Fracture Micromechanisms Evaluation of High-Strength Cast Irons Under Thermomechanical Fatigue Conditions von Bon, Douglas G., Ferreira, Marcio Henrique, Bose Filho, Waldek Wladimir, Guesser, Wilson Luiz

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Reduced Bone Density and Vertebral Fractures in Smokers. Men and COPD Patients at Increased Risk von Jaramillo, Joshua D, Wilson, Carla, Stinson, Douglas S, Stinson, Douglas J, Lynch, David A, Bowler, Russell P, Lutz, Sharon, Bon, Jessica M, Arnold, Ben, McDonald, Merry-Lynn N, Washko, George R, Wan, Emily S, DeMeo, Dawn L, Foreman, Marilyn G, Soler, Xavier, Lindsay, Sarah E, Lane, Nancy E, Genant, Harry K, Silverman, Edwin K, Hokanson, John E, Make, Barry J, Crapo, James D, Regan, Elizabeth A

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Assessment of 2q23.1 Microdeletion Syndrome Implicates MBD5 as a Single Causal Locus of Intellectual Disability, Epilepsy, and Autism Spectrum Disorder von Talkowski, Michael E., Mullegama, Sureni V., Rosenfeld, Jill A., van Bon, Bregje W.M., Shen, Yiping, Repnikova, Elena A., Gastier-Foster, Julie, Thrush, Devon Lamb, Kathiresan, Sekar, Ruderfer, Douglas M., Chiang, Colby, Hanscom, Carrie, Ernst, Carl, Lindgren, Amelia M., Morton, Cynthia C., An, Yu, Astbury, Caroline, Brueton, Louise A., Lichtenbelt, Klaske D., Ades, Lesley C., Fichera, Marco, Romano, Corrado, Innis, Jeffrey W., Williams, Charles A., Bartholomew, Dennis, Van Allen, Margot I., Parikh, Aditi, Zhang, Lilei, Wu, Bai-Lin, Pyatt, Robert E., Schwartz, Stuart, Shaffer, Lisa G., de Vries, Bert B.A., Gusella, James F., Elsea, Sarah H.

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A HIGH-VELOCITY CLOUD IMPACT FORMING A SUPERSHELL IN THE MILKY WAY von Park, Geumsook, Koo, Bon-Chul, Kang, Ji-hyun, Gibson, Steven J., Peek, J. E. G., Douglas, Kevin A., Korpela, Eric J., Heiles, Carl E.

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YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction von Gabriele, Michele, Vulto-van Silfhout, Anneke T., Germain, Pierre-Luc, Vitriolo, Alessandro, Kumar, Raman, Douglas, Evelyn, Haan, Eric, Kosaki, Kenjiro, Takenouchi, Toshiki, Rauch, Anita, Steindl, Katharina, Frengen, Eirik, Misceo, Doriana, Pedurupillay, Christeen Ramane J., Stromme, Petter, Rosenfeld, Jill A., Shao, Yunru, Craigen, William J., Schaaf, Christian P., Rodriguez-Buritica, David, Farach, Laura, Friedman, Jennifer, Thulin, Perla, McLean, Scott D., Nugent, Kimberly M., Morton, Jenny, Nicholl, Jillian, Andrieux, Joris, Stray-Pedersen, Asbjørg, Chambon, Pascal, Patrier, Sophie, Lynch, Sally A., Kjaergaard, Susanne, Tørring, Pernille M., Brasch-Andersen, Charlotte, Ronan, Anne, van Haeringen, Arie, Anderson, Peter J., Powis, Zöe, Brunner, Han G., Pfundt, Rolph, Schuurs-Hoeijmakers, Janneke H.M., van Bon, Bregje W.M., Lelieveld, Stefan, Gilissen, Christian, Nillesen, Willy M., Vissers, Lisenka E.L.M., Gecz, Jozef, Koolen, David A., Testa, Giuseppe, de Vries, Bert B.A.

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Long-term effects of curcumin in the non-human primate brain von Koo, Bang-Bon, Calderazzo, Samantha, Bowley, Bethany G.E., Kolli, Alekha, Moss, Mark B., Rosene, Douglas L., Moore, Tara L.

