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1Academic Journal
المؤلفون: Christiansen, E., Hansen, S.V.F., Urban, C., Hudson, B.D., Wargent, E.T., Grundmann, M., Jenkins, L., Zaibi, M., Stocker, C.J., Ullrich, S., Kostenis, E., Kassack, M.U., Milligan, G., Cawthorne, M.A., Ulven, T.
وصف الملف: text
Relation: https://eprints.gla.ac.uk/81349/1/81349.pdf; Christiansen, E. et al. (2013) Discovery of TUG-770: a highly potent free fatty acid receptor 1 (FFA1/GPR40) agonist for treatment of type 2 diabetes. ACS Medicinal Chemistry Letters , 4(5), pp. 441-445. (doi:10.1021/ml4000673 )
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2Academic Journal
المؤلفون: Christiansen, E., Due-Hansen, M.E., Urban, C., Grundmann, M., Schmidt, J., Hansen, S.V.F., Hudson, B.D., Zaibi, M., Markussen, S.B., Hagesaether, E., Milligan, G., Cawthorne, M.A., Kostenis, E., Kassack, M.U., Ulven, T.
Relation: Christiansen, E. et al. (2013) Discovery of a potent and selective free fatty acid receptor 1 agonist with low lipophilicity and high oral bioavailability. Journal of Medicinal Chemistry , 56(3), pp. 982-992. (doi:10.1021/jm301470a )
الاتاحة: https://eprints.gla.ac.uk/78018/
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3Academic Journal
المؤلفون: Christiansen, E., Due-Hansen, M.E., Urban, C., Grundmann, M., Schröder, R., Hudson, B.D., Milligan, G., Cawthorne, M.A., Kostenis, E., Kassack, M.U., Ulven, T.
Relation: Christiansen, E. et al. (2012) Free fatty acid receptor 1 (FFA1/GPR40) agonists: mesylpropoxy appendage lowers lipophilicity and improves ADME properties. Journal of Medicinal Chemistry , 55(14), pp. 6624-6628. (doi:10.1021/jm3002026 )
الاتاحة: https://eprints.gla.ac.uk/69361/
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4Academic Journal
المؤلفون: Kornum B.R., Kawashima M., Faraco J., Lin L., Rico T.J., Hesselson S., Axtell R.C., Kuipers H., Weiner K., Hamacher A., Kassack M.U., Han F., Knudsen S., Li J., Dong X., Winkelmann J., Plazzi G., Nevsimalova S., Hong S.C., Honda Y., Honda M., Hogl B., Ton T.G., Montplaisir J., Bourgin P., Kemlink D., Huang Y.S., Warby S., Einen M., Eshragh J.L., Miyagawa T., Desautels A., Ruppert E., Hesla P.E., Poli F., Pizza F., Frauscher B., Jeong J.H., Lee S.P., Strohl K.P., Longstreth W.T. Jr., Kvale M., Dobrovolna M., Ohayon M.M., Nepom G.T., Wichmann H.E., Rouleau G.A., Gieger C., Levinson D.F., Gejman P.V., Meitinger T., Peppard P., Young T., Jennum P., Steinman L., Tokunaga K., Kwok P.Y., Risch N., Hallmayer J., Mognot E.
المساهمون: Kornum, B. R., Kawashima, M., Faraco, J., Lin, L., Rico, T. J., Hesselson, S., Axtell, R. C., Kuipers, H., Weiner, K., Hamacher, A., Kassack, M. U., Han, F., Knudsen, S., Li, J., Dong, X., Winkelmann, J., Plazzi, G., Nevsimalova, S., Hong, S. C., Honda, Y., Honda, M., Hogl, B., Ton, T. G., Montplaisir, J., Bourgin, P., Kemlink, D., Huang, Y. S., Warby, S., Einen, M., Eshragh, J. L., Miyagawa, T., Desautels, A., Ruppert, E., Hesla, P. E., Poli, F., Pizza, F., Frauscher, B., Jeong, J. H., Lee, S. P., Strohl, K. P., Longstreth, W. T. Jr., Kvale, M., Dobrovolna, M., Ohayon, M. M., Nepom, G. T., Wichmann, H. E., Rouleau, G. A., Gieger, C., Levinson, D. F., Gejman, P. V., Meitinger, T., Peppard, P., Young, T., Jennum, P., Steinman, L., Tokunaga, K., Kwok, P. Y., Risch, N., Hallmayer, J., Mognot, E.
