Search Results - "Swahn, Marie"

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    Characterization of AZD4694, a novel fluorinated Aβ plaque neuroimaging PET radioligand by Juréus, Anders, Swahn, Britt-Marie, Sandell, Johan, Jeppsson, Fredrik, Johnson, Allan E, Johnström, Peter, Neelissen, Jan A.M, Sunnemark, Dan, Farde, Lars, Svensson, Samuel P.S

    Published in Journal of neurochemistry (01-08-2010)
    “…J. Neurochem. (2010) 114, 784-794. Positron emission tomography (PET) radioligands that bind selectively to β-amyloid plaques (Aβ) are promising imaging tools…”
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    Video Radiology Reports: A Valuable Tool to Improve Patient-Centered Radiology by Recht, Michael P, Westerhoff, Malte, Doshi, Ankur M, Young, Matthew, Ostrow, Dana, Swahn, Dawn-Marie, Krueger, Sebastian, Thesen, Stefan

    Published in American journal of roentgenology (1976) (01-09-2022)
    “…Improved communication between radiologists and patients is a key component of patient-centered radiology. The purpose of this study was to create…”
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    Decreased Tongue Volume Post Radiation by Garber, David, Rotsides, Janine, Abu-Ghanem, Sara, Bandler, Ilana, Smith, Amy, Oyfe, Irina, Swahn, Dawn-Marie, Hagiwara, Mari, Amin, Milan, Johnson, Aaron M.

    Published in Annals of otology, rhinology & laryngology (01-08-2020)
    “…Objectives: To evaluate volume changes within the tongue post chemoradiation therapy (CRT) Study Design: Retrospective review Setting: Academic Medical Center…”
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    Creation of Novel Cores for β‑Secretase (BACE-1) Inhibitors: A Multiparameter Lead Generation Strategy by Viklund, Jenny, Kolmodin, Karin, Nordvall, Gunnar, Swahn, Britt-Marie, Svensson, Mats, Gravenfors, Ylva, Rahm, Fredrik

    Published in ACS medicinal chemistry letters (10-04-2014)
    “…In order to find optimal core structures as starting points for lead optimization, a multiparameter lead generation workflow was designed with the goal of…”
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    Design and synthesis of 2′-anilino-4,4′-bipyridines as selective inhibitors of c-Jun N-terminal kinase-3 by Swahn, Britt-Marie, Xue, Yafeng, Arzel, Erwan, Kallin, Elisabet, Magnus, Angelika, Plobeck, Niklas, Viklund, Jenny

    Published in Bioorganic & medicinal chemistry letters (01-03-2006)
    “…The design and synthesis of new c-Jun N-terminal kinase-3 inhibitors (JNK3) with selectivity against JNK1 and p38α are reported. Compound 18 displayed the best…”
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    Design and synthesis of 6-anilinoindazoles as selective inhibitors of c-Jun N-terminal kinase-3 by Swahn, Britt-Marie, Huerta, Fernando, Kallin, Elisabet, Malmström, Jonas, Weigelt, Tatjana, Viklund, Jenny, Womack, Patrick, Xue, Yafeng, Öhberg, Liselotte

    Published in Bioorganic & medicinal chemistry letters (15-11-2005)
    “…The structure-based design and synthesis of a new series of c-Jun N-terminal kinase-3 inhibitors 4 with selectivity against JNK1 and p38α is reported. The…”
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    Liver X receptor agonists with selectivity for LXRβ; N-aryl-3,3,3-trifluoro-2-hydroxy-2-methylpropionamides by Swahn, Britt-Marie, Macsari, Istvan, Viklund, Jenny, Öhberg, Liselotte, Sjödin, Johanna, Neelissen, Jan, Lindquist, Johanna

    Published in Bioorganic & medicinal chemistry letters (01-04-2009)
    “…The synthesis and SAR of a new series of LXR agonist is reported. The N-Aryl-3,3,3-trifluoro-2-hydroxy-2-methyl-propionamide hits were found in a limited…”
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    New heteroaryl-spaced phosphono α-amino acids are competitive NMDA antagonists with analgesic activity by Swahn, Britt-Marie, Claesson, Alf, Pelcman, Benjamin, Besidski, Yevgeni, Molin, Håkan, Sandberg, Mats P., Berge, Odd-Geir

    Published in Bioorganic & medicinal chemistry letters (23-07-1996)
    “…The synthesis and the NMDA receptor binding affinities of α-amino-3-(phosphonomethyl)-2-naphthalene-propanoic acid,…”
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    Two non-racemic preparations of a piperidine-based NMDA antagonist with analgesic activity by Swahn, Britt-Marie, Edvinsson, Karin M., Kallin, Elisabet, Larsson, Ulf, Berge, Odd-Geir, Molin, Håkan, Pelcman, Benjamin, Claesson, Alf

    Published in Bioorganic & medicinal chemistry (01-07-1997)
    “…(2 R,3 S,1′ R)-3-(1-Hydroxy-2-phosphonoethyl)-2-piperidinecarboxylic acid 1 has been synthesized by two different methods. The NMDA receptor binding affinities…”
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