Sphingolipids: membrane microdomains in brain development, function and neurological diseases von Olsen, Anne S. B., Færgeman, Nils J.

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Increased short-term risk of thrombo-embolism or death after interruption of warfarin treatment in patients with atrial fibrillation von RAUNSØ, Jakob, SELMER, Christian, GISLASON, Gunnar H, TORP-PEDERSEN, Christian, LOCK HANSEN, Morten, BJERRING OLESEN, Jonas, GITZ CHARLOT, Mette, OLSEN, Anne-Marie S, BRETLER, Ditte-Marie, DALSGAARD NIELSEN, Jørn, DOMINGUEZ, Helena, GADSBØLL, Niels, KØBER, Lars

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Clopidogrel discontinuation after myocardial infarction and risk of thrombosis: a nationwide cohort study von CHARLOT, Mette, HOUGAARD NIELSEN, Lars, TORP-PEDERSEN, Christian, LINDHARDSEN, Jesper, AHLEHOFF, Ole, OLSEN, Anne-Marie S, LOCK HANSEN, Morten, HANSEN, Peter Riis, MADSEN, Jan Kyst, KØBER, Lars, GISLASON, Gunnar H

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Ongoing treatment with non-steroidal anti-inflammatory drugs at time of admission is associated with poorer prognosis in patients with first-time acute myocardial infarction von Lamberts, Morten, Fosbøl, Emil L, Olsen, Anne-Marie S, Hansen, Morten L, Folke, Frederik, Kristensen, Søren L, Olesen, Jonas B, Hansen, Peter R, Køber, Lars, Torp-Pedersen, Christian, Gislason, Gunnar H

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Inactivation of the EGF‐TM7 receptor EMR4 after the Pan‐Homo divergence von Hamann, Jörg, Kwakkenbos, Mark J., de Jong, Esther C., Heus, Henk, Olsen, Anne S., van Lier, René A.W.

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A serine/threonine kinase gene defective in Peutz-Jeghers syndrome von Aaltonen, Lauri A, Hemminki, Akseli, Markie, David, Tomlinson, Ian, Avizienyte, Egle, Roth, Stina, Loukola, Anu, Bignell, Graham, Warren, William, Aminoff, Maria, Höglund, Pia, Järvinen, Heikki, Kristo, Paula, Pelin, Katarina, Ridanpää, Maaret, Salovaara, Reijo, Toro, Tumi, Bodmer, Walter, Olschwang, Sylviane, Olsen, Anne S, Stratton, Michael R, de la Chapelle, Albert

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Human Chromosome 19 and Related Regions in Mouse: Conservative and Lineage-Specific Evolution von Dehal, Paramvir, Predki, Paul, Olsen, Anne S., Kobayashi, Art, Folta, Peg, Lucas, Susan, Land, Miriam, Terry, Astrid, Carol L. Ecale Zhou, Rash, Sam, Zhang, Qing, Gordon, Laurie, Kim, Joomyeong, Elkin, Christopher, Pollard, Martin J., Richardson, Paul, Rokhsar, Dan, Uberbacher, Ed, Hawkins, Trevor, Branscomb, Elbert, Stubbs, Lisa

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Reduced ceramide synthase 2 activity causes progressive myoclonic epilepsy von Mosbech, Mai‐Britt, Olsen, Anne S. B., Neess, Ditte, Ben‐David, Oshrit, Klitten, Laura L., Larsen, Jan, Sabers, Anne, Vissing, John, Nielsen, Jørgen E., Hasholt, Lis, Klein, Andres D., Tsoory, Michael M., Hjalgrim, Helle, Tommerup, Niels, Futerman, Anthony H., Møller, Rikke S., Færgeman, Nils J.

