Differential Response of Gestational Tissues to TLR3 Viral Priming Prior to Exposure to Bacterial TLR2 and TLR2/6 Agonists von Rasheed, Zahirrah B M, Lee, Yun S, Kim, Sung H, Rai, Ranjit K, Ruano, Camino S M, Anucha, Eberechi, Sullivan, Mark H F, MacIntyre, David A, Bennett, Phillip R, Sykes, Lynne

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Bacteria and inflammatory cells in fetal membranes do not always cause preterm labor von STEEL, Jennifer H, MALATOS, Sotiris, KENNEA, Nigel, EDWARDS, A. David, MILES, Lynda, DUGGAN, Philip, REYNOLDS, Peter R, FELDMAN, Robert G, SULLIVAN, Mark H. F

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Bacteria in placenta and fetal membranes von Sullivan, Mark H.F., MD, PhD

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The effects of non-steroidal anti-inflammatory compounds on human myometrial contractility von Sawdy, Robert J, Sullivan, Mark H.F, Bennett, Phillip R

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Expression of the Human Neuropeptide Tyrosine Y1 Receptor von Wharton, John, Gordon, Lee, Byrne, Johanna, Herzog, Herbert, Selbie, Lisa A., Moore, Kevin, Mark H. F. Sullivan, Elder, Murdoch G., Moscoso, Gonzalo, Taylor, Kenneth M., Shine, John, Polak, Julia M.

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Retrospective analysis of platelet numbers and volumes in normal pregnancy and in pre‐eclampsia von Ahmed, Yusuf, Iddekinge, Basil, Paul, Carolyn, Sullivan, Mark H. F., Elder, Murdoch G.

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Changes in decidual stromal cell function associated with labour von KHAN, HAROON, ISHIHARA, OSAMU, SULLIVAN, MARK H. F., ELDER, MURDOCH G.

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An inhibitor of type-1 cyclo-oxygenase in tissues from human pregnancy von Willix-Payne, Dawn J., Sun, Mei-Yi, Elder, Murdoch G., Bennett, Phillip R., Sullivan, Mark H. F.

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Limited Transfer of Prostaglandin E2 Across the Fetal Membrane before and after Labor von Roseblade, Christopher K., Sullivan, Mark H.F., Khan, Haroon, Lumb, Michael R., Elder, Murdoch G.

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Control of Fetal Membrane Prostaglandin E2 Production by Bacteria von Helmig, Rikke, Roseblade, Christopher K., Uldbjerg, Niels, Elder, Murdoch G., Sullivan, Mark H. F.

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Veliparib with First-Line Chemotherapy and as Maintenance Therapy in Ovarian Cancer von Coleman, Robert L, Fleming, Gini F, Brady, Mark F, Swisher, Elizabeth M, Steffensen, Karina D, Friedlander, Michael, Okamoto, Aikou, Moore, Kathleen N, Efrat Ben-Baruch, Noa, Werner, Theresa L, Cloven, Noelle G, Oaknin, Ana, DiSilvestro, Paul A, Morgan, Mark A, Nam, Joo-Hyun, Leath, Charles A, Nicum, Shibani, Hagemann, Andrea R, Littell, Ramey D, Cella, David, Baron-Hay, Sally, Garcia-Donas, Jesus, Mizuno, Mika, Bell-McGuinn, Katherine, Sullivan, Danielle M, Bach, Bruce A, Bhattacharya, Sudipta, Ratajczak, Christine K, Ansell, Peter J, Dinh, Minh H, Aghajanian, Carol, Bookman, Michael A

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Obesity remodels activity and transcriptional state of a lateral hypothalamic brake on feeding von Rossi, Mark A, Basiri, Marcus L, McHenry, Jenna A, Kosyk, Oksana, Otis, James M, van den Munkhof, Hanna E, Bryois, Julien, Hübel, Christopher, Breen, Gerome, Guo, Wilson, Bulik, Cynthia M, Sullivan, Patrick F, Stuber, Garret D

