Molecular cloning and characterization of an invertebrate cellular retinoic acid binding protein von Mansfield, S.G. (Intron LLC, Durham, NC.), Cammer, S, Alexander, S.C, Muehleisen, D.P, Gray, R.S, Tropsha, A, Bollenbacher, W.E

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Life cycle expression of a bombyxin-like neuropeptide in the tobacco hornworm, Manduca sexta von Nogueira, Brigid V, Muehleisen, David P, Whisenton, Lavern R, Gray, Rosemary S, Bollenbacher, Walter E

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Immunoaffinity purification of the neuropeptide prothoracicotropic hormone from Manduca sexta von Muehleisen, David P., Gray, Rosemary S., Katahira, Eva J., Thomas, Mark K., Bollenbacher, Walter E.

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The Biology of the Prothoracicotropic Hormone Peptidergic Neurons in an Insect von BOLLENBACHER, WALTER E., GRAY, ROSEMARY S., MUEHLEISEN, DAVID P., REGAN, SHEILA A., WESTBROOK, ANNE L.

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The prothoracicotropic hormone (PTTH) of the commercial silkmoth, Bombyx mori, in the CNS of the tobacco hornworm, Manduca sexta von Gray, Rosemary S., Muehleisen, David P., Katahira, Eva J., Bollenbacher, Walter E.

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A 28-kDa cerebral neuropeptide from Manduca sexta : relationship to the insect prothoracicotropic hormone von GRAY, R. S, MUEHLEISEN, D. P, KATAHIRA, E. J, BOLLENBACHER, W. E

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A 28-kDa cerebral neuropeptide fromManduca sexta: Relationship to the insect prothoracicotropic hormone von Gray, Rosemary S., Muehleisen, David P., Katahira, Eva J., Bollenbacher, Walter E.

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Effects of cotton allelochemicals on toxicity of insecticides and induction of detoxifying enzymes in bollworm (Lepidoptera: noctuidae) von MUEHLEISEN, D. P, BENEDICT, J. H, PLAPP, F. W. JR, CARINO, F. A

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High affinity TCDD binding to fat body cytosolic proteins of the bollworm, Heliothis zea von Muehleisen, David P., Plapp, F.W., Benedict, J.H., Carino, F.A.

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High-affinity juvenile hormone binding to fat body cytosolic proteins of the bollworm, Heliothis zea: Characterization and interaction with allelochemicals and xenobiotics von Muehleisen, David P., Plapp, F.W., Benedict, J.H., Carino, F.A.

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Synthesis of deuterated and tritiated gossypol von Stipanovic, Robert D., Williams, Howard J., Muehleisen, David P., Plapp Jr, F. W.

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Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease von Deloukas, Panagiotis, Hamshere, Marian L, Lovestone, Simon, Mead, Simon, Nöthen, Markus M, Gerrish, Amy, O'Donovan, Michael, Hüll, Michael, Hardy, John, Hampel, Harald, Passmore, Peter A, Engelborghs, Sebastiaan, Abraham, Richard, Thomas, Charlene, Moskvina, Valentina, Brayne, Carol, Lawlor, Brian, Bass, Nicholas J, McQuillin, Andrew, Holmans, Peter A, Jones, Nicola, Pahwa, Jaspreet Singh, Morgan, Kevin, Klopp, Norman, Schürmann, Britta, Carrasquillo, Minerva M, Jessen, Frank, Tsolaki, Magda, McGuinness, Bernadette, Van Broeckhoven, Christine, De Deyn, Peter P, Cruchaga, Carlos, Mayo, Kevin, Wichmann, H-Erich, Brown, Kristelle S, Fox, Nick, Proitsi, Petroula, Mühleisen, Thomas W, Lupton, Michelle K, Lynch, Aoibhinn, Williams, Julie, Singleton, Andrew B, Moebus, Susanne, Dowzell, Kimberley, Livingston, Gill, Powell, John, Todd, Stephen, Wiltfang, Jens, Kornhuber, Johannes, Shaw, Christopher E, Pankratz, V Shane, Owen, Michael J, Holmes, Clive, Kehoe, Patrick G, Al-Chalabi, Ammar, Morgan, Angharad R, Heuser, Isabella, Williams, Amy, Mann, David, Gurling, Hugh, Kauwe, John S K, Goate, Alison M, Frölich, Lutz, Rubinsztein, David C, Love, Seth, Rossor, Martin, Rujescu, Dan, Hollingworth, Paul, Bettens, Karolien, Younkin, Steven G, Nowotny, Petra, Dichgans, Martin, Smith, A David, Collinge, John, van den Bussche, Hendrik, Gwilliam, Rhian, Guerreiro, Rita, Jöckel, Karl-Heinz, Sims, Rebecca, Morris, John C, Gill, Michael, Craig, David, Sleegers, Kristel, Harold, Denise, Stretton, Alexandra, Maier, Wolfgang