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An integrated metric physical map of human chromosome 19 von Ashworth, Linda K, Batzer, Mark A, Brandriff, Brigitte, Branscomb, Elbert, de Jong, Pieter, Garcia, Emilio, Garnes, Jeffrey A, Gordon, Laurie A, Lamerdin, Jane E, Lennon, Greg, Mohrenweiser, Harvey, Olsen, Anne S, Slezak, Tom, Carrano, Anthony V

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Evolution of the mammalian G protein α subunit multigene family von Wilkie, Thomas M, Gilbert, Debra J, Olsen, Anne S, Chen, Xiao-Ning, Amatruda, Thomas T, Korenberg, Julie R, Trask, Barbara J, de Jong, Pieter, Reed, Randall R, Simon, Melvin I, Jenkins, Nancy A, Copeland, Neal G

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Chromosomal Localization of the Human and Mouse Hyaluronan Synthase Genes von Spicer, Andrew P., Seldin, Michael F., Olsen, Anne S., Brown, Nicholas, Wells, Dan E., Doggett, Norman A., Itano, Naoki, Kimata, Koji, Inazawa, Joji, McDonald, John A.

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Location of mouse and human genes corresponding to conserved canine olfactory receptor gene subfamilies von Carver, E A, Issel-Tarver, L, Rine, J, Olsen, A S, Stubbs, L

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Physical mapping of EMR1 and CD97 in human Chromosome 19 and assignment of Cd97 to mouse Chromosome 8 suggest an ancient genomic duplication von Carver, E A, Hamann, J, Olsen, A S, Stubbs, L

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Assembly of a 1-Mb Restriction-Mapped Cosmid Contig Spanning the Candidate Region for Finnish Congenital Nephrosis (NPHS1) in 19q13.1 von Olsen, Anne S., Georgescu, Anca, Johnson, Stephanie, Carrano, Anthony V.

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The GCN2 eIF2α Kinase Is Required for Adaptation to Amino Acid Deprivation in Mice von Zhang, Peichuan, McGrath, Barbara C., Reinert, Jamie, Olsen, DeAnne S., Lei, Li, Gill, Sangeeta, Wek, Sheree A., Vattem, Krishna M., Wek, Ronald C., Kimball, Scot R., Jefferson, Leonard S., Cavener, Douglas R.

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The spectrum of thyroid disease and risk of new onset atrial fibrillation: a large population cohort study von Selmer, Christian, Olesen, Jonas Bjerring, Hansen, Morten Lock, Lindhardsen, Jesper, Olsen, Anne-Marie Schjerning, Madsen, Jesper Clausager, Faber, Jens, Hansen, Peter Riis, Pedersen, Ole Dyg, Torp-Pedersen, Christian, Gislason, Gunnar Hilmar

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Domains of eIF1A that mediate binding to eIF2, eIF3 and eIF5B and promote ternary complex recruitment in vivo von Olsen, DeAnne S., Savner, Erin M., Mathew, Amy, Zhang, Fan, Krishnamoorthy, Thanuja, Phan, Lon, Hinnebusch, Alan G.

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Human hypoxanthine phosphoribosyltransferase. Purification and properties von Olsen, Anne S, Milman, Gregory

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A serine/threonine kinase gene defective in Peutz–Jeghers syndrome von Hemminki, Akseli, Markie, David, Tomlinson, Ian, Avizienyte, Egle, Roth, Stina, Loukola, Anu, Bignell, Graham, Warren, William, Aminoff, Maria, Höglund, Pia, Järvinen, Heikki, Kristo, Paula, Pelin, Katarina, Ridanpää, Maaret, Salovaara, Reijo, Toro, Tumi, Bodmer, Walter, Olschwang, Sylviane, Olsen, Anne S., Stratton, Michael R., de la Chapelle, Albert, Aaltonen, Lauri A.

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Identification and characterization of the human homologue of the short PDE4A cAMP-specific phosphodiesterase RD1 (PDE4A1) by analysis of the human HSPDE4A gene locus located at ch... von Sullivan, M, Rena, G, Begg, F, Gordon, L, Olsen, A S, Houslay, M D

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