Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Carolyn R. Vitek"'
Autor:
Matheus V. M. B. Wilke, Eric W. Klee, Radhika Dhamija, Fernando C. Fervenza, Brittany Thomas, Nelson Leung, Marie C. Hogan, Megan M. Hager, Kayla J. Kolbert, Jennifer L. Kemppainen, Elle C. Loftus, Katie M. Leitzen, Carolyn R. Vitek, Tammy McAllister, Konstantinos N. Lazaridis, Filippo Pinto e Vairo
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-9 (2024)
Abstract Background Though next-generation sequencing (NGS) tests like exome sequencing (ES), genome sequencing (GS), and panels derived from exome and genome data (EGBP) are effective for rare diseases, the ideal diagnostic approach is debated. Limi
Externí odkaz:
https://doaj.org/article/972503d913ba4e5d89b1ba27347069e3
Autor:
Eric T, Matey, Ashley Kate, Ragan, Lance J, Oyen, Carolyn R, Vitek, Stacy L, Aoudia, Ahmed K, Ragab, Kelliann C, Fee-Schroeder, John L, Black, Ann M, Moyer, Wayne T, Nicholson, Sofia, Shrestha, Tammy M, McAllister, Jason P, Sinnwell, Stephanie S, Faubion, Konstantinos N, Lazaridis
Publikováno v:
The pharmacogenomics journal. 22(1)
The Pharmacogenomics (PGx) Profile Service was a proof-of-concept project to implement PGx in patient care at Mayo Clinic.Eighty-two healthy individuals aged 18 and older underwent genotyping of CYP1A2, CYP2C9, CYP2C19, CYP2D6, CYP3A4, CYP3A5, SLCO1B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::69377d18c2b770482dab3c3d8a1e78bf
https://pubmed.ncbi.nlm.nih.gov/34671112
https://pubmed.ncbi.nlm.nih.gov/34671112