Resultats de la cerca - Mirjam C. G. N. van den Hout
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Split Pool Ligation-based Single-cell Transcriptome sequencing (SPLiT-seq) data processing pipeline comparison per Lucas Kuijpers, Bastian Hornung, Mirjam C. G. N. van den Hout - van Vroonhoven, Wilfred F. J. van IJcken, Frank Grosveld, Eskeatnaf Mulugeta
Publicat 2024Artigo -
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Next generation sequencing of SNPs for non-invasive prenatal diagnosis: challenges and feasibility as illustrated by an application to β-thalassaemia per Thessalia Papasavva, Wilfred F. J. van IJcken, Christel Kockx, Mirjam C. G. N. van den Hout, Petros Kountouris, Loukas Kythreotis, Eleni Ι. Kalogirou, Frank Grosveld, Marina Kleanthous
Publicat 2013Artigo -
3
Dynamic long-range chromatin interactions control<i>Myb</i>proto-oncogene transcription during erythroid development per Ralph Stadhouders, Supat Thongjuea, Charlotte Andrieu‐Soler, Robert‐Jan Palstra, Jan Christian Bryne, Anita van den Heuvel, Mary E. Stevens, Ernie de Boer, Christel Kockx, Antoine van der Sloot, Mirjam C. G. N. van den Hout, Wilfred F. J. van IJcken, Dirk Eick, Boris Lenhard, Frank Grosveld, Éric Soler
Publicat 2011Artigo -
4
Whole-transcriptome analysis of endothelial to hematopoietic stem cell transition reveals a requirement for Gpr56 in HSC generation per Parham Solaimani Kartalaei, Tomoko Yamada-Inagawa, Chris S. Vink, Emma de Pater, Reinier van der Linden, Jonathon Marks-Bluth, Anthon van der Sloot, Mirjam C. G. N. van den Hout, Tomomasa Yokomizo, M. Lucila van Schaick-Solernó, Ruud Delwel, John E. Pimanda, Wilfred F. J. van IJcken, Elaine Dzierzak
Publicat 2014Artigo -
5
Exome sequencing and functional analyses suggest that SIX6 is a gene involved in an altered proliferation–differentiation balance early in life and optic nerve degeneration at old... per Adriana I. Iglesias, Henriët Springelkamp, Herma van der Linde, Lies‐Anne Severijnen, Najaf Amin, Ben A. Oostra, Christel Kockx, Mirjam C. G. N. van den Hout, Wilfred F. J. van IJcken, Albert Hofman, André G. Uitterlinden, Robert M. Verdijk, Caroline C. W. Klaver, Rob Willemsen, Cornelia M. van Duijn
Publicat 2013Artigo -
6
Engram-specific transcriptome profiling of contextual memory consolidation per Priyanka Rao‐Ruiz, Jonathan J. Couey, Ivo M. Marcelo, Christian G. Bouwkamp, Denise E. Slump, Mariana R. Matos, Rolinka J. van der Loo, Gabriela J. Martins, Mirjam C. G. N. van den Hout, Wilfred F. J. van IJcken, Rui M. Costa, Michel C. van den Oever, Steven A. Kushner
Publicat 2019Artigo -
7
CTCF chromatin residence time controls three-dimensional genome organization, gene expression and DNA methylation in pluripotent cells per Widia Soochit, Frank Sleutels, Grégoire Stik, Marek Bartkuhn, Sreya Basu, Silvia C. Hernández, Sarra Merzouk, Enrique Vidal, Ruben Boers, Joachim Boers, Michael van der Reijden, Bart Geverts, Wiggert A. van Cappellen, Mirjam C. G. N. van den Hout, Zeliha Özgür, Wilfred F. J. van IJcken, Joost Gribnau, Rainer Renkawitz, Thomas Graf, Adriaan B. Houtsmuller, Frank Grosveld, Ralph Stadhouders, Niels Galjart
