Search Results - "Shei, Gan-Ju" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Alteration of Lymphocyte Trafficking by Sphingosine-1-Phosphate Receptor Agonists

Alteration of Lymphocyte Trafficking by Sphingosine-1-Phosphate Receptor Agonists

by Mandala, Suzanne, Hajdu, Richard, Bergstrom, James, Quackenbush, Elizabeth, Xie, Jenny, Milligan, James, Thornton, Rosemary, Shei, Gan-Ju, Card, Deborah, Keohane, CarolAnn, Rosenbach, Mark, Hale, Jeffrey, Lynch, Christopher L., Rupprecht, Kathleen, Parsons, William, Rosen, Hugh
Published in Science (American Association for the Advancement of Science) (12.04.2002)

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Characterization of a Novel Sphingosine 1-Phosphate Receptor, Edg-8

Characterization of a Novel Sphingosine 1-Phosphate Receptor, Edg-8

by Im, Dong-Soon, Heise, Christopher E., Ancellin, Nicolas, O'Dowd, Brian F., Shei, Gan-ju, Heavens, Robert P., Rigby, Michael R., Hla, Timothy, Mandala, Suzanne, McAllister, George, George, Susan R., Lynch, Kevin R.
Published in The Journal of biological chemistry (12.05.2000)

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Potent S1P receptor agonists replicate the pharmacologic actions of the novel immune modulator FTY720

Potent S1P receptor agonists replicate the pharmacologic actions of the novel immune modulator FTY720

by Hale, Jeffrey J., Neway, William, Mills, Sander G., Hajdu, Richard, Ann Keohane, Carol, Rosenbach, Mark, Milligan, James, Shei, Gan-Ju, Chrebet, Gary, Bergstrom, James, Card, Deborah, Koo, Gloria C., Koprak, Sam L., Jackson, Jesse J., Rosen, Hugh, Mandala, Suzanne
Published in Bioorganic & medicinal chemistry letters (21.06.2004)

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Synthesis, stereochemical determination and biochemical characterization of the enantiomeric phosphate esters of the novel immunosuppressive agent FTY720

Synthesis, stereochemical determination and biochemical characterization of the enantiomeric phosphate esters of the novel immunosuppressive agent FTY720

by Hale, Jeffrey J., Yan, Lin, Neway, William E., Hajdu, Richard, Bergstrom, James D., Milligan, James A., Shei, Gan-Ju, Chrebet, Gary L., Thornton, Rosemary A., Card, Deborah, Rosenbach, Mark, HughRosen, Mandala, Suzanne
Published in Bioorganic & medicinal chemistry (15.09.2004)

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Phytosphingosine 1-phosphate: a high affinity ligand for the S1P4/Edg-6 receptor

Phytosphingosine 1-phosphate: a high affinity ligand for the S1P4/Edg-6 receptor

by Rios Candelore, Mari, Wright, Michael J, Tota, Laurie M, Milligan, James, Shei, Gan-ju, Bergstrom, James D, Mandala, Suzanne M
Published in Biochemical and biophysical research communications (01.09.2002)

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The Yeast HML I Silencer Defines a Heterochromatin Domain Boundary by Directional Establishment of Silencing

The Yeast HML I Silencer Defines a Heterochromatin Domain Boundary by Directional Establishment of Silencing

by Bi, Xin, Braunstein, Miriam, Shei, Gan-Ju, Broach, James R.
Published in Proceedings of the National Academy of Sciences - PNAS (12.10.1999)

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Discovery of Potent 3,5-Diphenyl-1,2,4-oxadiazole Sphingosine-1-phosphate-1 (S1P1) Receptor Agonists with Exceptional Selectivity against S1P2 and S1P3

Discovery of Potent 3,5-Diphenyl-1,2,4-oxadiazole Sphingosine-1-phosphate-1 (S1P1) Receptor Agonists with Exceptional Selectivity against S1P2 and S1P3

by Li, Zhen, Chen, Weirong, Hale, Jeffrey J, Lynch, Christopher L, Mills, Sander G, Hajdu, Richard, Keohane, Carol Ann, Rosenbach, Mark J, Milligan, James A, Shei, Gan-Ju, Chrebet, Gary, Parent, Stephen A, Bergstrom, James, Card, Deborah, Forrest, Michael, Quackenbush, Elizabeth J, Wickham, L. Alexandra, Vargas, Hugo, Evans, Rose M, Rosen, Hugh, Mandala, Suzanne
Published in Journal of medicinal chemistry (06.10.2005)

