VIAF

Virtual International Authority File

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Leader     00000nz a2200037n 45 0
001     WKP|Q59160197  (VIAF cluster)  (Authority/Source Record)
003     WKP
005     20241121000046.0
008     241121nneanz||abbn n and d
035 ‎‡a  (WKP)Q59160197‏
024 ‎‡a  0000-0003-0671-7312‏ ‎‡2  orcid‏
024 ‎‡a  56042377900‏ ‎‡2  scopus‏
024 ‎‡a  57192923840‏ ‎‡2  scopus‏
035 ‎‡a  (OCoLC)Q59160197‏
100 0 ‎‡a  Yan Wang‏ ‎‡c  researcher ORCID ID = 0000-0003-0671-7312‏ ‎‡9  en‏
670 ‎‡a  Author's (+/-)-Lucidumone, a COX-2 Inhibitory Caged Fungal Meroterpenoid from Ganoderma lucidum‏
670 ‎‡a  Author's 1,4-Bis(5-(naphthalen-1-yl)thiophen-2-yl)naphthalene, a small molecule, functions as a novel anti-HIV-1 inhibitor targeting the interaction between integrase and cellular Lens epithelium-derived growth factor.‏
670 ‎‡a  Author's A fluorescence-based high-throughput assay to identify inhibitors of tyrosylprotein sulfotransferase activity.‏
670 ‎‡a  Author's Acetylshikonin, a Novel AChE Inhibitor, Inhibits Apoptosis via Upregulation of Heme Oxygenase-1 Expression in SH-SY5Y Cells‏
670 ‎‡a  Author's Antiviral activities of whey proteins‏
670 ‎‡a  Author's Bovine Lactoferrampin, Human Lactoferricin, and Lactoferrin 1-11 Inhibit Nuclear Translocation of HIV Integrase‏
670 ‎‡a  Author's Characterization of miR-210 in 3T3-L1 adipogenesis.‏
670 ‎‡a  Author's Differential regulation of lipid metabolism genes in the brain of acetylcholinesterase knockout mice‏
670 ‎‡a  Author's Discovery of FDA-approved drugs as inhibitors of fatty acid binding protein 4 using molecular docking screening‏
670 ‎‡a  Author's Enzyme kinetic and molecular docking studies for the inhibitions of miltirone on major human cytochrome P450 isozymes.‏
670 ‎‡a  Author's FRET-based assay using a three-way junction DNA substrate to identify inhibitors of human cytomegalovirus pUL89 endonuclease activity‏
670 ‎‡a  Author's Ganoderma cochlear Metabolites as Probes to Identify a COX-2 Active Site and as in Vitro and in Vivo Anti-Inflammatory Agents‏
670 ‎‡a  Author's Herbalog: A tool for target-based identification of herbal drug efficacy through molecular docking.‏
670 ‎‡a  Author's Inhibition of Human Cytomegalovirus pUL89 Terminase Subunit Blocks Virus Replication and Genome Cleavage‏
670 ‎‡a  Author's Lung tissue distribution of drugs as a key factor for COVID-19 treatment‏
670 ‎‡a  Author's Miltirone Is a Dual Inhibitor of P-Glycoprotein and Cell Growth in Doxorubicin-Resistant HepG2 Cells‏
670 ‎‡a  Author's MiR-25 suppresses 3T3-L1 adipogenesis by directly targeting KLF4 and C/EBPα.‏
670 ‎‡a  Author's Molecular docking and enzyme kinetic studies of dihydrotanshinone on metabolism of a model CYP2D6 probe substrate in human liver microsomes‏
670 ‎‡a  Author's Overexpression of CXCR4 synergizes with LL-37 in the metastasis of breast cancer cells‏
670 ‎‡a  Author's Pimozide, a novel fatty acid binding protein 4 inhibitor, promotes adipogenesis of 3T3-L1 cells by activating PPARγ.‏
670 ‎‡a  Author's Silibinin, a novel chemokine receptor type 4 antagonist, inhibits chemokine ligand 12-induced migration in breast cancer cells.‏
670 ‎‡a  Author's Synthesis, β -catenin Translocation Capability and ALP Activation Activity of 7H-thiazolo[3,2-b]-1,2,4-triazin-7-one Derivatives.‏
909 ‎‡a  (scopus) 57192923840‏ ‎‡9  1‏
909 ‎‡a  (scopus) 56042377900‏ ‎‡9  1‏
909 ‎‡a  (orcid) 0000000306717312‏ ‎‡9  1‏
919 ‎‡a  bovinelactoferrampinhumanlactoferricinandlactoferrin111inhibitnucleartranslocationofhivintegrase‏ ‎‡A  Bovine Lactoferrampin, Human Lactoferricin, and Lactoferrin 1-11 Inhibit Nuclear Translocation of HIV Integrase‏ ‎‡9  1‏
919 ‎‡a  differentialregulationoflipidmetabolismgenesinthebrainofacetylcholinesteraseknockoutmice‏ ‎‡A  Differential regulation of lipid metabolism genes in the brain of acetylcholinesterase knockout mice‏ ‎‡9  1‏
919 ‎‡a  +lucidumoneacox2inhibitorycagedfungalmeroterpenoidfromganodermalucidum‏ ‎‡A  (+/-)-Lucidumone, a COX-2 Inhibitory Caged Fungal Meroterpenoid from Ganoderma lucidum‏ ‎‡9  1‏
919 ‎‡a  ganodermacochlearmetabolitesasprobestoidentifyacox2activesiteandasinvitroandinvivoantiinflammatoryagents‏ ‎‡A  Ganoderma cochlear Metabolites as Probes to Identify a COX-2 Active Site and as in Vitro and in Vivo Anti-Inflammatory Agents‏ ‎‡9  1‏