Publicat 2021Artigo -
8
PLD3 variants in population studies per Sven J. van der Lee, Henne Holstege, Tsz Hang Wong, Jóhanna Jakobsdóttir, Joshua C. Bis, Vincent Chouraki, Jeroen van Rooij, Megan L. Grove, Albert V. Smith, Najaf Amin, Seung-Hoan Choi, Alexa Beiser, Melissa E. Garcia, Wilfred F. J. van IJcken, Yolande A.L. Pijnenburg, Eva Louwersheimer, Rutger W. W. Brouwer, Mirjam C. G. N. van den Hout, Edwin Oole, Gudny Eirkisdottir, Daniel Levy, Jerome I. Rotter, Valur Emilsson, Christopher J. O’Donnell, Thor Aspelund, André G. Uitterlinden, Lenore J. Launer, Albert Hofman, Eric Boerwinkle, Bruce M. Psaty, Anita L. DeStefano, Philip Scheltens, Sudha Seshadri, John C. van Swieten, Vilmundur Guðnason, Wiesje M. van der Flier, M. Arfan Ikram, Cornelia M. van Duijn
Publicat 2015Carta -
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Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes per Hongsheng Gui, Duco Schriemer, William Cheng, Rajendra Chauhan, Guillermo Antiñolo, Courtney Berrios, Marta Bleda, Alice S. Brooks, Rutger W. W. Brouwer, Alan J. Burns, Stacey S. Cherny, Joaquı́n Dopazo, Bart J. L. Eggen, Paola Griseri, Binta Jalloh, Thuy-Linh Le, Vincent Chi Hang Lui, Berta Luzón‐Toro, Ivana Matera, Esw Ngan, Anna Pelet, Macarena Ruiz‐Ferrer, Pak C. Sham, Iain T. Shepherd, Man-Ting So, Yunia Sribudiani, Clara Sze-Man Tang, Mirjam C. G. N. van den Hout, Herma C. van der Linde, Tjakko J. van Ham, Wilfred F. J. van IJcken, Joanne Verheij, Jeanne Amiel, Salud Borrego, Isabella Ceccherini, Aravinda Chakravarti, Stanislas Lyonnet, Paul Kwong Hang Tam, Maria‐Mercè Garcia‐Barceló, Robert M.W. Hofstra
Publicat 2017Artigo -
10
Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects per Terry Vrijenhoek, Ken Kraaijeveld, Martin Elferink, Joep de Ligt, Elcke Kranendonk, Gijs W.E. Santen, Isaäc J. Nijman, Derek Butler, Godelieve R.F. Claes, Adalberto Costessi, Wim Dorlijn, Winfried van Eyndhoven, Dicky Halley, Mirjam C. G. N. van den Hout, Steven van Hove, Lennart Johansson, Jan D.H. Jongbloed, Rick Kamps, Christel Kockx, Bart de Koning, Marjolein Kriek, Ronald Lekanne dit Deprez, Hans Lunstroo, Marcel M.A.M. Mannens, Olaf R.F. Mook, Marcel Nelen, M.C. Ploem, Marco Rijnen, Jasper J. Saris, Richard J. Sinke, Erik A. Sistermans, Marjon van Slegtenhorst, Frank Sleutels, Nienke van der Stoep, Marianne van Tienhoven, Martijn Vermaat, Maartje J. Vogel, Quinten Waisfisz, Janneke Weiss, Arthur van den Wijngaard, Wilbert van Workum, Helger Ijntema, Bert van der Zwaag, Wilfred F. J. van IJcken, Johan T. den Dunnen, Joris A. Veltman, Raoul C. M. Hennekam, Edwin Cuppen
Publicat 2015Artigo
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Matèries relacionades
Biology
Gene
Genetics
Exome sequencing
Gene expression
Medicine
Transcription factor
Cell biology
Computational biology
DNA sequencing
Environmental health
Exome
Mutation
Population
Transcriptome
Chromatin
Enhancer
Genotype
Neuroscience
Phenotype
Single-nucleotide polymorphism
Zebrafish
Allele
Allele frequency
Alternative medicine
Anatomy
CREB
CTCF
Candidate gene
ChIA-PET