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Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability von Grozeva, Detelina, Carss, Keren, Spasic-Boskovic, Olivera, Tejada, Maria-Isabel, Gecz, Jozef, Shaw, Marie, Corbett, Mark, Haan, Eric, Thompson, Elizabeth, Friend, Kathryn, Hussain, Zaamin, Hackett, Anna, Field, Michael, Renieri, Alessandra, Stevenson, Roger, Schwartz, Charles, Floyd, James A.B., Bentham, Jamie, Cosgrove, Catherine, Keavney, Bernard, Bhattacharya, Shoumo, Hurles, Matthew, Raymond, F. Lucy

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Machine Learning Characterization of COPD Subtypes: Insights From the COPDGene Study von Castaldi, Peter J, Boueiz, Adel, Yun, Jeong, Estepar, Raul San Jose, Ross, James C, Washko, George, Cho, Michael H, Hersh, Craig P, Kinney, Gregory L, Young, Kendra A, Regan, Elizabeth A, Lynch, David A, Criner, Gerald J, Dy, Jennifer G, Rennard, Stephen I, Casaburi, Richard, Make, Barry J, Crapo, James, Silverman, Edwin K, Hokanson, John E

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Development of a Blood-based Transcriptional Risk Score for Chronic Obstructive Pulmonary Disease von Moll, Matthew, Boueiz, Adel, Ghosh, Auyon J, Saferali, Aabida, Lee, Sool, Xu, Zhonghui, Yun, Jeong H, Hobbs, Brian D, Hersh, Craig P, Sin, Don D, Tal-Singer, Ruth, Silverman, Edwin K, Cho, Michael H, Castaldi, Peter J

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DNA Tests in Prolific Sheep from Eight Countries Provide New Evidence on Origin of the Booroola (FecB) Mutation von DAVIS, George H, GALLOWAY, Susan M, INOUNU, Ismeth, TIESNAMURTI, Bess, MARTYNIUK, Elzbieta, EYTHORSDOTTIR, Emma, MULSANT, Philippe, LECERF, Frederic, HANRAHAN, James P, BRADFORD, G. Eric, WILSON, Theresa, ROSS, Ian K, GREGAN, Scott M, WARD, Jamie, NIMBKAR, Bon V, GHALSASI, Pradip M, NIMBKAR, Chanda, GRAY, G. Douglas, SUBANDRIYO

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A deep learning system for detection of early Barrett's neoplasia: a model development and validation study von Fockens, K N, Jong, M R, Jukema, J B, Boers, T G W, Kusters, C H J, van der Putten, J A, Pouw, R E, Duits, L C, Montazeri, N S M, van Munster, S N, Weusten, B L A M, Alvarez Herrero, L, Houben, M H M G, Nagengast, W B, Westerhof, J, Alkhalaf, A, Mallant-Hent, R C, Scholten, P, Ragunath, K, Seewald, S, Elbe, P, Baldaque-Silva, F, Barret, M, Ortiz Fernández-Sordo, J, Villarejo, G Moral, Pech, O, Beyna, T, van der Sommen, F, de With, P H, de Groof, A J, Bergman, J J

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Emission and chemistry of organic carbon in the gas and aerosol phase at a sub-urban site near Mexico City in March 2006 during the MILAGRO study von de Gouw, J. A., Welsh-Bon, D., Warneke, C., Kuster, W. C., Alexander, L., Baker, A. K., Beyersdorf, A. J., Blake, D. R., Canagaratna, M., Celada, A. T., Huey, L. G., Junkermann, W., Onasch, T. B., Salcido, A., Sjostedt, S. J., Sullivan, A. P., Tanner, D. J., Vargas, O., Weber, R. J., Worsnop, D. R., Yu, X. Y., Zaveri, R.

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I-GALFA: The Inner-Galaxy ALFA Low-Latitude H I Survey von Koo, Bon-Chul, Gibson, Steven J., Kang, Ji-hyun, Douglas, Kevin A., Park, Geumsook, Peek, Joshua E. G., Korpela, Eric J., Heiles, Carl E., Bania, Thomas M.

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DNA Tests in Prolific Sheep from Eight Countries Provide New Evidence on Origin of the Booroola (FecB) Mutation1 von Davis, George H, Galloway, Susan M, Ross, Ian K, Gregan, Scott M, Ward, Jamie, Nimbkar, Bon V, Ghalsasi, Pradip M, Nimbkar, Chanda, Douglas Gray, G, Subandriyo, Inounu, Ismeth, Tiesnamurti, Bess, Martyniuk, Elzbieta, Eythorsdottir, Emma, Mulsant, Philippe, Lecerf, Frederic, Hanrahan, James P, Eric Bradford, G, Wilson, Theresa

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A High-Velocity Cloud Impact Forming a Supershell in the Milky Way von Park, Geumsook, Bon-Chul Koo, Ji-hyun, Kang, Gibson, Steven J, Peek, J E G, Douglas, Kevin A, Korpela, Eric J, Heiles, Carl E