مصطلحات موضوعية: P2RY11, narcolepsy, narcolepsy with cataplexy, genome-wide association
Relation: info:eu-repo/semantics/altIdentifier/pmid/21170044; info:eu-repo/semantics/altIdentifier/wos/WOS:000285683500018; volume:43; issue:1; firstpage:66; lastpage:71; numberofpages:6; journal:NATURE GENETICS; http://hdl.handle.net/11380/1206082; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-78651245467
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5
المؤلفون: Marie Dobrovolna, Alex Desautels, Thomas Meitinger, Birgit Frauscher, Jing Li, William T. Longstreth, Yutaka Honda, Sung-Pil Lee, Birgit Högl, Stine Knudsen, Makoto Honda, Fabio Pizza, Pui-Yan Kwok, Neil Risch, Karin Weiner, Elisabeth Ruppert, Mali Einen, Seung-Chul Hong, Sona Nevsimalova, Lawrence Steinman, Birgitte Rahbek Kornum, Ling Lin, Juliette Faraco, Taku Miyagawa, Fang Han, David Kemlink, Joachim Hallmayer, Pablo V. Gejman, Mark N. Kvale, Terry Young, Alexandra Hamacher, Emmanuel Mignot, Matthias U. Kassack, H-Erich Wichmann, Gerald T. Nepom, Robert C. Axtell, Jasmin L Eshragh, Thomas J Rico, Juliane Winkelmann, Jong-Hyun Jeong, Jacques Montplaisir, Minae Kawashima, Christian Gieger, Maurice M. Ohayon, Patrice Bourgin, Giuseppe Plazzi, Xiaosong Dong, Francesca Poli, Hedwich F. Kuipers, Kingman P. Strohl, Simon C. Warby, Paul E. Peppard, Yu-Shu Huang, Stephanie Hesselson, Katsushi Tokunaga, Poul Jennum, Douglas F. Levinson, Thanh G.N. Ton, Guy A. Rouleau, Per Egil Hesla
المساهمون: Kornum B.R., Kawashima M., Faraco J., Lin L., Rico T.J., Hesselson S., Axtell R.C., Kuipers H., Weiner K., Hamacher A., Kassack M.U., Han F., Knudsen S., Li J., Dong X., Winkelmann J., Plazzi G., Nevsimalova S., Hong S.C., Honda Y., Honda M., Hogl B., Ton T.G., Montplaisir J., Bourgin P., Kemlink D., Huang Y.S., Warby S., Einen M., Eshragh J.L., Miyagawa T., Desautels A., Ruppert E., Hesla P.E., Poli F., Pizza F., Frauscher B., Jeong J.H., Lee S.P., Strohl K.P., Longstreth W.T. Jr., Kvale M., Dobrovolna M., Ohayon M.M., Nepom G.T., Wichmann H.E., Rouleau G.A., Gieger C., Levinson D.F., Gejman P.V., Meitinger T., Peppard P., Young T., Jennum P., Steinman L., Tokunaga K., Kwok P.Y., Risch N., Hallmayer J., Mognot E.
المصدر: Nature genetics
Nature genetics, vol 43, iss 1مصطلحات موضوعية: Genome-wide association study, Medical and Health Sciences, P2RY11, narcolepsy, narcolepsy with cataplexy, genome-wide association, 0302 clinical medicine, Receptors, Ethnicity, Odds Ratio, 2.1 Biological and endogenous factors, Pandemrix, Aetiology, African Americans, 0303 health sciences, Single Nucleotide, Biological Sciences, Asians, Asian Continental Ancestry Group, European Continental Ancestry Group, Ethnic Groups, Biology, Peripheral blood mononuclear cell, Polymorphism, Single Nucleotide, White People, Article, 03 medical and health sciences, Asian People, Genetics, medicine, Humans, Genetic Predisposition to Disease, Polymorphism, Allele, Alleles, 030304 developmental biology, Narcolepsy, Autoimmune disease, Purinergic P2, Whites, Receptors, Purinergic P2, Human Genome, Case-control study, Genetic Variation, medicine.disease, Brain Disorders, Black or African American, Case-Control Studies, Immunology, 030217 neurology & neurosurgery, CD8, Developmental Biology, Genome-Wide Association Study
وصف الملف: ELETTRONICO; application/pdf