يعرض 1 - 11 نتائج من 11 نتيجة بحث عن '"Wenling Kao"', وقت الاستعلام: 0.41s تنقيح النتائج
  1. 1
    Supplementary Table 3 from Comparison of Human and Rat Uterine Leiomyomata: Identification of a Dysregulated Mammalian Target of Rapamycin Pathway

    المؤلفون: Cheryl L. Walker, Richard C. Winneker, Magid Abou-Gharbia, Jerauld S. Skotnicki, Wenling Kao, Eugene L. Brown, Russell R. Broaddus, Bhuvanesh Dave, Adrienne S. McCampbell, Wei Liu, Kathryn A. Saraf, Ewa Wilson, Michelle L. Kimberland, Monette M. Cotreau, Sung E. Choe, Heather A. Harris, Scott A. Jelinsky, Judy S. Crabtree

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8eeadc07c3d5cb2cba812ec3e00abad0
    https://doi.org/10.1158/0008-5472.22377996.v1

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  2. 2
    Supplementary Table 1 from Comparison of Human and Rat Uterine Leiomyomata: Identification of a Dysregulated Mammalian Target of Rapamycin Pathway

    المؤلفون: Cheryl L. Walker, Richard C. Winneker, Magid Abou-Gharbia, Jerauld S. Skotnicki, Wenling Kao, Eugene L. Brown, Russell R. Broaddus, Bhuvanesh Dave, Adrienne S. McCampbell, Wei Liu, Kathryn A. Saraf, Ewa Wilson, Michelle L. Kimberland, Monette M. Cotreau, Sung E. Choe, Heather A. Harris, Scott A. Jelinsky, Judy S. Crabtree

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39ee0312576692d2359aa6868e077996
    https://doi.org/10.1158/0008-5472.22378002

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  3. 3
    Supplementary Methods from Comparison of Human and Rat Uterine Leiomyomata: Identification of a Dysregulated Mammalian Target of Rapamycin Pathway

    المؤلفون: Cheryl L. Walker, Richard C. Winneker, Magid Abou-Gharbia, Jerauld S. Skotnicki, Wenling Kao, Eugene L. Brown, Russell R. Broaddus, Bhuvanesh Dave, Adrienne S. McCampbell, Wei Liu, Kathryn A. Saraf, Ewa Wilson, Michelle L. Kimberland, Monette M. Cotreau, Sung E. Choe, Heather A. Harris, Scott A. Jelinsky, Judy S. Crabtree

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::689bedcffbc5615d69e975e9371d9425
    https://doi.org/10.1158/0008-5472.22378005.v1

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  4. 4
    Supplementary Table 2 from Comparison of Human and Rat Uterine Leiomyomata: Identification of a Dysregulated Mammalian Target of Rapamycin Pathway

    المؤلفون: Cheryl L. Walker, Richard C. Winneker, Magid Abou-Gharbia, Jerauld S. Skotnicki, Wenling Kao, Eugene L. Brown, Russell R. Broaddus, Bhuvanesh Dave, Adrienne S. McCampbell, Wei Liu, Kathryn A. Saraf, Ewa Wilson, Michelle L. Kimberland, Monette M. Cotreau, Sung E. Choe, Heather A. Harris, Scott A. Jelinsky, Judy S. Crabtree

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::653d89c66861b9901cc0faf0967526fa
    https://doi.org/10.1158/0008-5472.22377999

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  5. 5
    Supplementary Table 4 from Comparison of Human and Rat Uterine Leiomyomata: Identification of a Dysregulated Mammalian Target of Rapamycin Pathway

    المؤلفون: Cheryl L. Walker, Richard C. Winneker, Magid Abou-Gharbia, Jerauld S. Skotnicki, Wenling Kao, Eugene L. Brown, Russell R. Broaddus, Bhuvanesh Dave, Adrienne S. McCampbell, Wei Liu, Kathryn A. Saraf, Ewa Wilson, Michelle L. Kimberland, Monette M. Cotreau, Sung E. Choe, Heather A. Harris, Scott A. Jelinsky, Judy S. Crabtree

