Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Heather Workman"'
Autor:
Meghan Towne, Melissa Holman, Margo Gallegos, Heather Workman, Amybeth Weaver, Heather Zimmermann
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100622- (2023)
Externí odkaz:
https://doaj.org/article/8a912f8f592f4c87afcf8eeef5693426
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 36:447-456
The ability to rapidly and consistently measure aqueous solubility in a preclinical environment is critical to the successful identification of promising discovery compounds. The advantage of an early solubility screen is timely attrition of compound
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a18c0d1a3e065124655109319bcd4b3
https://doi.org/10.1016/j.jpba.2004.07.022
https://doi.org/10.1016/j.jpba.2004.07.022
Publikováno v:
Journal of Chromatography A. 1037:445-454
Capillary electrophoresis affords a simple, automated approach for the measurement of pKa values in the range 2-11 at a throughput of less than 1 h per sample per instrument. Agreement with literature values is usually within 0.20 log units with a pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f7232ba0da459c337cea4deb6ac9c13
https://doi.org/10.1016/j.chroma.2004.02.087
https://doi.org/10.1016/j.chroma.2004.02.087
Autor:
Hannie Kremer, Guy Van Camp, Katherine Lachlan, Isabelle Schrauwen, Thomas L. Casavant, Leticia Olavarrieta, Adam P. DeLuca, Carla Nishimura, Bruce W. Tompkins, Carmelo Morales-Angulo, Fernando Mayo, Patrick L. M. Huygen, Richard J.H. Smith, Ignacio del Castillo, Maarten Van Wesemael, Terry A. Braun, Felipe Moreno, Michael S. Hildebrand, Kyle R. Taylor, Ángeles Mencía, Silvia Modamio-Høybjør, M A Moreno-Pelayo, Matías Morín, A. Eliot Shearer, Corey W. Goodman, Nicole C. Meyer, Heather Workman
Publikováno v:
Human Mutation, 32, 7, pp. 825-34
Human mutation
Human Mutation, 32, 825-34
Human mutation
Human Mutation, 32, 825-34
Item does not contain fulltext The prevalence of DFNA8/DFNA12 (DFNA8/12), a type of autosomal dominant nonsyndromic hearing loss (ADNSHL), is unknown as comprehensive population-based genetic screening has not been conducted. We therefore completed u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::deeb3ee61d67b7c48a85bd11d678726d
https://hdl.handle.net/2066/96779
https://hdl.handle.net/2066/96779
Autor:
Lee Ann K. Damian, Todd Leander Hicks, Glenda McDonald Christian, Elissa Berner, Mark D. Farley, Heather Workman, Candace F. Zickler, Eileen F. Kasten, Stephen P. Schmidt, Manuel Freeman
Publikováno v:
Current problems in pediatric and adolescent health care. 38(5)
u u m l t f F o b A rcheological data and ancient historical records document the presence of cleft lip and palate and even attempts to surgically epair the cleft defect. Current estimates suggest hat as many as 6500 babies are born each year in he U
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::026d594125b70e78a971aff4363e2bf7
https://pubmed.ncbi.nlm.nih.gov/18423348
https://pubmed.ncbi.nlm.nih.gov/18423348