Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Svetlana Gavrilov"'
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e70149 (2013)
Members of the T-box family of transcription factors are important regulators orchestrating the complex regionalization of the developing mammalian heart. Individual mutations in Tbx20 and Tbx3 cause distinct congenital heart abnormalities in the mou
Externí odkaz:
https://doaj.org/article/6ae811f8319b4351adc24a831f2795e7
Autor:
Svetlana Gavrilov, Darja Marolt, Nataki C. Douglas, Robert W. Prosser, Imran Khalid, Mark V. Sauer, Donald W. Landry, Gordana Vunjak-Novakovic, Virginia E. Papaioannou
Publikováno v:
Stem Cells International, Vol 2011 (2011)
We report the derivation and characterization of two new human embryonic stem cells (hESC) lines (CU1 and CU2) from embryos with an irreversible loss of integrated organismic function. In addition, we analyzed retrospective data of morphological prog
Externí odkaz:
https://doaj.org/article/5c3c130cebf24fc89935f6afa2c9b3dc
Autor:
Rohit Prakash, Svetlana Gavrilov, Laina Freyer, Raymond Wang, Anna-Katerina Hadjantonakis, Elizabeth Lacy, Peter Romanienko, Néstor Saiz, Maria Jasin
Publikováno v:
DNA Repair (Amst)
RAD51 paralogs are key components of the homologous recombination (HR) machinery. Mouse mutants have been reported for four of the canonical RAD51 paralogs, and each of these mutants exhibits embryonic lethality, although at different gestational sta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a77473c56004fa0421b4b6104fac8835
https://doi.org/10.1016/j.dnarep.2021.103227
https://doi.org/10.1016/j.dnarep.2021.103227
Autor:
Ana Potic, Stefanie Perrier, Tijana Radovic, Svetlana Gavrilovic, Jelena Ostojic, Luan T. Tran, Isabelle Thiffault, Tomi Pastinen, Raphael Schiffmann, Geneviève Bernard
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-17 (2023)
Abstract Background Neurodegeneration due to cerebral folate transport deficiency is a rare autosomal recessive disorder caused by biallelic pathogenic variants in FOLR1. Onset typically occurs in late infancy and is characterized by psychomotor regr
Externí odkaz:
https://doaj.org/article/069bc339519c472a91b38f2db7cff481
Autor:
Irene M. Ghobrial, Jane Wilkinson, Viktor A. Adalsteinsson, Elizabeth D. Lightbody, Steven E. Labkoff, Hearn Jay Cho, Teni Dowdell, Daniel Auclair, Jennifer Yesil, Salomon Manier, Svetlana Gavrilov, Justin Rhoades, Romanos Sklavenitis-Pistofidis, Carrie Cibulskis, Annette S. Kim, Mark Bustoros, Shaadi Mehr, Niall J. Lennon, Keith L. Ligon, Cody J. Boehner
Publikováno v:
Blood. 136:33-33
Direct-to-Patient (DTP) Multiple Myeloma (MM) research studies have been launched recently, including PCROWD (NCT02269592), PROMISE (NCT03689595) and the MMRF CureCloud Research Initiative (NCT03657251), aimed at enrolling thousands of individuals fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29c7de605f01db3b12dfee84a83c9f5e
https://doi.org/10.1182/blood-2020-136865
https://doi.org/10.1182/blood-2020-136865
Autor:
