Zobrazeno 1 - 10
of 369
pro vyhledávání: '"McKenzie W"'
Autor:
Cheng, C. -J., Lim, S. H., Fujino, S., McKenzie, W. R., Nagarajan, V., Munroe, P. R., Takeuchi, I., Salamanca-Riba, L., Misirlioglu, I. B.
We investigate the microstructural evolution in a ferroelectric to antiferroelectric phase transition at the morphotropic phase boundary in the Bi(1-x)SmxFeO3 system. Continuous Sm3+ substitution on the A-site induces short-range anti-parallel cation
Externí odkaz:
http://arxiv.org/abs/0803.0777
Publikováno v:
The Educational and Developmental Psychologist; July 2023, Vol. 40 Issue: 2 p214-231, 18p
IntroductionClinical education has moved to a “competency-based” model with an emphasis on workplace-based learning and assessment which, in turn, depends on feedback to be effective. Further, the understanding of feedback has changed from inform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e0d4a445208c12de55195cbc0a58480
https://doi.org/10.1101/2021.01.24.21250413
https://doi.org/10.1101/2021.01.24.21250413
Autor:
Colleen C. Muraresku, Elizabeth M. McCormick, Lydia Rockart, T. Blaine Crowley, Stephanie Asher, Amanda Back, Sarah M. Baldino, Emma Bedoukian, Allison D. Britt, Natalie Burrill, Cara Cacioppo, Dana Farengo Clark, Mary Egan Clark, Laura Conway, Laynie Dratch, Holly A. Dubbs, Nicole M. Engelhardt, Natalie Ginn, Christopher Gray, Tiff Hartman, Evan R. Hathaway, Katherine L. Helbig, Lily Hoffman-Andrews, Stefanie Kasperski, Beth A. Keena, Kierstin N. Keller, Jessica M. Long, Lauren Lulis, Laina Lusk, Daniel E. McGinn, Rebecca Mueller, Rache A. Paul, Lisa Pilchman, Jacquelyn Powers, Sarah E. Raible, Sara Reichert, Alyssa L. Rippert, Angela G. Arnold, Sarah M. Ruggiero, Erica Schindewolf, Katie Rose Sullivan, Shannon Terek, Bekah Wang, McKenzie Wells, Natalia Wisniewski, Renee Wright, Elisabeth McCarty Wood, Stacy Woyciechowski, Kristin Zelley, Kathleen D. Valverde, Donna M. McDonald-McGinn
Publikováno v:
Genes, Vol 15, Iss 7, p 867 (2024)
Purpose: Genetic counselors (GCs) increasingly play key roles in advancing genomic medicine through innovative research. Here, we examine one large cohort of GCs’ evolving contributions to the literature, with the goal of facilitating worldwide pro
Externí odkaz:
https://doaj.org/article/59c3bef6795540fa99ac77b828440db8
Autor:
Mario Cuk, Busra Unal, Andjela Bevanda, Connor P. Hayes, McKenzie Walker, Feruza Abraamyan, Robert Beluzic, Kristina Crkvenac Gornik, David Ozretic, Maja Prutki, Qian Nie, Honey V. Reddi, Arezou A. Ghazani
Publikováno v:
Genes, Vol 15, Iss 7, p 946 (2024)
Purpose: An investigation for the co-occurrence of two unrelated genetic disorders of muscular dystrophy and Prader-Willi syndrome (PWS) (OMIM#176270) using joint whole genome sequencing (WGS). Methods: Trio WGS joint analysis was performed to invest
Externí odkaz:
https://doaj.org/article/3819776ae52e4e0d994a2fbf3e6b0fcc
Autor:
Nihat B. Agaoglu, Busra Unal, Connor P. Hayes, McKenzie Walker, Ozden Hatirnaz Ng, Levent Doganay, Nisan D. Can, Huma Q. Rana, Arezou A. Ghazani
Publikováno v:
Cancer Medicine, Vol 13, Iss 3, Pp n/a-n/a (2024)
Abstract Objective Turkish genome is underrepresented in large genomic databases. This study aims to evaluate the effect of allele frequency in the Turkish population in determining the clinical utility of germline findings in breast cancer, includin
Externí odkaz:
https://doaj.org/article/0e8c822e43624d2f9734ff8febc97f18
Autor:
Raymond A. Isidro, Anu Chittenden, McKenzie Walker, Alison Schwartz, Diane R. Koeller, Connor P. Hayes, Busra Unal, Monica Devi Manam, Ryan M. Buehler, Danielle K. Manning, Lynette M. Sholl, Mark S. Redston, Matthew B. Yurgelun, Huma Q. Rana, Judy E. Garber, Arezou A. Ghazani
Publikováno v:
Frontiers in Oncology, Vol 13 (2024)
The presence of variants of uncertain significance (VUS) in DNA mismatch repair (MMR) genes leads to uncertainty in the clinical management of patients being evaluated for Lynch syndrome (LS). Currently, there is no platform to systematically use tum
Externí odkaz:
https://doaj.org/article/6d8a9b32038a4cdca4bc04f27dba67f4
Autor:
Layne N. Rodden, Kellie McIntyre, Medina Keita, Mckenzie Wells, Courtney Park, Victoria Profeta, Amy Waldman, Christian Rummey, Laura J. Balcer, David R. Lynch
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 8, Pp 1397-1406 (2023)
Abstract Objective Friedreich ataxia (FRDA) is an inherited condition caused by a GAA triplet repeat (GAA‐TR) expansion in the FXN gene. Clinical features of FRDA include ataxia, cardiomyopathy, and in some, vision loss. In this study, we character
Externí odkaz:
https://doaj.org/article/507dec434b804a3ca00e4ca193e6156b