Resultados da busca - Jennifer M. Martin

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  1. 1
    Latent membrane protein of Epstein-Barr virus induces cellular phenotypes independently of expression of Bcl-2

    Latent membrane protein of Epstein-Barr virus induces cellular phenotypes independently of expression of Bcl-2 por Jennifer M. Martin, Deborah J. Veis, S J Korsmeyer, Bill Sugden

    Publicado em 1993
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  2. 2
    The Immunophilin FKBP12 Functions as a Common Inhibitor of the TGFβ Family Type I Receptors

    The Immunophilin FKBP12 Functions as a Common Inhibitor of the TGFβ Family Type I Receptors por Tongwen Wang, Bi-Yu Li, Paul D. Danielson, Paresh C. Shah, Sybil Rockwell, Robert J. Lechleider, Jennifer M. Martin, Thomas F. Manganaro, Patricia K. Donahoe

    Publicado em 1996
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  3. 3
    A novel Smad nuclear interacting protein, SNIP1, suppresses p300-dependent TGF-β signal transduction

    A novel Smad nuclear interacting protein, SNIP1, suppresses p300-dependent TGF-β signal transduction por Richard H. Kim, David Wang, Michael Tsang, Jennifer M. Martin, Carla Huff, Mark P. de Caestecker, W. Tony Parks, Xianwang Meng, Robert J. Lechleider, Tongwen Wang, Anita B. Roberts

    Publicado em 2000
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  4. 4
    Sorting Nexin 6, a Novel SNX, Interacts with the Transforming Growth Factor-β Family of Receptor Serine-Threonine Kinases

    Sorting Nexin 6, a Novel SNX, Interacts with the Transforming Growth Factor-β Family of Receptor Serine-Threonine Kinases por W. Tony Parks, David B. Frank, Carla Huff, Carol Renfrew Haft, Jennifer M. Martin, Xianwang Meng, Mark P. de Caestecker, James G. McNally, Amit R. Reddi, Simeon I. Taylor, Anita B. Roberts, Tongwen Wang, Robert J. Lechleider

    Publicado em 2001
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  5. 5
    First Genotype–Phenotype Study in TBX4 Syndrome: Gain-of-Function Mutations Causative for Lung Disease

    First Genotype–Phenotype Study in TBX4 Syndrome: Gain-of-Function Mutations Causative for Lung Disease por Matina Prapa, Mauro Lago‐Docampo, Emilia M. Swietlik, David Montani, Mélanie Eyries, Marc Humbert, Carrie L. Welch, Wendy K. Chung, Rolf M.F. Berger, Harm Jan Bogaard, Olivier Danhaive, Pilar Escribano Subías, Henning Gall, Barbara Girerd, Ignacio Hernández‐González, Simon Holden, David Hunt, Samara M.A. Jansen, Wilhelmina S. Kerstjens‐Frederikse, David G. Kiely, Pablo Lapunzina, John McDermott, Shahin Moledina, Joanna Pepke‐Żaba, Gary Polwarth, Gwen Schotte, Jair Tenorio, A. A. Roger Thompson, John Wharton, Stephen J. Wort, Karyn Mégy, Rutendo Mapeta, Carmen Treacy, Jennifer M. Martin, Wei Li, Andrew J. Swift, Paul D. Upton, Nicholas W. Morrell, Stefan Gräf, Diana Valverde

    Publicado em 2022
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  6. 6
    Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

    Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH por Na Zhu, Emilia M. Swietlik, Carrie L. Welch, Michael W. Pauciulo, Jacob Hagen, Xueya Zhou, Yicheng Guo, Johannes Karten, Divya Pandya, Tobias Tilly, Katie A. Lutz, Jennifer M. Martin, Carmen Treacy, Erika B. Rosenzweig, Usha Krishnan, Anna W. Coleman, Claudia Gonzaga‐Jauregui, Allan Lawrie, Richard C. Trembath, Martin R. Wilkins, Russel Hirsch, R.J. White, Marc A. Simon, David B. Badesch, Erika B. Rosenzweig, Charles D. Burger, Murali M. Chakinala, Thenappan Thenappan, Greg Elliott, Robert W. Simms, Harrison W. Farber, Robert P. Frantz, Jean Elwing, Nicholas S. Hill, D. Dunbar Ivy, James Klinger, Steven D. Nathan, Ronald J. Oudiz, Ivan M. Robbins, Robert Schilz, Terry Fortin, Jeffrey Wilt, Delphine Yung, Eric D. Austin, Ferhaan Ahmad, Nitin Bhatt, Tim Lahm, Adaani Frost, Zeenat Safdar, Zia Ur Rehman, Robert Walter, Fernando Torres, Sahil Bakshi, Stephen L. Archer, Rahul Argula, Christopher F. Barnett, Raymond L. Benza, Ankit A. Desai, Veeranna Maddipati, Harm Jan Bogaard, Colin Church, Gerry Coghlin, Robin Condliffe, Mélanie Eyries, Henning Gall, Stefano Ghio, Barbara Girerd, Simon Holden, Luke Howard, Marc Humbert, David G. Kiely, Gábor Kovács, Jim Lordan, Rajiv D. Machado, Robert V. MacKenzie Ross, Colm McCabe, Jennifer M. Martin, Shahin Moledina, David Montani, Horst Olschewski, Christopher J. Penkett, Joanna Pepke‐Żaba, Laura Price, Christopher J. Rhodes, Werner Seeger, Florent Soubrier, Laura Southgate, Jay Suntharalingam, Andrew J. Swift, Mark Toshner, Carmen Treacy, Anton Vonk Noordegraaf, John Wharton, Jim M. Wild, Stephen J. Wort, Harm Jan Bogaard, Colin Church, Gerry Coghlin, Robin Condliffe, Mélanie Eyries

    Publicado em 2021
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  7. 7
    Loss-of-Function <i>ABCC8</i> Mutations in Pulmonary Arterial Hypertension

    Loss-of-Function <i>ABCC8</i> Mutations in Pulmonary Arterial Hypertension por Michael S. Bohnen, Lijiang Ma, Na Zhu, Hongjian Qi, Conor McClenaghan, Claudia Gonzaga‐Jauregui, Frederick E. Dewey, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Aris Baras, Kevin J. Sampson, Marta Bleda, Charaka Hadinnapola, Matthias Haimel, Harm Jan Bogaard, Colin Church, Gerry Coghlan, Paul A. Corris, Mélanie Eyries, J. Simon R. Gibbs, Barbara Girerd, Arjan C. Houweling, Marc Humbert, Christophe Guignabert, David G. Kiely, Allan Lawrie, Rob V. Mackenzie Ross, Jennifer M. Martin, David Montani, Andrew J. Peacock, Joanna Pepke‐Żaba, Florent Soubrier, Jay Suntharalingam, Mark Toshner, Carmen Treacy, Richard C. Trembath, Anton Vonk Noordegraaf, John Wharton, Martin R. Wilkins, Stephen J. Wort, Katherine Yates, Stefan Gräf, Nicholas W. Morrell, Usha Krishnan, Erika B. Rosenzweig, Yufeng Shen, Colin G. Nichols, Robert S. Kass, Wendy K. Chung

    Publicado em 2018
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  8. 8
    Characterization of <i>GDF2</i> Mutations and Levels of BMP9 and BMP10 in Pulmonary Arterial Hypertension