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b903ae166d34c4e3599343618f33d9a2
    https://doi.org/10.1158/0008-5472.22377993.v1

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  6. 6
    Small molecule antagonists of the gonadotropin-releasing hormone (GnRH) receptor: Structure–activity relationships of small heterocyclic groups appended to the 2-phenyl-4-piperazinyl-benzimidazole template

    المؤلفون: Lloyd M. Garrick, John F. Mehlmann, Diane B. Hauze, Joshua E. Cottom, Daniel M. Green, Jeffrey C. Pelletier, Murty Chengalvala, Irene Feingold, Joseph T. Lundquist, John F. Rogers, Charles William Mann, Linda Shanno, Jay E. Wrobel, Christine Huselton, Wenling Kao, Kees Kenneth L

    المصدر: Bioorganic & Medicinal Chemistry Letters. 19:1986-1990

    مصطلحات موضوعية: medicine.medical_specialty, Benzimidazole, Time Factors, Clinical Biochemistry, Administration, Oral, Pharmaceutical Science, Gonadotropin-releasing hormone, Peptide hormone, Biochemistry, Piperazines, Structure-Activity Relationship, chemistry.chemical_compound, Heterocyclic Compounds, Oral administration, Internal medicine, Drug Discovery, medicine, Animals, Receptor, Molecular Biology, Volume of distribution, Chemistry, Organic Chemistry, Antagonist, Luteinizing Hormone, Rats, Bioavailability, Endocrinology, Models, Animal, Molecular Medicine, Benzimidazoles, Receptors, LHRH

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98e42c70637294bea6edaaf45f2b6b18
    https://doi.org/10.1016/j.bmcl.2009.02.043

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  7. 7
    2-Phenyl-4-piperazinylbenzimidazoles: Orally active inhibitors of the gonadotropin releasing hormone (GnRH) receptor

    المؤلفون: Murty V. Chengalvala, Linda Shanno, Charles William Mann, Josh Cottom, Diane B. Hauze, Jay E. Wrobel, Irene Feingold, Jeffrey C. Pelletier, Gregory S. Kopf, Daniel M. Green, John A. Rogers, Wenling Kao, Christine Huselton, John F. Mehlmann, Joseph T. Lundquist, Lloyd M. Garrick, James W. Jetter

    المصدر: Bioorganic & Medicinal Chemistry. 16:6617-6640

    مصطلحات موضوعية: Male, endocrine system, medicine.medical_specialty, medicine.drug_class, Clinical Biochemistry, Administration, Oral, Pharmaceutical Science, Gonadotropin-releasing hormone, Methylation, Biochemistry, Piperazines, Gonadotropin-releasing hormone antagonist, Rats, Sprague-Dawley, Structure-Activity Relationship, Prostate cancer, In vivo, Internal medicine, Drug Discovery, medicine, Animals, Humans, Structure–activity relationship, Receptor, Piperazine, Molecular Biology, Leuteinizing hormone, Molecular Structure, Chemistry, Organic Chemistry, Antagonist, Luteinizing Hormone, medicine.disease, Glycolates, Rats, Cross-Linking Reagents, Endocrinology, Molecular Medicine, Benzimidazoles, Receptors, LHRH, hormones, hormone substitutes, and hormone antagonists

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11f80d1947f55d3348918157d5792d53
    https://doi.org/10.1016/j.bmc.2008.05.024

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  8. 8
    Synthesis of (bis)Sulfonic acid, (bis)Benzamides as follicle-Stimulating hormone (FSH) antagonists

    المؤلفون: Jill L. Hardenburg, John Rogers, Darlene C. Deecher, Francisco J. López, Emily S. Shen, Brian J. Arey, Jay Wrobel, James W Jetter, M. Claudia Perez, Daniel M. Green, Wenling Kao

