Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Tiana M Scott"'
Autor:
Diana G Calvopina-Chavez, Robyn E Howarth, Audrey K Memmott, Oscar H Pech Gonzalez, Caleb B Hafen, Kyson T Jensen, Alex B Benedict, Jessica D Altman, Brittany S Burnside, Justin S Childs, Samuel W Dallon, Alexa C DeMarco, Kirsten C Flindt, Sarah A Grover, Elizabeth Heninger, Christina S Iverson, Abigail K Johnson, Jack B Lopez, McKay A Meinzer, Brook A Moulder, Rebecca I Moulton, Hyrum S Russell, Tiana M Scott, Yuka Shiobara, Mason D Taylor, Kathryn E Tippets, Kayla M Vainerere, Isabella C Von Wallwitz, Madison Wagley, Megumi S Wiley, Naomi J Young, Joel S Griffitts
Publikováno v:
PLoS ONE, Vol 18, Iss 1, p e0279936 (2023)
The genetic and molecular basis of flagellar motility has been investigated for several decades, with innovative research strategies propelling advances at a steady pace. Furthermore, as the phenomenon is examined in diverse bacteria, new taxon-speci
Externí odkaz:
https://doaj.org/article/1f8ccdcb3272414db56cdce9b7aa4280
Autor:
Tiana M. Scott, Antonio Solis-Leal, J. Brandon Lopez, Richard A. Robison, Bradford K. Berges, Brett E. Pickett
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 12 (2022)
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was first reported in Wuhan, China in December 2019 and caused a global pandemic resulting in millions of deaths and tens of millions of patients positive tests. While studies have shown a
Externí odkaz:
https://doaj.org/article/0d1c676111714d158744c48755ae2925
Publikováno v:
F1000Research, Vol 10 (2021)
Background: Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), the etiological agent of coronavirus disease-2019 (COVID-19), is a novel Betacoronavirus that was first reported in Wuhan, China in December of 2019. The virus has since caused
Externí odkaz:
https://doaj.org/article/593270438fb7483794a24a92a666fbf9
Autor:
Naomi Rapier-Sharman, John Krapohl, Ethan J. Beausoleil, Kennedy T. L. Gifford, Benjamin R. Hinatsu, Curtis S. Hoffmann, Makayla Komer, Tiana M. Scott, Brett E. Pickett
Publikováno v:
Data, Vol 6, Iss 7, p 75 (2021)
Publicly available RNA-sequencing (RNA-seq) data are a rich resource for elucidating the mechanisms of human disease; however, preprocessing these data requires considerable bioinformatic expertise and computational infrastructure. Analyzing multiple
Externí odkaz:
https://doaj.org/article/ab137def0747499bbfa4ef75f295c8e9
Autor:
Lei Wang, Mauricio R. Delgado, Margarita Saenz, Hongzheng Dai, Daryl A. Scott, Kathryn Curry, Bo Yuan, Anh Dang, Wenmiao Zhu, John Lattier, Rui Xiao, Suneeta Madan-Khetarpal, Linyan Meng, Tiana M. Scott, Pilar L. Magoulas, Haley Streff, Jessica Sebastian, Jill A. Rosenfeld, Haowei Du, Seema R. Lalani, James R. Lupski, Jennifer E. Posey, Ronit Marom, Vipulkumar Patel, Weimin Bi, Neil A. Hanchard, Chun-An Chen, Shayna Svihovec, Pengfei Liu, Fan Xia, Christine M. Eng
Publikováno v:
Genet Med
PURPOSE: The BRG1/BRM-associated factor (BAF) complex is a chromatin remodeling complex playing a critical role in gene regulation. Defects in the genes encoding the BAF subunits lead to BAFopathies, a group of neurodevelopmental disorders with exten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05592fed7a1530f5c5f05dde2d8fd381
https://doi.org/10.1016/j.gim.2021.09.017
https://doi.org/10.1016/j.gim.2021.09.017
Autor:
Diana G. Calvopina-Chavez, Robyn E. Howarth, Audrey K. Memmott, Oscar H. Pech Gonzalez, Caleb B. Hafen, Kyson T. Jensen, Alex B. Benedict, Jessica D. Altman, Brittany S. Burnside, Justin S. Childs, Samuel W. Dallon, Alexa C. DeMarco, Kirsten C. Flindt, Sarah A. Grover, Elizabeth Heninger, Christina S. Iverson, Abigail K. Johnson, Jack B. Lopez, McKay A. Meinzer, Brook A. Moulder, Rebecca I. Moulton, Hyrum S. Russell, Tiana M. Scott, Yuka Shiobara, Mason D. Taylor, Kathryn E. Tippets, Kayla M. Vainerere, Isabella C. Von Wallwitz, Madison Wagley, Megumi S. Wiley, Naomi J. Young, Joel S. Griffitts
Publikováno v:
PloS one. 18(1)
The genetic and molecular basis of flagellar motility has been investigated for several decades, with innovative research strategies propelling advances at a steady pace. Furthermore, as the phenomenon is examined in diverse bacteria, new taxon-speci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::468f7f28808ea60bc9e0a71b9325e28d