    Characterization of <i>GDF2</i> Mutations and Levels of BMP9 and BMP10 in Pulmonary Arterial Hypertension por Joshua Hodgson, Emilia M. Swietlik, Richard M. Salmon, Charaka Hadinnapola, Ivana Nikolić, John Wharton, Jingxu Guo, James Liley, Matthias Haimel, Marta Bleda, Laura Southgate, Rajiv D. Machado, Jennifer M. Martin, Carmen Treacy, Katherine Yates, Louise C. Daugherty, Olga Shamardina, Deborah Whitehorn, Simon Holden, Harm Jan Bogaard, Colin Church, Gerry Coghlan, Robin Condliffe, Paul A. Corris, Cesare Danesino, Mélanie Eyries, Henning Gall, Stefano Ghio, Hossein Ardeschir Ghofrani, J. Simon R. Gibbs, Barbara Girerd, Arjan C. Houweling, Luke Howard, Marc Humbert, David G. Kiely, Gábor Kovács, Allan Lawrie, Robert V. MacKenzie Ross, Shahin Moledina, David Montani, Andrea Olschewski, Horst Olschewski, Willem H. Ouwehand, Andrew J. Peacock, Joanna Pepke‐Żaba, Inga Prokopenko, Christopher J. Rhodes, Laura Scelsi, Werner Seeger, Florent Soubrier, Jay Suntharalingam, Mark Toshner, Richard C. Trembath, Anton Vonk Noordegraaf, Stephen J. Wort, Martin R. Wilkins, Paul B. Yu, Wei Li, Stefan Gräf, Paul D. Upton, Nicholas W. Morrell

    Publicado em 2019
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  9. 9
    Identification of rare sequence variation underlying heritable pulmonary arterial hypertension

    Identification of rare sequence variation underlying heritable pulmonary arterial hypertension por Stefan Gräf, Matthias Haimel, Marta Bleda, Charaka Hadinnapola, Laura Southgate, Wei Li, Joshua Hodgson, Bin Liu, Richard M. Salmon, Mark Southwood, Rajiv D. Machado, Jennifer M. Martin, Carmen Treacy, Katherine Yates, Louise C. Daugherty, Olga Shamardina, Deborah Whitehorn, Simon Holden, Micheala A. Aldred, Harm Jan Bogaard, Colin Church, Gerry Coghlan, Robin Condliffe, Paul A. Corris, Cesare Danesino, Mélanie Eyries, Henning Gall, Stefano Ghio, Hossein Ardeschir Ghofrani, J. Simon R. Gibbs, Barbara Girerd, Arjan C. Houweling, Luke Howard, Marc Humbert, David G. Kiely, Gábor Kovács, Robert V. MacKenzie Ross, Shahin Moledina, David Montani, Michael Newnham, Andrea Olschewski, Horst Olschewski, Andrew J. Peacock, Joanna Pepke‐Żaba, Inga Prokopenko, Christopher J. Rhodes, Laura Scelsi, Werner Seeger, Florent Soubrier, Dan F. Stein, Jay Suntharalingam, Emilia M. Swietlik, Mark Toshner, David A. van Heel, Anton Vonk Noordegraaf, Quinten Waisfisz, John Wharton, Stephen J. Wort, Willem H. Ouwehand, Nicole Soranzo, Allan Lawrie, Paul D. Upton, Martin R. Wilkins, Richard C. Trembath, Nicholas W. Morrell

    Publicado em 2018
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  10. 10
    Mining the Plasma Proteome for Insights into the Molecular Pathology of Pulmonary Arterial Hypertension

