Effect of compost on erodibility of loamy sand under simulated rainfall von Arthur, E., Cornelis, W.M., Vermang, J., De Rocker, E.

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Amending a loamy sand with three compost types: impact on soil quality von Arthur, E, Cornelis, W.M, Vermang, J, De Rocker, E

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LOCKING KEY FOR COUPLING von ANDREW J. VACCARO, DONALD E. DE ROCKER

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ECONOMISCHE RIBBENBETONVLOER von R.G. DE ROCKER

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SEALING RING von SAMUEL KAUFMAN, DONALD E. DE ROCKER, HERBERT A. CONRAD

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SEALING RING von SAMUEL KAUFMAN, DONALD E. DE ROCKER, HERBERT A. CONRAD

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Zebrafish Collagen Type I: Molecular and Biochemical Characterization of the Major Structural Protein in Bone and Skin von Gistelinck, C., Gioia, R., Gagliardi, A., Tonelli, F., Marchese, L., Bianchi, L., Landi, C., Bini, L., Huysseune, A., Witten, P. E., Staes, A., Gevaert, K., De Rocker, N., Menten, B., Malfait, F., Leikin, S., Carra, S., Tenni, R., Rossi, A., De Paepe, A., Coucke, P., Willaert, A., Forlino, A.

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Poly(D,l-lactide-co-glycolide) particles are metabolised by the gut microbiome and elevate short chain fatty acids von McCoubrey, Laura E., Ferraro, Fabiana, Seegobin, Nidhi, Verin, Jérémy, Alfassam, Haya A., Awad, Atheer, Marzorati, Massimo, Verstrepen, Lynn, Ghyselinck, Jonas, De Munck, Julie, De Medts, Jelle, Steppe, Evi, De Vleeschhauwer, Valerie, De Rocker, Gilles, Droesbeke, Alexandra, De Rijck, Melanie, Vanthoor, Sara, Moens, Frédéric, Siepmann, Juergen, Siepmann, Florence, Gaisford, Simon, Orlu, Mine, Basit, Abdul W.

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Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly von Braun, Daniela A, Rao, Jia, Mollet, Geraldine, Schapiro, David, Daugeron, Marie-Claire, Tan, Weizhen, Gribouval, Olivier, Boyer, Olivia, Revy, Patrick, Jobst-Schwan, Tilman, Schmidt, Johanna Magdalena, Lawson, Jennifer A, Schanze, Denny, Ashraf, Shazia, Ullmann, Jeremy F P, Hoogstraten, Charlotte A, Boddaert, Nathalie, Collinet, Bruno, Martin, Gaëlle, Liger, Dominique, Lovric, Svjetlana, Furlano, Monica, Guerrera, I Chiara, Sanchez-Ferras, Oraly, Hu, Jennifer F, Boschat, Anne-Claire, Sanquer, Sylvia, Menten, Björn, Vergult, Sarah, De Rocker, Nina, Airik, Merlin, Hermle, Tobias, Shril, Shirlee, Widmeier, Eugen, Gee, Heon Yung, Choi, Won-Il, Sadowski, Carolin E, Pabst, Werner L, Warejko, Jillian K, Daga, Ankana, Basta, Tamara, Matejas, Verena, Scharmann, Karin, Kienast, Sandra D, Behnam, Babak, Beeson, Brendan, Begtrup, Amber, Bruce, Malcolm, Ch'ng, Gaik-Siew, Lin, Shuan-Pei, Chang, Jui-Hsing, Chen, Chao-Huei, Cho, Megan T, Gaffney, Patrick M, Gipson, Patrick E, Hsu, Chyong-Hsin, Kari, Jameela A, Ke, Yu-Yuan, Kiraly-Borri, Cathy, Lai, Wai-ming, Lemyre, Emmanuelle, Littlejohn, Rebecca Okashah, Masri, Amira, Moghtaderi, Mastaneh, Nakamura, Kazuyuki, Ozaltin, Fatih, Praet, Marleen, Prasad, Chitra, Roeder, Elizabeth R, Rump, Patrick, Schnur, Rhonda E, Shiihara, Takashi, Sinha, Manish D, Soliman, Neveen A, Soulami, Kenza, Sweetser, David A, Tsai, Wen-Hui, Tsai, Jeng-Daw, Topaloglu, Rezan, Vester, Udo, Viskochil, David H, Vatanavicharn, Nithiwat, Wierenga, Klaas J, Wolf, Matthias T F, Wong, Sik-Nin, Leidel, Sebastian A, Truglio, Gessica, Dedon, Peter C, Poduri, Annapurna, Mane, Shrikant, Lifton, Richard P, Bouchard, Maxime, Kannu, Peter, Chitayat, David, Magen, Daniella, Callewaert, Bert, van Tilbeurgh, Herman, Zenker, Martin, Antignac, Corinne, Hildebrandt, Friedhelm

