Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Emily M. Coonrod"'
Autor:
Andrew D. Huber, Jennifer J. Wolf, Dandan Liu, Anna T. Gres, Jing Tang, Kelsey N. Boschert, Maritza N. Puray-Chavez, Dallas L. Pineda, Thomas G. Laughlin, Emily M. Coonrod, Qiongying Yang, Juan Ji, Karen A. Kirby, Zhengqiang Wang, Stefan G. Sarafianos
Publikováno v:
mSphere, Vol 3, Iss 2 (2018)
ABSTRACT Heteroaryldihydropyrimidines (HAPs) are compounds that inhibit hepatitis B virus (HBV) replication by modulating viral capsid assembly. While their biophysical effects on capsid assembly in vitro have been previously studied, the effect of H
Externí odkaz:
https://doaj.org/article/d21fb67e4b2b429c9a5549748928bef6
Autor:
Emily M. Coonrod, Jacob D. Durtschi, Chad VanSant Webb, Karl V. Voelkerding, Attila Kumánovics
Publikováno v:
BioTechniques, Vol 57, Iss 4, Pp 204-207 (2014)
Next-generation sequencing (NGS) of multigene panels performed for genetic clinical diagnostics requires 100% coverage of all targeted genes. In the genetic diagnostics laboratory, coverage gaps are typically filled with Sanger sequencing after NGS d
Externí odkaz:
https://doaj.org/article/f2a902ea98294ff3baded9d56c70302f
Autor:
Rebecca L. Margraf, Qin Zhou, Karl V. Voelkerding, Jacob D. Durtschi, Xiao He, Emily M. Coonrod, Attila Kumánovics, Hemant R. Joshi, Harry R. Hill, Julie Asch
Publikováno v:
Journal of Allergy and Clinical Immunology. 147:1504-1507.e8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebcb648603b2a05f4db94b4b616fe589
https://doi.org/10.1016/j.jaci.2020.09.036
https://doi.org/10.1016/j.jaci.2020.09.036
Autor:
Danielle Groat, Jorge L. Contreras, Bianca Rich, Emily M. Coonrod, Willard H. Dere, Chad VanSant-Webb, Adam P. Bress
Publikováno v:
SSRN Electronic Journal.
The emergence of precision medicine and population health reveals a potential divergence of perspective among experts in these fields. Personalizing diagnostic and therapeutic interventions to address the needs of individual patients raises the spect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e4e232c32021693655bf14c37b7b38d
https://doi.org/10.2139/ssrn.3280424
https://doi.org/10.2139/ssrn.3280424
Autor:
Joshua McElwee, Emily M. Coonrod, Diane J. Nugent, Jolan E. Walter, Lindsey B. Rosen, Jacob D. Durtschi, Krisztian Csomos, Rebecca Baker, Harry R. Hill, Nancy H. Augustine, Yu Nee Lee, Juan C. Ravell, Luigi D. Notarangelo, Attila Kumánovics, David Buchbinder, Sarah K. Browne, Karl V. Voelkerding, Yu Zhang
Publikováno v:
Journal of Clinical Immunology. 35:119-124
Combined immunodeficiency (CID) presents a unique challenge to clinicians. Two patients presented with the prior clinical diagnosis of common variable immunodeficiency (CVID) disorder marked by an early age of presentation, opportunistic infections,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65490add906320e9ccec6bec867feef2
https://doi.org/10.1007/s10875-014-0121-5
https://doi.org/10.1007/s10875-014-0121-5
Autor:
John M. Opitz, Kalyan C. Mallempati, Tara M. Newcomb, Karl V. Voelkerding, Emily M. Coonrod, Rebecca L. Margraf, Attila Kumánovics, John C. Carey, Ben E. Katz, Kathryn J. Swoboda, Holly Zhou, Jacob D. Durtschi
Publikováno v:
American Journal of Medical Genetics Part A. 164:17-28
Three related males presented with a newly recognized x-linked syndrome associated with neurodegeneration, cutaneous abnormalities, and systemic iron overload. Linkage studies demonstrated that they shared a haplotype on Xp21.3-Xp22.2 and exome seque
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b1a2062bcb56b715f0f5d909d7072d2
https://doi.org/10.1002/ajmg.a.36189
https://doi.org/10.1002/ajmg.a.36189
Autor:
Wilfred Wu, Nancy H. Augustine, Harry R. Hill, Emily M. Coonrod, Karl V. Voelkerding, Guy A. Zimmerman, Zechariah F. Franks, Karin Chen, Adi V. Gundlapalli, Andrew S. Weyrich, Rebecca L. Margraf, Jacob D. Durtschi, Perry G. Ridge, Lynn B. Jorde, Attila Kumánovics, John F. Bohnsack, Nahla M. Heikal
Publikováno v:
The American Journal of Human Genetics. 93:812-824
Common variable immunodeficiency (CVID) is a heterogeneous disorder characterized by antibody deficiency, poor humoral response to antigens, and recurrent infections. To investigate the molecular cause of CVID, we carried out exome sequence analysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b57a1b8dab5f9f3d40657ec571c5b894
https://doi.org/10.1016/j.ajhg.2013.09.009
https://doi.org/10.1016/j.ajhg.2013.09.009
Publikováno v:
Archives of Pathology & Laboratory Medicine. 137:415-433
Context.—Advances in sequencing technology with the commercialization of next-generation sequencing (NGS) has substantially increased the feasibility of sequencing human genomes and exomes. Next-generation sequencing has been successfully applied t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a65fafb0e1a3e86f1f97d163b61308e
https://doi.org/10.5858/arpa.2012-0107-ra
https://doi.org/10.5858/arpa.2012-0107-ra
Autor:
Jorge L. Contreras, James Tabery, Willard H. Dere, Emily M. Coonrod, Jeffrey R. Botkin, Leslie P. Francis
Publikováno v:
SSRN Electronic Journal.
Precision medicine is being developed today within a complex landscape of medicine, science, public policy, law, and ethics. In December 2016, the University of Utah School of Medicine, Huntsman Cancer Institute and S.J. Quinney College of Law held t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4148dc4908452903fdc65ac1488bfb05
https://doi.org/10.2139/ssrn.3074961
https://doi.org/10.2139/ssrn.3074961
Publikováno v:
Molecular Pathology in Clinical Practice ISBN: 9783319196732
High-throughput, massively parallel DNA sequencing, more commonly termed “next-generation sequencing,” is an innovation in sequencing that emerged during the past decade. Next-generation sequencing (NGS) is not a single technology, but rather sev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e94c197121dbba1164a274657f54553
https://doi.org/10.1007/978-3-319-19674-9_59
https://doi.org/10.1007/978-3-319-19674-9_59