    Mining the Plasma Proteome for Insights into the Molecular Pathology of Pulmonary Arterial Hypertension por Lars Harbaum, Christopher J. Rhodes, John Wharton, Allan Lawrie, Jason H. Karnes, Ankit A. Desai, William C. Nichols, Marc Humbert, David Montani, Barbara Girerd, Olivier Sitbon, Mario Boehm, Tatyana Novoyatleva, Ralph T. Schermuly, Hossein Ardeschir Ghofrani, Mark Toshner, David G. Kiely, Luke Howard, Emilia M. Swietlik, Stefan Gräf, Maik Pietzner, Nicholas W. Morrell, Martin R. Wilkins, Laura Southgate, Rajiv D. Machado, Jennifer M. Martin, W.H. Ouwehand, MW Pauciulo, Amit Arora, Katie Lutz, Ferhaan Ahmad, SL Archer, R Argula, ED Austin, D Badesch, Sahil Bakshi, Chris Barnett, R.L. Benza, Navin Bhatt, CD Burger, Murali M. Chakinala, Jean Elwing, Terry Fortin, R. P. Frantz, A. Frost, J. Garcia, John B. Harley, Hua He, NS Hill, Raphael Hirsch, D. Dunbar Ivy, James R. Klinger, Tim Lahm, Keith Marsolo, L. Martin, SD Nathan, RJ Oudiz, Zia Ur Rehman, Ivan M. Robbins, DM Roden, E.B. Rosenzweig, Ghulam Saydain, Robert Schilz, RW Simms, Marcel Simon, Huadong Tang, AY Tchourbanov, Thenappan Thenappan, F. Torres, AK Walsworth, RE Walter, R.J. White, J Wilt, Delphine Yung, Rick A. Kittles, Jurjan Aman, Jo Knight, KB Hanscombe, Henning Gall, Alexis Ulrich, HJ Bogaard, Colin Church, JG Coghlan, R Condliffe, PA Corris, Cesare Danesino, C. Gregory Elliott, André Franke, Stefano Ghio, J. Simon R. Gibbs, AC. Houweling, György Kovács, Matthias Laudes, R Mackenzie Ross, Shahin Moledina, Michael Newnham, Andrea Olschewski, Horst Olschewski, AJ Peacock, Joanna Pepke‐Żaba

    Publicado em 2022
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  11. 11
    Phenotypic Characterization of <i>EIF2AK4</i> Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension

    Phenotypic Characterization of <i>EIF2AK4</i> Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension por Charaka Hadinnapola, Marta Bleda, Matthias Haimel, Nicholas Screaton, Andrew J. Swift, Peter Dorfmüller, Stephen Preston, Mark Southwood, Jules Hernández‐Sánchez, Jennifer M. Martin, Carmen Treacy, Katherine Yates, Harm Jan Bogaard, Colin Church, Gerry Coghlan, Robin Condliffe, Paul A. Corris, Simon Gibbs, Barbara Girerd, Simon Holden, Marc Humbert, David G. Kiely, Allan Lawrie, Rajiv D. Machado, Robert Ross, Shahin Moledina, David Montani, Michael Newnham, Andrew J. Peacock, Joanna Pepke‐Żaba, Paula Rayner-Matthews, Olga Shamardina, Florent Soubrier, Laura Southgate, Jay Suntharalingam, Mark Toshner, Richard C. Trembath, Anton Vonk Noordegraaf, Martin R. Wilkins, Stephen J. Wort, John Wharton, Stefan Gräf, Nicholas W. Morrell, Timothy J. Aitman, David Bennett, Mark J. Caulfield, Patrick F. Chinnery, Daniel P. Gale, Ania Koziell, Taco W. Kuijpers, Michael Laffan, Eamonn R. Maher, Hugh S. Markus, Willem H. Ouwehand, David J. Perry, F. Lucy Raymond, Irene Roberts, Kenneth G. C. Smith, Adrian J. Thrasher, Hugh Watkins, Catherine Williamson, Geoffrey Woods, Sofie Ashford, John R. Bradley, Debra Fletcher, Tracey Hammerton, Roger James, Nathalie Kingston, Willem H. Ouwehand, Christopher J. Penkett, F. Lucy Raymond, Kathleen Stirrups, Marijke Veltman, Timothy M. Young, Sofie Ashford, Matthew A. Brown, Emma Clement, John Davis, Eleanor Dewhurst, Marie Erwood, Amy Frary, Rachel Linger, Sofia Papadia, Karola Rehnström, Hannah Stark, David Allsup, Steve Austin, Tamam Bakchoul, Tadbir K. Bariana, Paula Bolton‐Maggs, Elizabeth Chalmers, Peter Collins, Wendy N. Erber, Tamara Everington, Rémi Favier, Kathleen Freson, Bruce Furie, Michael Gattens, Keith Gomez, Daniel Greene

