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of 5
pro vyhledávání: '"Traci Toy"'
Autor:
Marc A Harper, Zugen Chen, Traci Toy, Iara M P Machado, Stanley F Nelson, James C Liao, Christopher J Lee
Publikováno v:
PLoS ONE, Vol 6, Iss 2, p e16517 (2011)
Random mutagenesis and phenotype screening provide a powerful method for dissecting microbial functions, but their results can be laborious to analyze experimentally. Each mutant strain may contain 50-100 random mutations, necessitating extensive fun
Externí odkaz:
https://doaj.org/article/aaf6e814031f4c118da4a417748398bf
Autor:
Shanna L. White, Thomas D. Lee, Traci Toy, Judith E. Carroll, Lilian Polsky, Beatriz Campo Fernandez, Alejandra Davila, Donald B. Kohn, Vivian Y. Chang
Publikováno v:
Blood advances, vol 6, iss 21
Autologous stem cell transplant with gene therapy (ASCT-GT) provides curative therapy while reducing pretransplant immune-suppressive conditioning and eliminating posttransplant immune suppression. Clonal hematopoiesis of indeterminate potential (CHI
Autor:
Sureni V, Mullegama, Michael O, Alberti, Cora, Au, Yan, Li, Traci, Toy, Vanina, Tomasian, Rena R, Xian
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1897
Nucleic acid isolation is often the starting point for all downstream experiments in biomedical research. It is therefore the most crucial step in any molecular technique. DNA and RNA extraction follow protocols with standardized reagents, many of wh
Autor:
Traci Toy, Zugen Chen, Iara M. P. Machado, Marc Harper, James C. Liao, Stanley F. Nelson, Christopher Lee
Publikováno v:
PLoS ONE, Vol 6, Iss 2, p e16517 (2011)
PLoS ONE
PLoS ONE
Random mutagenesis and phenotype screening provide a powerful method for dissecting microbial functions, but their results can be laborious to analyze experimentally. Each mutant strain may contain 50–100 random mutations, necessitating extensive f
Autor:
Brent L. Fogel, Stanley F. Nelson, Sibel Kantarci, Traci Toy, Samuel P. Strom, Kingshuk Das, Perry B. Shieh, Christina G.S. Palmer, Hane Lee, Fabiola Quintero-Rivera, Derek Wong, Michelle Fox, Vivian Y. Chang, Joshua L. Deignan, Wayne W. Grody, Katrina M. Dipple, Michael Yourshaw, Naghmeh Dorrani, Julian A. Martinez-Agosto, Bret Harry, Eric Vilain
Publikováno v:
JAMA, vol 312, iss 18
ImportanceClinical exome sequencing (CES) is rapidly becoming a common molecular diagnostic test for individuals with rare genetic disorders.ObjectiveTo report on initial clinical indications for CES referrals and molecular diagnostic rates for diffe