Kết quả tìm kiếm - Jason D. Heaney
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High-Fat Diet-Induced Complement Activation Mediates Intestinal Inflammation and Neoplasia, Independent of Obesity Bằng Stephanie K. Doerner, Edimara S. Reis, Elaine S. Leung, Justine S. Ko, Jason D. Heaney, Nathan A. Berger, John D. Lambris, Joseph H. Nadeau
Được phát hành 2016Artigo -
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Mice With a Deletion in the Gene for CCAAT/Enhancer-Binding Protein β Are Protected Against Diet-Induced Obesity Bằng Carrie A. Millward, Jason D. Heaney, David S. Sinasac, Eric Chun‐Pu Chu, Ilya Bederman, Danielle A. Gilge, Stephen F. Previs, Colleen M. Croniger
Được phát hành 2006Artigo -
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Phosphoenolpyruvate carboxykinase (Pck1) helps regulate the triglyceride/fatty acid cycle and development of insulin resistance in mice Bằng Carrie A. Millward, David DeSantis, Chang-Wen Hsieh, Jason D. Heaney, Sorana Pisano, Yael Olswang, Lea Reshef, Michelle Beidelschies, Michelle Puchowicz, Colleen M. Croniger
Được phát hành 2010Artigo -
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IL-33 activates tumor stroma to promote intestinal polyposis Bằng Rebecca L. Maywald, Stephanie K. Doerner, Luca Pastorelli, Carlo De Salvo, Susan M. Benton, Emily P. Dawson, Denise G. Lanza, Nathan A. Berger, Sanford D. Markowitz, Heinz‐Josef Lenz, Joseph H. Nadeau, Theresa T. Pizarro, Jason D. Heaney
Được phát hành 2015Artigo -
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Comparative analysis of single-stranded DNA donors to generate conditional null mouse alleles Bằng Denise G. Lanza, Angelina Gaspero, Isabel Lorenzo, Lan Liao, Ping Zheng, Ying Wang, Yu Deng, Chonghui Cheng, Chuansheng Zhang, John R. Seavitt, Francesco J. DeMayo, Jianming Xu, Mary E. Dickinson, Arthur L. Beaudet, Jason D. Heaney
Được phát hành 2018Artigo -
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Whole genome analysis for 163 gRNAs in Cas9-edited mice reveals minimal off-target activity Bằng Kevin A. Peterson, Sam Khalouei, Nour Hanafi, Joshua A. Wood, Denise G. Lanza, Lauri G. Lintott, Brandon Willis, John R. Seavitt, Robert E. Braun, Mary E. Dickinson, Jacqueline K. White, K. C. Kent Lloyd, Jason D. Heaney, Stephen A. Murray, Arun Ramani, Lauryl M. J. Nutter
Được phát hành 2023Artigo -
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Targeting AAV vectors to the central nervous system by engineering capsid–receptor interactions that enable crossing of the blood–brain barrier Bằng Qin Huang, Albert T. Chen, Ken Y. Chan, Hikari Sorensen, Andrew J. Barry, Bahar Azari, Qingxia Zheng, Thomas Beddow, Binhui Zhao, Isabelle G. Tobey, Cynthia Moncada-Reid, Fatma-Elzahraa Eid, Christopher J. Walkey, M. Cecilia Ljungberg, William R. Lagor, Jason D. Heaney, Yujia A. Chan, Benjamin E. Deverman
Được phát hành 2023Artigo -
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GSDMB is increased in IBD and regulates epithelial restitution/repair independent of pyroptosis Bằng Nitish Rana, Giuseppe Privitera, Hannah Kondolf, Katarzyna Bulek, Susana Lechuga, Carlo De Salvo, Daniele Corridoni, Agne Antanaviciute, Rebecca L. Maywald, Alexander M. Hurtado, Junjie Zhao, Emina H. Huang, Xiaoxia Li, E. Ricky Chan, Alison Simmons, Giorgos Bamias, Derek W. Abbott, Jason D. Heaney, Andrei I. Ivanov, Theresa T. Pizarro