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Two novel beta synuclein specific assays for the detection of Alzheimer’s disease von Bayoumy, Sherif, Goossens, Julie, De Rocker, Charlotte, Verberk, Inge M.W., Teunissen, Charlotte E., Vanmechelen, Eugeen

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Canadian Thoracic Society recommendations for management of chronic obstructive pulmonary disease - 2007 update von O'Donnell, Denis E, Aaron, Shaw, Bourbeau, Jean, Hernandez, Paul, Marciniuk, Darcy D, Balter, Meyer, Ford, Gordon, Gervais, Andre, Goldstein, Rogers, Hodder, Rick, Kaplan, Alan, Keenan, Sean, Lacasse, Yves, Maltais, Francois, Road, Jeremy, Rocker, Graeme, Sin, Don, Sinuff, Tasmin, Voduc, Nha

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Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity von De Rocker, Nina, Vergult, Sarah, Koolen, David, Jacobs, Eva, Hoischen, Alexander, Zeesman, Susan, Bang, Birgitte, Béna, Frédérique, Bockaert, Nele, Bongers, Ernie M., de Ravel, Thomy, Devriendt, Koenraad, Giglio, Sabrina, Faivre, Laurence, Joss, Shelagh, Maas, Saskia, Marle, Nathalie, Novara, Francesca, Nowaczyk, Malgorzata J.M., Peeters, Hilde, Polstra, Abeltje, Roelens, Filip, Rosenberg, Carla, Thevenon, Julien, Tümer, Zeynep, Vanhauwaert, Suzanne, Varvagiannis, Konstantinos, Willaert, Andy, Willemsen, Marjolein, Willems, Marjolaine, Zuffardi, Orsetta, Coucke, Paul, Speleman, Frank, Eichler, Evan E., Kleefstra, Tjitske, Menten, Björn

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Massively parallel sequencing for early molecular diagnosis in Leber congenital amaurosis von Coppieters, Frauke, De Wilde, Bram, Lefever, Steve, De Meester, Ellen, De Rocker, Nina, Van Cauwenbergh, Caroline, Pattyn, Filip, Meire, Françoise, Leroy, Bart P., Hellemans, Jan, Vandesompele, Jo, De Baere, Elfride

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Mutations Affecting the SAND Domain of DEAF1 Cause Intellectual Disability with Severe Speech Impairment and Behavioral Problems von Vulto-van Silfhout, Anneke T., Rajamanickam, Shivakumar, Jensik, Philip J., Vergult, Sarah, de Rocker, Nina, Newhall, Kathryn J., Raghavan, Ramya, Reardon, Sara N., Jarrett, Kelsey, McIntyre, Tara, Bulinski, Joseph, Ownby, Stacy L., Huggenvik, Jodi I., McKnight, G. Stanley, Rose, Gregory M., Cai, Xiang, Willaert, Andy, Zweier, Christiane, Endele, Sabine, de Ligt, Joep, van Bon, Bregje W.M., Lugtenberg, Dorien, de Vries, Petra F., Veltman, Joris A., van Bokhoven, Hans, Brunner, Han G., Rauch, Anita, de Brouwer, Arjan P.M., Carvill, Gemma L., Hoischen, Alexander, Mefford, Heather C., Eichler, Evan E., Vissers, Lisenka E.L.M., Menten, Björn, Collard, Michael W., de Vries, Bert B.A.

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Failure of anticoagulant thromboprophylaxis: risk factors in medical-surgical critically ill patients von Lim, Wendy, Meade, Maureen, Lauzier, Francois, Zarychanski, Ryan, Mehta, Sangeeta, Lamontagne, Francois, Dodek, Peter, McIntyre, Lauralyn, Hall, Richard, Heels-Ansdell, Diane, Fowler, Robert, Pai, Menaka, Guyatt, Gordon, Crowther, Mark A, Warkentin, Theodore E, Devereaux, P J, Walter, Stephen D, Muscedere, John, Herridge, Margaret, Turgeon, Alexis F, Geerts, William, Finfer, Simon, Jacka, Michael, Berwanger, Otavio, Ostermann, Marlies, Qushmaq, Ismael, Friedrich, Jan O, Cook, Deborah J

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Mutations Affecting the SAND Domain of DEAF1 Cause Intellectual Disability with Severe Speech Impairment and Behavioral Problems von Vulto-van Silfhout, Anneke T., Rajamanickam, Shivakumar, Jensik, Philip J., Vergult, Sarah, de Rocker, Nina, Newhall, Kathryn J., Raghavan, Ramya, Reardon, Sara N., Jarrett, Kelsey, McIntyre, Tara, Bulinski, Joseph, Ownby, Stacy L., Huggenvik, Jodi I., McKnight, G. Stanley, Rose, Gregory M., Cai, Xiang, Willaert, Andy, Zweier, Christiane, Endele, Sabine, de Ligt, Joep, van Bon, Bregje W.M., Lugtenberg, Dorien, de Vries, Petra F., Veltman, Joris A., van Bokhoven, Hans, Brunner, Han G., Rauch, Anita, de Brouwer, Arjan P.M., Carvill, Gemma L., Hoischen, Alexander, Mefford, Heather C., Eichler, Evan E., Vissers, Lisenka E.L.M., Menten, Björn, Collard, Michael W., de Vries, Bert B.A.

