Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Lindsay Meyers"'
Autor:
Shannon Hateley, Angelica Lopez-Izquierdo, Chuanchau J. Jou, Scott Cho, Joshua G. Schraiber, Shiya Song, Colin T. Maguire, Natalia Torres, Michael Riedel, Neil E. Bowles, Cammon B. Arrington, Brett J. Kennedy, Susan P. Etheridge, Shuping Lai, Chase Pribble, Lindsay Meyers, Derek Lundahl, Jake Byrnes, Julie M. Granka, Christopher A. Kauffman, Gordon Lemmon, Steven Boyden, W. Scott Watkins, Mary Anne Karren, Stacey Knight, J. Brent Muhlestein, John F. Carlquist, Jeffrey L. Anderson, Kenneth G. Chahine, Khushi U. Shah, Catherine A. Ball, Ivor J. Benjamin, Mark Yandell, Martin Tristani-Firouzi
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-10 (2021)
Many rare high-impact variants have been associated with disease, but the origins and functional impact are not always explored. Here, the authors trace the ancestry of a rare high impact atrial fibrillation allele in KCNQ1, and use iPSC-derived card
Externí odkaz:
https://doaj.org/article/fc7dba9c47974f5aa229e04e2b3a9d14
Autor:
Lindsey Gakenheimer‐Smith, Lindsay Meyers, Derek Lundahl, Shaji C. Menon, T. Jared Bunch, Briana L. Sawyer, Martin Tristani‐Firouzi, Susan P. Etheridge
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 6, Pp n/a-n/a (2021)
Abstract Background Pathogenic variants in the L‐type Ca2+ channel gene CACNA1C cause a multi‐system disorder that includes severe long QT syndrome (LQTS), congenital heart disease, dysmorphic facial features, syndactyly, abnormal immune function
Externí odkaz:
https://doaj.org/article/f5daaacb8149408f84f1957a87494717
Autor:
Juliana M Ruzante, Katherine Olin, Breda Munoz, Jeff Nawrocki, Rangaraj Selvarangan, Lindsay Meyers
Publikováno v:
PLoS ONE, Vol 16, Iss 4, p e0250767 (2021)
Acute gastrointestinal infection (AGI) represents a significant public health concern. To control and treat AGI, it is critical to quickly and accurately identify its causes. The use of novel multiplex molecular assays for pathogen detection and iden
Externí odkaz:
https://doaj.org/article/64bca9ec75bd4bd4ae3d480a33341a0c
Autor:
Mark A. Poritz, Anne J. Blaschke, Carrie L. Byington, Lindsay Meyers, Kody Nilsson, David E. Jones, Stephanie A. Thatcher, Thomas Robbins, Beth Lingenfelter, Elizabeth Amiott, Amy Herbener, Judy Daly, Steven F. Dobrowolski, David H. -F. Teng, Kirk M. Ririe
Publikováno v:
PLoS ONE, Vol 6, Iss 11 (2011)
Externí odkaz:
https://doaj.org/article/96631b77deda413c8b218bf44403a887
Autor:
Mark A Poritz, Anne J Blaschke, Carrie L Byington, Lindsay Meyers, Kody Nilsson, David E Jones, Stephanie A Thatcher, Thomas Robbins, Beth Lingenfelter, Elizabeth Amiott, Amy Herbener, Judy Daly, Steven F Dobrowolski, David H-F Teng, Kirk M Ririe
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e26047 (2011)
The ideal clinical diagnostic system should deliver rapid, sensitive, specific and reproducible results while minimizing the requirements for specialized laboratory facilities and skilled technicians. We describe an integrated diagnostic platform, th
Externí odkaz:
https://doaj.org/article/e7ad8b4b51a1448aad5d2451b0503fca
Autor:
Mounia Tannour-Louet, Shuo Han, Sean T Corbett, Jean-Francois Louet, Svetlana Yatsenko, Lindsay Meyers, Chad A Shaw, Sung-Hae L Kang, Sau Wai Cheung, Dolores J Lamb
Publikováno v:
PLoS ONE, Vol 5, Iss 10, p e15392 (2010)
Disorders of sexual development (DSD), ranging in severity from genital abnormalities to complete sex reversal, are among the most common human birth defects with incidence rates reaching almost 3%. Although causative alterations in key genes control
Externí odkaz:
https://doaj.org/article/cd0441f0a0334b3ab05d6a4f4ef04f3a
Autor:
W. Scott Watkins, Derek Lundahl, Steven E. Boyden, Shiya Song, Mary Anne Karren, J. Brent Muhlestein, Shannon Hateley, Chuanchau J. Jou, Colin T. Maguire, Jeffrey L. Anderson, Khushi U Shah, Susan P. Etheridge, Kenneth G. Chahine, Brett Kennedy, Martin Tristani-Firouzi, Gordon Lemmon, Lindsay Meyers, Ivor J. Benjamin, Stacey Knight, Chase Pribble, Catherine A. Ball, Shuping Lai, Christopher A. Kauffman, Scott Cho, Cammon B. Arrington, Natalia S. Torres, Michael Riedel, Joshua G. Schraiber, John F. Carlquist, Jake K. Byrnes, Julie M. Granka, Neil E. Bowles, Mark Yandell, Angelica Lopez-Izquierdo
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-10 (2021)
Nature Communications
Nature Communications
The genetic architecture of atrial fibrillation (AF) encompasses low impact, common genetic variants and high impact, rare variants. Here, we characterize a high impact AF-susceptibility allele, KCNQ1 R231H, and describe its transcontinental geograph
Autor:
Emily Leann Griffin, Sara Fitzgerald-Butt, Katie L. Ziegler, Matthew J Thomas, Allison F. Schartman, Benjamin M. Helm, Erin Syverson, Hannah E. Ison, Kristyne M. Stone, Erin M. Demo, Amy R. Shikany, Ashley Parrott, Lindsay Meyers, Kristi K Fitzgerald
Publikováno v:
Journal of Genetic Counseling. 31:9-33
Congenital heart disease (CHD) is an indication which spans multiple specialties across various genetic counseling practices. This practice resource aims to provide guidance on key considerations when approaching counseling for this particular indica
Autor:
Jeff Nawrocki, Camille V Cook, Michaela Powell, Katherine Olin, Martin C. Holdrege, Lindsay Meyers, Andrew Hemmert, Thomas Charles Robbins, Charles Benjamin Cox, Joel Hartsell, Christine C. Ginocchio, Jay Jones
Publikováno v:
Open Forum Infectious Diseases
Background The initial focus of the US public health response to coronavirus disease 2019 (COVID-19) was the implementation of numerous social distancing policies. While COVID-19 was the impetus for imposing these policies, it is not the only respira
Autor:
Kevin Messacar, Bryan T. Grenfell, Sang Woo Park, Margarita Pons-Salort, Lindsay Meyers, Jeremy Farrar
Publikováno v:
medRxiv
article-version (status) pre
article-version (number) 1
article-version (status) pre
article-version (number) 1
The lack of active surveillance for enterovirus D68 (EV-D68) in the US has hampered the ability to assess the relationship with predominantly biennial epidemics of acute flaccid myelitis (AFM), a rare but serious neurological condition. Using novel s