Resultats de la cerca - Geert Geeven
- Mostrar 1 - 19 resultats de 19
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Characterization and dynamics of pericentromere-associated domains in mice per Patrick J. Wijchers, Geert Geeven, Michael Eyres, Atze J. Bergsma, Mark Janssen, Marjon J.A.M. Verstegen, Yun Zhu, Yori Schell, Carlo Vermeulen, Elzo de Wit, Wouter de Laat
Publicat 2015Artigo -
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Enhancers reside in a unique epigenetic environment during early zebrafish development per Lucas Kaaij, Michal Mokrý, Meng Zhou, Michael U. Musheev, Geert Geeven, Adrien S. J. Melquiond, António Miguel de Jesus Domingues, Wouter de Laat, Christof Niehrs, Andrew D. Smith, René F. Ketting
Publicat 2016Artigo -
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Hominin-specific regulatory elements selectively emerged in oligodendrocytes and are disrupted in autism patients per Bas Castelijns, Mirna Baak, Ilia Sarah Timpanaro, Caroline R.M. Wiggers, Marit W. Vermunt, Peng Shang, Ivanela Kondova, Geert Geeven, Valerio Bianchi, Wouter de Laat, Niels Geijsen, Menno P. Creyghton
Publicat 2020Artigo -
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YAP Drives Growth by Controlling Transcriptional Pause Release from Dynamic Enhancers per Giorgio Giacomo Galli, Matteo Carrara, Wei-Chien Yuan, Christian Valdes‐Quezada, Basanta Gurung, Brian J. Pepe-Mooney, Tinghu Zhang, Geert Geeven, Nathanael S. Gray, Wouter de Laat, Raffaele Calogero, Fernando D. Camargo
Publicat 2015Artigo -
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The role of confined placental mosaicism in fetal growth restriction: A retrospective cohort study per Geerke M. Eggenhuizen, Attie T. J. I. Go, Zoë Sauter, Mariëtte J.V. Hoffer, Monique C. Haak, Geert Geeven, Karin E. M. Diderich, Marieke Joosten, Myrthe van den Born, Malgorzata I. Srebniak, Diane Van Opstal
Publicat 2024Artigo -
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Large-Scale Identification of Coregulated Enhancer Networks in the Adult Human Brain per Marit W. Vermunt, Peter Reinink, Jeroen Korving, Ewart de Bruijn, Paul M. Creyghton, Onur Basak, Geert Geeven, Pim W. Toonen, Nico Lansu, Charles Meunier, Sebastiaan van Heesch, Hans Clevers, Wouter de Laat, Edwin Cuppen, Menno P. Creyghton
Publicat 2014Artigo -
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Early detection of active Human CytomegaloVirus (hCMV) infection in pregnant women using data generated for noninvasive fetal aneuploidy testing per Brigitte H. W. Faas, Galuh Astuti, Willem J. G. Melchers, A. Reuss, Christian Gilissen, Merryn Macville, Stijn A.I. Ghesquiere, Leonieke M.H. Houben, Malgorzata I. Srebniak, Geert Geeven, Janette Rahamat‐Langendoen, Erik A. Sistermans, Jasper Linthorst
Publicat 2024Artigo -
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Cause and Consequence of Tethering a SubTAD to Different Nuclear Compartments per Patrick J. Wijchers, Peter H.L. Krijger, Geert Geeven, Yun Zhu, Annette Denker, Marjon J.A.M. Verstegen, Christian Valdes‐Quezada, Carlo Vermeulen, Mark Janssen, Hans Teunissen, Lisette C.M. Anink-Groenen, Pernette J. Verschure, Wouter de Laat
Publicat 2016Artigo -
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Genome-wide profiling of p53-regulated enhancer RNAs uncovers a subset of enhancers controlled by a lncRNA per Nicolas Léveillé, Carlos A. Melo, Koos Rooijers, Ángel Díaz‐Lagares, Sónia A. Melo, Gözde Korkmaz, Rui Lopes, Farhad Akbari Moqadam, Ana Maia, Patrick J. Wijchers, Geert Geeven, Monique L. den Boer, Raghu Kalluri, Wouter de Laat, Manel Esteller, Reuven Agami
Publicat 2015Artigo -
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Local compartment changes and regulatory landscape alterations in histone H1-depleted cells per Geert Geeven, Yun Zhu, Byung Ju Kim, Boris Bartholdy, Seung-Min Yang, Todd S. Macfarlan, Wesley D. Gifford, Samuel L. Pfaff, Marjon J.A.M. Verstegen, Hugo Pinto, Marit W. Vermunt, Menno P. Creyghton, Patrick J. Wijchers, J Stamatoyannopoulos, Arthur I. Skoultchi, Wouter de Laat
Publicat 2015Artigo -