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Specific Glial Functions Contribute to Schizophrenia Susceptibility von GOUDRIAAN, Andrea, DE LEEUW, Christiaan, RIPKE, Stephan, HULTMAN, Christina M, SKLAR, Pamela, SULLIVAN, Patrick F, SMIT, August B, POSTHUMA, Danielle, VERHEIJEN, Mark H. G

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Identification of common genetic risk variants for autism spectrum disorder von Grove, Jakob, Ripke, Stephan, Als, Thomas D., Mattheisen, Manuel, Walters, Raymond K., Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A., Anney, Richard, Awashti, Swapnil, Belliveau, Rich, Bettella, Francesco, Buxbaum, Joseph D., Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Christensen, Jane H., Churchhouse, Claire, Dellenvall, Karin, Demontis, Ditte, De Rubeis, Silvia, Devlin, Bernie, Djurovic, Srdjan, Dumont, Ashley L., Goldstein, Jacqueline I., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Hope, Sigrun, Howrigan, Daniel P., Huang, Hailiang, Hultman, Christina M., Klei, Lambertus, Maller, Julian, Martin, Joanna, Martin, Alicia R., Moran, Jennifer L., Nyegaard, Mette, Nærland, Terje, Palmer, Duncan S., Palotie, Aarno, Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, dPoterba, Timothy, Poulsen, Jesper Buchhave, Pourcain, Beate St, Qvist, Per, Rehnström, Karola, Reichenberg, Abraham, Reichert, Jennifer, Robinson, Elise B., Roeder, Kathryn, Roussos, Panos, Saemundsen, Evald, Sandin, Sven, Satterstrom, F. Kyle, Davey Smith, George, Stefansson, Hreinn, Steinberg, Stacy, Stevens, Christine R., Sullivan, Patrick F., Turley, Patrick, Walters, G. Bragi, Xu, Xinyi, Stefansson, Kari, Geschwind, Daniel H., Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Neale, Benjamin M., Daly, Mark J., Børglum, Anders D.

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Understanding racial HIV/STI disparities in black and white men who have sex with men: a multilevel approach von Sullivan, Patrick S, Peterson, John, Rosenberg, Eli S, Kelley, Colleen F, Cooper, Hannah, Vaughan, Adam, Salazar, Laura F, Frew, Paula, Wingood, Gina, Diclemente, Ralph, del Rio, Carlos, Mulligan, Mark, Sanchez, Travis H

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A polygenic burden of rare disruptive mutations in schizophrenia von Purcell, Shaun M., Moran, Jennifer L., Fromer, Menachem, Ruderfer, Douglas, Solovieff, Nadia, Roussos, Panos, O’Dushlaine, Colm, Chambert, Kimberly, Bergen, Sarah E., Kähler, Anna, Duncan, Laramie, Stahl, Eli, Genovese, Giulio, Fernández, Esperanza, Collins, Mark O., Komiyama, Noboru H., Choudhary, Jyoti S., Magnusson, Patrik K. E., Banks, Eric, Shakir, Khalid, Garimella, Kiran, Fennell, Tim, DePristo, Mark, Grant, Seth G. N., Haggarty, Stephen J., Gabriel, Stacey, Scolnick, Edward M., Lander, Eric S., Hultman, Christina M., Sullivan, Patrick F., McCarroll, Steven A., Sklar, Pamela

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Explaining racial disparities in HIV incidence in black and white men who have sex with men in Atlanta, GA: a prospective observational cohort study von Sullivan, Patrick S., DVM, PhD, Rosenberg, Eli S., PhD, Sanchez, Travis H., DVM, MPH, Kelley, Colleen F., MD, Luisi, Nicole, MPH, Cooper, Hannah L., ScD, Diclemente, Ralph J., PhD, Wingood, Gina M., PhD, Frew, Paula M., PhD, Salazar, Laura F., PhD, del Rio, Carlos, MD, Mulligan, Mark J., MD, Peterson, John L., PhD