    Publicado em 2017
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  12. 12
    De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures

    De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures por Yoko Itō, Keren Carss, Sofia Duarte, Taila Hartley, Boris Keren, Manju A. Kurian, Isabelle Marey, Perinne Charles, Carla Mendonça, Caroline Nava, Rolph Pfundt, Alba Sanchis‐Juan, Hans van Bokhoven, Anthony van Essen, Conny M.A. van Ravenswaaij‐Arts, Kym M. Boycott, Kristin D. Kernohan, Sarah Dyack, F. Lucy Raymond, Timothy J. Aitman, David Bennett, Mark J. Caulfield, Patrick F. Chinnery, Daniel P. Gale, Ania Koziell, Taco W. Kuijpers, Michael Laffan, Eamonn R. Maher, Hugh S. Markus, Nicholas W. Morrell, Willem H. Ouwehand, David J. Perry, F. Lucy Raymond, Irene Roberts, Kenneth G. C. Smith, Adrian J. Thrasher, Hugh Watkins, Catherine Williamson, Geoffrey Woods, Sofie Ashford, John R. Bradley, Debra Fletcher, Tracey Hammerton, Roger James, Nathalie Kingston, Christopher J. Penkett, Kathleen Stirrups, Marijke Veltman, Tim Young, Matthew A. Brown, Emma Clement, John Davis, Eleanor Dewhurst, Helen Dolling, Marie Erwood, Amy Frary, Rachel Linger, Jennifer M. Martin, Sofia Papadia, Karola Rehnström, Hannah Stark, David Allsup, Steve Austin, Tamam Bakchoul, Tadbir K. Bariana, Paula Bolton‐Maggs, Elizabeth Chalmers, Janine Collins, Peter Collins, Wendy N. Erber, Tamara Everington, Rémi Favier, Kathleen Freson, Bruce Furie, Michael Gattens, Johanna Gebhart, Keith Gomez, Daniel Greene, Andreas Greinacher, Paolo Gresele, Daniel Hart, Johan W. M. Heemskerk, Yvonne Henskens, Rashid Kazmi, David Keeling, Anne M. Kelly, Michele P. Lambert, Claire Lentaigne, Ri Liesner, Μichael Μakris, Sarah Mangles, Mary Mathias, Carolyn M. Millar, Andrew Mumford, Paquita Nurden, Jeanette Payne, John Pasi, Kathelijne Peerlinck, Shoshana Revel‐Vilk, Michael Richards

    Publicado em 2018
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  13. 13
    Bayesian Inference Associates Rare <i>KDR</i> Variants With Specific Phenotypes in Pulmonary Arterial Hypertension

    Bayesian Inference Associates Rare <i>KDR</i> Variants With Specific Phenotypes in Pulmonary Arterial Hypertension por Emilia M. Swietlik, Daniel Greene, Na Zhu, Karyn Mégy, Marcella Cogliano, Smitha Rajaram, Divya Pandya, Tobias Tilly, Katie A. Lutz, Carrie L. Welch, Michael W. Pauciulo, Laura Southgate, Jennifer M. Martin, Carmen Treacy, Christopher J. Penkett, Jonathan Stephens, Harm Jan Bogaard, Colin Church, Gerry Coghlan, Anna W. Coleman, Robin Condliffe, Christina A. Eichstaedt, Mélanie Eyries, Henning Gall, Stefano Ghio, Barbara Girerd, Ekkehard Grünig, Simon Holden, Luke Howard, Marc Humbert, David G. Kiely, Gábor Kovács, Jim Lordan, Rajiv D. Machado, Robert V. MacKenzie Ross, Colm McCabe, Shahin Moledina, David Montani, Horst Olschewski, Joanna Pepke‐Żaba, Laura Price, Christopher J. Rhodes, Werner Seeger, Florent Soubrier, Jay Suntharalingam, Mark Toshner, Anton Vonk Noordegraaf, John Wharton, Jim M. Wild, Stephen J. Wort, Allan Lawrie, Martin R. Wilkins, Richard C. Trembath, Yufeng Shen, Wendy K. Chung, Andrew J. Swift, William C. Nichols, Nicholas W. Morrell, Stefan Gräf, Stephen Abbs, Lara Abulhoul, Julian Adlard, Munaza Ahmed, Timothy J. Aitman, Hana Alachkar, David Allsup, Philip Ancliff, Richard Antrobus, Ruth Armstrong, Gavin Arno, Sofie Ashford, William J. Astle, Anthony Attwood, Paul Aurora, Christian Babbs, Chiara Bacchelli, Tamam Bakchoul, Siddharth Banka, Tadbir K. Bariana, Julian Barwell, Joana Batista, Helen Baxendale, Phil Beales, David Bennett, Agnieszka Bierżyńska, Tina Biss, Maria Bitner‐Glindzicz, Graeme Black, Marta Bleda, Iulia Blesneac, Detlef Böckenhauer, Sara Boyce, John R. Bradley, Gerome Breen, Paul Brennan, Carole Brewer, Matthew Brown, Andrew C. Browning, Michael J. Browning, Rachel Buchan

