Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Rebecca E Steiner"'
Autor:
Rocío Canals, Roy R Chaudhuri, Rebecca E Steiner, Siân V Owen, Natalia Quinones-Olvera, Melita A Gordon, Michael Baym, Michael Ibba, Jay C D Hinton
Publikováno v:
PLoS Pathogens, Vol 15, Iss 9, p e1007948 (2019)
We have used a transposon insertion sequencing (TIS) approach to establish the fitness landscape of the African Salmonella enterica serovar Typhimurium ST313 strain D23580, to complement our previous comparative genomic and functional transcriptomic
Externí odkaz:
https://doaj.org/article/b2d83a68e52043c9a34d009f7e7e3d08
Autor:
A. Gregory Matera, Rebecca E. Steiner, C. Allie Mills, Benjamin D. McMichael, Laura E. Herring, Eric L. Garcia
Publikováno v:
Frontiers in RNA Research, Vol 2 (2024)
IntroductionMolecular chaperones and co-chaperones are highly conserved cellular components that perform a variety of duties related to the proper three-dimensional folding of the proteome. The web of factors that carries out this essential task is c
Externí odkaz:
https://doaj.org/article/9428fafe243740aeb08226fc03eb62c2
Autor:
Eric L. Garcia, Rebecca E. Steiner, Amanda C. Raimer, Laura E. Herring, A. Gregory Matera, Ashlyn M. Spring
Publikováno v:
BMC Biology, Vol 22, Iss 1, Pp 1-18 (2024)
Abstract Background Spinal muscular atrophy (SMA) is a devastating neuromuscular disease caused by hypomorphic loss of function in the survival motor neuron (SMN) protein. SMA presents across a broad spectrum of disease severity. Unfortunately, genet
Externí odkaz:
https://doaj.org/article/36f3f1bc6c894a5db9335516db4577d4
Autor:
Michael Ibba, Ian J Pavelich, Ricardo C. Guerrero-Ferreira, Pooja Srinivas, Christine M. Dunham, Puneet Juneja, Rebecca E. Steiner
Publikováno v:
Nucleic Acids Research
High fidelity during protein synthesis is accomplished by aminoacyl-tRNA synthetases (aaRSs). These enzymes ligate an amino acid to a cognate tRNA and have proofreading and editing capabilities that ensure high fidelity. Phenylalanyl-tRNA synthetase
Autor:
Rebecca E. Steiner, Michael Ibba
Publikováno v:
IUBMB Life. 71:1150-1157
Translation is the most error-prone process in protein synthesis; however, it is important that accuracy is maintained because erroneous translation has been shown to affect all domains of life. Translational quality control is maintained by both pro
Autor:
Melita A. Gordon, Siân V. Owen, Michael Ibba, Roy R. Chaudhuri, Natalia Quinones-Olvera, Jay C. D. Hinton, Rocío Canals, Rebecca E. Steiner
We have used a transposon insertion sequencing (TIS) approach to establish the fitness landscape of the AfricanSalmonella entericaserovar Typhimurium ST313 strain D23580, to complement our previous comparative genomic and functional transcriptomic st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e409836249c1330d0753abf84ce726de
Accurate translation of the genetic code is maintained in part by aminoacyl-tRNA synthetases (aaRS) proofreading mechanisms that ensure correct attachment of a cognate amino acid to a transfer RNA (tRNA). During environmental stress, such as oxidativ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b593a95d72a90cba7ac124f4d71631b
https://europepmc.org/articles/PMC6525502/
https://europepmc.org/articles/PMC6525502/
Autor:
Norikio Salamon, Tyler Mark Pierson, Supreet K. Sahai, John M. Graham, Rebecca E. Steiner, Michael Ibba, Margaret G. Au
Publikováno v:
Annals of clinical and translational neurology, vol 5, iss 9
Annals of Clinical and Translational Neurology, Vol 5, Iss 9, Pp 1128-1133 (2018)
Annals of Clinical and Translational Neurology, Vol 5, Iss 9, Pp 1128-1133 (2018)
Mutations in FARS2, the gene encoding the mitochondrial phenylalanine‐tRNA synthetase (mtPheRS), have been linked to a range of phenotypes including epileptic encephalopathy, developmental delay, and motor dysfunction. We report a 9‐year‐old bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45116ed8de028dbec1f2b3d86d869f60
https://escholarship.org/uc/item/7vd123v5
https://escholarship.org/uc/item/7vd123v5
Autor:
Rebecca E. Steiner, Michael Ibba
Publikováno v:
Biochemistry. 57(18)
Autor:
Supreet K. Sahai, Rebecca E. Steiner, Margaret G. Au, John M. Graham, Noriko Salamon, Michael Ibba, Tyler M. Pierson
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 5, Iss 9, Pp 1128-1133 (2018)
Abstract Mutations in FARS2, the gene encoding the mitochondrial phenylalanine‐tRNA synthetase (mtPheRS), have been linked to a range of phenotypes including epileptic encephalopathy, developmental delay, and motor dysfunction. We report a 9‐year
Externí odkaz:
https://doaj.org/article/43e4647c5fe14af28f7805a0655f19d9