, distribution to the placenta and impact of placental compromise

Kiserud, T. ; Ebbing, C. ; Kessler, J. ; Rasmussen, S.

Ultrasound in obstetrics & gynecology, 2006-08, Vol.28 (2), p.126-136 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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