Compile Data Set for Download or QSAR
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Found 89 with Last Name = 'maltais' and Initial = 'r'
TargetSteryl-sulfatase(Homo sapiens (Human))
Chu De Qu£Bec - Research Center

Curated by ChEMBL
LigandPNGBDBM50369432(CHEMBL1627465)
Affinity DataIC50:  0.0300nMAssay Description:Irreversible inhibition of human steroid sulfatase expressed in HEK293 cells using [3H] E1S as substrate after 2 hrs by liquid scintillation counting...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Chu De Qu£Bec - Research Center

Curated by ChEMBL
LigandPNGBDBM50545255(CHEMBL4643348)
Affinity DataIC50:  0.0400nMAssay Description:Irreversible inhibition of human steroid sulfatase expressed in HEK293 cells using [3H] E1S as substrate after 2 hrs by liquid scintillation counting...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Chu De Qu£Bec - Research Center

Curated by ChEMBL
LigandPNGBDBM50168219(CHEMBL3805209)
Affinity DataIC50:  0.0500nMAssay Description:Inhibition of steroid sulfatase (unknown origin) expressed in HEK293 cells assessed as reduction in transformation of [3H]-E1S to E1 after 2 hrs by l...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Chu De Qu£Bec - Research Center

Curated by ChEMBL
LigandPNGBDBM50369432(CHEMBL1627465)
Affinity DataIC50:  0.800nMAssay Description:Inhibition of steroid sulfatase (unknown origin) expressed in HEK293 cells using [3H] E1S as substrate after 2 hrs by scintillation counting methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Chu De Qu£Bec - Research Center

Curated by ChEMBL
LigandPNGBDBM50545254(CHEMBL4639657)
Affinity DataIC50:  2.10nMAssay Description:Irreversible inhibition of steroid sulfatase (unknown origin) expressed in HEK293 cells using [3H] E1S as substrate after 2 hrs by scintillation coun...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Chu De Qu£Bec - Research Center

Curated by ChEMBL
LigandPNGBDBM50193084(CHEMBL3910182)
Affinity DataIC50:  3.90nMAssay Description:Inhibition of steroid sulfatase (unknown origin) expressed in HEK293 cells assessed as reduction in transformation of [3H]-E1S to E1 after 2 hrs by l...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50350421(CHEMBL1813731)
Affinity DataIC50:  6nMAssay Description:Inhibition of 17betaHSD3 (unknown origin) transfected in HEK293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50350421(CHEMBL1813731)
Affinity DataIC50:  6nMAssay Description:Inhibition of 17Beta-HSD3 expressed in intact HEK293 cells assessed as transformation of [14C]-4-androstene-3,17-dione into [14C]-testosterone in pre...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Chu De Qu£Bec - Research Center

Curated by ChEMBL
LigandPNGBDBM50193082(CHEMBL3953180)
Affinity DataIC50:  8.90nMAssay Description:Inhibition of steroid sulfatase (unknown origin) expressed in HEK293 cells assessed as reduction in transformation of [3H]-E1S to E1 after 2 hrs by l...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
Chu De Qu£Bec-Research Center (Chul)

Curated by ChEMBL
LigandPNGBDBM50350421(CHEMBL1813731)
Affinity DataIC50:  13nMAssay Description:Inhibition of 17beta-HSD3 in rat testes microsomes using [14C]-4-androstene-3,17-dione as substrate after 2 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Chu De Qu£Bec - Research Center

Curated by ChEMBL
LigandPNGBDBM50193083(CHEMBL3981927)
Affinity DataIC50:  17nMAssay Description:Inhibition of steroid sulfatase (unknown origin) expressed in HEK293 cells assessed as reduction in transformation of [3H]-E1S to E1 after 2 hrs by l...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Laval University

Curated by ChEMBL
LigandPNGBDBM151585(US11739089, Compound Ketoconazole | US8987315, Ket...)
Affinity DataIC50:  24nMAssay Description:Inhibition of CYP3A4 (unknown origin) by fluorescence assayMore data for this Ligand-Target Pair
TargetCytochrome P450 3A4(Homo sapiens (Human))
Laval University

