Composto formulacao farmaceutica uso de um composto e processos para a preparacao de um composto e para tratamento de um individuo humano ou animal que esteja sofrendo de um distur... von GEORGE STUART COCKERRILL, KATHYRN JANE SMITH, MALCOLM CLIVE CARTER, STEPHEN BARRY GUNTRIP

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Erratum to Gene Set Enrichment Analyses Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy. Am J Ophthalmol 2022;233:111-123 von Sobrin, Lucia, Susarla, Gayatri, Stanwyck, Lynn, Rouhana, John M., Li, Ashley, Pollack, Samuela, Igo, Robert P., Jensen, Richard A., Li, Xiaohui, Ng, Maggie C.Y., Smith, Albert V., Kuo, Jane Z., Taylor, Kent D., Freedman, Barry I., Bowden, Donald W., Penman, Alan, Chen, Ching J., Craig, Jamie E., Adler, Sharon G., Chew, Emily Y., Cotch, Mary Frances, Yaspan, Brian, Mitchell, Paul, Wang, Jie Jin, Klein, Barbara E.K., Wong, Tien Y., Rotter, Jerome I., Burdon, Kathyrn P., Iyengar, Sudha K., Segrè, Ayellet V.

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Gene Set Enrichment Analsyes Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy von Sobrin, Lucia, Susarla, Gayatri, Stanwyck, Lynn, Rouhana, John M., Li, Ashley, Pollack, Samuela, Igo Jr, Robert P., Jensen, Richard A., Li, Xiaohui, Ng, Maggie C.Y., Smith, Albert V., Kuo, Jane Z., Taylor, Kent D., Freedman, Barry I., Bowden, Donald W., Penman, Alan, Chen, Ching J., Craig, Jamie E., Adler, Sharon G., Chew, Emily Y., Cotch, Mary Frances, Yaspan, Brian, Mitchell, Paul, Wang, Jie Jin, Klein, Barbara E.K., Wong, Tien Y., Rotter, Jerome I., Burdon, Kathyrn P., Iyengar, Sudha K., Segrè, Ayellet V.

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The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions von Rahmioglu, Nilufer, Mortlock, Sally, Ghiasi, Marzieh, Moller, Peter L, Stefansdottir, Lilja, Galarneau, Genevieve, Turman, Constance, Danning, Rebecca, Law, Matthew H, Sapkota, Yadav, Christofidou, Paraskevi, Skarp, Sini, Giri, Ayush, Banasik, Karina, Krassowski, Michal, Lepamets, Maarja, Marciniak, Blazej, Noukas, Margit, Perro, Danielle, Sliz, Eeva, Sobalska-Kwapis, Marta, Thorleifsson, Gudmar, Topbas-Selcuki, Nura F, Vitonis, Allison, Westergaard, David, Arnadottir, Ragnheidur, Burgdorf, Kristoffer S, Campbell, Archie, Cheuk, Cecilia S.K, Clementi, Caterina, Cook, James, De Vivo, Immaculata, DiVasta, Amy, Dorien, O, Donoghue, Jacqueline F, Edwards, Todd, Fontanillas, Pierre, Fung, Jenny N, Geirsson, Reynir T, Girling, Jane E, Harkki, Paivi, Harris, Holly R, Healey, Martin, Heikinheimo, Oskari, Holdsworth-Carson, Sarah, Hostettler, Isabel C, Houlden, Henry, Houshdaran, Sahar, Irwin, Juan C, Jarvelin, Marjo-Riitta, Kamatani, Yoichiro, Kennedy, Stephen H, Kepka, Ewa, Kettunen, Johannes, Kubo, Michiaki, Kulig, Bartosz, Kurra, Venla, Laivuori, Hannele, Laufer, Marc R, Lindgren, Cecilia M, MacGregor, Stuart, Mangino, Massimo, Martin, Nicholas G, Matalliotaki, Charoula, Matalliotakis, Michail, Murray, Alison D, Ndungu, Anne, Nezhat, Camran, Olsen, Catherine M, Opoku-Anane, Jessica, Padmanabhan, Sandosh, Paranjpe, Manish, Peters, Maire, Polak, Grzegorz, Porteous, David J, Rabban, Joseph, Rexrode, Kathyrn M, Romanowicz, Hanna, Saare, Merli, Saavalainen, Liisu, Schork, Andrew J, Sen, Sushmita, Shafrir, Amy L, Siewierska-Gorska, Anna, Slomka, Marcin, Smith, Blair H, Smolarz, Beata, Szaflik, Tomasz, Szyllo, Krzysztof, Takahashi, Atsushi, Terry, Kathryn L, Tomassetti, Carla, Treloar, Susan A, Vanhie, Arne, Vincent, Katy, Vo, Kim C, Werring, David J, Zeggini, Eleftheria, Zervou, Maria, Stefansson, Kari