https://pubmed.ncbi.nlm.nih.gov/36598925
https://pubmed.ncbi.nlm.nih.gov/36598925
Autor:
Erin Conboy, Catherine Nowak, Karen Stals, Elliot S. Stolerman, Brett Bostwick, Tiana M. Scott, Emma Wakeling, Cyril Mignot, Sian Ellard, Brittany C. Michel, Kayla Treat, Berrak Ugur, Jill A. Rosenfeld, Caroline Nava, Sally Ann Lynch, Victoria M. Pratt, Hugo J. Bellen, Aiko Otsubo, Michael F. Wangler, Jennifer Gass, John Herriges, Jennifer B. Phillips, Gaetan Lesca, Bo Yuan, Shinya Yamamoto, Scott Barish, Marjon van Slegtenhorst, Jessica Douglas, Dihong Zhou, Patrick Edery, David R. Murdock, Jeremy Wegner, Jose Camacho, Marie Faoucher, Boris Keren, Camerun Washington, Elena Perenthaler, Kendra Engleman, Francesco Vetrini, Anita Nikoncuk, Alfredo M. Valencia, Daryl A. Scott, Cigall Kadoch, Isabelle Thiffault, Tahsin Stefan Barakat, Chun-An Chen, Lance H. Rodan, Raymond J. Louie, Hongzheng Dai, Alice S. Brooks, Nazar Mashtalir, Monte Westerfield, Nora Shannon
Publikováno v:
Am J Hum Genet
American Journal of Human Genetics, 107(6), 1096-1112. Cell Press
American Journal of Human Genetics, 107(6), 1096-1112. Cell Press
SWI/SNF-related intellectual disability disorders (SSRIDDs) are rare neurodevelopmental disorders characterized by developmental disability, coarse facial features, and fifth digit/nail hypoplasia that are caused by pathogenic variants in genes that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63a2119984a12b57df62077f22734a60
https://doi.org/10.1016/j.ajhg.2020.11.003
https://doi.org/10.1016/j.ajhg.2020.11.003
Autor:
Yoel Gofin, Tianyun Wang, Madelyn A. Gillentine, Tiana M. Scott, Aliska M. Berry, Mahshid S. Azamian, Casie Genetti, Pankaj B. Agrawal, Jonathan Picker, Monica H. Wojcik, Mauricio R. Delgado, Sally A. Lynch, Stephen W. Scherer, Jennifer L. Howe, Carlos A. Bacino, Stephanie DiTroia, Grace E. VanNoy, Anne O'Donnell‐Luria, Seema R. Lalani, William D. Graf, Jill A. Rosenfeld, Evan E. Eichler, Rachel K. Earl, Daryl A. Scott
Publikováno v:
Hum Mutat
PAX5 is a transcription factor associated with abnormal posterior midbrain and cerebellum development in mice. PAX5 is highly loss-of-function intolerant and missense constrained, and has been identified as a candidate gene for autism spectrum disord
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::592fe4dad054b12b1afb2086078722c3
https://pubmed.ncbi.nlm.nih.gov/35094443
https://pubmed.ncbi.nlm.nih.gov/35094443
Autor:
Hernandez P, Gilbert-Dussardier B, Boris Keren, Ai X, Eric L. Bogenschutz, J. Wells, Zeynep Coban-Akdemir, Julia Wynn, Frédéric Frénois, Contreras Htm, Lupski, Andres Hernandez-Garcia, Ropers Hh, Lu Qiao, Florence Petit, Yonath H, Richard S. Maser, Anne-Sophie Jourdain, Delrue M, Giampietro Pf, Clark Rd, Wendy K. Chung, Harrison Brand, McCulley D, Tiana M. Scott, Mauro Longoni, Bult Cj, Patricia K. Donahoe, Barbara R. Pober, Frances A. High, Rebecca Hernan, Maria Loscertales, Yufeng Shen, Daryl A. Scott, Devisme L, Dysart Mj, Daniel G. Calame, Hu H
Congenital diaphragmatic hernia (CDH) is a relatively common and genetically heterogeneous structural birth defect associated with high mortality and morbidity. We describe eight unrelated families with a novel X-linked condition characterized by dia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b87ddad8d2b0da56dd83ec489239f18
https://doi.org/10.1101/2021.07.07.21259278
https://doi.org/10.1101/2021.07.07.21259278
Autor:
Kennedy T. L. Gifford, Makayla Komer, Tiana M. Scott, John Krapohl, Ethan Beausoleil, Brett E. Pickett, Curtis S. Hoffmann, Benjamin R. Hinatsu, Naomi Rapier-Sharman
Publikováno v:
Data, Vol 6, Iss 75, p 75 (2021)
Publicly available RNA-sequencing (RNA-seq) data are a rich resource for elucidating the mechanisms of human disease; however, preprocessing these data requires considerable bioinformatic expertise and computational infrastructure. Analyzing multiple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cbab4bacb2375f6a61fb296d70252a9
https://www.mdpi.com/2306-5729/6/7/75
https://www.mdpi.com/2306-5729/6/7/75