Resultados de procura - Patrick Devine

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  1. 1
    Quality of Life and Symptomatology Before and After Nissen Fundoplication

    Quality of Life and Symptomatology Before and After Nissen Fundoplication por Byars, John-Patrick Devine, Pursnani, Kishore, Mughal, Muntzer

    Publicado 2010
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  2. 2
    Requirement for chitin biosynthesis in epithelial tube morphogenesis

    Requirement for chitin biosynthesis in epithelial tube morphogenesis por W. Patrick Devine, Barry Lubarsky, Ken Shaw, Stefan Luschnig, Lisa Messina, Mark A. Krasnow

    Publicado 2005
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  3. 3
    Early patterning and specification of cardiac progenitors in gastrulating mesoderm

    Early patterning and specification of cardiac progenitors in gastrulating mesoderm por W. Patrick Devine, Joshua D. Wythe, Matthew George, Kazuko Koshiba‐Takeuchi, Benoit G. Bruneau

    Publicado 2014
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  4. 4
    Heart enhancers with deeply conserved regulatory activity are established early in zebrafish development

    Heart enhancers with deeply conserved regulatory activity are established early in zebrafish development por Xuefei Yuan, Mengyi Song, Patrick Devine, Benoit G. Bruneau, Ian C. Scott, Michael D. Wilson

    Publicado 2018
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  5. 5
    Cortical Neurons Require Otx1 for the Refinement of Exuberant Axonal Projections to Subcortical Targets

    Cortical Neurons Require Otx1 for the Refinement of Exuberant Axonal Projections to Subcortical Targets por James M. Weimann, Y.Alex Zhang, Margaret Levin, W. Patrick Devine, Philippe Brûlet, Susan K. McConnell

    Publicado 1999
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  6. 6
    Loss of p16 expression is a sensitive marker of CDKN2A homozygous deletion in malignant meningiomas

    Loss of p16 expression is a sensitive marker of CDKN2A homozygous deletion in malignant meningiomas por Vivian Tang, Rufei Lu, Kanish Mirchia, Jessica Van Ziffle, Patrick Devine, Julieann Lee, Joanna J. Phillips, Arie Perry, David R. Raleigh, Calixto‐Hope G. Lucas, David A. Solomon

    Publicado 2023
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  7. 7
    ETS Factors Regulate Vegf-Dependent Arterial Specification

    ETS Factors Regulate Vegf-Dependent Arterial Specification por Joshua D. Wythe, Lan Dang, W. Patrick Devine, Émilie Boudreau, Stanley T Artap, Daniel He, William Schachterle, Didier Y. R. Stainier, Peter Oettgen, Brian L. Black, Benoit G. Bruneau, Jason E. Fish

    Publicado 2013
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  8. 8
    Genetic ancestry and diagnostic yield of exome sequencing in a diverse population

    Genetic ancestry and diagnostic yield of exome sequencing in a diverse population por Yusuph Mavura, Nuriye Sahin‐Hodoglugil, Uğur Hodoğlugil, Mark Kvale, Pierre‐Marie Martin, Jessica Van Ziffle, W. Patrick Devine, Sara Ackerman, Barbara A. Koenig, Pui‐Yan Kwok, Mary E. Norton, Anne Slavotinek, Neil Risch

    Publicado 2024
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  9. 9
    Next-Generation Sequencing of Retinoblastoma Identifies Pathogenic Alterations beyond RB1 Inactivation That Correlate with Aggressive Histopathologic Features

    Next-Generation Sequencing of Retinoblastoma Identifies Pathogenic Alterations beyond RB1 Inactivation That Correlate with Aggressive Histopathologic Features por Armin R. Afshar, Melike Pekmezci, Michele M. Bloomer, Nicola J. Cadenas, Meredith Stevers, Anuradha Banerjee, Ritu Roy, Adam B. Olshen, Jessica Van Ziffle, Courtney Onodera, W. Patrick Devine, James P. Grenert, Boris C. Bastian, David A. Solomon, Bertil Damato

    Publicado 2019
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  10. 10
    Identification of high-risk human papillomavirus and Rb/E2F pathway genomic alterations in mutually exclusive subsets of colorectal neuroendocrine carcinoma

    Identification of high-risk human papillomavirus and Rb/E2F pathway genomic alterations in mutually exclusive subsets of colorectal neuroendocrine carcinoma por Eliah R. Shamir, W. Patrick Devine, Melike Pekmezci, Sarah E. Umetsu, Gregor Krings, Scot Federman, Soo‐Jin Cho, Tara A. Saunders, Kuang‐Yu Jen, Emily K. Bergsland, Kirk D. Jones, Grace Kim, Sanjay Kakar, Charles Y. Chiu, Nancy M. Joseph

    Publicado 2018
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  11. 11
    Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis

    Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis por Teresa N. Sparks, Billie R. Lianoglou, Rebecca Adami, Ilina D. Pluym, Kerry Holliman, Jennifer Duffy, Sarah L. Downum, Sachi Patel, Amanda Faubel, Nina M. Boe, Nancy T. Field, Aisling Murphy, Louise C. Laurent, Jennifer Jolley, Cherry Uy, Anne Slavotinek, Patrick Devine, Uğur Hodoğlugil, Jessica Van Ziffle, Stephan Sanders, Tippi C. MacKenzie, Mary E. Norton