Được phát hành 2022Artigo -
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A GREB1-steroid receptor feedforward mechanism governs differential GREB1 action in endometrial function and endometriosis Bằng Sangappa B. Chadchan, Pooja Popli, Zian Liao, Eryk Andreas, Michelle Dias, Tianyuan Wang, Stephanie Gunderson, Patricia T. Jimenez, Denise G. Lanza, Rainer B. Lanz, Charles E. Foulds, Diana Monsivais, Francesco J. DeMayo, Hari Krishna Yalamanchili, Emily S. Jungheim, Jason D. Heaney, John P. Lydon, Kelle H. Moley, Bert W. O’Malley, Ramakrishna Kommagani
Được phát hành 2024Artigo -
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A Comprehensive Atlas of AAV Tropism in the Mouse Bằng Christopher J. Walkey, Kathy J. Snow, Jote Bulcha, Aaron R. Cox, Alexa Martinez, M. Cecilia Ljungberg, Denise G. Lanza, Marco De Giorgi, Marcel Chuecos, Michele Alves‐Bezerra, Carlos Flores Suarez, Sean M. Hartig, Susan G. Hilsenbeck, Chih‐Wei Hsu, Ethan Saville, Yaned Gaitan, J. Duryea, Seth Hannigan, Mary E. Dickinson, Oleg Mirochnitchenko, Dan Wang, Cathleen Lutz, Jason D. Heaney, Guangping Gao, Stephen A. Murray, William R. Lagor
Được phát hành 2025Artigo -
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The Deep Genome Project Bằng K. C. Kent Lloyd, David J. Adams, Gareth Baynam, Arthur L. Beaudet, Fátima Bosch, Kym M. Boycott, Robert E. Braun, Mark J. Caulfield, Ronald D. Cohn, Mary E. Dickinson, Michael S. Dobbie, Ann M. Flenniken, Paul Flicek, Sanjeev Galande, Xiang Gao, Anne Grobler, Jason D. Heaney, Yann Hérault, Martin Hrabé de Angelis, James R. Lupski, Stanislas Lyonnet, Ann‐Marie Mallon, Fabio Mammano, Calum A. MacRae, Roderick R. McInnes, Colin McKerlie, Terrence F. Meehan, Stephen A. Murray, Lauryl M. J. Nutter, Yuichi Obata, Helen Parkinson, Michael S. Pepper, Radislav Sedláček, Je Kyung Seong, Toshihiko Shiroishi, Damian Smedley, Glauco P. Tocchini‐Valentini, David Valle, Chi‐Kuang Leo Wang, Sara Wells, Jacqueline K. White, Wolfgang Wurst, Ying Xu, Steve D. M. Brown
Được phát hành 2020Editorial -
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Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features Bằng Teresa Santiago‐Sim, Lindsay C. Burrage, Frédéric Ebstein, Mari Tokita, Marcus J. Miller, Weimin Bi, Alicia Braxton, Jill A. Rosenfeld, Maher Shahrour, Andrea Lehmann, Benjamin Cogné, Sébastien Küry, Thomas Besnard, Bertrand Isidor, Stéphane Bézieau, Isabelle Hazart, Honey Nagakura, LaDonna Immken, Rebecca O. Littlejohn, Elizabeth Roeder, Bülent Kara, Katia Hardies, Sarah Weckhuysen, Patrick May, Johannes R. Lemke, Orly Elpeleg, Bassam Abu‐Libdeh, Kiely N. James, Jennifer L. Silhavy, Mahmoud Y. Issa, Maha S. Zaki, Joseph G. Gleeson, John R. Seavitt, Mary E. Dickinson, M. Cecilia Ljungberg, Sara Wells, Sara Johnson, Lydia Teboul, Christine M. Eng, Yaping Yang, Peter‐Michael Kloetzel, Jason D. Heaney, Magdalena Walkiewicz, Zaid Afawi, Rudi Balling, Nina Barišić, Stéphanie Baulac, Dana Craiu, Peter De Jonghe, Rosa Guerrero, Renzo Guerrini, Ingo Helbig, Helle Hjalgrim, Johanna Jähn, Karl Martin Klein, Eric LeGuern, Holger Lerche, Carla Marini, Hiltrud Muhle, Felix Rosenow, José M. Serratosa, Katalin Štěrbová, Arvid Suls, Rikke S. Møller, Pasquale Striano, Yvonne G. Weber, Federico Zara
