Canlyniadau Chwilio - Jonathan J. Wilde

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  1. 1
    Genetic, Epigenetic, and Environmental Contributions to Neural Tube Closure

    Genetic, Epigenetic, and Environmental Contributions to Neural Tube Closure gan Jonathan J. Wilde, Juliette R. Petersen, Lee Niswander

    Cyhoeddwyd 2014
    Cael y testun llawn
    Revisão
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  2. 2
    Microcephaly disease gene Wdr62 regulates mitotic progression of embryonic neural stem cells and brain size

    Microcephaly disease gene Wdr62 regulates mitotic progression of embryonic neural stem cells and brain size gan Jian-Fu Chen, Ying Zhang, Jonathan J. Wilde, Kirk C. Hansen, Fan Lai, Lee Niswander

    Cyhoeddwyd 2014
    Cael y testun llawn Cael y testun llawn
    Artigo
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  3. 3
    Prime editing primarily induces undesired outcomes in mice

    Prime editing primarily induces undesired outcomes in mice gan Tomomi Aida, Jonathan J. Wilde, Lixin Yang, Yuanyuan Hou, Mengqi Li, Dongdong Xu, Jianbang Lin, Peimin Qi, Zhonghua Lu, Guoping Feng

    Cyhoeddwyd 2020
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    Pré-impressão
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  4. 4
    Efficient embryonic homozygous gene conversion via RAD51-enhanced interhomolog repair

    Efficient embryonic homozygous gene conversion via RAD51-enhanced interhomolog repair gan Jonathan J. Wilde, Tomomi Aida, Ricardo C.H. del Rosario, Tobias Kaiser, Peimin Qi, Martin Wienisch, Qiangge Zhang, Steven M. Colvin, Guoping Feng

    Cyhoeddwyd 2021
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    Artigo
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  5. 5
    Scribble is required for normal epithelial cell–cell contacts and lumen morphogenesis in the mammalian lung

    Scribble is required for normal epithelial cell–cell contacts and lumen morphogenesis in the mammalian lung gan Laura L. Yates, Carsten Schnatwinkel, Lee Hazelwood, Lauren Chessum, Anju Paudyal, Helen Hilton, M. Rosario Romero, Jonathan J. Wilde, Debora Bogani, Jeremy Sanderson, Caroline J. Formstone, J. Murdoch, Lee Niswander, Andy Greenfield, Charlotte Dean

    Cyhoeddwyd 2012
    Cael y testun llawn
    Artigo
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  6. 6
    Circuit-specific gene therapy reverses core symptoms in a primate Parkinson’s disease model

    Circuit-specific gene therapy reverses core symptoms in a primate Parkinson’s disease model gan Yefei Chen, Zexuan Hong, Jingyi Wang, Kunlin Liu, Jing Liu, Jianbang Lin, Shijing Feng, Tianhui Zhang, Liang Shan, Taian Liu, Pinyue Guo, Yunping Lin, Tian Li, Qian Chen, Xiaodan Jiang, Anan Li, Xiang Li, Yuantao Li, Jonathan J. Wilde, Bao Jin, Ji Dai, Zhonghua Lu

    Cyhoeddwyd 2023
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    Artigo
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  7. 7
    Autism-associated CHD8 controls reactive gliosis and neuroinflammation via remodeling chromatin in astrocytes

    Autism-associated CHD8 controls reactive gliosis and neuroinflammation via remodeling chromatin in astrocytes gan Platon Megagiannis, Mei Yuan, Rachel Yan, Yuan Lin, Jonathan J. Wilde, Hailey Eckersberg, Rahul Suresh, Xinzhu Tan, Hong Chen, W. Todd Farmer, Kuwook Cha, Phuong Uyen Le, Hélène Catoire, Daniel Rochefort, Tony Kwan, Brian A. Yee, Patrick A. Dion, Arjun Krishnaswamy, Jean‐François Cloutier, Stefano Stifani, Kevin Petrecca, G Yeo, Keith K. Murai, Guoping Feng, Guy A. Rouleau, Trey Ideker, Neville E. Sanjana, Yang Zhou

    Cyhoeddwyd 2024
    Cael y testun llawn
    Artigo
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  8. 8
    RAD21 Mutations Cause a Human Cohesinopathy