    المصدر: Bioorganic & Medicinal Chemistry. 10:639-656

    مصطلحات موضوعية: Male, endocrine system, Stereochemistry, medicine.drug_class, Clinical Biochemistry, Nitro compound, Pharmaceutical Science, Carboxamide, Sulfonic acid, Transfection, Biochemistry, Chemical synthesis, Rats, Sprague-Dawley, Inhibitory Concentration 50, Mice, Radioligand Assay, Structure-Activity Relationship, chemistry.chemical_compound, Thyroid-stimulating hormone, Testis, Drug Discovery, Cyclic AMP, Tumor Cells, Cultured, medicine, Animals, Humans, Receptor, Molecular Biology, Progesterone, Benzoic acid, chemistry.chemical_classification, Granulosa Cells, Chemistry, Organic Chemistry, Estrogen Antagonists, Receptors, Thyrotropin, Progesterone secretion, Rats, Benzamides, Receptors, FSH, Molecular Medicine, Female, Follicle Stimulating Hormone, Sulfonic Acids, Dimerization

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfa4a53329a75a805c02c0a70c3199dd
    https://doi.org/10.1016/s0968-0896(01)00324-8

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  9. 9
    USE OF AN ISOPROPYL ESTER MOIETY AS A SULFONIC ACID PROTECTING GROUP IN A GREATLY IMPROVED SYNTHESIS OF AN ARYLSULFONIC ACID-BASED FOLLICLE STIMULATING HORMONE ANTAGONIST

    المؤلفون: Daniel M. Green, Wenling Kao, Jay E. Wrobel, John Rogers

    المصدر: Synthetic Communications. 32:2695-2704

    مصطلحات موضوعية: chemistry.chemical_classification, Follicle-stimulating hormone, Chemistry, Organic Chemistry, Antagonist, Organic chemistry, Moiety, Sulfonic acid, Protecting group, Isopropyl

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::fd5bbb42f69515aa917cb0aa91e29f38
    https://doi.org/10.1081/scc-120006035

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  10. 10
    5-Alkylated thiazolidinones as follicle-stimulating hormone (FSH) receptor agonists

    المؤلفون: John A. Rogers, Jamin Chi, Gi-Chung Chen, Li Di, James W. Jetter, M. Claudia Perez, Emily S. Shen, Wenling Kao, Jay E. Wrobel

    المصدر: Bioorganicmedicinal chemistry. 14(16)

    مصطلحات موضوعية: Agonist, endocrine system, Alkylation, medicine.drug_class, Stereochemistry, Clinical Biochemistry, Substituent, Pharmaceutical Science, Hamster, CHO Cells, Biochemistry, Chemical synthesis, Cell Line, chemistry.chemical_compound, Follicle-stimulating hormone, Structure-Activity Relationship, Cricetinae, Drug Discovery, medicine, Cyclic AMP, Animals, Humans, Luciferases, Molecular Biology, Chinese hamster ovary cell, Organic Chemistry, Ovary, Biological activity, Recombinant Proteins, chemistry, Molecular Medicine, Receptors, FSH, Female, Thiazolidinediones, Follicle Stimulating Hormone, Follicle-stimulating hormone receptor

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f99e8f500b9ac15e85d181f3013c88d
    https://pubmed.ncbi.nlm.nih.gov/16675221

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  11. 11
    Synthesis of (+)-16-thioketal and 16-keto prostaglandins

    المؤلفون: Richard W. Rees, Wenling Kao

    المصدر: Prostaglandins. 16(3)

    مصطلحات موضوعية: Thioketal, Prostaglandins E, Synthetic, chemistry.chemical_compound, Chemistry, Endocrinology, chemistry, Chemical Phenomena, Stereochemistry, Guinea Pigs, Animals, lipids (amino acids, peptides, and proteins), Biological Assay, Biochemistry

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38545b13234a349392d4034113b875b9
    https://pubmed.ncbi.nlm.nih.gov/725078

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