Zobrazeno 1 - 10
of 91
pro vyhledávání: '"P. E. Morrow"'
Autor:
Joy E. Morrow
Publikováno v:
Polish Journal of English Studies, Vol 9, Iss 2, Pp 26-39 (2023)
Letters in literature intimately convey information to both the characters and the reader; letters in literature also represent captured moments that the characters can revisit over and over again to relive memories of themselves and the letter’s a
Externí odkaz:
https://doaj.org/article/7bf0f598b8a74a799771c59ec9f2318f
Autor:
Yingjie Zhao, Yujue Wang, Lijie Shi, Donna M. McDonald-McGinn, T. Blaine Crowley, Daniel E. McGinn, Oanh T. Tran, Daniella Miller, Jhih-Rong Lin, Elaine Zackai, H. Richard Johnston, Eva W. C. Chow, Jacob A. S. Vorstman, Claudia Vingerhoets, Therese van Amelsvoort, Doron Gothelf, Ann Swillen, Jeroen Breckpot, Joris R. Vermeesch, Stephan Eliez, Maude Schneider, Marianne B. M. van den Bree, Michael J. Owen, Wendy R. Kates, Gabriela M. Repetto, Vandana Shashi, Kelly Schoch, Carrie E. Bearden, M. Cristina Digilio, Marta Unolt, Carolina Putotto, Bruno Marino, Maria Pontillo, Marco Armando, Stefano Vicari, Kathleen Angkustsiri, Linda Campbell, Tiffany Busa, Damian Heine-Suñer, Kieran C. Murphy, Declan Murphy, Sixto García-Miñaúr, Luis Fernández, International 22q11.2 Brain and Behavior Consortium (IBBC), Zhengdong D. Zhang, Elizabeth Goldmuntz, Raquel E. Gur, Beverly S. Emanuel, Deyou Zheng, Christian R. Marshall, Anne S. Bassett, Tao Wang, Bernice E. Morrow
Publikováno v:
npj Genomic Medicine, Vol 8, Iss 1, Pp 1-15 (2023)
Abstract Congenital heart disease (CHD) affecting the conotruncal region of the heart, occurs in 40–50% of patients with 22q11.2 deletion syndrome (22q11.2DS). This syndrome is a rare disorder with relative genetic homogeneity that can facilitate i
Externí odkaz:
https://doaj.org/article/8c4a618d8f784a9c9f58db40b2e0cf57
Autor:
Betelehem Solomon Bera, Taylor V. Thompson, Eric Sosa, Hiroko Nomaru, David Reynolds, Robert A. Dubin, Shahina B. Maqbool, Deyou Zheng, Bernice E. Morrow, John M. Greally, Masako Suzuki
Publikováno v:
Epigenetics & Chromatin, Vol 16, Iss 1, Pp 1-13 (2023)
Abstract Background Single-cell technologies to analyze transcription and chromatin structure have been widely used in many research areas to reveal the functions and molecular properties of cells at single-cell resolution. Sample multiplexing techni
Externí odkaz:
https://doaj.org/article/f1b57dbd9eda4373b99c5082f8dfd9c5
Autor:
Christopher De Bono, Yang Liu, Alexander Ferrena, Aneesa Valentine, Deyou Zheng, Bernice E. Morrow
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-20 (2023)
Cardiac neural crest must differentiate and migrate correctly to achieve proper cardiovascular development. Here, the authors use single cell analyses to show how these cells are altered non-autonomously by loss of Tbx1, the major gene for 22q11.2 de
Externí odkaz:
https://doaj.org/article/eeff170cd5784f0e87176312e4001630
Autor:
Franck F. Rahaghi, Vivien M. Hsu, Robert J. Kaner, Maureen D. Mayes, Ivan O. Rosas, Rajan Saggar, Virginia D. Steen, Mary E. Strek, Elana J. Bernstein, Nitin Bhatt, Flavia V. Castelino, Lorinda Chung, Robyn T. Domsic, Kevin R. Flaherty, Nishant Gupta, Bashar Kahaleh, Fernando J. Martinez, Lee E. Morrow, Teng Moua, Nina Patel, Oksana A. Shlobin, Brian D. Southern, Elizabeth R. Volkmann, Dinesh Khanna