    Publicado 2020
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  12. 12
    Modeling Human TBX5 Haploinsufficiency Predicts Regulatory Networks for Congenital Heart Disease

    Modeling Human TBX5 Haploinsufficiency Predicts Regulatory Networks for Congenital Heart Disease por Irfan S. Kathiriya, Kavitha S. Rao, Giovanni Iacono, W. Patrick Devine, Andrew P. Blair, Swetansu K. Hota, Michael H. Lai, Bayardo I. Garay, Reuben Thomas, Henry Gong, Lauren K. Wasson, Piyush Goyal, Tatyana Sukonnik, Kevin Hu, Güneş Akgün, Laure D. Bernard, Brynn N. Akerberg, Fei Gu, Kai Li, Matthew L Speir, Maximilian Haeussler, William T. Pu, Joshua M. Stuart, Christine E. Seidman, J G Seidman, Holger Heyn, Benoit G. Bruneau

    Publicado 2020
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  13. 13
    Neoadjuvant Osimertinib for the Treatment of Stage I-IIIA Epidermal Growth Factor Receptor–Mutated Non–Small Cell Lung Cancer: A Phase II Multicenter Study

    Neoadjuvant Osimertinib for the Treatment of Stage I-IIIA Epidermal Growth Factor Receptor–Mutated Non–Small Cell Lung Cancer: A Phase II Multicenter Study por Collin M. Blakely, Anatoly Urisman, Matthew A. Gubens, Claire K. Mulvey, Greg M. Allen, Stephen Shiboski, Julia Rotow, Turja Chakrabarti, D. Lucas Kerr, Jacqueline V. Aredo, Bianca Bacaltos, Megan Gee, Lisa Tan, Kirk D. Jones, W. Patrick Devine, Robert C. Doebele, Dara L. Aisner, Tejas Patil, Erin L. Schenk, Trever G. Bivona, Jonathan W. Riess, Melissa H. Coleman, Johannes R. Kratz, David M. Jablons

    Publicado 2024
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  14. 14
    Myxoid glioneuronal tumor, <i>PDGFRA</i> p.K385‐mutant: clinical, radiologic, and histopathologic features

    Myxoid glioneuronal tumor, <i>PDGFRA</i> p.K385‐mutant: clinical, radiologic, and histopathologic features por Calixto‐Hope G. Lucas, Javier Villanueva-Meyer, Nicholas Whipple, Nancy Ann Oberheim Bush, Tabitha Cooney, Susan M. Chang, Michael McDermott, Mitchel S. Berger, Elaine Cham, Peter P. Sun, Angelica R. Putnam, Hong Zhou, Robert J. Bollo, Samuel Cheshier, Matthew M. Poppe, Kar‐Ming Fung, Sarah Sung, Chad A. Glenn, Xuemo Fan, Serguei Bannykh, Jethro Hu, Moise Danielpour, Rong Li, Elizabeth Alva, James M. Johnston, Jessica Van Ziffle, Courtney Onodera, Patrick Devine, James P. Grenert, Julieann C. Lee, Melike Pekmezci, Tarık Tihan, Andrew W. Bollen, Arie Perry, David A. Solomon

    Publicado 2019
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  15. 15
    Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population

    Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population por Anne Slavotinek, Shannon Rego, Nuriye Sahin‐Hodoglugil, Mark Kvale, Billie R. Lianoglou, Tiffany Yip, Hannah Hoban, Simon Outram, Beatrice Anguiano, Flavia Chen, Jeremy Michelson, Roberta Cilio, Cynthia J. Curry, Renata C. Gallagher, Marisa Gardner, Rachel Kuperman, Bryce A. Mendelsohn, Elliott H. Sherr, Joseph T.C. Shieh, Jonathan B. Strober, Allison Tam, Jessica Tenney, William A. Weiss, Amy Whittle, Garrett Chin, Amanda Faubel, Hannah Prasad, Yusuph Mavura, Jessica Van Ziffle, W. Patrick Devine, Uğur Hodoğlugil, Pierre‐Marie Martin, Teresa N. Sparks, Barbara A. Koenig, Sara Ackerman, Neil Risch, Pui‐Yan Kwok, Mary E. Norton

    Publicado 2023
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  16. 16
    Pediatric bithalamic gliomas have a distinct epigenetic signature and frequent EGFR exon 20 insertions resulting in potential sensitivity to targeted kinase inhibition