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Dna tests in prolific sheep from eight countries provide new evidence on origin of the booroola (fecb) mutation1 von Davis, George H, Galloway, Susan M, Ross, Ian K, Gregan, Scott M, Ward, Jamie, Nimbkar, Bon V, Ghalsasi, Pradip M, Nimbkar, Chanda, Gray, G. Douglas, Subandriyo, Inounu, Ismeth, Tiesnamurti, Bess, Martyniuk, Elzbieta, Eythorsdottir, Emma, Mulsant, Philippe, Lecerf, Frederic, Hanrahan, James P, Bradford, G. Eric, Wilson, Theresa

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YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction von Gabriele, M., Vulto-van Silfhout, A.T., Germain, P.L., Vitriolo, A., Kumar, R., Douglas, E., Haan, E., Kosaki, K., Takenouchi, T., Rauch, A., Steindl, K., Frengen, E., Misceo, D., Pedurupillay, C.R.J., Stromme, P., Rosenfeld, J.A., Shao, Y.R., Craigen, W.J., Schaaf, C.P., Rodriguez-Buritica, D., Farach, L., Friedman, J., Thulin, P., McLean, S.D., Nugent, K.M., Morton, J., Nicholl, J., Andrieux, J., Stray-Pedersen, A., Chambon, P., Patrier, S., Lynch, S.A., Kjaergaard, S., Torring, P.M., Brasch-Andersen, C., Ronan, A., Haeringen, A. van, Anderson, P.J., Powis, Z., Brunner, H.G., Pfundt, R., Schuurs-Hoeijmakers, J.H.M., Bon, B.W.M. van, Lelieveld, S., Gilissen, C., Nillesen, W.M., Vissers, L.E.L.M., Gecz, J., Koolen, D.A., Testa, G., Vries, B.B.A. de

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Hi Shells and Supershells in the I-GALFA Hi 21-cm Line Survey: I. Fast-Expanding Hi Shells Associated with Supernova Remnants von Park, Geumsook, Bon-Chul Koo, Gibson, Steven J, Ji-hyun, Kang, Lane, Daria C, Douglas, Kevin A, Peek, Joshua E G, Korpela, Eric J, Heiles, Carl E, Newton, Jonathan H

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De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability von Kury, S., Woerden, G.M. van, Besnard, T., Onori, M.P., Latypova, X., Towne, M.C., Cho, M.T., Prescott, T.E., Ploeg, M.A., Sanders, S., Stessman, H.A.F., Pujol, A., Distel, ben, Robak, L.A., Bernstein, J.A., Denomme-Pichon, A.S., Lesca, G., Sellars, E.A., Berg, J., Carre, W., Busk, O.L., Bon, B.W.M. van, Waugh, J.L., Deardorff, M., Hoganson, G.E., Bosanko, K.B., Johnson, D.S., Dabir, T., Holla, O.L., Sarkar, A., Tveten, K., Bellescize, J. de, Braathen, G.J., Terhal, P.A., Grange, D.K., Haeringen, A. van, Lam, C., Mirzaa, G., Burton, J., Bhoj, E.J., Douglas, J., Santani, A.B., Nesbitt, A.I., Helbig, K.L., Andrews, M.V., Begtrup, A., Tang, S., Gassen, K.L.I. van, Juusola, J., Foss, K., Enns, G.M., Moog, U., Hinderhofer, K., Paramasivam, N., Lincoln, S., Kusako, B.H., Lindenbaum, P., Charpentier, E., Nowak, C.B., Cherot, E., Simonet, T., Ruivenkamp, C.A.L., Hahn, S., Brownstein, C.A., Xia, F., Schmitt, S., Deb, W., Bonneau, D., Nizon, M., Quinquis, D., Chelly, J., Rudolf, G., Sanlaville, D., Parent, P., Gilbert-Dussardier, B., Toutain, A., Peart-Vissers, L.E.L.M., Boisseau, P., Vincent, M., Grabrucker, A.M., Dubourg, C., Tan, W.H., Verbeek, N.E., Granzow, M., Santen, G.W.E., Shendure, J., Isidor, B., Pasquier, L., Redon, R., Yang, Y.P., State, M.W., Kleefstra, T., Cogne, B., Petrovski, S., Retterer, K., Eichler, E.E., Agrawal, P.B., Bezieau, S., Odent, S., Elgersma, Y.

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I-GALFA: The Inner-Galaxy ALFA Low-Latitude H I Survey von Bon-Chul Koo, Gibson, Steven J, Ji-hyun, Kang, Douglas, Kevin A, Park, Geumsook, Peek, Joshua E G, Korpela, Eric J, Heiles, Carl E, Bania, Thomas M

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