×
验证码:
换一张
Forgotten Password?
Stay signed in
Login With UMPASS
English
|
繁體
Login With UMPASS
Log In
ALL
ORCID
TI
AU
PY
SU
KW
TY
JN
DA
IN
PB
FP
ST
SM
Study Hall
Image search
Paste the image URL
Home
Faculties & Institutes
Scholars
Publications
Subjects
Statistics
News
Search in the results
Faculties & Institutes
Institute of Chi... [1]
Authors
CHEN XIN [1]
Document Type
Journal article [10]
Date Issued
2019 [1]
2017 [2]
2016 [1]
2013 [1]
2011 [1]
2005 [1]
More...
Language
英語English [9]
Source Publication
Acta Pharmacolog... [1]
BIOCHEMICAL PHAR... [1]
Biochemical Jour... [1]
Biochemical Phar... [1]
Bioorganic and M... [1]
DRUG DEVELOPMENT... [1]
More...
Indexed By
SCIE [3]
Funding Organization
Funding Project
×
Knowledge Map
UM
Start a Submission
Submissions
Unclaimed
Claimed
Attach Fulltext
Bookmarks
Browse/Search Results:
1-10 of 10
Help
Selected(
0
)
Clear
Items/Page:
5
10
15
20
25
30
35
40
45
50
55
60
65
70
75
80
85
90
95
100
Sort:
Select
Journal Impact Factor Ascending
Journal Impact Factor Descending
Title Ascending
Title Descending
Author Ascending
Author Descending
Issue Date Ascending
Issue Date Descending
WOS Cited Times Ascending
WOS Cited Times Descending
Submit date Ascending
Submit date Descending
Formyl Peptide Receptor 2 Deficiency Improves Cognition and Attenuates Tau Hyperphosphorylation and Astrogliosis in a Mouse Model of Alzheimer's Disease
Journal article
Zhang, Haibo, Wang, Ding, Gong, Ping, Lin, Aihua, Zhang, Yan, Ye, Richard D., Yu, Yang. Formyl Peptide Receptor 2 Deficiency Improves Cognition and Attenuates Tau Hyperphosphorylation and Astrogliosis in a Mouse Model of Alzheimer's Disease[J]. Journal of Alzheimer's Disease, 2019, 67(1), 169-179.
Authors:
Zhang, Haibo
;
Wang, Ding
;
Gong, Ping
;
Lin, Aihua
;
Zhang, Yan
; et al.
Favorite
|
TC[WOS]:
19
TC[Scopus]:
18
IF:
3.4
/
4.2
|
Submit date:2022/05/23
Alzheimer's Disease
Astrocyte Activation
Formyl Peptide Receptor 2
Tau Phosphorylation
4-Aroyl-3-hydroxy-5-phenyl-1H-pyrrol-2(5H)-ones as N-formyl peptide receptor 1 (FPR1) antagonists
Journal article
Kirpotina, Liliya N., Schepetkin, Igor A., Khlebnikov, Andrei I., Ruban, Olga I., Ge, Yunjun, Ye, Richard D., Kominsky, Douglas J., Quinn, Mark T.. 4-Aroyl-3-hydroxy-5-phenyl-1H-pyrrol-2(5H)-ones as N-formyl peptide receptor 1 (FPR1) antagonists[J]. BIOCHEMICAL PHARMACOLOGY, 2017, 142, 120-132.
Authors:
Kirpotina, Liliya N.
;
Schepetkin, Igor A.
;
Khlebnikov, Andrei I.
;
Ruban, Olga I.
;
Ge, Yunjun
; et al.
Favorite
|
TC[WOS]:
29
TC[Scopus]:
28
IF:
5.3
/
5.2
|
Submit date:2018/10/30
Antagonist Formyl Peptide Receptor
1h-pyrrol-2(5h)-one
Neutrophil
Molecular Modeling
Synthesis of Five- and Six-Membered N-Phenylacetamido Substituted Heterocycles as Formyl Peptide Receptor Agonists
Journal article
Vergelli, Claudia, Schepetkin, Igor A., Ciciani, Giovanna, Cilibrizzi, Agostino, Crocetti, Letizia, Giovannoni, Maria Paola, Guerrini, Gabriella, Iacovone, Antonella, Kirpotina, Liliya N., Ye, Richard D., Quinn, Mark T.. Synthesis of Five- and Six-Membered N-Phenylacetamido Substituted Heterocycles as Formyl Peptide Receptor Agonists[J]. DRUG DEVELOPMENT RESEARCH, 2017, 78(1), 49-62.
Authors:
Vergelli, Claudia
;
Schepetkin, Igor A.
;
Ciciani, Giovanna
;
Cilibrizzi, Agostino
;
Crocetti, Letizia
; et al.
View
|
Adobe PDF
|
Favorite
|
TC[WOS]:
8
TC[Scopus]:
8
IF:
3.5
/
4.0
|
Submit date:2018/10/30
Formyl Peptide Receptor
Agonist
Pyridazin-3(2h)-one
Neutrophil
ca2+flux
2-Arylacetamido-4-phenylamino-5-substituted pyridazinones as formyl peptide receptors agonists
Journal article
Vergelli C., Schepetkin I.A., Ciciani G., Cilibrizzi A., Crocetti L., Giovannoni M.P., Guerrini G., Iacovone A., Kirpotina L.N., Khlebnikov A.I., Ye R.D., Quinn M.T.. 2-Arylacetamido-4-phenylamino-5-substituted pyridazinones as formyl peptide receptors agonists[J]. Bioorganic and Medicinal Chemistry, 2016, 24(11), 2530-2543.