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A Rational Utilization of High-Throughput Screening Affords Selective, Orally Bioavailable 1-Benzyl-3-carboxyazetidine Sphingosine-1-phosphate-1 Receptor Agonists

A Rational Utilization of High-Throughput Screening Affords Selective, Orally Bioavailable 1-Benzyl-3-carboxyazetidine Sphingosine-1-phosphate-1 Receptor Agonists

by Hale, Jeffrey J, Lynch, Christopher L, Neway, William, Mills, Sander G, Hajdu, Richard, Keohane, Carol Ann, Rosenbach, Mark J, Milligan, James A, Shei, Gan-Ju, Parent, Stephen A, Chrebet, Gary, Bergstrom, James, Card, Deborah, Ferrer, Marc, Hodder, Peter, Strulovici, Berta, Rosen, Hugh, Mandala, Suzanne
Published in Journal of medicinal chemistry (30.12.2004)

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Selecting against S1P3 enhances the acute cardiovascular tolerability of 3-(N-benzyl)aminopropylphosphonic acid S1P receptor agonists

Selecting against S1P3 enhances the acute cardiovascular tolerability of 3-(N-benzyl)aminopropylphosphonic acid S1P receptor agonists

by Hale, Jeffrey J., Doherty, George, Toth, Leslie, Mills, Sander G., Hajdu, Richard, Ann Keohane, Carol, Rosenbach, Mark, Milligan, James, Shei, Gan-Ju, Chrebet, Gary, Bergstrom, James, Card, Deborah, Forrest, Michael, Sun, Shu-Yu, West, Sarah, Xie, Huijuan, Nomura, Naomi, Rosen, Hugh, Mandala, Suzanne
Published in Bioorganic & medicinal chemistry letters (05.07.2004)

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SAR studies of 3-arylpropionic acids as potent and selective agonists of sphingosine-1-phosphate receptor-1 (S1P 1) with enhanced pharmacokinetic properties

SAR studies of 3-arylpropionic acids as potent and selective agonists of sphingosine-1-phosphate receptor-1 (S1P 1) with enhanced pharmacokinetic properties

by Yan, Lin, Huo, Pei, Hale, Jeffrey J., Mills, Sander G., Hajdu, Richard, Keohane, Carol A., Rosenbach, Mark J., Milligan, James A., Shei, Gan-Ju, Chrebet, Gary, Bergstrom, James, Card, Deborah, Mandala, Suzanne M.
Published in Bioorganic & medicinal chemistry letters (01.02.2007)

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Discovery of 3-arylpropionic acids as potent agonists of sphingosine-1-phosphate receptor-1 (S1P 1) with high selectivity against all other known S1P receptor subtypes

Discovery of 3-arylpropionic acids as potent agonists of sphingosine-1-phosphate receptor-1 (S1P 1) with high selectivity against all other known S1P receptor subtypes

by Yan, Lin, Huo, Pei, Doherty, George, Toth, Lesile, Hale, Jeffrey J., Mills, Sander G., Hajdu, Richard, Keohane, Carol A., Rosenbach, Mark J., Milligan, James A., Shei, Gan-Ju, Chrebet, Gary, Bergstrom, James, Card, Deborah, Quackenbush, Elizabeth, Wickham, Alexandra, Mandala, Suzanne M.
Published in Bioorganic & medicinal chemistry letters (15.07.2006)

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2-Aryl(pyrrolidin-4-yl)acetic acids are potent agonists of sphingosine-1-phosphate (S1P) receptors

2-Aryl(pyrrolidin-4-yl)acetic acids are potent agonists of sphingosine-1-phosphate (S1P) receptors

by Yan, Lin, Budhu, Richard, Huo, Pei, Lynch, Christopher L., Hale, Jeffrey J., Mills, Sander G., Hajdu, Richard, Keohane, Carol A., Rosenbach, Mark J., Milligan, James A., Shei, Gan-Ju, Chrebet, Gary, Bergstrom, James, Card, Deborah, Mandala, Suzanne M.
Published in Bioorganic & medicinal chemistry letters (01.07.2006)

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2,5-Disubstituted pyrrolidine carboxylates as potent, orally active sphingosine-1-phosphate (S1P) receptor agonists

