Rong L. He

发表

Characterization of a Mutation in the Phox Homology Domain of the NADPH Oxidase Component p40phox Identifies A Mechanism for Negative Regulation of Superoxide Production*

M. Dinauer, R. Ye, R. Minshall, 2007, Journal of Biological Chemistry.

Studies of Benzamide‐ and Thiol‐Based Histone Deacetylase Inhibitors in Models of Oxidative‐Stress‐Induced Neuronal Death: Identification of Some HDAC3‐Selective Inhibitors

B. Langley, A. Kozikowski, Yufeng Chen, 2009, ChemMedChem.

Normal Cell Surface Expression and Selective Loss of Functions Resulting from Phe110 to Ser and Cys126 to Trp Substitutions in the Formyl Peptide Receptor

R. Ye, M. Nanamori, Rong L. He, 2004, Immunological investigations.

Serum amyloid A induces IL-8 secretion through a G protein-coupled receptor, FPRL1/LXA4R.

R. Ye, Rong L. He, H. Sang, 2003, Blood.

Differential signaling of formyl peptide receptor-like 1 by Trp-Lys-Tyr-Met-Val-Met-CONH2 or lipoxin A4 in human neutrophils.

J. Kwak, P. Suh, R. Ye, 2003, Molecular pharmacology.

Reconstitution of Chemotactic Peptide-Induced Nicotinamide Adenine Dinucleotide Phosphate (Reduced) Oxidase Activation in Transgenic COS-phox Cells1

M. Dinauer, R. Ye, M. Nanamori, 2004, The Journal of Immunology.

Cutting Edge: TLR2 Is a Functional Receptor for Acute-Phase Serum Amyloid A1

R. Ye, Jun Tian, Ni Cheng, 2008, The Journal of Immunology.

receptor, FPRL1/LXA4R Serum amyloid A induces IL-8 secretion through a G protein-coupled

R. Ye, Rong L. He, H. Sang, 2011 .

Mouse Neutrophils as Potent Chemoattractants for aureus Staphylococcus and Listeria monocytogenes Identification of Formyl Peptides from

R. Ye, P. Murphy, Ji-Liang Gao, 2008 .

A Ca2+-binding domain in RyR1 that interacts with the calmodulin binding site and modulates channel activity.

S. Hamilton, L. Xiong, Rong L. He, 2006, Biophysical journal.

Stereoselective HDAC Inhibition from Cysteine‐Derived Zinc‐Binding Groups

Kyle V. Butler, K. McLaughlin, B. Langley, 2009, ChemMedChem.

CHARACTERIZATION OF A MUTATION IN THE PX DOMAIN OF THE NADPH OXIDASE COMPONENT p 40 PHOX IDENTIFIES A MECHANISM FOR NEGATIVE REGULATION OF SUPEROXIDE PRODUCTION *

M. Dinauer, R. Ye, R. Minshall, 2007 .

Dinucleotide Phosphate Oxidase Activation of Nicotinamide Adenine and Rapid phox uced Phosphorylation of p47 Formyl-Methionyl-Leucyl-Phenylalanine-IndActivation Loop Phosphorylation in d A Critical Role of Protein Kinase C

M. Dinauer, R. Ye, Jun Tian, 2022 .

Isoxazole moiety in the linker region of HDAC inhibitors adjacent to the Zn-chelating group: effects on HDAC biology and antiproliferative activity.

A. Kozikowski, D. Billadeau, Doris N Luchini, 2009, Bioorganic & medicinal chemistry letters.

Activation in Transgenic COS-phox Cells Dinucleotide Phosphate ( Reduced ) Oxidase Peptide-Induced Nicotinamide Adenine Reconstitution of Chemotactic

M. Dinauer, R. Ye, M. Nanamori, 2004 .

Synthesis and antituberculosis activity of novel mefloquine-isoxazole carboxylic esters as prodrugs.

S. Franzblau, J. Mao, B. Wan, 2010, Bioorganic & medicinal chemistry letters.

Further structure-activity relationship studies of piperidine-based monoamine transporter inhibitors: effects of piperidine ring stereochemistry on potency. Identification of norepinephrine transporter selective ligands and broad-spectrum transporter inhibitors.

Kenneth M. Johnson, A. Kozikowski, Kelly M. Giberson, 2005, Journal of medicinal chemistry.

Novel chemoattractant peptides for human leukocytes.

J. Kwak, S. Ryu, P. Suh, 2003, Biochemical pharmacology.

Differential activation of formyl peptide receptor signaling by peptide ligands.

Sung Ho Ryu, Jong-Young Kwak, Pann-Ghill Suh, 2003, Molecular pharmacology.

Identification, synthesis, and pharmacological evaluation of tetrahydroindazole based ligands as novel antituberculosis agents.

