Zobrazeno 21 - 30
of 50
pro vyhledávání: '"Wouter Steyaert"'
Autor:
Paul C. Marcogliese, Vandana Shashi, Rebecca C. Spillmann, Nicholas Stong, Jill A. Rosenfeld, Mary Kay Koenig, Julián A. Martínez-Agosto, Matthew Herzog, Agnes H. Chen, Patricia I. Dickson, Henry J. Lin, Moin U. Vera, Noriko Salamon, John M. Graham, Damara Ortiz, Elena Infante, Wouter Steyaert, Bart Dermaut, Bruce Poppe, Hyung-Lok Chung, Zhongyuan Zuo, Pei-Tseng Lee, Oguz Kanca, Fan Xia, Yaping Yang, Edward C. Smith, Joan Jasien, Sujay Kansagra, Gail Spiridigliozzi, Mays El-Dairi, Robert Lark, Kacie Riley, Dwight D. Koeberl, Katie Golden-Grant, Shinya Yamamoto, Michael F. Wangler, Ghayda Mirzaa, Dimitri Hemelsoet, Brendan Lee, Stanley F. Nelson, David B. Goldstein, Hugo J. Bellen, Loren D.M. Pena, Steven Callens, Paul Coucke, Wim Terryn, Rudy Van Coster, David R. Adams, Mercedes E. Alejandro, Patrick Allard, Mahshid S. Azamian, Carlos A. Bacino, Ashok Balasubramanyam, Hayk Barseghyan, Gabriel F. Batzli, Alan H. Beggs, Babak Behnam, Anna Bican, David P. Bick, Camille L. Birch, Devon Bonner, Braden E. Boone, Bret L. Bostwick, Lauren C. Briere, Donna M. Brown, Matthew Brush, Elizabeth A. Burke, Lindsay C. Burrage, Shan Chen, Gary D. Clark, Terra R. Coakley, Joy D. Cogan, Cynthia M. Cooper, Heidi Cope, William J. Craigen, Precilla D’Souza, Mariska Davids, Jyoti G. Dayal, Esteban C. Dell’Angelica, Shweta U. Dhar, Ani Dillon, Katrina M. Dipple, Laurel A. Donnell-Fink, Naghmeh Dorrani, Daniel C. Dorset, Emilie D. Douine, David D. Draper, David J. Eckstein, Lisa T. Emrick, Christine M. Eng, Ascia Eskin, Cecilia Esteves, Tyra Estwick, Carlos Ferreira, Brent L. Fogel, Noah D. Friedman, William A. Gahl, Emily Glanton, Rena A. Godfrey, Sarah E. Gould, Jean-Philippe F. Gourdine, Catherine A. Groden, Andrea L. Gropman, Melissa Haendel, Rizwan Hamid, Neil A. Hanchard, Lori H. Handley, Matthew R. Herzog, Ingrid A. Holm, Jason Hom, Ellen M. Howerton, Yong Huang, Howard J. Jacob, Mahim Jain, Yong-hui Jiang, Jean M. Johnston, Angela L. Jones, Isaac S. Kohane, Donna M. Krasnewich, Elizabeth L. Krieg, Joel B. Krier, Seema R. Lalani, C. Christopher Lau, Jozef Lazar, Brendan H. Lee, Hane Lee, Shawn E. Levy, Richard A. Lewis, Sharyn A. Lincoln, Allen Lipson, Sandra K. Loo, Joseph Loscalzo, Richard L. Maas, Ellen F. Macnamara, Calum A. MacRae, Valerie V. Maduro, Marta M. Majcherska, May Christine V. Malicdan, Laura A. Mamounas, Teri A. Manolio, Thomas C. Markello, Ronit Marom, Julian A. Martínez-Agosto, Shruti Marwaha, Thomas May, Allyn McConkie-Rosell, Colleen E. McCormack, Alexa T. McCray, Matthew Might, Paolo M. Moretti, Marie Morimoto, John J. Mulvihill, Jennifer L. Murphy, Donna M. Muzny, Michele E. Nehrebecky, Stan F. Nelson, J. Scott Newberry, John H. Newman, Sarah K. Nicholas, Donna Novacic, Jordan S. Orange, J. Carl Pallais, Christina G.S. Palmer, Jeanette C. Papp, Neil H. Parker, John A. Phillips, Jennifer E. Posey, John H. Postlethwait, Lorraine Potocki, Barbara N. Pusey, Chloe M. Reuter, Amy K. Robertson, Lance H. Rodan, Jacinda B. Sampson, Susan L. Samson, Kelly Schoch, Molly C. Schroeder, Daryl A. Scott, Prashant Sharma, Rebecca Signer, Edwin K. Silverman, Janet S. Sinsheimer, Kevin S. Smith, Kimberly Splinter, Joan M. Stoler, Jennifer A. Sullivan, David A. Sweetser, Cynthia J. Tifft, Camilo Toro, Alyssa A. Tran, Tiina K. Urv, Zaheer M. Valivullah, Eric Vilain, Tiphanie P. Vogel, Colleen E. Wahl, Nicole M. Walley, Chris A. Walsh, Patricia A. Ward, Katrina M. Waters, Monte Westerfield, Anastasia L. Wise, Lynne A. Wolfe, Elizabeth A. Worthey, Guoyun Yu, Diane B. Zastrow, Allison Zheng
Publikováno v:
American journal of human genetics. 103(3)
Interferon regulatory factor 2 binding protein-like (IRF2BPL) encodes a member of the IRF2BP family of transcriptional regulators. Currently the biological function of this gene is obscure, and the gene has not been associated with a Mendelian diseas
Publikováno v:
Clinical Genetics. 90:263-269
Woodhouse Sakati syndrome (WSS, MIM 241080) is a rare autosomal recessive genetic condition characterized by alopecia, hypogonadism, hearing impairment, diabetes mellitus, learning disabilities and extrapydamidal manifestations. Sequence variants in
Autor:
Martine Biervliet, Elena Makareeva, Aileen M. Barnes, Anne De Paepe, Andy Willaert, Fransiska Malfait, Wouter Steyaert, Joan C. Marini, Sanne D'hondt, Eckhard Witten, Sofie Symoens, Kris Vleminckx, Paul Coucke, Julie De Backer, Brecht Guillemyn, Ann Huysseune, Gabriele Gillessen-Kaesbach, Delfien Syx, Sergey Leikin, Charlotte Gistelinck