    Pediatric bithalamic gliomas have a distinct epigenetic signature and frequent EGFR exon 20 insertions resulting in potential sensitivity to targeted kinase inhibition por Gourish Mondal, Julieann C. Lee, Ajay Ravindranathan, Javier Villanueva-Meyer, Quynh T. Tran, Sariah J. Allen, Jairo Barreto, Rohit Gupta, Pamela Doo, Jessica Van Ziffle, Courtney Onodera, Patrick Devine, James P. Grenert, David Samuel, Rong Li, Laura K. Metrock, Lee‐Way Jin, Reuben Antony, Mouied Alashari, Samuel Cheshier, Nicholas Whipple, Carol S. Bruggers, Corey Raffel, Nalin Gupta, Cassie Kline, Alyssa Reddy, Anu Banerjee, Matthew D. Hall, Minesh P. Mehta, Ziad Khatib, Ossama Maher, Carole Brathwaite, Melike Pekmezci, Joanna J. Phillips, Andrew W. Bollen, Tarık Tihan, John T. Lucas, Alberto Broniscer, Mitchel S. Berger, Arie Perry, Brent A. Orr, David A. Solomon

    Publicado 2020
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  17. 17
    Novel <i>SOX10</i> indel mutations drive schwannomas through impaired transactivation of myelination gene programs

    Novel <i>SOX10</i> indel mutations drive schwannomas through impaired transactivation of myelination gene programs por Erik A. Williams, Ajay Ravindranathan, Rohit Gupta, Nicholas Stevers, Abigail K. Suwala, Chibo Hong, Somang Kim, Jimmy Yuan, Jasper Wu, Jairo Barreto, Calixto‐Hope G. Lucas, Emily Chan, Melike Pekmezci, Philip E. LeBoit, Thaddeus W. Mully, Arie Perry, Andrew W. Bollen, Jessica Van Ziffle, W. Patrick Devine, Alyssa Reddy, Nalin Gupta, Kristen M. Basnet, Robert J.B. Macaulay, Patrick Malafronte, Han Lee, William H. Yong, Kevin Jon Williams, Tareq A. Juratli, Douglas A. Mata, Richard S.P. Huang, Matthew Hiemenz, Dean C. Pavlick, Garrett M. Frampton, Tyler Janovitz, Jeffrey S. Ross, Susan M. Chang, Mitchel S. Berger, Line Jacques, Jun S. Song, J Costello, David A. Solomon

    Publicado 2023
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  18. 18
    Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome

    Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome por Federico Tessadori, Karen Duran, Karen Knapp, Matthias Fellner, Sarah Smithson, Ana Beleza‐Meireles, Mariet W. Elting, Quinten Waisfisz, Anne O’Donnell‐Luria, C. Nowak, Jessica Douglas, Anne Ronan, Theresa Brunet, Urania Kotzaeridou, Shayna Svihovec, Margarita Sáenz, Isabelle Thiffault, Florencia Del Viso, Patrick Devine, Shannon Rego, Jessica Tenney, Arie van Haeringen, Claudia Ruivenkamp, Saskia Koene, Stephen P. Robertson, Charulata Deshpande, Rolph Pfundt, Nienke E. Verbeek, Jiddeke M. van de Kamp, Janneke M.M. Weiss, Anna Ruiz, Elisabeth Gabau, Ehud Banne, Alexander Pepler, Armand Bottani, Sacha Laurent, Michel Guipponi, Emilia Bijlsma, Ange‐Line Bruel, Arthur Sorlin, Mary Willis, Zöe Powis, Thomas Smol, Catherine Vincent‐Delorme, Diana Baralle, Estelle Colin, Nicole Revençu, Eduardo Calpena, Andrew O.M. Wilkie, Maya Chopra, Valérie Cormier‐Daire, Boris Keren, Alexandra Afenjar, Marcello Niceta, Antonio Terracciano, Nicola Specchio, Marco Tartaglia, Marlène Rio, Giulia Barcia, Sophie Rondeau, Cindy Colson, Jeroen Bakkers, Peter D. Mace, Louise S. Bicknell, Gijs van Haaften

    Publicado 2022
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  19. 19
    De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy

    De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy por Chiara Klöckner, Heinrich Sticht, Pia Zacher, Bernt Popp, Holly E. Babcock, Dewi P. Bakker, Katy Barwick, Michaela Bonfert, Carsten G. Bönnemann, Eva H. Brilstra, Wendy K. Chung, Angus Clarke, Patrick Devine, Sandra Donkervoort, Jamie L. Fraser, Jennifer Friedman, Alyssa Gates, Jamal Ghoumid, Emma Hobson, Gabriella Horváth, Jennifer Keller‐Ramey, Boris Keren, Manju A. Kurian, Virgina Lee, Kathleen A. Leppig, Johan Lundgren, Marie McDonald, Heather M. McLaughlin, Amy McTague, Heather C. Mefford, Cyril Mignot, Mohamad A. Mikati, Caroline Nava, F. Lucy Raymond, Julian R. Sampson, Alba Sanchis-Juan, Vandana Shashi, Joseph T.C. Shieh, Marwan Shinawi, Anne Slavotinek, Tommy Stödberg, Nicholas Stong, Jennifer A. Sullivan, Ashley C. Taylor, Tomi L. Toler, Marie-José van den Boogaard, Saskia N. van der Crabben, Koen L.I. van Gassen, Richard H. van Jaarsveld, Jessica Van Ziffle, Alexandrea Wadley, Matias Wagner, Kristen Wigby, Saskia B. Wortmann, Yuri A. Zárate, Rikke S. Møller, Johannes R. Lemke, Konrad Platzer

    Publicado 2020
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