Curated by ChEMBL
LigandPNGBDBM151585(US11739089, Compound Ketoconazole | US8987315, Ket...)
Affinity DataIC50:  25nMAssay Description:Inhibition of CYP3A4 (unknown origin) using AMMC by fluorescence assayMore data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 1(Homo sapiens (Human))
Laval University

Curated by ChEMBL
LigandPNGBDBM50373700(CHEMBL410242)
Affinity DataIC50:  27nMAssay Description:Inhibition of 17-beta HSD1 in human T47D cells assessed as transformation of [14C]E1 to [14C]E2 after 24 hrs by thin layer chromatographyMore data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 1(Homo sapiens (Human))
Laval University

Curated by ChEMBL
LigandPNGBDBM50373700(CHEMBL410242)
Affinity DataIC50:  27nMAssay Description:Inhibition of 17beta-HSD1 in human T47D cells assessed as decrease in transformation of [14C]estrone to [14C]-estradiol after 24 hrs by thin layer ch...More data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Chu De Qu£Bec - Research Center

Curated by ChEMBL
LigandPNGBDBM50366532(CHEMBL518966)
Affinity DataIC50:  28nMAssay Description:Reversible inhibition of steroid sulfatase in human JEG3 cells using [3H] E1S as substrate by scintillation counting methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
Chu De Qu£Bec-Research Center (Chul)

Curated by ChEMBL
LigandPNGBDBM50111763(CHEMBL3605211)
Affinity DataIC50:  28nMAssay Description:Inhibition of 17beta-HSD3 in rat testes microsomes using [14C]-4-androstene-3,17-dione as substrate after 2 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50108810(CHEMBL347019 | N-Adamantan-2-ylmethyl-N-(3-hydroxy...)
Affinity DataIC50:  35nMAssay Description:Concentration to inhibit 50% activity of the Type-3 17-beta- hydroxysteroid dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Chu De Qu£Bec - Research Center

Curated by ChEMBL
LigandPNGBDBM50366532(CHEMBL518966)
Affinity DataIC50:  45nMAssay Description:Inhibition of steroid sulfatase (unknown origin) expressed in HEK293 cells using [3H] E1S as substrate after 2 hrs by scintillation counting methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50350422(CHEMBL1813912)
Affinity DataIC50:  51nMAssay Description:Inhibition of 17Beta-HSD3 expressed in intact HEK293 cells assessed as transformation of [14C]-4-androstene-3,17-dione into [14C]-testosterone in pre...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50108814(CHEMBL158995 | Cyclopropanecarboxylic acid (3-hydr...)
Affinity DataIC50:  57nMAssay Description:The ability to inhibit the Type-3 17-beta- hydroxysteroid dehydrogenase activity in transfected human embryonic kidney (HEK)-293 cells experiment 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50093902((3R,10S,13S)-3-Benzyl-3-hydroxy-10,13-dimethyl-hex...)
Affinity DataIC50:  57nMAssay Description:The ability to inhibit the Type-3 17-beta- hydroxysteroid dehydrogenase activity in transfected human embryonic kidney (HEK)-293 cells experiment 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50108810(CHEMBL347019 | N-Adamantan-2-ylmethyl-N-(3-hydroxy...)
Affinity DataIC50:  57nMAssay Description:Concentration to inhibit 50% activity of the Type-3 17-beta- hydroxysteroid dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
Chu De Qu£Bec-Research Center (Chul)

Curated by ChEMBL
LigandPNGBDBM50528377(CHEMBL4451878)
Affinity DataIC50:  60nMAssay Description:Inhibition of 17beta-HSD3 in Sprague-Dawley rat testes microsomal fraction assessed as reduction in [14C]-testosterone formation from [14C]-4-androst...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 1(Homo sapiens (Human))
Laval University