    Publicado em 2020
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  14. 14
    Biological heterogeneity in idiopathic pulmonary arterial hypertension identified through unsupervised transcriptomic profiling of whole blood

    Biological heterogeneity in idiopathic pulmonary arterial hypertension identified through unsupervised transcriptomic profiling of whole blood por Sokratis Kariotis, Emmanuel Jammeh, Emilia M. Swietlik, Josephine Pickworth, Christopher J. Rhodes, P. Morales Otero, John Wharton, James Iremonger, Mark Dunning, Divya Pandya, Thomas S. Mascarenhas, Niamh Errington, A. A. Roger Thompson, Casey E. Romanoski, Franz Rischard, Joe G. N. Garcia, Jason X.‐J. Yuan, Tae-Hwi Schwantes An, Ankit A. Desai, Gerry Coghlan, Jim Lordan, Paul A. Corris, Luke Howard, Robin Condliffe, David G. Kiely, Colin Church, Joanna Pepke‐Żaba, Mark Toshner, Stephen J. Wort, Stefan Gräf, Nicholas W. Morrell, Martin R. Wilkins, Allan Lawrie, Dennis Wang, Marta Bleda, Charaka Hadinnapola, Matthias Haimel, Kate Auckland, Tobias Tilly, Jennifer M. Martin, Katherine Yates, Carmen Treacy, Margaret Day, Alan Greenhalgh, Debbie Shipley, Andrew J. Peacock, Val Irvine, Fiona Kennedy, Shahin Moledina, Lynsay MacDonald, Eleni Tamvaki, Anabelle Barnes, Victoria Cookson, Latifa Chentouf, Souad Ali, Shokri Othman, Lavanya Ranganathan, J. Simon R. Gibbs, Rosa DaCosta, Joy Pinguel, Natalie Dormand, Alice Parker, Della Stokes, Dipa Ghedia, Yvonne Tan, Tanaka Ngcozana, Ivy Wanjiku, Gary Polwarth, Rob V. Mackenzie Ross, Jay Suntharalingam, Mark Grover, Ali Kirby, Ali Grove, Katie White, Annette Seatter, Amanda Creaser-Myers, Sara J. Walker, Stephen Roney, Charles Elliot, Athanasios Charalampopoulos, Ian Sabroe, Abdul Hameed, Iain Armstrong, Neil Hamilton, Alexander Rothman, Andrew J. Swift, Jim M. Wild, Florent Soubrier, Mélanie Eyries, Marc Humbert, David Montani, Barbara Girerd, Laura Scelsi, Stefano Ghio, Henning Gall, Hossein Ardeschir Ghofrani, Harm Jan Bogaard, Anton Vonk Noordegraaf, Arjan C. Houweling, Anna Huis in’t Veld

    Publicado em 2021
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