919 ‎‡a  herbalogatoolfortargetbasedidentificationofherbaldrugefficacythroughmoleculardocking‏ ‎‡A  Herbalog: A tool for target-based identification of herbal drug efficacy through molecular docking.‏ ‎‡9  1‏
919 ‎‡a  inhibitionofhumancytomegaloviruspul89terminasesubunitblocksvirusreplicationandgenomecleavage‏ ‎‡A  Inhibition of Human Cytomegalovirus pUL89 Terminase Subunit Blocks Virus Replication and Genome Cleavage‏ ‎‡9  1‏
919 ‎‡a  discoveryoffdaapproveddrugsasinhibitorsoffattyacidbindingprotein4usingmoleculardockingscreening‏ ‎‡A  Discovery of FDA-approved drugs as inhibitors of fatty acid binding protein 4 using molecular docking screening‏ ‎‡9  1‏
919 ‎‡a  synthesisβcatenintranslocationcapabilityandalpactivationactivityof7hthiazolo124triazin71derivatives‏ ‎‡A  Synthesis, β -catenin Translocation Capability and ALP Activation Activity of 7H-thiazolo[3,2-b]-1,2,4-triazin-7-one Derivatives.‏ ‎‡9  1‏
919 ‎‡a  miltironeisadualinhibitorofpglycoproteinandcellgrowthindoxorubicinresistanthepg2cells‏ ‎‡A  Miltirone Is a Dual Inhibitor of P-Glycoprotein and Cell Growth in Doxorubicin-Resistant HepG2 Cells‏ ‎‡9  1‏
919 ‎‡a  lungtissuedistributionofdrugsasakeyfactorforcovid19treatment‏ ‎‡A  Lung tissue distribution of drugs as a key factor for COVID-19 treatment‏ ‎‡9  1‏
919 ‎‡a  14bis5naphthalen1ylthiophen2ylnaphthaleneasmallmoleculefunctionsasanovelantihiv1inhibitortargetingtheinteractionbetweenintegraseandcellularlensepitheliumderivedgrowthfactor‏ ‎‡A  1,4-Bis(5-(naphthalen-1-yl)thiophen-2-yl)naphthalene, a small molecule, functions as a novel anti-HIV-1 inhibitor targeting the interaction between integrase and cellular Lens epithelium-derived growth factor.‏ ‎‡9  1‏
919 ‎‡a  fluorescencebasedhighthroughputassaytoidentifyinhibitorsoftyrosylproteinsulfotransferaseactivity‏ ‎‡A  A fluorescence-based high-throughput assay to identify inhibitors of tyrosylprotein sulfotransferase activity.‏ ‎‡9  1‏
919 ‎‡a  silibininanovelchemokinereceptortype4antagonistinhibitschemokineligand12inducedmigrationinbreastcancercells‏ ‎‡A  Silibinin, a novel chemokine receptor type 4 antagonist, inhibits chemokine ligand 12-induced migration in breast cancer cells.‏ ‎‡9  1‏
919 ‎‡a  enzymekineticandmoleculardockingstudiesfortheinhibitionsofmiltironeonmajorhumancytochromep450isozymes‏ ‎‡A  Enzyme kinetic and molecular docking studies for the inhibitions of miltirone on major human cytochrome P450 isozymes.‏ ‎‡9  1‏
919 ‎‡a  pimozideanovelfattyacidbindingprotein4inhibitorpromotesadipogenesisof3t3l1cellsbyactivatingpparγ‏ ‎‡A  Pimozide, a novel fatty acid binding protein 4 inhibitor, promotes adipogenesis of 3T3-L1 cells by activating PPARγ.‏ ‎‡9  1‏
919 ‎‡a  overexpressionofcxcr4synergizeswithll37inthemetastasisofbreastcancercells‏ ‎‡A  Overexpression of CXCR4 synergizes with LL-37 in the metastasis of breast cancer cells‏ ‎‡9  1‏
919 ‎‡a  moleculardockingandenzymekineticstudiesofdihydrotanshinoneonmetabolismofamodelcyp2d6probesubstrateinhumanlivermicrosomes‏ ‎‡A  Molecular docking and enzyme kinetic studies of dihydrotanshinone on metabolism of a model CYP2D6 probe substrate in human liver microsomes‏ ‎‡9  1‏
919 ‎‡a  mir25suppresses3t3l1adipogenesisbydirectlytargetingklf4and100ebpα‏ ‎‡A  MiR-25 suppresses 3T3-L1 adipogenesis by directly targeting KLF4 and C/EBPα.‏ ‎‡9  1‏
919 ‎‡a  fretbasedassayusinga3wayjunctiondnasubstratetoidentifyinhibitorsofhumancytomegaloviruspul89endonucleaseactivity‏ ‎‡A  FRET-based assay using a three-way junction DNA substrate to identify inhibitors of human cytomegalovirus pUL89 endonuclease activity‏ ‎‡9  1‏
919 ‎‡a  characterizationofmir210in3t3l1adipogenesis‏ ‎‡A  Characterization of miR-210 in 3T3-L1 adipogenesis.‏ ‎‡9  1‏
919 ‎‡a  antiviralactivitiesofwheyproteins‏ ‎‡A  Antiviral activities of whey proteins‏ ‎‡9  1‏
919 ‎‡a  acetylshikoninanovelacheinhibitorinhibitsapoptosisviaupregulationofhemeoxygenase1expressioninshsy5ycells‏ ‎‡A  Acetylshikonin, a Novel AChE Inhibitor, Inhibits Apoptosis via Upregulation of Heme Oxygenase-1 Expression in SH-SY5Y Cells‏ ‎‡9  1‏
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997 ‎‡a  0 0 lived 0 0‏ ‎‡9  1‏