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Large recurrent microdeletions associated with schizophrenia von Tosato, Sarah, Peltonen, Leena, Kiemeney, Lambertus A, Nöthen, Markus M, Sigurdsson, Asgeir, Fraser, Gillian, Sigmundsson, Thordur, Ophoff, Roel A, Ullum, Henrik, Li, Tao, Stefansson, Kari, Bramon, Elvira, Djurovic, Srdjan, Walshe, Muriel, Bjornsson, Asgeir, Suvisaari, Jaana, Gylfason, Arnaldur, Tuulio-Henriksson, Annamarie, Sabatti, Chiara, Andreassen, Ole A, Kong, Augustine, Collier, David A, Ingason, Andres, Sigurdsson, Engilbert, Jonasdottir, Adalbjorg, Haraldsson, Magnus, Pietiläinen, Olli P. H, Walker, Nicholas, Hartmann, Annette, Halldorsson, Bjarni V, St Clair, David, Ruggeri, Mirella, Vasilescu, Catalina, Need, Anna C, Jakobsen, Klaus D, Gudbjartsson, Daniel, Di Forti, Marta, Melle, Ingrid, Toulopoulou, Timi, Mühleisen, Thomas W, Jonasdottir, Aslaug, Stefansson, Hreinn, Franke, Barbara, Steinberg, Stacy, Blondal, Thorarinn, Rietschel, Marcella, Vassos, Evangelos, Rujescu, Dan, Buizer-Voskamp, Jacobine E, Goldstein, David B, Cichon, Sven, Freimer, Nelson B, Petursson, Hannes, Werge, Thomas, Magnusdottir, Brynja B, Murray, Robin, Francks, Clyde, Gulcher, Jeffrey R, Crombie, Caroline, Giegling, Ina, Möller, Hans-Jürgen, Wang, August G, Hansen, Thomas, Olesen, Jes, Paunio, Tiina, Thorsteinsdottir, Unnur, Lonnqvist, Jouko, Shianna, Kevin V, Georgi, Alexander, Ge, Dongliang, Mattiasdottir, Sigurborg, Thorgeirsson, Thorgeir E, Matthews, Paul M, Fossdal, Ragnheidur, Muglia, Pierandrea

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The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma von Weinhold, Niels, Johnson, David C, Chubb, Daniel, Chen, Bowang, Försti, Asta, Hosking, Fay J, Broderick, Peter, Ma, Yussanne P, Dobbins, Sara E, Hose, Dirk, Walker, Brian A, Davies, Faith E, Kaiser, Martin F, Li, Ni L, Gregory, Walter A, Jackson, Graham H, Witzens-Harig, Mathias, Neben, Kai, Hoffmann, Per, Nöthen, Markus M, Mühleisen, Thomas W, Eisele, Lewin, Ross, Fiona M, Jauch, Anna, Goldschmidt, Hartmut, Houlston, Richard S, Morgan, Gareth J, Hemminki, Kari

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Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk von Broderick, Peter, Chubb, Daniel, Johnson, David C, Weinhold, Niels, Försti, Asta, Lloyd, Amy, Olver, Bianca, Ma, Yussanne P, Dobbins, Sara E, Walker, Brian A, Davies, Faith E, Gregory, Walter A, Child, J Anthony, Ross, Fiona M, Jackson, Graham H, Neben, Kai, Jauch, Anna, Hoffmann, Per, Mühleisen, Thomas W, Nöthen, Markus M, Moebus, Susanne, Tomlinson, Ian P, Goldschmidt, Hartmut, Hemminki, Kari, Morgan, Gareth J, Houlston, Richard S

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A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia von Ingason, Andrés, Giegling, Ina, Cichon, Sven, Hansen, Thomas, Rasmussen, Henrik B., Nielsen, Jimmi, Jürgens, Gesche, Muglia, Pierandrea, Hartmann, Annette M., Strengman, Eric, Vasilescu, Catalina, Mühleisen, Thomas W., Djurovic, Srdjan, Melle, Ingrid, Lerer, Bernard, Möller, Hans-Jürgen, Francks, Clyde, Pietiläinen, Olli P.H., Lonnqvist, Jouko, Suvisaari, Jaana, Tuulio-Henriksson, Annamari, Walshe, Muriel, Vassos, Evangelos, Di Forti, Marta, Murray, Robin, Bonetto, Chiara, Tosato, Sarah, Cantor, Rita M., Rietschel, Marcella, Craddock, Nick, Owen, Michael J., Peltonen, Leena, Andreassen, Ole A., Nöthen, Markus M., St Clair, David, Ophoff, Roel A., O'Donovan, Michael C., Collier, David A., Werge, Thomas, Rujescu, Dan