Curated by ChEMBL
LigandPNGBDBM50400509(CHEMBL2203397)
Affinity DataIC50:  68nMAssay Description:Inhibition of 17-beta HSD1 in human T47D cells assessed as transformation of [14C]E1 to [14C]E2 after 24 hrs by thin layer chromatographyMore data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 1(Homo sapiens (Human))
Laval University

Curated by ChEMBL
LigandPNGBDBM50400509(CHEMBL2203397)
Affinity DataIC50:  68nMAssay Description:Inhibition of 17beta-HSD1 in human T47D cells assessed as decrease in transformation of [14C]estrone to [14C]-estradiol after 24 hrs by thin layer ch...More data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Chu De Qu£Bec - Research Center

Curated by ChEMBL
LigandPNGBDBM50545253(CHEMBL4632735)
Affinity DataIC50:  69nMAssay Description:Reversible inhibition of steroid sulfatase (unknown origin) expressed in HEK293 cells using [3H] E1S as substrate after 2 hrs by scintillation counti...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50108813(2-[9a,11a-dimethyl-1,2'-dioxospiro[perhydrocyclope...)
Affinity DataIC50:  74nMAssay Description:Concentration to inhibit 50% activity of the Type-3 17-beta- hydroxysteroid dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50108811(3-[(Adamantan-2-ylmethyl-butyl-amino)-methyl]-3-hy...)
Affinity DataIC50:  80nMAssay Description:Concentration to inhibit 50% activity of the Type-3 17-beta- hydroxysteroid dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
Chu De Qu£Bec-Research Center (Chul)

Curated by ChEMBL
LigandPNGBDBM50443289(CHEMBL3088217)
Affinity DataIC50:  80nMAssay Description:Inhibition of 17beta-HSD3 in Sprague-Dawley rat testes microsomal fraction assessed as reduction in [14C]-testosterone formation from [14C]-4-androst...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50108812(CHEMBL160184 | Cyclopropanecarboxylic acid cyclohe...)
Affinity DataIC50:  85nMAssay Description:Concentration to inhibit 50% activity of the Type-3 17-beta- hydroxysteroid dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50350421(CHEMBL1813731)
Affinity DataIC50:  85nMAssay Description:Inhibition of 17betaHSD3 (unknown origin) transfected in human LNCAP cells assessed as conversion of [14C]-4-androstene-3,17-dione into [14C]-testost...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
Chu De Qu£Bec-Research Center (Chul)

Curated by ChEMBL
LigandPNGBDBM50111764(CHEMBL3605212)
Affinity DataIC50:  88nMAssay Description:Inhibition of 17beta-HSD3 in rat testes microsomes using [14C]-4-androstene-3,17-dione as substrate after 2 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
Chu De Qu£Bec-Research Center (Chul)

Curated by ChEMBL
LigandPNGBDBM17639((1S,2S,5R,7S,10R,11S,15S)-5-hydroxy-2,15-dimethylt...)
Affinity DataIC50:  90nMAssay Description:Inhibition of 17beta-HSD3 in rat testes microsomes using [14C]-4-androstene-3,17-dione as substrate after 2 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50443289(CHEMBL3088217)
Affinity DataIC50:  90nMAssay Description:Inhibition of 17beta-HSD3 (unknown origin) expressed in human LNCAP cells assessed as reduction in [14C]-testosterone formation from [14C]-4-androste...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 1(Homo sapiens (Human))
Laval University

Curated by ChEMBL
LigandPNGBDBM50400509(CHEMBL2203397)
Affinity DataIC50:  97nMAssay Description:Inhibition of 17-beta HSD1 in human T47D cellsMore data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50093902((3R,10S,13S)-3-Benzyl-3-hydroxy-10,13-dimethyl-hex...)
Affinity DataIC50:  98nMAssay Description:The ability to inhibit the Type-3 17-beta- hydroxysteroid dehydrogenase activity in transfected human embryonic kidney (HEK)-293 cells experiment 3More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50528381(CHEMBL4468509)
Affinity DataIC50:  100nMAssay Description:Inhibition of 17beta-HSD3 (unknown origin) expressed in human LNCAP cells assessed as reduction in [14C]-testosterone formation from [14C]-4-androste...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
Chu De Qu£Bec-Research Center (Chul)

