Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Sarah M Gubara"'
Autor:
Sthefano Araya, Alexander H Chang, Civanni Moss, Sarah M Gubara, Maria T Gebreyesus, Kenneth Jordan, Karen J Ruth, Pablo Baltodano, Sameer A Patel
Publikováno v:
Aesthetic Surgery Journal Open Forum, Vol 6 (2024)
Abstract BackgroundAutologous fat grafting (AFG) is a widely used surgical technique that involves extracting a patient's own adipose tissue and transferring it to different areas of the body. This practice is still evolving. Guidelines for antibiot
Externí odkaz:
https://doaj.org/article/3c4363f87add455c9b90d3e069b62c84
Autor:
Alejandro Orlowski, Michael G. Katz, Sarah M. Gubara, Anthony S. Fargnoli, Kenneth M. Fish, Thomas Weber
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 16, Iss , Pp 192-203 (2020)
Gene therapy with adeno-associated virus (AAV)-based vectors shows great promise for the gene therapeutic treatment of a broad array of diseases. In fact, the treatment of genetic diseases with AAV vectors is currently the only in vivo gene therapy a
Externí odkaz:
https://doaj.org/article/15ad95b43f0f4dd189705de14587d1d1
Autor:
Jeko M. Madjarov, Michael G. Katz, Sarah M. Gubara, Svetozar Madzharov, Kevin Reames, Sophia Madjarova, Francis Robicsek
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 14, Iss 1, Pp 1-5 (2019)
Abstract Background A strategy for the surgical repair of ruptured Kommerell diverticulum has not yet been established. The aim of this study is to demonstrate that this entity could be associated with a number of other cardiac anomalies and this les
Externí odkaz:
https://doaj.org/article/5911bad94df344c0aa12f5130452e4cd
Autor:
Michael G. Katz, Anthony S. Fargnoli, Sarah M. Gubara, Kenneth Fish, Thomas Weber, Charles R. Bridges, Roger J. Hajjar, Kiyotake Ishikawa
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 6, Iss 1, p 8 (2019)
Advances in DNA- and RNA-based technologies have made gene therapy suitable for many lung diseases, especially those that are hereditary. The main objective of gene therapy is to deliver an adequate amount of gene construct to the intended target cel
Externí odkaz:
https://doaj.org/article/eba4073123d04bceba63aab9a23938bf
Autor:
Sima T. Tarzami, Lahouaria Hadri, Carly Jones, Michael G. Katz, Erik Kohlbrenner, Malik Bisserier, Yassine Abdeldjebbar, Julio Cortijo, Jane A. Leopold, Roger J. Hajjar, Sarah M. Gubara, Elena Chepurko, Javier Milara, Carlos Bueno-Beti, Yassine Sassi
Publikováno v:
Mol Ther
Inhibition of pulmonary fibrosis (PF) by restoring sarco/endoplasmic reticulum calcium ATPase 2a isoform (SERCA2a) expression using targeted gene therapy may be a potentially powerful new treatment approach for PF. Here, we found that SERCA2a express
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af386ca1bd609b36edf5a1628757c4f4
https://doi.org/10.1016/j.ymthe.2019.11.027
https://doi.org/10.1016/j.ymthe.2019.11.027
Autor:
Anthony S. Fargnoli, Jonathan A Cohen, Sophia Madjarova, Sarah M. Gubara, Hylton P Gordon, Michael G. Katz, Virginia L. Gillespie, Shahood Fazal
Publikováno v:
Comp Med
Ischemic myocardial disease is a major cause of death among humans worldwide; it results in scarring and pallor of the myocardium and triggers an inflammatory response that contributes to impaired left ventricular function. This response includes and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::131ab3e21c116299adc64c60f3e0148c
https://pubmed.ncbi.nlm.nih.gov/34082856
