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Found 153 with Last Name = 'wortman' and Initial = 'm'
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM12915(2-(4-Morpholinyl)-8-phenyl-4H-1-benzopyran-4-one |...)
Affinity DataIC50:  200nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM12915(2-(4-Morpholinyl)-8-phenyl-4H-1-benzopyran-4-one |...)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278545(2-((4-fluoro-2-methylphenylamino)methyl)-6-morphol...)
Affinity DataIC50:  5.00E+3nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278506(2-((4-fluoro-2-methylphenoxy)methyl)-6-morpholinoi...)
Affinity DataIC50:  7.00E+3nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278503(2-((4-fluoro-2-methylphenoxy)methyl)-N-hydroxy-6-m...)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278504(2-((4-fluoro-2-methylphenoxy)methyl)-6-morpholinoi...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278543((2-((4-fluoro-2-methylphenylamino)methyl)-6-morpho...)
Affinity DataIC50:  2.00E+4nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278506(2-((4-fluoro-2-methylphenoxy)methyl)-6-morpholinoi...)
Affinity DataIC50:  2.30E+4nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278613(6-((4-fluoro-2-methylphenylamino)methyl)-2,4'-bipy...)
Affinity DataIC50:  2.90E+4nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278545(2-((4-fluoro-2-methylphenylamino)methyl)-6-morphol...)
Affinity DataIC50:  3.40E+4nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278659(2-morpholinoisonicotinic acid | CHEMBL449172)
Affinity DataIC50:  3.60E+4nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278616(2-((4-fluoro-2-methylphenylamino)methyl)-6-(3-hydr...)
Affinity DataIC50:  4.20E+4nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278613(6-((4-fluoro-2-methylphenylamino)methyl)-2,4'-bipy...)
Affinity DataIC50:  4.20E+4nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278660(CHEMBL450243 | ethyl 2-morpholinoisonicotinate)
Affinity DataIC50:  5.10E+4nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278544(2-((4-fluoro-2-methylphenylamino)methyl)-6-morphol...)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278576(2-((4-fluoro-2-methylphenylamino)methyl)-6-(3-hydr...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278578(2-((4-fluoro-2-methylphenylamino)methyl)-6-(2-hydr...)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278579(2-(bis(2-hydroxyethyl)amino)-6-((4-fluoro-2-methyl...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278614(6-((4-fluoro-2-methylphenylamino)methyl)-2,3'-bipy...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278615(2-((4-fluoro-2-methylphenylamino)methyl)-6-(4-hydr...)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278616(2-((4-fluoro-2-methylphenylamino)methyl)-6-(3-hydr...)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278617(2-((4-fluoro-2-methylphenylamino)methyl)-6-(2-hydr...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278656(2-chloro-6-((4-fluoro-2-methylphenylamino)methyl)i...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278657(2-((4-fluoro-2-methylphenylamino)methyl)-N-(2-hydr...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278658((2-((4-fluoro-2-methylphenylamino)methyl)-6-(3-hyd...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278577(2-((4-fluoro-2-methylphenylamino)methyl)-6-((2-hyd...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278656(2-chloro-6-((4-fluoro-2-methylphenylamino)methyl)i...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278659(2-morpholinoisonicotinic acid | CHEMBL449172)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278660(CHEMBL450243 | ethyl 2-morpholinoisonicotinate)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278658((2-((4-fluoro-2-methylphenylamino)methyl)-6-(3-hyd...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278657(2-((4-fluoro-2-methylphenylamino)methyl)-N-(2-hydr...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278617(2-((4-fluoro-2-methylphenylamino)methyl)-6-(2-hydr...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278615(2-((4-fluoro-2-methylphenylamino)methyl)-6-(4-hydr...)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278614(6-((4-fluoro-2-methylphenylamino)methyl)-2,3'-bipy...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278579(2-(bis(2-hydroxyethyl)amino)-6-((4-fluoro-2-methyl...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278578(2-((4-fluoro-2-methylphenylamino)methyl)-6-(2-hydr...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278577(2-((4-fluoro-2-methylphenylamino)methyl)-6-((2-hyd...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278576(2-((4-fluoro-2-methylphenylamino)methyl)-6-(3-hydr...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278575(2-((4-fluoro-2-methylphenylamino)methyl)-6-(pyrrol...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278547(2-((4-fluoro-2-methylphenylamino)methyl)-6-(piperi...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278546(2-((4-fluoro-2-methylphenylamino)methyl)-6-(pipera...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278544(2-((4-fluoro-2-methylphenylamino)methyl)-6-morphol...)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibition of PI3Kgamma by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50278546(2-((4-fluoro-2-methylphenylamino)methyl)-6-(pipera...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of PI3Kalpha by luminescent kinase glo assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMelanocyte-stimulating hormone receptor(Mus musculus)
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50301125((S)-2-((R)-2-((S)-2-cinnamamido-3-(1H-imidazol-5-y...)
Affinity DataEC50:  1.20E+3nMAssay Description:Agonistic activity against mouse MC1RMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMelanocyte-stimulating hormone receptor(Mus musculus)
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50301126((S)-2-((R)-2-((S)-2-(3-(2-fluorophenyl)acrylamido)...)
Affinity DataEC50:  1.16E+3nMAssay Description:Agonistic activity against mouse MC1RMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMelanocyte-stimulating hormone receptor(Mus musculus)
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50301127((S)-2-((R)-2-((S)-3-(1H-imidazol-5-yl)-2-(3-(2-met...)
Affinity DataEC50:  1.69E+3nMAssay Description:Agonistic activity against mouse MC1RMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMelanocyte-stimulating hormone receptor(Mus musculus)
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50301128((R)-2-((R)-2-((S)-3-(1H-imidazol-5-yl)-2-(3-(4-met...)
Affinity DataEC50:  3.66E+3nMAssay Description:Agonistic activity against mouse MC1RMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMelanocyte-stimulating hormone receptor(Mus musculus)
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50301129((S)-2-((R)-2-((S)-2-(3-(3-chlorophenyl)acrylamido)...)
Affinity DataEC50:  660nMAssay Description:Agonistic activity against mouse MC1RMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMelanocyte-stimulating hormone receptor(Mus musculus)
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50301130((S)-2-((R)-2-((S)-3-(1H-imidazol-5-yl)-2-(3-(3-(tr...)
Affinity DataEC50:  310nMAssay Description:Agonistic activity against mouse MC1RMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMelanocyte-stimulating hormone receptor(Mus musculus)
University Of Cincinnati

Curated by ChEMBL
LigandPNGBDBM50301131((S)-5-guanidino-2-((R)-2-((S)-2-(3-(3-hydroxypheny...)
Affinity DataEC50:  274nMAssay Description:Agonistic activity against mouse MC1RMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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