Được phát hành 2017Artigo -
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Systematic ocular phenotyping of 8,707 knockout mouse lines identifies genes associated with abnormal corneal phenotypes Bằng Thao Vo, Denise M. Imai-Leonard, Benjamin A. Yang, Andrew Briere, Andy Shao, M. Isabel Casanova, David J. Adams, Takanori Amano, Oana V. Amarie, Zorana Berberovic, Lynette Bower, Robert E. Braun, Steve D. M. Brown, Samantha Burrill, Soo Young Cho, Sharon Clementson-Mobbs, Abigail D’Souza, Mary E. Dickinson, Mohammad Eskandarian, Ann M. Flenniken, Helmut Fuchs, Valerie Gailus-Durner, Jason D. Heaney, Yann Hérault, Martin Hrabě de Angelis, Chih‐Wei Hsu, Jin Sun, Russell Joynson, Yeon Kyung Kang, Haerim Kim, Hiroshi Masuya, Hamid Méziane, Steve Murray, Ki-Hoan Nam, Hyuna Noh, Lauryl M. J. Nutter, Marcela Pálková, Jan Procházka, Miles Joseph Raishbrook, Fabrice Riet, Jennifer Ryan, Jason Salazar, Zachery Seavey, John R. Seavitt, Radislav Sedláček, Mohammed Selloum, Kyoung Yul Seo, Je Kyung Seong, Hae-Sol Shin, Toshihiko Shiroishi, Michelle Stewart, Karen L. Svenson, Masaru Tamura, Heather Tolentino, Uchechukwu Udensi, Sara Wells, Jacqueline K. White, Amelia Willett, Janine M. Wotton, Wolfgang Wurst, Atsushi Yoshiki, Louise Lanoue, K. C. Kent Lloyd, Brian C. Leonard, Michel Roux, Colin McKerlie, Ala Moshiri
Được phát hành 2025Artigo -
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The NIH Somatic Cell Genome Editing program Bằng Krishanu Saha, Erik J. Sontheimer, Philip J. Brooks, Melinda R. Dwinell, Charles A. Gersbach, David R. Liu, Stephen A. Murray, Shengdar Q. Tsai, Ross C. Wilson, Daniel G. Anderson, Aravind Asokan, Jillian F. Banfield, Krystof S. Bankiewicz, Gang Bao, Jeff W. M. Bulte, Nenad Bursac, Jarryd M. Campbell, Daniel F. Carlson, Elliot L. Chaikof, Zheng‐Yi Chen, R. Holland Cheng, Karl J. Clark, David T. Curiel, James E. Dahlman, Benjamin E. Deverman, Mary E. Dickinson, Jennifer A. Doudna, Stephen C. Ekker, Marina E. Emborg, Guoping Feng, Benjamin Freedman, David M. Gamm, Guangping Gao, Ionita Ghiran, Peter M. Glazer, Shaoqin Gong, Jason D. Heaney, Jon D. Hennebold, J. Travis Hinson, Anastasia Khvorova, Samira Kiani, William R. Lagor, Kit S. Lam, Kam W. Leong, Jon E. Levine, Jennifer A. Lewis, Cathleen Lutz, Danith H. Ly, Samantha Maragh, Paul B. McCray, Todd C. McDevitt, Oleg Mirochnitchenko, Ryuji Morizane, Niren Murthy, Randall S. Prather, John A. Ronald, Subhojit Roy, Sushmita Roy, Venkata Sabbisetti, W. Mark Saltzman, Philip J. Santangelo, David J. Segal, Hyunjin Shim, Melissa C. Skala, Alice F. Tarantal, John C. Tilton, George A. Truskey, Moriel Vandsburger, Jonathan K. Watts, Kevin D. Wells, Scot A. Wolfe, Qiaobing Xu, Wen Xue, Guohua Yi, Jiangbing Zhou
Được phát hành 2021Revisão -
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Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy Bằng Nadine Spielmann, Gregor Miller, Tudor I. Oprea, Chih‐Wei Hsu, Gisela Fobo, Goar Frishman, Corinna Montrone, Hamed Haseli Mashhadi, Jeremy Mason, Violeta Muñoz‐Fuentes, Stefanie Leuchtenberger, Andreas Ruepp, Matias Wagner, Dominik S. Westphal, Cordula M. Wolf, Agnes Görlach, Adrián Sanz‐Moreno, Yi-Li Cho, Raffaele Teperino, Stefan Brandmaier, Sapna Sharma, Isabella Galter, Manuela