https://pubmed.ncbi.nlm.nih.gov/34082856
Autor:
Michael G. Katz, Anthony S. Fargnoli, Charles R. Bridges, Roger J. Hajjar, Sarah M. Gubara, Elena Chepurko
Publikováno v:
Heart Fail Rev
Rodent surgical animal models of heart failure (HF) are critically important for understanding the proof of principle of the cellular alterations underlying the development of the disease as well as evaluating therapeutics. Robust, reproducible roden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd9f4d3edf31dec196f6c56f77431868
https://doi.org/10.1007/s10741-019-09783-4
https://doi.org/10.1007/s10741-019-09783-4
Autor:
Kenneth Fish, Sarah M. Gubara, Anthony S. Fargnoli, Thomas Weber, Michael G. Katz, Alejandro Orlowski
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Molecular Therapy: Methods & Clinical Development, Vol 16, Iss, Pp 192-203 (2020)
Molecular Therapy. Methods & Clinical Development
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Molecular Therapy: Methods & Clinical Development, Vol 16, Iss, Pp 192-203 (2020)
Molecular Therapy. Methods & Clinical Development
Gene therapy with adeno-associated virus (AAV)-based vectors shows great promise for the gene therapeutic treatment of a broad array of diseases. In fact, the treatment of genetic diseases with AAV vectors is currently the only in vivo gene therapy a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53b596abfe63856da1a208c5e416bc33
https://linkinghub.elsevier.com/retrieve/pii/S2329050120300152
https://linkinghub.elsevier.com/retrieve/pii/S2329050120300152
Autor:
Pierfrancesco Agostoni, Amir Landesberg, Wayne Balkan, Monisha Banerjee, C. Adam Banks, Yaron Barac, Colin M. Barker, Harini Bejjanki, Laura Besola, C.V.C. Bouten, Charles R Bridges, Simone Budassi, Daniel Burkhoff, Francesco Burzotta, Tharian S. Cherian, Tony Chour, Karen L. Christman, David Cleveland, Andrea Colli, David K.C. Cooper, Darryl R Davis, Burcin Ekser, Anthony S Fargnoli, Alessandro Fiocco, Giulio Folino, Mario Gössl, Tiffany A. Garbutt, Gino Gerosa, Livia Gheorghe, Sarah M Gubara, Rebecca T. Hahn, Roger J Hajjar, Nadira Hamid, Hidetaka Hara, Joshua M. Hare, Camila Hochman-Mendez, Hayato Iwase, Ahmad-Fawad Jebran, Michael G Katz, Amir Kazory, Chad Kliger, L. Klouda, Abhilash Koratala, Ingo Kutschka, Po-Feng Lee, Andrew J. Lenneman, Scott M. Lilly, Jiandong Liu, E.B. Lurier, Eduardo Marbán, Matteo Nadali, Evgenios Neofytou, Vincent J Nijenhuis, Francis D. Pagani, Luigi Pirelli, Sumanth D. Prabhu, Nicola Pradegan, Li Qian, Indranee N. Rajapreyar, Michael J. Reardon, Giulio Russo, Luiz C. Sampaio, Paul Sorajja, Liang Tang, Doris A. Taylor, Guy Topaz, Carlo Trani, Justin Trapana, Roderick Tung, Udi Nussinovitch, Gaurav A. Upadhyay, Anezi Uzendu, Jan van der Heyden, Marguerite B. Vigliani, Raymond M. Wang, Tessa M.F. Watt, Joseph C. Wu, Yair Feld, Wolfram-Hubertus Zimmermann, Carlo Zivelonghi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b01d0e5b227f87b57b4d3bc5db5f0fe
https://doi.org/10.1016/b978-0-12-813706-2.00031-2
https://doi.org/10.1016/b978-0-12-813706-2.00031-2
Gene-based therapy is a relatively novel treatment which has the ability to target intracellular disease-specific manifestations in the setting of cardiac dysfunction. Gene transfer offers an option to treat the mutated or failing cardiomyocytes via
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e0d5afac7cc22ea186928d3d8645a45
https://doi.org/10.1016/b978-0-12-813706-2.00016-6
https://doi.org/10.1016/b978-0-12-813706-2.00016-6