Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Andrew J. Catomeris"'
Autor:
Allison N Dammann, Anna B Chamby, Andrew J Catomeris, Kyle M Davidson, Hervé Tettelin, Jan-Peter van Pijkeren, Kathyayini P Gopalakrishna, Mary F Keith, Jordan L Elder, Adam J Ratner, Thomas A Hooven
Publikováno v:
PLoS Pathogens, Vol 17, Iss 3, p e1009116 (2021)
Streptococcus agalactiae (group B Streptococcus; GBS) remains a dominant cause of serious neonatal infections. One aspect of GBS that renders it particularly virulent during the perinatal period is its ability to invade the chorioamniotic membranes a
Externí odkaz:
https://doaj.org/article/3493e7f3e0ba42799bba78ade439f8e2
Autor:
Andrew J, Catomeris, Brian G, Ballios, Riccardo, Sangermano, Naomi E, Wagner, Jason I, Comander, Eric A, Pierce, Emily M, Place, Kinga M, Bujakowska, Rachel M, Huckfeldt
Publikováno v:
Ophthalmic Genet
BACKGROUND: Variants in RCBTB1 were recently described to cause a retinal dystrophy with only eight families described to date and a predominant phenotype of macular atrophy and peripheral reticular degeneration. Here, we further evaluate the genotyp
Autor:
Andrew J. Catomeris, Brian G. Ballios, Riccardo Sangermano, Naomi E. Wagner, Jason I. Comander, Eric A. Pierce, Emily M. Place, Kinga M. Bujakowska, Rachel M. Huckfeldt
Publikováno v:
Ophthalmic Genetics. 43:332-339
Autor:
Brian S. Cole, Eglé Galdikaité-Braziené, Katherine R. Chao, Sherwin Nassiri, Broad Cmg, Kinga M. Bujakowska, Joey Pagliarulo, Matthew Maher, Stephanie DiTroia, Seraphim Himes, Naomi E Wagner, Andrew J. Catomeris, Eric A. Pierce, Charles Ferguson, Erin Zampaglione, Eleina M. England, Emily Place
Publikováno v:
Genet Med
PurposeIn Mendelian disease diagnosis, variant analysis is a repetitive, error-prone, and time-consuming process. To address this, we have developed the Mendelian Analysis Toolkit (MATK), a configurable automated variant ranking program.MethodsMATK a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8ee69f52576d89554bcab5aaf189345
https://doi.org/10.1101/2021.04.09.21255188
https://doi.org/10.1101/2021.04.09.21255188
Autor:
Allison N. Dammann, Mary F. Keith, Jan-Peter van Pijkeren, Andrew J. Catomeris, Adam J. Ratner, Thomas A. Hooven, Anna B. Chamby, Hervé Tettelin, Jordan L. Elder, Kyle M. Davidson, Kathyayini P. Gopalakrishna
Publikováno v:
PLoS Pathogens
PLoS Pathogens, Vol 17, Iss 3, p e1009116 (2021)
PLoS Pathogens, Vol 17, Iss 3, p e1009116 (2021)
Streptococcus agalactiae (group B Streptococcus; GBS) remains a dominant cause of serious neonatal infections. One aspect of GBS that renders it particularly virulent during the perinatal period is its ability to invade the chorioamniotic membranes a
Autor:
Sean C. Daugherty, Thomas A. Hooven, Maryam Bonakdar, Sandra Ott, Hervé Tettelin, Ivette Santana-Cruz, Andrew J. Catomeris, Adam J. Ratner, Luke J. Tallon
Publikováno v:
Infection and Immunity
Streptococcus agalactiae (group B Streptococcus [GBS]) causes serious infections in neonates. We previously reported a transposon sequencing (Tn-seq) system for performing genomewide assessment of gene fitness in GBS. In order to identify molecular m
Autor:
Luke J. Tallon, Duncan J. Maskell, Hervé Tettelin, Sandra Ott, Andrew J. Catomeris, Tara M. Randis, Adam J. Ratner, Leor H. Akabas, Thomas A. Hooven, Ivette Santana-Cruz, Sarah Peters
Publikováno v:
BMC Genomics
Background Next-generation sequencing of transposon-genome junctions from a saturated bacterial mutant library (Tn-seq) is a powerful tool that permits genome-wide determination of the contribution of genes to fitness of the organism under a wide ran