Publikováno v:
The American Journal of Human Genetics. 97:521-534
The evolutionarily conserved transmembrane anterior posterior transformation 1 protein, encoded by TAPT1, is involved in murine axial skeletal patterning, but its cellular function remains unknown. Our study demonstrates that TAPT1 mutations underlie
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1865
Due to its simple nature, the clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 technique is massively used nowadays to modify genomic loci in a wide range of model systems. The possibility to interrogate gene function on a geno
Autor:
Felke Steijns, Tjorven Audenaert, Wouter Steyaert, Paul Coucke, Julie De Backer, Ilse Meerschaut, Bert Callewaert, Sofie Symoens, Marjolijn Renard, Laura Muiño-Mosquera, Anne De Paepe
Publikováno v:
Circulation: Genomic and Precision Medicine. 11
Background:The introduction of next-generation sequencing techniques has substantially increased the identification of new genetic variants and hence the necessity of accurate variant interpretatio...
Autor:
Dimitri Hemelsoet, Patricia I. Dickson, Nicholas Stong, Rebecca C. Spillmann, Yaping Yang, Hyunglok Chung, Katie Golden-Grant, Brendan Lee, Hugo J. Bellen, Dwight D. Koeberl, Mays A. El-Dairi, Wouter Steyaert, Bart Dermaut, Stanley F. Nelson, Robert K. Lark, Oguz Kanca, Mary Kay Koenig, Ghayda M. Mirzaa, Michael F. Wangler, Henry J. Lin, Paul C. Marcogliese, Shinya Yamamoto, Joan Jasien, Matthew R. Herzog, Sujay Kansagra, Elena Infante, Fan Xia, Zhen Zuo, Loren D.M. Pena, Ah Chen, Edward C. Smith, Bruce Poppe, Jill A. Rosenfeld, Vandana Shashi, Kacie Riley, Moin Vera, Noriko Salamon, Pei-Tseng Lee, David Goldstein, Damara Ortiz, Gail A. Spiridigliozzi, Julian A. Martinez-Agosto
The Interferon Regulatory Factor 2 Binding Protein Like (IRF2BPL) gene encodes a member of the IRF2BP family of transcriptional regulators. Currently the biological function of this gene is obscure, and the gene has not been associated with a Mendeli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce0253daea36cb4ece5b5297a029841d
Publikováno v:
Methods in Molecular Biology ISBN: 9781493987832
Due to its simple nature, the clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 technique is massively used nowadays to modify genomic loci in a wide range of model systems. The possibility to interrogate gene function on a geno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eda496f1f5f30e22846adccb5306ba72
https://doi.org/10.1007/978-1-4939-8784-9_6
https://doi.org/10.1007/978-1-4939-8784-9_6
© 2018 IEEE. CMOS transistors have become nanometer devices and operating frequencies (fmax) of transistors keep increasing with each technology node. Today, in 28 nm and 40 nm CMOS, sub-THz circuits can be implemented in standard CMOS. By using non
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::948db0312ef0e8f4e8f8697c5a167513
https://lirias.kuleuven.be/handle/123456789/631402
https://lirias.kuleuven.be/handle/123456789/631402
Autor:
Wouter Steyaert, Anne De Paepe, Paul Coucke, Bert Callewaert, Hanna De Saffel, Andy Willaert, Annekatrien Boel
Publikováno v:
DISEASE MODELS & MECHANISMS
Disease Models & Mechanisms, Vol 11, Iss 10 (2018)
Disease Models & Mechanisms
Disease Models & Mechanisms, Vol 11, Iss 10 (2018)
Disease Models & Mechanisms
Targeted genome editing by CRISPR/Cas9 is extremely well fitted to generate gene disruptions, although precise sequence replacement by CRISPR/Cas9-mediated homology-directed repair (HDR) suffers from low efficiency, impeding its use for high-throughp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f8d968130bf6eaaccf5d3d43e388648
https://hdl.handle.net/1854/LU-8602691
https://hdl.handle.net/1854/LU-8602691
Autor:
Laura, Muiño-Mosquera, Felke, Steijns, Tjorven, Audenaert, Ilse, Meerschaut, Anne, De Paepe, Wouter, Steyaert, Sofie, Symoens, Paul, Coucke, Bert, Callewaert, Marjolijn, Renard, Julie, De Backer
Publikováno v:
Circulation. Genomic and precision medicine. 11(6)
The introduction of next-generation sequencing techniques has substantially increased the identification of new genetic variants and hence the necessity of accurate variant interpretation. In 2015, the American College of Medical Genetics and Genomic