Cody J. Boehner, Steven E. Labkoff, Annette S. Kim, Teni Dowdell, Daniel Auclair, Romanos Sklavenitis Pistofidis, Jane Wilkinson, Svetlana Gavrilov, Irene M. Ghobrial, Jihye Park, Jennifer Yesil, Salomon Manier, Viktor A. Adalsteinsson, Keith L. Ligon, Mark Bustoros, Shaadi Mehr, Niall J. Lennon, Carrie Cibulskis
Publikováno v:
Clinical Cancer Research. 26:A38-A38
Direct-to-patient (DTP) multiple myeloma (MM) research studies have been launched recently, including PCROWD (NCT02269592), PROMISE (NCT03689595), and the MMRF CureCloud Research Initiative (NCT03657251), aimed at enrolling thousands of individuals f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89007d259bb9f3717fa0a6853eab80d5
https://doi.org/10.1158/1557-3265.liqbiop20-a38
https://doi.org/10.1158/1557-3265.liqbiop20-a38
Autor:
Rachit Agarwal, Jon D. Ahlstrom, Rafiq Ahmad, Emilio I. Alarcon, Alejandro J. Almarza, Graça Almeida-Porada, Manuel Almeida, Melissa Alvarado-Velez, James M. Anderson, Judith Arcidiacono, Anthony Atala, Stephen F. Badylak, Wayne Balkan, Brian G. Ballios, Pedro M. Baptista, M. Douglas Baumann, Supinder S. Bedi, Ravi V. Bellamkonda, Nicole M. Bergmann, Helen M. Blau, Joel D. Boerckel, Andres M. Bratt-Leal, James C. Brown, Scott Brubaker, Isabelle Brunette, Gisele A. Calderon, Arnold I. Caplan, David G. Castner, Cynthia Chang, Aditya Chawla, Xuguang Chen, Paul Cohen, Michael J. Cooke, Joshua S. Copus, Vitor M. Correlo, Charles S. Cox, Abritee Dahl, Richard M. Day, Paolo De Coppi, Mahesh C. Dodla, Jennifer H. Elisseeff, Juliet A. Emamaullee, Adam Esa, Yunlan Fang, Heather J. Faust, John P. Fisher, Matthew B. Fisher, Elvis L. Francois, Andrés J. García, Svetlana Gavrilov, Dan Gazit, Zulma Gazit, Christopher V. Gemmiti, Gregory J. Gillispie, Sarah E. Gilpin, W.T. Godbey, Andrea Gray, Ronald M. Green, May Griffith, Robert E. Guldberg, Qiongyu Guo, Geoffrey C. Gurtner, Michael C. Hacker, Issa A. Hanna, Joshua M. Hare, Konstantinos E. Hatzistergos, Ralf-Peter Herber, Jöns Hilborn, H. David Humes, Joshua G. Hunsberger, Kenjiro Iwasa, John D. Jackson, Margaret L. Jackson, Hae Lin Jang, John A. Jansen, Josephine Johnston, Carl Jorns, Huijun Kang, David L. Kaplan, David S. Kaplan, Adam J. Katz, Matthew W. Kelley, Kelsey Kennedy, Ali Khademhosseini, Gilson Khang, Jinho Kim, Rachel H. Klein, Irina Klimanskaya, Paul S. Knoepfler, In Kap Ko, Yash M. Kolambkar, Jan Krieghoff, Nathan W. Kucko, Manoj Kumar, Joanne Kurtzberg, Anna Kwilas, Donald W. Landry, Mark T. Langhans, Robert Lanza, Giacomo Lanzoni, Sang Jin Lee, Sander C.G. Leeuwenburgh, Kam W. Leong, Rui Liang, Volha Liaudanskaya, Hang Lin, Michael T. Longaker, Hermann P. Lorenz, Jeanne F. Loring, Shi-Jiang Lu, Alberto Lue, Peter X. Ma, Renata S. Magalhaes, Serena Mandla, Clement D. Marshall, Manuela Martins-Green, Devon E. Mason, Jonquil R. Mau, Richard McFarland, Melissa K. McHale, James C. Melville, Jason R. Meyers, Antonios G. Mikos, Jordan S. Miller, Paul A. Mittermiller, Hideki Miyachi, Shinka Miyamoto, Nelson Monteiro, Alessandra L. Moore, Sara Morini, Philipp T. Moser, Vivek J. Mukhatyar, Mark Murdock, Aaron Nagiel, Gail K. Naughton, Allison Nauta, Javier Navarro, Jared M. Newton, Aparna Nori, Teruo Okano, Joaquim M. Oliveira, Harald C. Ott, Jagannath Padmanabhan, Kristin M. Page, Anil Kumar Pallickaveedu Rajan Asari, Virginia