Risultati della ricerca - Leslie Smoot
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Double outlet right ventricle: aetiologies and associations di Dita Obler, Amy L. Juraszek, Leslie Smoot, Marvin R. Natowicz
Pubblicazione 2008Revisão -
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Connection between Elastin Haploinsufficiency and Increased Cell Proliferation in Patients with Supravalvular Aortic Stenosis and Williams-Beuren Syndrome di Zsolt Urbán, Sheila Riazi, Thomas L. Seidl, J. Katahira, Leslie Smoot, David Chitayat, Charles D. Boyd, Aleksander Hinek
Pubblicazione 2002Artigo -
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Impact of ABO-Incompatible Listing on Wait-List Outcomes Among Infants Listed for Heart Transplantation in the United States di Christopher S. Almond, Kimberlee Gauvreau, Ravi R. Thiagarajan, Gary Piercey, Elizabeth D. Blume, Leslie Smoot, Francis Fynn‐Thompson, Tajinder P. Singh
Pubblicazione 2010Artigo -
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Safety and early outcomes using a corticosteroid-avoidance immunosuppression protocol in pediatric heart transplant recipients di Tajinder P. Singh, Carey Faber, Elizabeth D. Blume, Sarah Worley, Christopher S. Almond, Leslie Smoot, Shay Dillis, Colleen Nasman, Gerard J. Boyle
Pubblicazione 2010Artigo -
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Outcomes After Primary Transcatheter Therapy in Infants and Young Children With Severe Bilateral Peripheral Pulmonary Artery Stenosis di Jonathan W. Cunningham, Doff B. McElhinney, Kimberlee Gauvreau, Lisa Bergersen, Ronald V. Lacro, Audrey C. Marshall, Leslie Smoot, James E. Lock
Pubblicazione 2013Artigo -
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Mechanisms of Premature Vascular Aging in Children With Hutchinson-Gilford Progeria Syndrome di Marie Gerhard‐Herman, Leslie Smoot, Nicole Wake, Mark W. Kieran, Monica E. Kleinman, David T. Miller, Armin Schwartzman, Anita Giobbie‐Hurder, Donna Neuberg, Leslie B. Gordon
Pubblicazione 2011Artigo -
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Integrin β3 inhibition is a therapeutic strategy for supravalvular aortic stenosis di Ashish Misra, Abdul Q. Sheikh, Abhishek Kumar, Jiesi Luo, Jiasheng Zhang, Robert B. Hinton, Leslie Smoot, Paige Kaplan, Zsolt Urbán, Yibing Qyang, George Tellides, Daniel M. Greif
Pubblicazione 2016Artigo -
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Spectrum of heart disease associated with murine and human GATA4 mutation di Satish Rajagopal, Qing Ma, Dita Obler, Jie Shen, Ani Manichaikul, Aoy Tomita‐Mitchell, Kari Boardman, Christine Briggs, Vidu Garg, Deepak Srivastava, Elizabeth Goldmuntz, Karl W. Broman, D. Woodrow Benson, Leslie Smoot, William T. Pu
Pubblicazione 2007Artigo -
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Transcription factor genes <i>Smad4</i> and <i>Gata4</i> cooperatively regulate cardiac valve development di Ivan P. Moskowitz, Jun Wang, Michael Peterson, William T. Pu, Alexander C. Mackinnon, Leif Oxburgh, Gerald C. Chu, Molly Sarkar, Charles I. Berul, Leslie Smoot, Elizabeth J. Robertson, Robert J. Schwartz, Jonathan G. Seidman, Christine E. Seidman
Pubblicazione 2011Artigo -
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Mutations in Sarcomere Protein Genes as a Cause of Dilated Cardiomyopathy di Mitsuhiro Kamisago, Sapna Sharma, Steven R. DePalma, Scott D. Solomon, Pankaj Sharma, Barbara McDonough, Leslie Smoot, Mary P. Mullen, Paul K. Woolf, E. Douglas Wigle, J G Seidman, John A. Jarcho, Lawrence R. Shapiro, Christine E. Seidman
Pubblicazione 2000Artigo -