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Gene Set Enrichment Analyses Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy von Sobrin, Lucia, Susarla, Gayatri, Stanwyck, Lynn, Rouhana, John M., Li, Ashley, Pollack, Samuela, Igo, Robert P., Jensen, Richard A., Li, Xiaohui, Ng, Maggie C.Y., Smith, Albert V., Kuo, Jane Z., Taylor, Kent D., Freedman, Barry I., Bowden, Donald W., Penman, Alan, Chen, Ching J., Craig, Jamie E., Adler, Sharon G., Chew, Emily Y., Frances Cotch, Mary, Yaspan, Brian, Mitchell, Paul, Jin Wang, Jie, Klein, Barbara E.K., Wong, Tien Y., Rotter, Jerome I., Burdon, Kathyrn P., Iyengar, Sudha K., Segrè, Ayellet V.

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The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions von Mortlock, Sally, Møller, Peter L, Law, Matthew H, Sapkota, Yadav, Christofidou, Paraskevi, Skarp, Sini, Giri, Ayush, Banasik, Karina, Krassowski, Michal, Lepamets, Maarja, Marciniak, Błażej, Nõukas, Margit, Thorleifsson, Gudmar, Topbas-Selcuki, Nura F, Westergaard, David, Cheuk, Cecilia SK, Clementi, Caterina, Cook, James, De Vivo, Immaculata, Dorien, O, Donoghue, Jacqueline F, Edwards, Todd, Fontanillas, Pierre, Harkki, Paivi, Harris, Holly R, Healey, Martin, Heikinheimo, Oskari, Holdsworth-Carson, Sarah, Houlden, Henry, Irwin, Juan C, Jarvelin, Marjo-Riitta, Kamatani, Yoichiro, Kennedy, Stephen H, Kepka, Ewa, Kettunen, Johannes, Kubo, Michiaki, Kurra, Venla, Laufer, Marc R, MacGregor, Stuart, Mangino, Massimo, Matalliotaki, Charoula, Matalliotakis, Michail, Murray, Alison D, Ndungu, Anne, Nezhat, Camran, Opoku-Anane, Jessica, Padmanabhan, Sandosh, Paranjpe, Manish, Peters, Maire, Polak, Grzegorz, Porteous, David J, Rabban, Joseph, Romanowicz, Hanna, Saare, Merli, Saavalainen, Liisu, Schork, Andrew J, Sen, Sushmita, Shafrir, Amy L, Siewierska-Górska, Anna, Słomka, Marcin, Smith, Blair H, Szaflik, Tomasz, Szyłło, Krzysztof, Takahashi, Atsushi, Terry, Kathryn L, Tomassetti, Carla, Treloar, Susan A, Vincent, Katy, Vo, Kim C, Werring, David J, Zeggini, Eleftheria, Zervou, Maria I, DBDS Genomic Consortium, FinnGen Study, FinnGen Endometriosis Taskforce, Celmatix Research Team, 23andMe Research Team, Adachi, Sosuke, Ridker, Paul M, D'Hooghe, Thomas, Goulielmos, George N, Hapangama, Dharani K, Hayward, Caroline, Horne, Andrew W, Low, Siew-Kee, Martikainen, Hannu, Chasman, Daniel I, Rogers, Peter AW, Saunders, Philippa T, Velez-Edwards, Digna R, Kraft, Peter, Salumets, Andres, Nyholt, Dale R, Mägi, Reedik, Stefansson, Kari, Becker, Christian M, Nyegaard, Mette, Montgomery, Grant W, Morris, Andrew P, Zondervan, Krina T

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