Torthaí cuardaigh - Robert J. Roberts

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  1. 1
    The Development of the Newborn Rat Lung in Hyperoxia: A Dose-Response Study of Lung Growth, Maturation, and Changes in Antioxidant Enzyme Activities

    The Development of the Newborn Rat Lung in Hyperoxia: A Dose-Response Study of Lung Growth, Maturation, and Changes in Antioxidant Enzyme Activities de réir John R. Bucher, Robert J. Roberts

    Foilsithe / Cruthaithe 1981
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  2. 2
    Oxygen Toxicity: Comparison of Lung Biochemical Responses in Neonatal and Adult Rats

    Oxygen Toxicity: Comparison of Lung Biochemical Responses in Neonatal and Adult Rats de réir John Yam, Lee Frank, Robert J. Roberts

    Foilsithe / Cruthaithe 1978
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  3. 3
    Developmental Characteristics of Pulmonary Superoxide Dismutase: Relationship to Idiopathic Respiratory Distress Syndrome

    Developmental Characteristics of Pulmonary Superoxide Dismutase: Relationship to Idiopathic Respiratory Distress Syndrome de réir Anne P. Autor, Lee Frank, Robert J. Roberts

    Foilsithe / Cruthaithe 1976
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  4. 4
    Oxygen-Induced Alterations in Lung Vascular Development in the Newborn Rat

    Oxygen-Induced Alterations in Lung Vascular Development in the Newborn Rat de réir Robert J. Roberts, Kenneth M. Weesner, John R. Bucher

    Foilsithe / Cruthaithe 1983
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  5. 5
    Nitric Oxide-Induced Cytotoxicity: Involvement of Cellular Resistance to Oxidative Stress and the Role of Glutathione in Protection

    Nitric Oxide-Induced Cytotoxicity: Involvement of Cellular Resistance to Oxidative Stress and the Role of Glutathione in Protection de réir M. Whit Walker, Michael Kinter, Robert J. Roberts, Douglas R. Spitz

    Foilsithe / Cruthaithe 1995
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  6. 6
    Novel PRKAG2 Mutation Responsible for the Genetic Syndrome of Ventricular Preexcitation and Conduction System Disease With Childhood Onset and Absence of Cardiac Hypertrophy

    Novel PRKAG2 Mutation Responsible for the Genetic Syndrome of Ventricular Preexcitation and Conduction System Disease With Childhood Onset and Absence of Cardiac Hypertrophy de réir Michael H. Gollob, John J. Seger, Tanya N. Gollob, Terry Tapscott, Oscar Gonzales, Linda L. Bachinski, Robert J. Roberts

    Foilsithe / Cruthaithe 2001
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  7. 7
    A transgenic rabbit model for human hypertrophic cardiomyopathy

    A transgenic rabbit model for human hypertrophic cardiomyopathy de réir Ali J. Marian, Yun Wu, Do‐Sun Lim, Meghan McCluggage, Keith A. Youker, Quntao Yu, Ramón Brugada, Francesco J. DeMayo, Miguel A. Quiñones, Robert J. Roberts

    Foilsithe / Cruthaithe 1999
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  8. 8
    Comparative Genome-Wide Association Studies in Mice and Humans for Trimethylamine <i>N</i> -Oxide, a Proatherogenic Metabolite of Choline and <scp>l</scp> -Carnitine

    Comparative Genome-Wide Association Studies in Mice and Humans for Trimethylamine <i>N</i> -Oxide, a Proatherogenic Metabolite of Choline and <scp>l</scp> -Carnitine de réir Jaana Hartiala, Brian J. Bennett, W.H. Wilson Tang, Zeneng Wang, Alexandre F.R. Stewart, Robert J. Roberts, Ruth McPherson, Aldons J. Lusis, Stanley L. Hazen, Hooman Allayee

    Foilsithe / Cruthaithe 2014
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  9. 9
    Transgenic Mouse Model of Ventricular Preexcitation and Atrioventricular Reentrant Tachycardia Induced by an AMP-Activated Protein Kinase Loss-of-Function Mutation Responsible for Wolff-Parkinson-White Syndrome