Curated by ChEMBL
LigandPNGBDBM50528383(CHEMBL4445467)
Affinity DataIC50:  100nMAssay Description:Inhibition of 17beta-HSD3 in Sprague-Dawley rat testes microsomal fraction assessed as reduction in [14C]-testosterone formation from [14C]-4-androst...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
Chu De Qu£Bec-Research Center (Chul)

Curated by ChEMBL
LigandPNGBDBM50528381(CHEMBL4468509)
Affinity DataIC50:  110nMAssay Description:Inhibition of 17beta-HSD3 in Sprague-Dawley rat testes microsomal fraction assessed as reduction in [14C]-testosterone formation from [14C]-4-androst...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50350421(CHEMBL1813731)
Affinity DataIC50:  110nMAssay Description:Inhibition of 17-beta-HSD3 (unknown origin) expressed in human LNCaP cells using [14C]-4-androstene-3,17-dione as substrate assessed as reduction of ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
Chu De Qu£Bec-Research Center (Chul)

Curated by ChEMBL
LigandPNGBDBM50528382(CHEMBL4515514)
Affinity DataIC50:  120nMAssay Description:Inhibition of 17beta-HSD3 in Sprague-Dawley rat testes microsomal fraction assessed as reduction in [14C]-testosterone formation from [14C]-4-androst...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50121975((6-Methoxy-quinolin-4-yl)-(5-vinyl-1-aza-bicyclo[2...)
Affinity DataIC50:  120nMAssay Description:Inhibition of CYP2D6 (unknown origin) using AMMC by fluorescence assayMore data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50528383(CHEMBL4445467)
Affinity DataIC50:  130nMAssay Description:Inhibition of 17beta-HSD3 (unknown origin) expressed in human LNCAP cells assessed as reduction in [14C]-testosterone formation from [14C]-4-androste...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50528377(CHEMBL4451878)
Affinity DataIC50:  140nMAssay Description:Inhibition of 17beta-HSD3 (unknown origin) expressed in human LNCAP cells assessed as reduction in [14C]-testosterone formation from [14C]-4-androste...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50528377(CHEMBL4451878)
Affinity DataIC50:  140nMAssay Description:Inhibition of 17beta-HSD3 (unknown origin) expressed in human LNCAP cells assessed as reduction in [14C]-testosterone formation from [14C]-4-androste...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50235625(CHEMBL4076831)
Affinity DataIC50:  150nMAssay Description:Inhibition of 17-beta-HSD3 (unknown origin) expressed in human LNCaP cells using [14C]-4-androstene-3,17-dione as substrate assessed as reduction of ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 1(Homo sapiens (Human))
Laval University

Curated by ChEMBL
LigandPNGBDBM50495475(CHEMBL3108979)
Affinity DataIC50:  153nMAssay Description:Inhibition of 17-beta HSD1 in human T47D cells assessed as transformation of [14C]E1 to [14C]E2 after 24 hrs by thin layer chromatographyMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
Chu De Qu£Bec-Research Center (Chul)

Curated by ChEMBL
LigandPNGBDBM91713(Androst-4-en-3,17-dione, 2 | Androst-4-ene-3,17-di...)
Affinity DataIC50:  169nMAssay Description:Inhibition of 17beta-HSD3 in rat testes microsomes using [14C]-4-androstene-3,17-dione as substrate after 2 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chu De Qu£Bec-Research Center

Curated by ChEMBL
LigandPNGBDBM50528382(CHEMBL4515514)
Affinity DataIC50:  170nMAssay Description:Inhibition of 17beta-HSD3 (unknown origin) expressed in human LNCAP cells assessed as reduction in [14C]-testosterone formation from [14C]-4-androste...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
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