Authors:
Vergelli C.
;
Schepetkin I.A.
;
Ciciani G.
;
Cilibrizzi A.
;
Crocetti L.
; et al.
Favorite
|
TC[WOS]:
21
TC[Scopus]:
21
|
Submit date:2018/11/07
Agonist
Ca2++ Mobilization
Formyl Peptide Receptor (Fpr)
Neutrophil
Pyridazin-3(2h)-one
V101L of human formyl peptide receptor 1 (FPR1) increases receptor affinity and augments the antagonism mediated by cyclosporins
Journal article
Zhou C., Zhou Y., Wang J., Feng Y., Wang H., Xue J., Chen Y., Ye R.D., Wang M.-W.. V101L of human formyl peptide receptor 1 (FPR1) increases receptor affinity and augments the antagonism mediated by cyclosporins[J]. Biochemical Journal, 2013, 451(2), 245-255.
Authors:
Zhou C.
;
Zhou Y.
;
Wang J.
;
Feng Y.
;
Wang H.
; et al.
Favorite
|
TC[WOS]:
12
TC[Scopus]:
14
|
Submit date:2018/11/07
Cyclosporin
Formyl Peptide Receptor 1 (Fpr1)
Haplotype
Pharmacogenomics
Receptor Affinity
Single Nucleotide Polymorphism
Characterization of Quin-C1 for its anti-inflammatory property in a mouse model of bleomycin-induced lung injury
Journal article
He M., Cheng N., Gao W.-W., Zhang M., Zhang Y.-Y., Ye R.D., Wang M.-W.. Characterization of Quin-C1 for its anti-inflammatory property in a mouse model of bleomycin-induced lung injury[J]. Acta Pharmacologica Sinica, 2011, 32(5), 601-610.
Authors:
He M.
;
Cheng N.
;
Gao W.-W.
;
Zhang M.
;
Zhang Y.-Y.
; et al.
Favorite
|
TC[WOS]:
32
TC[Scopus]:
33
|
Submit date:2018/11/07
Anti-inflammation
Bleomycin
Cytokines
Formyl Peptide Receptor
Lung Injury
Quin-c1
Identification of functional domains in the formyl peptide receptor-like 1 for agonist-induced cell chemotaxis
Journal article
Le Y., Ye R.D., Gong W., Li J., Iribarren P., Wang J.M.. Identification of functional domains in the formyl peptide receptor-like 1 for agonist-induced cell chemotaxis[J]. FEBS Journal, 2005, 272(3), 769-778.
Authors:
Le Y.
;
Ye R.D.
;
Gong W.
;
Li J.
;
Iribarren P.
; et al.
Favorite
|
TC[WOS]:
34
TC[Scopus]:
34
|
Submit date:2018/11/07
Chemotaxis
Formyl Peptide Receptor
Formyl Peptide Receptor-like 1
Structure-function
Novel chemoattractant peptides for human leukocytes
Journal article
Bae Y.-S., Park E.-Y., Kim Y., He R., Ye R.D., Kwak J.-Y., Suh P.-G., Ryu S.H.. Novel chemoattractant peptides for human leukocytes[J]. Biochemical Pharmacology, 2003, 66(9), 1841-1851.
Authors:
Bae Y.-S.
;
Park E.-Y.
;
Kim Y.
;
He R.
;
Ye R.D.
; et al.
Favorite
|
TC[WOS]:
13
TC[Scopus]:
13
|
Submit date:2018/11/07
Chemotaxis
Formyl Peptide Receptor Like 1
Peptide
Phagocytes
Phospholipase A2
Superoxide
Characterization of chenodeoxycholic acid as an endogenous antagonist of the G-coupled formyl peptide receptors
Journal article
Chen X., Yang D., Shen W., Dong H.F., Wang J.M., Oppenheim J.J., Howard O.M.Z.. Characterization of chenodeoxycholic acid as an endogenous antagonist of the G-coupled formyl peptide receptors[J]. Inflammation Research, 2000, 49(12), 744-755.
Authors:
Chen X.
;
Yang D.
;
Shen W.
;
Dong H.F.
;
Wang J.M.
; et al.
Favorite
|
TC[WOS]:
52
TC[Scopus]:
52
|
Submit date:2018/11/06
Bile Acids
Chemotaxis
Chenodeoxycholic Acid
Formyl Peptide Receptor
Formyl Peptide Receptor Like 1. Calcium Flux
The N-formyl peptide receptor: A model for the study of chemoattractant receptor structure and function
Journal article
Prossnitz E.R., Ye R.D.. The N-formyl peptide receptor: A model for the study of chemoattractant receptor structure and function[J]. Pharmacology and Therapeutics, 1997, 74(1), 73-102.
Authors:
Prossnitz E.R.
;
Ye R.D.
Favorite
|
TC[WOS]:
225
TC[Scopus]:
230
|
Submit date:2018/11/07
Chemoattractants
G-protein-coupled Receptor
Inflammation
N-formyl Peptide
N-formyl Peptide Receptor