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Enhancer hubs and loop collisions identified from single-allele topologies per Amin Allahyar, Carlo Vermeulen, Britta A. M. Bouwman, Peter H.L. Krijger, Marjon J.A.M. Verstegen, Geert Geeven, Melissa van Kranenburg, Mark Pieterse, Roy Straver, Judith H.I. Haarhuis, Kees Jalink, Hans Teunissen, Ivo Renkens, Wigard P. Kloosterman, Benjamin D. Rowland, Elzo de Wit, Jeroen de Ridder, Wouter de Laat
Publicat 2018Artigo -
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Evaluation of Circulating Tumor DNA as a Liquid Biomarker in Uveal Melanoma per Daniël P. de Bruyn, Natasha M. van Poppelen, Tom Brands, Susanne C. van den Boom, Ellis L. Eikenboom, Anja Wagner, Monique M. van Veghel–Plandsoen, Geert Geeven, Berna Beverloo, Caroline M. van Rij, Robert M. Verdijk, Nicole C. Naus, Mette Bagger, Jens Folke Kiilgaard, Annelies de Klein, Erwin Brosens, Emine Kılıç
Publicat 2024Artigo -
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Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping per Carlo Vermeulen, Geert Geeven, Elzo de Wit, Marjon J.A.M. Verstegen, Rumo Jansen, Melissa van Kranenburg, Ewart de Bruijn, Sara L. Pulit, Evelien Kruisselbrink, Zahra Shahsavari, Davood Omrani, Fatemeh Zeinali, Hossein Najmabadi, Θεοδώρα Κάτσιλα, Christina Vrettou, George P. Patrinos, Joanne Traeger‐Synodinos, Erik Splinter, Jeffrey M. Beekman, Sima Kheradmand Kia, Gerard J. te Meerman, Hans Kristian Ploos van Amstel, Wouter de Laat
Publicat 2017Artigo -
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Pyruvate metabolism controls chromatin remodeling during CD4+ T cell activation per Enric Mocholí, Laura Russo, Keshav Gopal, Andrew G. Ramstead, Sophia M. Hochrein, Harmjan R. Vos, Geert Geeven, Adeolu Adegoke, Anna T. Hoekstra, Robert M. van Es, José M. Ramos Pittol, Sebastiaan J. Vastert, Jared Rutter, Timothy R. D. J. Radstake, Jorg van Loosdregt, Celia R. Berkers, Michal Mokrý, Colin C. Anderson, Ryan M. O’Connell, Martin Vaeth, John R. Ussher, Boudewijn Burgering, Paul J. Coffer
Publicat 2023Artigo -
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Web-accessible application for identifying pathogenic transcripts with RNA-seq: Increased sensitivity in diagnosis of neurodevelopmental disorders per Jordy Dekker, Rachel Schot, Michiel Bongaerts, Walter G. de Valk, Monique M. van Veghel–Plandsoen, Kathryn Monfils, Hannie Douben, Peter Elfferich, Esmee Kasteleijn, Leontine van Unen, Geert Geeven, Jasper J. Saris, Yvette van Ierland, Frans W. Verheijen, Marianne L. T. van der Sterre, Farah Sadeghi Niaraki, Daphne J. Smits, Hidde H. Huidekoper, Monique Williams, Martina Wilke, Virginie J. M. Verhoeven, Marieke Joosten, Anneke J.A. Kievit, Ingrid M.B.H. van de Laar, Lies H. Hoefsloot, Marianne Hoogeveen‐Westerveld, Mark Nellist, Grazia M.S. Mancini, Tjakko J. van Ham
Publicat 2023Artigo -
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AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model per Ruizhi Deng, Eva Medico Salsench, Anita Nikoncuk, Reshmi Ramakrishnan, Kristina Lanko, Nikolas A. Kühn, Herma C. van der Linde, Sarah Lor-Zade, Fatimah Albuainain, Yuwei Shi, Soheil Yousefi, Ivan Čapo, Evita Medici‐ van den Herik, Marjon van Slegtenhorst, Rick van Minkelen, Geert Geeven, Monique Mulder, George J. G. Ruijter, Dieter Lütjohann, Edwin H. Jacobs, Henry Houlden, Alistair T. Pagnamenta, Kay Metcalfe, Adam Jackson, Siddharth Banka, Lenika De Simone, Abigail Schwaede, Nancy L. Kuntz, Timothy Blake Palculict, Safdar Abbas, Muhammad Umair, Mohammed A. AlMuhaizea, Dilek Çolak, Hanan AlQudairy, Maysoon Alsagob, Catarina Pereira, Roberta Trunzo, Vasiliki Karageorgou, Aida M. Bertoli‐Avella, Peter Bauer, Arjan Bouman, Lies H. Hoefsloot, Tjakko J. van Ham, Mahmoud Y. Issa, Maha S. Zaki, Joseph G. Gleeson, Rob Willemsen, Namik Kaya, Stefan T. Arold, Reza Maroofian, Leslie E. Sanderson, Tahsin Stefan Barakat
Publicat 2023Artigo
Eines de cerca:
Matèries relacionades
Biology
Gene
Genetics
Computational biology
Enhancer
Gene expression
Genome
Chromatin
Cell biology
Medicine
Transcription factor
Chromatin remodeling
Chromosome
Chromosome conformation capture
Computer science
DNA methylation
Epigenetics
Epigenomics
Evolutionary biology
Fetus
Histone
Mathematics
Neuroscience
Pregnancy
Prenatal diagnosis
Aneuploidy
Biochemistry
CTCF
DNA
Gene silencing