E. Papaioannou, Jihoon Park, Samantha L. Payne, Gadi Pelled, Andrew Pepper, Elumalai Perumal, Melissa Petreaca, Christopher J. Pino, Alessandro Pirosa, Iris Pla-Palacín, Marta Pokrywczynska, Christopher D. Porada, Blaise D. Porter, Milica Radisic, Kunal J. Rambhia, F. Raquel Maia, Buddy D. Ratner, A.H. Reddi, Rui L. Reis, Laura Ricles, Camillo Ricordi, Muhammad Rizwan, Rebecca Robinson, Melanie Rodrigues, Benjamin B. Rothrauff, Hooman Sadri-Ardekani, Pilar Sainz-Arnal, Rangarajan Sambathkumar, Natalia Sánchez-Romero, Michelle Scarritt, Christopher M. Schneider, Steven D. Schwartz, Sarah Selem, Trinidad Serrano-Aulló, A.M. James Shapiro, Dmitriy Sheyn, Tatsuya Shimizu, Toshiharu Shinoka, Molly S. Shoichet, Toshihiro Shoji, Thomas Shupe, Andrew G. Sikora, Fiona Simpson, Aleksander Skardal, Daniel Skuk, Brandon T. Smith, Jihee Sohn, Shay Soker, Estela Solanas, Jeong Eun Song, Disha Sood, David L. Stocum, Stephen C. Strom, Jessica M. Sun, Hironobu Takahashi, Jacques P. Tremblay, Nirmalya Tripathy, John W. Tse, Rocky S. Tuan, Catherine M. Verfaillie, Gordana Vunjak-Novakovic, William R. Wagner, Yanling Wang, Emma Watson, Jennifer L. West, David F. Williams, James K. Williams, Mark E. Wong, Savio L-Y. Woo, Fiona M. Wood, Lei Xu, Doron C. Yakubovich, Yafeng Yang, Michael J. Yaszemski, Pamela C. Yelick, Evelyn K.F. Yim, Carolyn Yong, James J. Yoo, Simon Young, Nora Yucel, Rachel L. Zacharias, Yuanyuan Zhang, Ai Zhang, Jin Zhang, Yang Zhu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac096fc37570ea954939c3a07088a7fb
https://doi.org/10.1016/b978-0-12-809880-6.01002-x
https://doi.org/10.1016/b978-0-12-809880-6.01002-x
Publikováno v:
Gene expression patterns : GEP. 27
Background The dual-specificity T-box/basic helix-loop-helix leucine zipper transcription factor MGA is part of the MAX-interacting network of proteins. In the mouse, MGA is necessary for the survival of the pluripotent epiblast cells of the peri-imp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fba96e6cbaf178f519d9db5b3fedccfd
https://pubmed.ncbi.nlm.nih.gov/29066359
https://pubmed.ncbi.nlm.nih.gov/29066359
Autor:
Andrew Norden, Steven E. Labkoff, Carrie Cibulskis, Scott Longley, Shaadi Mehr, Jennifer Yesil, Anne Quinn Young, Kenneth C. Anderson, Christopher Williams, Teni Dowdell, Mary Derome, Daniel Auclair, Eugene Hui, Jane Wilkinson, Kevin M. Keogh, Kathryn Tanenbaum, Devon Bush, Svetlana Gavrilov
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 19:e56
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6eaa590dff3d1f5eb6ea0830ef8aa9a3
https://doi.org/10.1016/j.clml.2019.09.086
https://doi.org/10.1016/j.clml.2019.09.086
Autor:
Elizabeth Lacy, Svetlana Gavrilov
Publikováno v:
Current Opinion in Genetics & Development. 23:461-469
Ventral folding morphogenesis, a vital morphogenetic process in amniotes, mediates gut endoderm internalization, linear heart tube formation, ventral body wall closure and encasement of the fetus in extraembryonic membranes. Aberrant ventral folding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::117b81f598a6f22129d3eee4339e63c2
https://doi.org/10.1016/j.gde.2013.04.001
https://doi.org/10.1016/j.gde.2013.04.001