A. Kozikowski, S. Franzblau, M. Beconi, 2010, Journal of medicinal chemistry.

Synthesis and biological evaluation of triazol-4-ylphenyl-bearing histone deacetylase inhibitors as anticancer agents.

A. Kozikowski, Rong L He, Yufeng Chen, 2010, Journal of medicinal chemistry.

Identification of Formyl Peptides from Listeria monocytogenes and Staphylococcus aureus as Potent Chemoattractants for Mouse Neutrophils1

R. Ye, P. Murphy, Rong L He, 2008, The Journal of Immunology.

The Synthetic Peptide Trp-Lys-Tyr-Met-Val-d-Met Is a Potent Chemotactic Agonist for Mouse Formyl Peptide Receptor1

Ji Ming Wang, R. Ye, Rong L He, 2000, The Journal of Immunology.

Kinetics and molecular docking studies of the inhibitions of angiotensin converting enzyme and renin activities by hemp seed (Cannabis sativa L.) peptides.

R. Aluko, Rong L He, A. Girgih, 2014, Journal of agricultural and food chemistry.

Human dendritic cells express functional formyl peptide receptor‐like‐2 (FPRL2) throughout maturation

R. Ye, Rong L He, J. Oppenheim, 2002, Journal of leukocyte biology.

Emodin Enhances Arsenic Trioxide-Induced Apoptosis via Generation of Reactive Oxygen Species and Inhibition of Survival Signaling

R. Ye, Jie Yang, Xue-ming Tang, 2004, Cancer Research.

Peptide Receptor Chemotactic Agonist for Mouse Formyl Trp-Lys-Tyr-Met-Val-d-Met Is a Potent The Synthetic Peptide and

Ji Ming Wang, R. Ye, Rong L He, 2000 .

Serum amyloid A induces G-CSF expression and neutrophilia via Toll-like receptor 2.

R. Ye, Ni Cheng, Jia Chen, 2009, Blood.

Modification of the side chain of micromolide, an anti-tuberculosis natural product.

A. Kozikowski, S. Franzblau, B. Wan, 2008, Bioorganic & medicinal chemistry letters.

Stereochemistry at the forefront in the design and discovery of novel anti-tuberculosis agents.

A. Kozikowski, Qingqing Huang, Rong L. He, 2011, Current topics in medicinal chemistry.

Piperidine-based nocaine/modafinil hybrid ligands as highly potent monoamine transporter inhibitors: efficient drug discovery by rational lead hybridization.

Kenneth M. Johnson, A. Kozikowski, Jia Zhou, 2004, Journal of medicinal chemistry.

beta-Arrestin1 interacts with the G-protein subunits beta1gamma2 and promotes beta1gamma2-dependent Akt signalling for NF-kappaB activation.

J. Benovic, R. Ye, Ming Yang, 2009, The Biochemical journal.

Serum Amyloid A Is an Endogenous Ligand That Differentially Induces IL-12 and IL-231

R. Ye, Z. Pan, Jia Chen, 2006, The Journal of Immunology.

Differential Roles of the NPXXY Motif in Formyl Peptide Receptor Signaling1

R. Ye, D. Browning, Rong L. He, 2001, The Journal of Immunology.

Sites on Calmodulin That Interact with the C-terminal Tail of Cav1.2 Channel*

J. Putkey, Q. Kleerekoper, S. Hamilton, 2005, Journal of Biological Chemistry.

Role of the increased noradrenergic neurotransmission in drug self-administration.

A. Kozikowski, Jia Zhou, W. Woolverton, 2006, Drug and alcohol dependence.

Structure-activity relationships of compounds targeting mycobacterium tuberculosis 1-deoxy-D-xylulose 5-phosphate synthase.

A. Kozikowski, S. Franzblau, D. Crick, 2008, Bioorganic & medicinal chemistry letters.

M. Dinauer, R. Ye, Jun Tian, 2007 .

The protective effect of Yi-Qi-Yang-Yin-Ye, a compound of traditional Chinese herbal medicine in diet-induced obese rats.

Rong L. He, Wei-jing Qu, Guang-wei He, 2008, The American journal of Chinese medicine.

Isoxazole moiety in the linker region of HDAC inhibitors adjacent to the Zn-chelating group: effects on HDAC biology and antiproliferative activity.

A. Kozikowski, D. Billadeau, Doris N Luchini, 2009, Bioorganic & medicinal chemistry letters.

Development of new brain imaging agents based upon nocaine-modafinil hybrid monoamine transporter inhibitors.

C. Halldin, J. Liow, V. Pike, 2006, Bioorganic & medicinal chemistry letters.

Survival Signaling Generation of Reactive Oxygen Species and Inhibition of Emodin Enhances Arsenic Trioxide-Induced Apoptosis via

R. Ye, Jie Yang, Xue-ming Tang, 2004 .