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Mutations in the evolutionarily highly conserved KEOPS complex genes cause nephrotic syndrome with microcephaly von Braun, Daniela A., Rao, Jia, Mollet, Geraldine, Schapiro, David, Daugeron, Marie-Claire, Tan, Weizhen, Gribouval, Olivier, Boyer, Olivia, Revy, Patrick, Jobst-Schwan, Tilman, Schmidt, Johanna Magdalena, Lawson, Jennifer A., Schanze, Denny, Ashraf, Shazia, Boddaert, Nathalie, Collinet, Bruno, Martin, Gaëlle, Liger, Dominique, Lovric, Svjetlana, Furlano, Monica, Guerrera, I. Chiara, Sanchez-Ferras, Oraly, Menten, Björn, Vergult, Sarah, De Rocker, Nina, Airik, Merlin, Hermle, Tobias, Shril, Shirlee, Widmeier, Eugen, Gee, Heon Yung, Choi, Won-Il, Sadowski, Carolin E., Pabst, Werner L., Warejko, Jillian, Daga, Ankana, LeBerre, Tamara Basta, Matejas, Verena, Behnam, Babak, Beeson, Brendan, Begtrup, Amber, Bruce, Malcolm, Ch'ng, Gaik-Siew, Lin, Shuan-Pei, Chang, Jui-Hsing, Chen, Chao-Huei, Cho, Megan T., Gipson, Patrick E., Hsu, Chyong-Hsin, Kari, Jameela A., Ke, Yu-Yuan, Kiraly-Borri, Cathy, Lai, Wai-ming, Lemyre, Emmanuelle, Littlejohn, Rebecca Okasha, Masri, Amira, Moghtaderi, Mastaneh, Nakamura, Kazuyuki, Praet, Marleen, Prasad, Chitra, Prytula, Agnieszka, Roeder, Elizabeth, Rump, Patrick, Schnur, Rhonda E., Shiihara, Takashi, Sinha, Manish, Soliman, Neveen A, Soulami, Kenza, Sweetser, David A., Tsai, Wen-Hui, Tsai, Jeng-Daw, Vester, Udo, Viskochil, David H., Vatanavicharn, Nithiwat, Waxler, Jessica L., Wolf, Matthias T.F., Wong, Sik-Nin, Poduri, Annapurna, Truglio, Gessica, Mane, Shrikant, Lifton, Richard P., Bouchard, Maxime, Kannu, Peter, Chitayat, David, Magen, Daniella, Calleweart, Bert, van Tilbeurgh, Herman, Zenker, Martin, Antignac, Corinne, Hildebrandt, Friedhelm

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Ultrasensitive Confocal Fluorescence Microscopy of C-Reactive Protein Interacting With FcγRIIa von Manolov, Dimitar E, Röcker, Carlheinz, Hombach, Vinzenz, Nienhaus, G Ulrich, Torzewski, Jan

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Mutations affecting the SAND domain of DEAF1 cause intellectual disability with severe speech impairment and behavioral problems von Vulto-van Silfhout, Anneke T, Rajamanickam, Shivakumar, Jensik, Philip J, Vergult, Sarah, de Rocker, Nina, Newhall, Kathryn J, Raghavan, Ramya, Reardon, Sara N, Jarrett, Kelsey, McIntyre, Tara, Bulinski, Joseph, Ownby, Stacy L, Huggenvik, Jodi I, McKnight, G Stanley, Rose, Gregory M, Cai, Xiang, Willaert, Andy, Zweier, Christiane, Endele, Sabine, de Ligt, Joep, van Bon, Bregje W M, Lugtenberg, Dorien, de Vries, Petra F, Veltman, Joris A, van Bokhoven, Hans, Brunner, Han G, Rauch, Anita, de Brouwer, Arjan P M, Carvill, Gemma L, Hoischen, Alexander, Mefford, Heather C, Eichler, Evan E, Vissers, Lisenka E L M, Menten, Björn, Collard, Michael W, de Vries, Bert B A

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Verfahren zum Backen von Kuchen von ROECKER, HANS., 35315 HOMBERG, DE

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