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1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans von Sonderby, Ida E, van der Meer, Dennis, Moreau, Clara, Kaufmann, Tobias, Walters, G. Bragi, Ellegaard, Maria, Abdellaoui, Abdel, Ames, David, Amunts, Katrin, Andersson, Micael, Armstrong, Nicola J, Bernard, Manon, Blackburn, Nicholas B, Blangero, John, Boomsma, Dorret I, Brodaty, Henry, Brouwer, Rachel M, Buelow, Robin, Boen, Rune, Cahn, Wiepke, Calhoun, Vince D, Caspers, Svenja, Ching, Christopher R.K, Cichon, Sven, Ciufolini, Simone, Crespo-Facorro, Benedicto, Curran, Joanne E, Dale, Anders M, Dalvie, Shareefa, Dazzan, Paola, de Geus, Eco J.C, de Zubicaray, Greig I, de Zwarte, Sonja M.C, Desrivieres, Sylvane, Doherty, Joanne L, Donohoe, Gary, Draganski, Bogdan, Ehrlich, Stefan, Eising, Else, Espeseth, Thomas, Fejgin, Kim, Fisher, Simon E, Fladby, Tormod, Frei, Oleksandr, Frouin, Vincent, Fukunaga, Masaki, Gareau, Thomas, Ge, Tian, Glahn, David C, Grabe, Hans J, Groenewold, Nynke A, Gustafsson, Omar, Haavik, Jan, Haberg, Asta K, Hall, Jeremy, Hashimoto, Ryota, Hehir-Kwa, Jayne Y, Hibar, Derrek P, Hillegers, Manon H.J, Hoffmann, Per, Holleran, Laurena, Holmes, Avram J, Homuth, Georg, Hottenga, Jouke-Jan, Hulshoff Pol, Hilleke E, Ikeda, Masashi, Jahanshad, Neda, Jockwitz, Christiane, Johansson, Stefan, Joensson, Erik G, Jorgensen, Niklas R, Kikuchi, Masataka, Knowles, Emma E.M, Kumar, Kuldeep, Le Hellard, Stephanie, Leu, Costin, Linden, David E.J, Liu, Jingyu, Lundervold, Arvid, Lundervold, Astri Johansen, Maillard, Anne M, Martin, Nicholas G, Martin-Brevet, Sandra, Mather, Karen A, Mathias, Samuel R, McMahon, Katie L, McRae, Allan F, Medland, Sarah E, Meyer-Lindenberg, Andreas, Moberget, Torgeir, Modenato, Claudia, Sanchez, Jennifer Monereo, Morris, Derek W, Muehleisen, Thomas W, Murray, Robin M, Nielsen, Jacob, Nordvik, Jan E, Nyberg, Lars, Loohuis, Loes M. Olde, Ophoff, Roel A

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Replication Study and Meta-Analysis in European Samples Supports Association of the 3p21.1 Locus with Bipolar Disorder von Vassos, Evangelos, Steinberg, Stacy, Cichon, Sven, Breen, Gerome, Sigurdsson, Engilbert, Andreassen, Ole A, Djurovic, Srdjan, Morken, Gunnar, Grigoroiu-Serbanescu, Maria, Diaconu, Carmen C, Czerski, Piotr M, Hauser, Joanna, Babadjanova, Gulja, Abramova, Lilia I, Mühleisen, Thomas W, Nöthen, Markus M, Rietschel, Marcella, McGuffin, Peter, St. Clair, David, Gustafsson, Omar, Melle, Ingrid, Pietiläinen, Olli P.H, Ruggeri, Mirella, Tosato, Sarah, Werge, Thomas, Ophoff, Roel A, Rujescu, Dan, Børglum, Anders D, Mors, Ole, Mortensen, Preben B, Demontis, Ditte, Hollegaard, Mads V, van Winkel, Ruud, Kenis, Gunter, De Hert, Marc, Réthelyi, János M, Bitter, István, Rubino, I. Alex, Golimbet, Vera, Kiemeney, Lambertus A, van den Berg, Leonard H, Franke, Barbara, Jönsson, Erik G, Farmer, Anne, Stefansson, Hreinn, Stefansson, Kari, Collier, David A

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Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease von Harold, Denise, Abraham, Richard, Hollingworth, Paul, Sims, Rebecca, Gerrish, Amy, Hamshere, Marian L, Pahwa, Jaspreet Singh, Moskvina, Valentina, Dowzell, Kimberley, Williams, Amy, Jones, Nicola, Thomas, Charlene, Stretton, Alexandra, Morgan, Angharad R, Lovestone, Simon, Powell, John, Proitsi, Petroula, Lupton, Michelle K, Brayne, Carol, Rubinsztein, David C, Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Morgan, Kevin, Brown, Kristelle S, Passmore, Peter A, Craig, David, McGuinness, Bernadette, Todd, Stephen, Holmes, Clive, Mann, David, Smith, A David, Love, Seth, Kehoe, Patrick G, Hardy, John, Mead, Simon, Fox, Nick, Rossor, Martin, Collinge, John, Maier, Wolfgang, Jessen, Frank, Schuermann, Britta, Heun, Reinhard, van den Bussche, Hendrik, Heuser, Isabella, Kornhuber, Johannes, Wiltfang, Jens, Dichgans, Martin, Frolich, Lutz, Hampel, Harald, et. al

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Genome-wide significant association between a ‘negative mood delusions’ dimension in bipolar disorder and genetic variation on chromosome 3q26.1 von Meier, S, Mattheisen, M, Vassos, E, Strohmaier, J, Treutlein, J, Josef, F, Breuer, R, Degenhardt, F, Mühleisen, T W, Müller-Myhsok, B, Steffens, M, Schmael, C, McMahon, F J, Nöthen, M M, Cichon, S, Schulze, T G, Rietschel, M

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