2,5-Disubstituted pyrrolidine carboxylates as potent, orally active sphingosine-1-phosphate (S1P) receptor agonists

by Colandrea, Vincent J., Legiec, Irene E., Huo, Pei, Yan, Lin, Hale, Jeffrey J., Mills, Sander G., Bergstrom, James, Card, Deborah, Chebret, Gary, Hajdu, Richard, Keohane, Carol Ann, Milligan, James A., Rosenbach, Mark J., Shei, Gan-Ju, Mandala, Suzanne M.
Published in Bioorganic & medicinal chemistry letters (01.06.2006)

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Design and synthesis of conformationally constrained 3-( N-alkylamino)propylphosphonic acids as potent agonists of sphingosine-1-phosphate (S1P) receptors

Design and synthesis of conformationally constrained 3-( N-alkylamino)propylphosphonic acids as potent agonists of sphingosine-1-phosphate (S1P) receptors

by Yan, Lin, Hale, Jeffrey J., Lynch, Christopher L., Budhu, Richard, Gentry, Amy, Mills, Sander G., Hajdu, Richard, Keohane, Carol Ann, Rosenbach, Mark J., Milligan, James A., Shei, Gan-Ju, Chrebet, Gary, Bergstrom, James, Card, Deborah, Rosen, Hugh, Mandala, Suzanne M.
Published in Bioorganic & medicinal chemistry letters (04.10.2004)

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The discovery of 3-(N-alkyl)aminopropylphosphonic acids as potent S1P receptor agonists

The discovery of 3-(N-alkyl)aminopropylphosphonic acids as potent S1P receptor agonists

by Hale, Jeffrey J., Doherty, George, Toth, Leslie, Li, Zhen, Mills, Sander G., Hajdu, Richard, Ann Keohane, Carol, Rosenbach, Mark, Milligan, James, Shei, Gan-Ju, Chrebet, Gary, Bergstrom, James, Card, Deborah, Rosen, Hugh, Mandala, Suzanne
Published in Bioorganic & medicinal chemistry letters (05.07.2004)

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Yeast silencers can act as orientation-dependent gene inactivation centers that respond to environmental signals

Yeast silencers can act as orientation-dependent gene inactivation centers that respond to environmental signals

by Shei, Gan-Ju, Broach, James R.
Published in Molecular and Cellular Biology (01.07.1995)

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Mutations in the HML E silencer of Saccharomyces cerevisiae yield metastable inheritance of transcriptional repression

Mutations in the HML E silencer of Saccharomyces cerevisiae yield metastable inheritance of transcriptional repression

by MAHONEY, D. J, MARQUARDT, R, SHEI, G.-J, ROSE, A. B, BROACH, J. R
Published in Genes & development (01.04.1991)

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Phytosphingosine 1-phosphate: a high affinity ligand for the S1P(4)/Edg-6 receptor

Phytosphingosine 1-phosphate: a high affinity ligand for the S1P(4)/Edg-6 receptor

by Candelore, Mari Rios, Wright, Michael J, Tota, Laurie M, Milligan, James, Shei, Gan-ju, Bergstrom, James D, Mandala, Suzanne M
Published in Biochemical and biophysical research communications (27.09.2002)

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Development of a cyclic adenosine monophosphate assay for Gi-coupled G protein-coupled receptors by utilizing the endogenous calcitonin activity in Chinese hamster ovary cells

Development of a cyclic adenosine monophosphate assay for Gi-coupled G protein-coupled receptors by utilizing the endogenous calcitonin activity in Chinese hamster ovary cells

by Wang, Yuren, Kong, Yan, Shei, Gan Ju, Kang, Liya, Cvijic, Mary Ellen
Published in Assay and drug development technologies (01.10.2011)

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Discovery of 3-arylpropionic acids as potent agonists of sphingosine-1-phosphate receptor-1 (S1P1) with high selectivity against all other known S1Preceptor subtypes

Discovery of 3-arylpropionic acids as potent agonists of sphingosine-1-phosphate receptor-1 (S1P1) with high selectivity against all other known S1Preceptor subtypes

by LIN YAN, PEI HUO, SHEI, Gan-Ju, CHREBET, Gary, BERGSTROM, James, CARD, Deborah, QUACKENBUSH, Elizabeth, WICKHAM, Alexandra, MANDALA, Suzanne M, DOHERTY, George, TOTH, Lesile, HALE, Jeffrey J, MILLS, Sander G, HAJDU, Richard, KEOHANE, Carol A, ROSENBACH, Mark J, MILLIGAN, James A
Published in Bioorganic & medicinal chemistry letters (2006)

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