    RAD21 Mutations Cause a Human Cohesinopathy gan Matthew A. Deardorff, Jonathan J. Wilde, Melanie Albrecht, Emma Dickinson, Stephanie Tennstedt, Diana Braunholz, Maren Mönnich, Yuqian Yan, Weizhen Xu, María Concepción Gil‐Rodríguez, Dinah Clark, Hákon Hákonarson, Sara Halbach, Laura Daniela Michelis, Abhinav Rampuria, Eva Rossier, Stephanie Spranger, Lionel Van Maldergem, Sally Ann Lynch, Gabriele Gillessen‐Kaesbach, Hermann‐Josef Lüdecke, Robert G. Ramsay, Michael J. McKay, Ian D. Krantz, Huiling Xu, Julia A. Horsfield, Frank J. Kaiser

    Cyhoeddwyd 2012
    Cael y testun llawn
    Artigo
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  9. 9
    HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle

    HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle gan Matthew A. Deardorff, Masashige Bando, Ryuichiro Nakato, Erwan Watrin, Takehiko Itoh, Masashi Minamino, Katsuya Saitoh, Makiko Komata, Yuki Katou, Dinah Clark, Kathryn Cole, Elfride De Baere, Christophe Decroos, Nataliya Di Donato, Sarah Ernst, Lauren J. Francey, Yolanda Gyftodimou, Kyotaro Hirashima, Melanie Hullings, Yuuichi Ishikawa, Christian Jaulin, Maninder Kaur, Tohru Kiyono, Patrick M. Lombardi, Laura Magnaghi-Jaulin, Geert Mortier, Naohito Nozaki, Michael B. Petersen, Hiroyuki Seimiya, Victoria Mok Siu, Yutaka Suzuki, Kentaro Takagaki, Jonathan J. Wilde, Patrick J. Willems, Claude Prigent, Gabriele Gillessen‐Kaesbach, D.W. Christianson, Frank J. Kaiser, Laird G. Jackson, Toru Hirota, Ian D. Krantz, Katsuhiko Shirahige

    Cyhoeddwyd 2012
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
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  10. 10
    Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance

    Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance gan Frank J. Kaiser, Morad Ansari, Diana Braunholz, María Concepción Gil‐Rodríguez, Christophe Decroos, Jonathan J. Wilde, Christopher T. Fincher, Maninder Kaur, Masashige Bando, David J. Amor, Paldeep S. Atwal, Melanie Bahlo, Christine M. Bowman, Jacquelyn J. Bradley, Han G. Brunner, Dinah Clark, Miguel Del Campo, Nataliya Di Donato, Peter Diakumis, Holly Dubbs, David A. Dyment, Juliane Eckhold, Sarah Ernst, José Carlos Ferreira, Lauren J. Francey, Ulrike Gehlken, Encarna Guillén‐Navarro, Yolanda Gyftodimou, Bryan D. Hall, Raoul C. M. Hennekam, Louanne Hudgins, Melanie Hullings, Jennifer M. Hunter, Helger G. Yntema, A. Micheil Innes, Antonie D. Kline, Zita Krūmiņa, Hane Lee, Kathleen A. Leppig, Sally Ann Lynch, Mark Mallozzi, Linda Mannini, Shane McKee, Sarju Mehta, Ieva Mičule, Shehla Mohammed, Ellen Moran, Geert Mortier, J. Moser, Sarah E. Noon, Naohito Nozaki, Luís Nunes, John Pappas, Lynette S. Penney, Antonio Pérez Aytés, Michael B. Petersen, Beatriz Puisac, Nicole Revençu, Elizabeth Roeder, Sulagna C. Saitta, Angela E. Scheuerle, Karen L. Schindeler, Victoria Mok Siu, Zornitza Stark, Samuel P. Strom, Heidi Thiese, Inga Vater, Patrick J. Willems, Kathleen A. Williamson, Louise C. Wilson, Hákon Hákonarson, Fabiola Quintero‐Rivera, Jolanta Wierzba, Antonio Musio, Gabriele Gillessen‐Kaesbach, Feliciano J. Ramos, Laird G. Jackson, Katsuhiko Shirahige, Juan Pié, D.W. Christianson, Ian D. Krantz, David Fitzpatrick, Matthew A. Deardorff

    Cyhoeddwyd 2014
    Cael y testun llawn
    Artigo
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