Publikováno v:
Respiratory Research, Vol 24, Iss 1, Pp 1-16 (2023)
Abstract Background Systemic sclerosis (SSc) is a rare, complex, connective tissue disorder. Interstitial lung disease (ILD) is common in SSc, occurring in 35–52% of patients and accounting for 20–40% of mortality. Evolution of therapeutic option
Externí odkaz:
https://doaj.org/article/f0f7c08666254d739a6ca421ab557bf3
Autor:
Bingruo Wu, Brian Wu, Sonia Benkaci, Lijie Shi, Pengfei Lu, Taeju Park, Bernice E. Morrow, Yidong Wang, Bin Zhou
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 18 (2023)
Background Endocardial cells are a major progenitor population that gives rise to heart valves through endocardial cushion formation by endocardial to mesenchymal transformation and the subsequent endocardial cushion remodeling. Genetic variants that
Externí odkaz:
https://doaj.org/article/b3a9b7dab43d42c88d1b61321aad4002
Autor:
Hiroko Nomaru, Yang Liu, Christopher De Bono, Dario Righelli, Andrea Cirino, Wei Wang, Hansoo Song, Silvia E. Racedo, Anelisa G. Dantas, Lu Zhang, Chen-Leng Cai, Claudia Angelini, Lionel Christiaen, Robert G. Kelly, Antonio Baldini, Deyou Zheng, Bernice E. Morrow
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-19 (2021)
Perturbations of the cardiopharyngeal mesoderm can lead to congenital defects in individuals with 22q11.2 deletion syndrome. Here the authors use single cell RNA-sequencing to identify a multilineage primed population within the mesoderm, marked by T
Externí odkaz:
https://doaj.org/article/f709a55fc0cc4c0b854e870ae4c8e741
Autor:
Nikhil Jagan, Lee E. Morrow, Ryan W. Walters, Robert W. Plambeck, Tej M. Patel, Douglas R. Moore, Mark A. Malesker
Publikováno v:
Annals of Intensive Care, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract Background Diametrically opposed positions exist regarding the deleterious effects of elevated lactate. There are data suggesting that it is a detrimental proxy for tissue hypoperfusion and anaerobic metabolism in sepsis and an alternative v
Externí odkaz:
https://doaj.org/article/c882a036803b4e71becff472582feab6
Autor:
F. Fitzal, M. Bolliger, D. Dunkler, L. Gambone, J. Heil, F. Riedel, J. de Boniface, C. André, Z. Matrai, D. Pukancsik, R.R. Paulinelli, V. Ostapenko, A. Burneckis, A. Ostapenko, E. Ostapenko, F. Meani, Y. Harder, M. Bonollo, A.S.M. Alberti, C. Tausch, B. Papassotiropoulos, R. Helfgott, D. Heck, H.J. Fehrer, M. Acko, P. Schrenk, G. Montagna, E. Trapp, G. Pristauz, C. Paliczek, J.U. Blohmer, S. Steffen, L. Romics, E. Morrow, K. Lorenz, M. Fehr, M. Ritter, W.P. Weber
Publikováno v:
Breast, Vol 56, Iss , Pp S71-S72 (2021)
Externí odkaz:
https://doaj.org/article/cbbc598ddbaa4b4396464191742397bc
Publikováno v:
Ecosphere, Vol 11, Iss 10, Pp n/a-n/a (2020)
Abstract The Attwater's prairie‐chicken (APC; Tympanuchus cupido attwateri) was listed as an endangered species in 1967, and since then multiple studies have addressed ecological and human factors that may have limited their population recovery. In
Externí odkaz:
https://doaj.org/article/1b3adf468aac45de94344cd337a4f11f