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	121.	Mini-hemagglutinin vaccination induces cross-reactive antibodies in pre-exposed NHP that protect mice against lethal influenza challenge. [electronic resource] by van der Lubbe, Joan E M Huizingh, Jeroen Verspuij, Johan W A Tettero, Lisanne Schmit-Tillemans, Sonja P R Mooij, Petra Mortier, Daniella Koopman, Gerrit Bogers, Willy M J M Dekking, Liesbeth Meijberg, Wim Kwaks, Ted Brandenburg, Boerries Tolboom, Jeroen T B M Schuitemaker, Hanneke Roozendaal, Ramon Kuipers, Harmjan Zahn, Roland C Publication details: NPJ vaccines 2018 In: NPJ vaccines vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	122.	Chromosome 1p21.3 microdeletions comprising DPYD and MIR137 are associated with intellectual disability. [electronic resource] by Willemsen, Marjolein H Vallès, Astrid Kirkels, Laurens A M H Mastebroek, Mathilde Olde Loohuis, Nikkie Kos, Aron Wissink-Lindhout, Willemijn M de Brouwer, Arjan P M Nillesen, Willy M Pfundt, Rolph Holder-Espinasse, Muriel Vallée, Louis Andrieux, Joris Coppens-Hofman, Marjolein C Rensen, Hanneke Hamel, Ben C J van Bokhoven, Hans Aschrafi, Armaz Kleefstra, Tjitske Producer: 20120308 In: Journal of medical genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	123.	Potent immune responses in rhesus macaques induced by nonviral delivery of a self-amplifying RNA vaccine expressing HIV type 1 envelope with a cationic nanoemulsion. [electronic resource] by Bogers, Willy M Oostermeijer, Herman Mooij, Petra Koopman, Gerrit Verschoor, Ernst J Davis, David Ulmer, Jeffrey B Brito, Luis A Cu, Yen Banerjee, Kaustuv Otten, Gillis R Burke, Brian Dey, Antu Heeney, Jonathan L Shen, Xiaoying Tomaras, Georgia D Labranche, Celia Montefiori, David C Liao, Hua-Xin Haynes, Barton Geall, Andrew J Barnett, Susan W Producer: 20150423 In: The Journal of infectious diseases vol. 211 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	124.	HSF2BP Interacts with a Conserved Domain of BRCA2 and Is Required for Mouse Spermatogenesis. [electronic resource] by Brandsma, Inger Sato, Koichi van Rossum-Fikkert, Sari E van Vliet, Nicole Sleddens, Esther Reuter, Marcel Odijk, Hanny van den Tempel, Nathalie Dekkers, Dick H W Bezstarosti, Karel Demmers, Jeroen A A Maas, Alex Lebbink, Joyce Wyman, Claire Essers, Jeroen van Gent, Dik C Baarends, Willy M Knipscheer, Puck Kanaar, Roland Zelensky, Alex N Producer: 20200730 In: Cell reports vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	125.	Systemic neutralizing antibodies induced by long interval mucosally primed systemically boosted immunization correlate with protection from mucosal SHIV challenge. [electronic resource] by Bogers, Willy M J M Davis, David Baak, Ilona Kan, Elaine Hofman, Sam Sun, Yide Mortier, Daniella Lian, Ying Oostermeijer, Herman Fagrouch, Zahra Dubbes, Rob van der Maas, Martin Mooij, Petra Koopman, Gerrit Verschoor, Ernst Langedijk, Johannes P M Zhao, Jun Brocca-Cofano, Egidio Robert-Guroff, Marjorie Srivastava, Indresh Barnett, Susan Heeney, Jonathan L Producer: 20090106 In: Virology vol. 382 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	126.	Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome. [electronic resource] by Vissers, Lisenka E L M Bonetti, Monica Paardekooper Overman, Jeroen Nillesen, Willy M Frints, Suzanna G M de Ligt, Joep Zampino, Giuseppe Justino, Ana Machado, José C Schepens, Marga Brunner, Han G Veltman, Joris A Scheffer, Hans Gros, Piet Costa, José L Tartaglia, Marco van der Burgt, Ineke Yntema, Helger G den Hertog, Jeroen Producer: 20151022 In: European journal of human genetics : EJHG vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	127.	