A. Östereicher, Lilly Zapf, Philipp Mayer‐Kuckuk, Jan Rozman, Lydia Teboul, Rosie Bunton-Stasyshyn, Heather Cater, Michelle Stewart, Skevoulla Christou, Henrik Westerberg, Amelia Willett, Janine M. Wotton, Willson Roper, Audrey E. Christiansen, Christopher Ward, Jason D. Heaney, Corey L. Reynolds, Jan Procházka, Lynette Bower, David Clary, Mohammed Selloum, Ghina Bou About, Olivia Wendling, Hugues Jacobs, Sophie Leblanc, Hamid Méziane, Tania Sorg, Enrique Audain, Arthur Gilly, Nigel W. Rayner, Juan Antonio Aguilar‐Pimentel, Lore Becker, Lillian Garrett, Sabine M. Hölter, Oana V. Amarie, Julia Calzada‐Wack, Tanja Klein‐Rodewald, Patricia da Silva‐Buttkus, Christoph Lengger, Claudia Stoeger, Raffaele Gerlini, Birgit Rathkolb, Daniela Mayr, John R. Seavitt, Angelina Gaspero, Jennie R. Green, Arturo Garza, Ritu Bohat, Leeyean Wong, Melissa L. McElwee, Sowmya Kalaga, Tara L. Rasmussen, Isabel Lorenzo, Denise G. Lanza, Rodney C. Samaco, Surabi Veeraragaven, Juan Gallegos, Petr Kašpárek, Silvia Petrezsélyová, Ruairidh King, Sara Johnson, James Cleak, Zsombor Szkoe-Kovacs, Gemma Codner, Matthew Mackenzie, Adam Caulder, Janet Kenyon, Wendy Gardiner, Hayley Phelps, Rhys Hancock, Claire Norris, Michayla Moore, Audrie Seluke, Rachel Urban, Coleen Kane, Leslie O. Goodwin, Kevin A. Peterson, Matthew Mckay
Được phát hành 2022Artigo -
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Human and mouse essentiality screens as a resource for disease gene discovery Bằng Pilar Cacheiro, Violeta Muñoz‐Fuentes, Stephen A. Murray, Mary E. Dickinson, Maja Bućan, Lauryl M. J. Nutter, Kevin A. Peterson, Hamed Haselimashhadi, Ann M. Flenniken, Hugh W. Morgan, Henrik Westerberg, Tomasz Konopka, Chih‐Wei Hsu, Audrey E. Christiansen, Denise G. Lanza, Arthur L. Beaudet, Jason D. Heaney, Helmut Fuchs, Valérie Gailus‐Durner, Tania Sorg, Jan Procházka, Vendula Novosadová, Christopher J. Lelliott, Hannah Wardle‐Jones, Sara Wells, Lydia Teboul, Heather Cater, Michelle Stewart, Tertius Hough, Wolfgang Wurst, Radislav Sedláček, David J. Adams, John R. Seavitt, Glauco P. Tocchini‐Valentini, Fabio Mammano, Robert E. Braun, Colin McKerlie, Yann Hérault, Martin Hrabé de Angelis, Ann‐Marie Mallon, K. C. Kent Lloyd, Steve D. M. Brown, Helen Parkinson, Terrence F. Meehan, Damian Smedley, J. C. Ambrose, P. Arumugam, E. L. Baple, Marta Bleda, F. Boardman-Pretty, J. M. Boissiere, C. R. Boustred, H. Brittain, Mark J. Caulfield, Gcf Chan, C. E. H. Craig, Louise C. Daugherty, A. de Burca, A. Devereau, Greg Elgar, Rebecca E. Foulger, Tom Fowler, P. Furió-Tarí, J.M. Hackett, Dina Halai, Angela Hamblin, Seton Henderson, J. E. Holman, Tim Hubbard, Kristina Ibáñez, Richard V. Jackson, Lesley Jones, Dalia Kasperavičiūtė, M. Kayikci, L. Lahnstein, Kim Lawson, S. E. A. Leigh, Ivone Leong, F. J. Lopez, F. Maleady-Crowe, Joanne Mason, Ellen M. McDonagh, L. Moutsianas, Michael Mueller, Nirupa Murugaesu, A. C. Need, Christopher A. Odhams, C. Patch, D. Perez-Gil, Dimitris Polychronopoulos, J. Pullinger, T. Rahim, Álvaro Rendón, Pablo Riesgo-Ferreiro, Tim Rogers, Mina Ryten, K Savage, K. Sawant, Richard H. Scott, A. Siddiq
Được phát hành 2020Artigo
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CRISPR
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Cas9
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