    Transgenic Mouse Model of Ventricular Preexcitation and Atrioventricular Reentrant Tachycardia Induced by an AMP-Activated Protein Kinase Loss-of-Function Mutation Responsible for... de réir Jasvinder Sidhu, Yadavendra S. Rajawat, Tapan G. Rami, Michael H. Gollob, Zhinong Wang, Ruiyong Yuan, Ali J. Marian, Francesco J. DeMayo, Donald E. Weilbacher, George E. Taffet, Joanna K. Davies, David Carling, Dirar S. Khoury, Robert J. Roberts

    Foilsithe / Cruthaithe 2004
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  10. 10
    Identification of a Gene Responsible for Familial Wolff–Parkinson–White Syndrome

    Identification of a Gene Responsible for Familial Wolff–Parkinson–White Syndrome de réir Michael H. Gollob, Martin S. Green, Anthony Tang, Tanya N. Gollob, Akihiko Karibe, Al-Sayegh Hassan, Ferhaan Ahmad, Ryan J. Lozado, Gopi Shah, Lameh Fananapazir, Linda L. Bachinski, Terry Tapscott, Oscar Gonzales, David Begley, Saidi Mohiddin, Robert J. Roberts

    Foilsithe / Cruthaithe 2001
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  11. 11
    Mutations in the Gene for Cardiac Myosin-Binding Protein C and Late-Onset Familial Hypertrophic Cardiomyopathy

    Mutations in the Gene for Cardiac Myosin-Binding Protein C and Late-Onset Familial Hypertrophic Cardiomyopathy de réir Hideshi Niimura, Linda L. Bachinski, Somkiat Sangwatanaroj, Hugh Watkins, Albert E. Chudley, William J. McKenna, Arni Kristinsson, Robert J. Roberts, Michael J. Sole, Barry J. Maron, Jonathan G. Seidman, Christine E. Seidman, Ludwig Thierfelder, John A. Jarcho, Aris Anastasakis, Pavlos Toutouzas, Eleanor Elstein, Choong‐Chin Liew, Jack Liew, John D. Mably, Harry Rakowski, E.Douglas Wigle, Minshun Zhao, Rosemarie Salerni, Halldóra Björnsdóttir

    Foilsithe / Cruthaithe 1998
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  12. 12
    Shared Genetic Susceptibility to Ischemic Stroke and Coronary Artery Disease

    Shared Genetic Susceptibility to Ischemic Stroke and Coronary Artery Disease de réir Martin Dichgans, Rainer Malik, Inke R. König, Jonathan Rosand, Robert Clarke, Sólveig Grétarsdóttir, Guðmar Þorleifsson, Braxton D. Mitchell, Themistocles L. Assimes, Christopher Levi, Christopher J O Donnell, Myriam Fornage, Unnur Þorsteinsdóttir, Bruce M. Psaty, Christian Hengstenberg, Sudha Seshadri, Jeanette Erdmann, Joshua C. Bis, Annette Peters, Giorgio B. Boncoraglio, Winfried März, James F. Meschia, Sekar Kathiresan, M. Arfan Ikram, Ruth McPherson, Kāri Stefánsson, Cathie Sudlow, Muredach P. Reilly, J. Thompson, Pankaj Sharma, Jemma C. Hopewell, John C. Chambers, Hugh Watkins, Peter M. Rothwell, Robert J. Roberts, Hugh S. Markus, Nilesh J. Samani, Martin Farrall, Heribert Schunkert, Andreas Gschwendtner, Steve Bevan, Yu‐Ching Chen, Anita L. DeStefano, Eugenio Parati, Thomas Quertermous, Andreas Ziegler, Eric Boerwinkle, Hilma Hólm, Marcus Fischer, Thorsten Kessler, Christina Willenborg, Reijo Laaksonen, Benjamin F. Voight, Alexandre F.R. Stewart, Daniel J. Rader, Alistair S. Hall, Jaspal S. Kooner

    Foilsithe / Cruthaithe 2013
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  13. 13
    Disruption at the <i>PTCHD1</i> Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability

    Disruption at the <i>PTCHD1</i> Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability de réir Abdul Noor, Annabel Whibley, Christian R. Marshall, Peter J. Gianakopoulos, Amélie Piton, Andrew R. Carson, M Orlic-Milacic, Anath C. Lionel, Daisuke Sato, Dalila Pinto, Irene Drmic, Carolyn Noakes, Lili Senman, Xiaoyun Zhang, Rong Mo, Julie Gauthier, Jennifer Crosbie, Alistair T. Pagnamenta, Jeffrey Munson, Annette Estes, Andreas Fiebig, André Franke, Stefan Schreiber, Alexandre F.R. Stewart, Robert J. Roberts, Ruth McPherson, Stephen J. Guter, Edwin H. Cook, Géraldine Dawson, Gerard D. Schellenberg, Agatino Battaglia, Elena Maestrini, Linda Jo Bone Jeng, Terry Hutchison, Evica Rajcan‐Separovic, Albert E. Chudley, M. E. Suzanne Lewis, Xudong Liu, J.J.A. Holden, Bridget A. Fernandez, Lonnie Zwaigenbaum, Susan E. Bryson, Wendy Roberts, Peter Szatmari, Louise Gallagher, Michael R. Stratton, Jozef Gécz, Angela F. Brady, Charles E. Schwartz, Russell Schachar, Anthony P. Monaco, Guy A. Rouleau, Chi‐chung Hui, F. Lucy Raymond, Stephen W. Scherer, John B. Vincent

    Foilsithe / Cruthaithe 2010
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  14. 14
    Genetic analysis for a shared biological basis between migraine and coronary artery disease

    Genetic analysis for a shared biological basis between migraine and coronary artery disease de réir Bendik S. Winsvold, Christopher P. Nelson, Rainer Malik, Padhraig Gormley, Verneri Anttila, Jason Vander Heiden, Katherine S. Elliott, L.M. Jacobsen, Priit Palta, Najaf Amin, Boukje de Vries, Eija Hämäläinen, Tobias Freilinger, M. Arfan Ikram, Thorsten Kessler, Markku Koiranen, Lannie Ligthart, George McMahon, Linda M. Pedersen, Christina Willenborg, Hong‐Hee Won, Jes Olesen, Ville Artto, Themistocles L. Assimes, Stefan Blankenberg, Dorret I. Boomsma, Lynn Cherkas, George Davey Smith, Stephen E. Epstein, Jeanette Erdmann, Michel D. Ferrari, Hartmut Göbel, Alistair S. Hall, Marjo‐Riitta Järvelin, Mikko Kallela, Jaakko Kaprio, Sekar Kathiresan, Terho Lehtimäki, Ruth McPherson, Winfried März, Dale R. Nyholt, Christopher J. O’Donnell, Lydia Quaye, Daniel J. Rader, Olli T. Raitakari, Robert J. Roberts, Heribert Schunkert, Markus Schürks, Alexandre F.R. Stewart, Gisela M. Terwindt, Unnur Þorsteinsdóttir, Arn M. J. M. van den Maagdenberg, Cornelia M. van Duijn, Maija Wessman, Tobias Kurth, Christian Kubisch, Martin Dichgans, Daniel I. Chasman, Chris Cotsapas, John‐Anker Zwart, Nilesh J. Samani, Aarno Palotie, Leonore J. Launer, George Davey Smith, George McMahon, Dale R. Nyholt, Alfons Macaya, Patricia Pozo‐Rosich, Bru Cormand, Jessica Fernandez, Marta Vila‐Pueyo, Cèlia Sintas, Jes Olesen, Anne Francke Christensen, Ann-Louise Esserlind, Najaf Amin, Tõnu Esko, Aarno Palotie, Mikko Kallela, Maija Wessman, Ville Artto, Verneri Anttila, Eija Hämäläinen, Priit Palta, Padhraig Gormley, E Garcia Cuenca, Jaakko Kaprio, Martin Dichgans, Hartmut Göbel, Christian Kubisch, Tobias Freilinger, Rainer Malik, Bertram Müller‐Myhsok, John‐Anker Zwart, Bendik S. Winsvold, L.M. Jacobsen, Linda M. Pedersen, Alice Pressman, Arn van den Maagdenberg, Gisela M. Terwindt

    Foilsithe / Cruthaithe 2015
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