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Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways von Howard, David M., Adams, Mark J., Shirali, Masoud, Clarke, Toni-Kim, Marioni, Riccardo E., Davies, Gail, Coleman, Jonathan R. I., Alloza, Clara, Shen, Xueyi, Barbu, Miruna C., Wigmore, Eleanor M., Gibson, Jude, Hagenaars, Saskia P., Lewis, Cathryn M., Ward, Joey, Smith, Daniel J., Sullivan, Patrick F., Haley, Chris S., Breen, Gerome, Deary, Ian J., McIntosh, Andrew M.

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Rare coding variants in ten genes confer substantial risk for schizophrenia von Singh, Tarjinder, Poterba, Timothy, Curtis, David, Akil, Huda, Al Eissa, Mariam, Barchas, Jack D., Bass, Nicholas, Bigdeli, Tim B., Breen, Gerome, Bromet, Evelyn J., Buckley, Peter F., Bunney, William E., Bybjerg-Grauholm, Jonas, Byerley, William F., Chapman, Sinéad B., Chen, Wei J., Churchhouse, Claire, Craddock, Nicholas, DeLisi, Lynn, Dodge, Sheila, Escamilla, Michael A., Eskelinen, Saana, Fanous, Ayman H., Faraone, Stephen V., Fiorentino, Alessia, Francioli, Laurent, Gabriel, Stacey B., Gage, Diane, Gagliano Taliun, Sarah A., Ganna, Andrea, Genovese, Giulio, Grove, Jakob, Hall, Mei-Hua, Heyne, Henrike O., Holi, Matti, Hougaard, David M., Howrigan, Daniel P., Huang, Hailiang, Hwu, Hai-Gwo, Kahn, René S., Kang, Hyun Min, Karczewski, Konrad J., Knowles, James A., Lee, Francis S., Lehrer, Douglas S., Lescai, Francesco, Marder, Stephen R., McCarroll, Steven A., McIntosh, Andrew M., Milani, Lili, Morley, Christopher P., Morris, Derek W., Mortensen, Preben Bo, Nordentoft, Merete, O’Brien, Niamh L., Olivares, Ana Maria, Ongur, Dost, Ouwehand, Willem H., Palmer, Duncan S., Paunio, Tiina, Quested, Digby, Rapaport, Mark H., Rees, Elliott, Rollins, Brandi, Satterstrom, F. Kyle, Schatzberg, Alan, Scolnick, Edward, Scott, Laura J., Sharp, Sally I., Sklar, Pamela, Smoller, Jordan W., Solomonson, Matthew, Stahl, Eli A., Stevens, Christine R., Suvisaari, Jaana, Watts, Nicholas A., Blackwood, Douglas H., Cohen, Bruce M., Corvin, Aiden P., Esko, Tõnu, Freimer, Nelson B., Glatt, Stephen J., Hultman, Christina M., McQuillin, Andrew, Palotie, Aarno, Pato, Carlos N., Pato, Michele T., Pulver, Ann E., St. Clair, David, Tsuang, Ming T., Vawter, Marquis P., Walters, James T., Werge, Thomas M., Ophoff, Roel A., Sullivan, Patrick F., Owen, Michael J., Boehnke, Michael, O’Donovan, Michael C., Neale, Benjamin M., Daly, Mark J.

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ASCL1 is a lineage oncogene providing therapeutic targets for high-grade neuroendocrine lung cancers von Augustyn, Alexander, Borromeo, Mark, Wang, Tao, Fujimoto, Junya, Shao, Chunii, Dospoy, Patrick D., Lee, Victoria, Tan, Christopher, Sullivan, James P., Larsen, Jill E., Girard, Luc, Behrens, Carmen, Wistuba, Ignacio I., Xie, Yang, Cobb, Melanie H., Gazdar, Adi F., Johnson, Jane E., Minna, John D.

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