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Elastin: mutational spectrum in supravalvular aortic stenosis di Kay Metcalfe, Agnes K Rucka, Leslie Smoot, Guenter Hofstadler, Gerald Tuzler, Pascal McKeown, Victoria Mok Siu, Anita Rauch, John Dean, N R Dennis, Ian O. Ellis, William Reardon, Cheryl Cytrynbaum, Lucy R. Osborne, John R.W. Yates, Andrew Read, Dian Donnai, Mayada Tassabehji
Pubblicazione 2000Artigo -
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Cardiovascular Pathology in Hutchinson-Gilford Progeria: Correlation With the Vascular Pathology of Aging di Michelle Olive, Ingrid A. Harten, Richard N. Mitchell, Jeanette Beers, Karima Djabali, Kan Cao, Michael R. Erdos, Cecilia D. Blair, Birgit Funke, Leslie Smoot, Marie Gerhard‐Herman, Jason T. Machan, Robert Kutys, Renu Virmani, Francis S. Collins, Thomas N. Wight, Elizabeth G. Nabel, Leslie B. Gordon
Pubblicazione 2010Artigo -
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Dissecting spatio‐temporal protein networks driving human heart development and related disorders di Kasper Lage, Kjeld Møllgård, Steven C. Greenway, Hiroko Wakimoto, Joshua M. Gorham, Christopher T. Workman, Eske Bendsen, Niclas Tue Hansen, Olga Rigina, Francisco S. Roque, Cornelia Wiese, Vincent M. Christoffels, Amy E. Roberts, Leslie Smoot, William T. Pu, Patricia K. Donahoe, Niels Tommerup, Søren Brunak, Christine E. Seidman, Jonathan G. Seidman, Lars Allan Larsen
Pubblicazione 2010Artigo -
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Genetic and environmental risk factors in congenital heart disease functionally converge in protein networks driving heart development di Kasper Lage, Steven C. Greenway, Jill A. Rosenfeld, Hiroko Wakimoto, Joshua M. Gorham, Ayellet V. Segrè, Amy E. Roberts, Leslie Smoot, William T. Pu, Alexandre C. Pereira, Sonia M Mesquita, Niels Tommerup, Søren Brunak, Blake C. Ballif, Lisa G. Shaffer, Patricia K. Donahoe, Mark J. Daly, Jonathan G. Seidman, Christine E. Seidman, Lars Allan Larsen
Pubblicazione 2012Artigo -
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Clinical Trial of the Protein Farnesylation Inhibitors Lonafarnib, Pravastatin, and Zoledronic Acid in Children With Hutchinson-Gilford Progeria Syndrome di Leslie B. Gordon, Monica E. Kleinman, Joseph M. Massaro, Ralph B. D’Agostino, Heather Shappell, Marie Gerhard‐Herman, Leslie Smoot, Catherine M. Gordon, Robert Cleveland, Ara Nazarian, Brian D. Snyder, Nicole J. Ullrich, V. Michelle Silvera, Marilyn G. Liang, Nicolle Quinn, David T. Miller, Susanna Y. Huh, Anne A. Dowton, Kelly Littlefield, Maya Mundkur Greer, Mark W. Kieran
Pubblicazione 2016Artigo -
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Clinical trial of a farnesyltransferase inhibitor in children with Hutchinson–Gilford progeria syndrome di Leslie B. Gordon, Monica E. Kleinman, David T. Miller, Donna Neuberg, Anita Giobbie‐Hurder, Marie Gerhard‐Herman, Leslie Smoot, Catherine M. Gordon, Robert Cleveland, Brian D. Snyder, Brian J. Fligor, W. Robert Bishop, Paul Statkevich, Amy Regen, Andrew L. Sonis, Susan Riley, Christine Ploski, Annette Correia, Nicolle Quinn, Nicole J. Ullrich, Ara Nazarian, Marilyn G. Liang, Susanna Y. Huh, Armin Schwartzman, Mark W. Kieran
Pubblicazione 2012Artigo
Strumenti per la ricerca:
Soggetti correlati
Internal medicine
Medicine
Biology
Gene
Genetics
Biochemistry
Cardiology
Mutation
Progeria
Endocrinology
Phenotype
Stenosis
Bioinformatics
Cardiomyopathy
Cell biology
Chemistry
Elastin
Embryonic stem cell
Heart failure
Missense mutation
Neuroscience
Pathology
Pediatrics
Supravalvular aortic stenosis
Transcription factor
Anatomy
Cognition
Cohort
Computational biology
Costello syndrome