GRECC Connect: Geriatrics Telehealth to Empower Health Care Providers and Improve Management of Older Veterans in Rural Communities. [electronic resource] by Pimentel, Camilla B Gately, Megan Barczi, Steven R Boockvar, Kenneth S Bowman, Ella H Caprio, Thomas V Colón-Emeric, Cathleen S Dang, Stuti Espinoza, Sara E Garner, Kimberly K Griffiths, Patricia C Howe, Judith L Lum, Hillary D Markland, Alayne D Rossi, Michelle I Thielke, Stephen M Valencia-Rodrigo, Willy M Moo, Lauren R Hung, William W Publication details: Federal practitioner : for the health care professionals of the VA, DoD, and PHS Oct 2019 In: Federal practitioner : for the health care professionals of the VA, DoD, and PHS vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	128.	Diagnostic genome profiling in mental retardation. [electronic resource] by de Vries, Bert B A Pfundt, Rolph Leisink, Martijn Koolen, David A Vissers, Lisenka E L M Janssen, Irene M Reijmersdal, Simon van Nillesen, Willy M Huys, Erik H L P G Leeuw, Nicole de Smeets, Dominique Sistermans, Erik A Feuth, Ton van Ravenswaaij-Arts, Conny M A van Kessel, Ad Geurts Schoenmakers, Eric F P M Brunner, Han G Veltman, Joris A Producer: 20051115 In: American journal of human genetics vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	129.	Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype. [electronic resource] by Martinelli, Simone De Luca, Alessandro Stellacci, Emilia Rossi, Cesare Checquolo, Saula Lepri, Francesca Caputo, Viviana Silvano, Marianna Buscherini, Francesco Consoli, Federica Ferrara, Grazia Digilio, Maria C Cavaliere, Maria L van Hagen, Johanna M Zampino, Giuseppe van der Burgt, Ineke Ferrero, Giovanni B Mazzanti, Laura Screpanti, Isabella Yntema, Helger G Nillesen, Willy M Savarirayan, Ravi Zenker, Martin Dallapiccola, Bruno Gelb, Bruce D Tartaglia, Marco Producer: 20100901 In: American journal of human genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	130.	Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy. [electronic resource] by Lugtenberg, Dorien Kleefstra, Tjitske Oudakker, Astrid R Nillesen, Willy M Yntema, Helger G Tzschach, Andreas Raynaud, Martine Rating, Dietz Journel, Hubert Chelly, Jamel Goizet, Cyril Lacombe, Didier Pedespan, Jean-Michel Echenne, Bernard Tariverdian, Gholamali O'Rourke, Declan King, Mary D Green, Andrew van Kogelenberg, Margriet Van Esch, Hilde Gecz, Jozef Hamel, Ben C J van Bokhoven, Hans de Brouwer, Arjan P M Producer: 20090508 In: European journal of human genetics : EJHG vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	131.	Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability. [electronic resource] by Kleefstra, Tjitske Kramer, Jamie M Neveling, Kornelia Willemsen, Marjolein H Koemans, Tom S Vissers, Lisenka E L M Wissink-Lindhout, Willemijn Fenckova, Michaela van den Akker, Willem M R Kasri, Nael Nadif Nillesen, Willy M Prescott, Trine Clark, Robin D Devriendt, Koenraad van Reeuwijk, Jeroen de Brouwer, Arjan P M Gilissen, Christian Zhou, Huiqing Brunner, Han G Veltman, Joris A Schenck, Annette van Bokhoven, Hans Producer: 20120920 In: American journal of human genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	132.	GATAD2B loss-of-function mutations cause a recognisable syndrome with intellectual disability and are associated with learning deficits and synaptic undergrowth in Drosophila. [electronic resource] by Willemsen, Marjolein H Nijhof, Bonnie Fenckova, Michaela Nillesen, Willy M Bongers, Ernie M H F Castells-Nobau, Anna Asztalos, Lenke Viragh, Erika van Bon, Bregje W M Tezel, Emre Veltman, Joris A Brunner, Han G de Vries, Bert B A de Ligt, Joep Yntema, Helger G van Bokhoven, Hans Isidor, Bertrand Le Caignec, Cédric Lorino, Elsa Asztalos, Zoltan Koolen, David A Vissers, Lisenka E L M Schenck, Annette Kleefstra, Tjitske Producer: 20140218 In: Journal of medical genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	133.	Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome. [electronic resource] by Koolen, David A Kramer, Jamie M Neveling, Kornelia Nillesen, Willy M Moore-Barton, Heather L Elmslie, Frances V Toutain, Annick Amiel, Jeanne Malan, Valérie Tsai, Anne Chun-Hui Cheung, Sau Wai Gilissen, Christian Verwiel, Eugene T P Martens, Sarah Feuth, Ton Bongers, Ernie M H F de Vries, Petra Scheffer, Hans Vissers, Lisenka E L M de Brouwer, Arjan P M Brunner, Han G Veltman, Joris A Schenck, Annette Yntema, Helger G de Vries, Bert B A Producer: 20120803 In: Nature genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	134.	Haploinsufficiency of MeCP2-interacting transcriptional co-repressor SIN3A causes mild intellectual disability by affecting the development of cortical integrity. [electronic resource] by Witteveen, Josefine S Willemsen, Marjolein H Dombroski, Thaís C D van Bakel, Nick H M Nillesen, Willy M van Hulten, Josephus A Jansen, Eric J R Verkaik, Dave Veenstra-Knol, Hermine E van Ravenswaaij-Arts, Conny M A Wassink-Ruiter, Jolien S Klein Vincent, Marie David, Albert Le Caignec, Cedric Schieving, Jolanda Gilissen, Christian Foulds, Nicola Rump, Patrick Strom, Tim Cremer, Kirsten Zink, Alexander M Engels, Hartmut de Munnik, Sonja A Visser, Jasper E Brunner, Han G Martens, Gerard J M Pfundt, Rolph Kleefstra, Tjitske Kolk, Sharon M Producer: 20170907 In: Nature genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	135.	Structure and immunogenicity of a stabilized HIV-1 envelope trimer based on a group-M consensus sequence. [electronic resource] by Sliepen, Kwinten Han, Byung Woo Bontjer, Ilja Mooij, Petra Garces, Fernando Behrens, Anna-Janina Rantalainen, Kimmo Kumar, Sonu Sarkar, Anita Brouwer, Philip J M Hua, Yuanzi Tolazzi, Monica Schermer, Edith Torres, Jonathan L Ozorowski, Gabriel van der Woude, Patricia de la Peña, Alba Torrents van Breemen, Mariëlle J Camacho-Sánchez, Juan Miguel Burger, Judith A Medina-Ramírez, Max González, Nuria Alcami, Jose LaBranche, Celia Scarlatti, Gabriella van Gils, Marit J Crispin, Max Montefiori, David C Ward, Andrew B Koopman, Gerrit Moore, John P Shattock, Robin J Bogers, Willy M Wilson, Ian A Sanders, Rogier W Producer: 20190617 In: Nature communications vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	136.	Variants in CUL4B are associated with cerebral malformations. [electronic resource] by Vulto-van Silfhout, Anneke T Nakagawa, Tadashi Bahi-Buisson, Nadia Haas, Stefan A Hu, Hao Bienek, Melanie Vissers, Lisenka E L M Gilissen, Christian Tzschach, Andreas Busche, Andreas Müsebeck, Jörg Rump, Patrick Mathijssen, Inge B Avela, Kristiina Somer, Mirja Doagu, Fatma Philips, Anju K Rauch, Anita Baumer, Alessandra Voesenek, Krysta Poirier, Karine Vigneron, Jacqueline Amram, Daniel Odent, Sylvie Nawara, Magdalena Obersztyn, Ewa Lenart, Jacek Charzewska, Agnieszka Lebrun, Nicolas Fischer, Ute Nillesen, Willy M Yntema, Helger G Järvelä, Irma Ropers, Hans-Hilger de Vries, Bert B A Brunner, Han G van Bokhoven, Hans Raymond, F Lucy Willemsen, Michèl A A P Chelly, Jamel Xiong, Yue Barkovich, A James Kalscheuer, Vera M Kleefstra, Tjitske de Brouwer, Arjan P M Producer: 20150910 In: Human mutation vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	137.	YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction. [electronic resource] by 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 Producer: 20170731 In: American journal of human genetics vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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