Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Stuart K. Archer"'
Autor:
Hieu T. Nim, Louis Dang, Harshini Thiyagarajah, Daniel Bakopoulos, Michael See, Natalie Charitakis, Tennille Sibbritt, Michael P. Eichenlaub, Stuart K. Archer, Nicolas Fossat, Richard E. Burke, Patrick P. L. Tam, Coral G. Warr, Travis K. Johnson, Mirana Ramialison
Publikováno v:
Genome Biology, Vol 22, Iss 1, Pp 1-21 (2021)
Abstract Background Congenital heart diseases are the major cause of death in newborns, but the genetic etiology of this developmental disorder is not fully known. The conventional approach to identify the disease-causing genes focuses on screening g
Externí odkaz:
https://doaj.org/article/b9ab3ed0c9654b1f902b20578e0de93f
Autor:
Julia C. Wilmanns, Raghav Pandey, Olivia Hon, Anjana Chandran, Jan M. Schilling, Elvira Forte, Qizhu Wu, Gael Cagnone, Preeti Bais, Vivek Philip, David Coleman, Heidi Kocalis, Stuart K. Archer, James T. Pearson, Mirana Ramialison, Joerg Heineke, Hemal H. Patel, Nadia A. Rosenthal, Milena B. Furtado, Mauro W. Costa
Publikováno v:
Molecular Metabolism, Vol 20, Iss , Pp 102-114 (2019)
Objective: Congenital heart disease (CHD) is the most frequent birth defect worldwide. The number of adult patients with CHD, now referred to as ACHD, is increasing with improved surgical and treatment interventions. However the mechanisms whereby AC
Externí odkaz:
https://doaj.org/article/54e4286b7710480bb545986201e5fddc
Autor:
Rebekah M Engel, Thierry Jardé, Karen Oliva, Genevieve Kerr, Wing Hei Chan, Sara Hlavca, David Nickless, Stuart K Archer, Raymond Yap, Pravin Ranchod, Stephen Bell, Ann Niap, Christine Koulis, Ashley Chong, Simon Wilkins, Trevor C Dale, Andrew J Hollins, Paul J McMurrick, Helen E Abud
Publikováno v:
Journal of Gastroenterology and Hepatology. 37:898-907
Background and Aim\ud Colorectal cancer (CRC) is the second leading cause of cancer death worldwide. To improve outcomes for these patients, we need to develop new treatment strategies. Personalized cancer medicine, where patients are treated based o
Autor:
Madara Ratnadiwakara, Stuart K Archer, Craig I Dent, Igor Ruiz De Los Mozos, Traude H Beilharz, Anja S Knaupp, Christian M Nefzger, Jose M Polo, Minna-Liisa Anko
Publikováno v:
eLife, Vol 7 (2018)
The establishment and maintenance of pluripotency depend on precise coordination of gene expression. We establish serine-arginine-rich splicing factor 3 (SRSF3) as an essential regulator of RNAs encoding key components of the mouse pluripotency circu
Externí odkaz:
https://doaj.org/article/f524e3ef382f48c884f4c109fc9e5eb6
Autor:
Denis V. Korneev, Moira K O'Bryan, Cody Oliveira, Jeremy J. Barr, Faye C. Morris, Michael Trim, Stuart K. Archer, Trevor Lithgow, Luisa Kielty, Xenia Kostoulias, Dinesh Subedi, Fernando Gordillo Altamirano, Anton Y. Peleg, Ruzeen Patwa, John H. Forsyth
Publikováno v:
Nature Microbiology. 6:157-161
We characterized two bacteriophages, ΦFG02 and ΦCO01, against clinical isolates of Acinetobacter baumannii and established that the bacterial capsule is the receptor for these phages. Phage-resistant mutants harboured loss-of-function mutations in
Autor:
Queenie Wing-Lei Wong, Candida Vaz, Qian Yi Lee, Tian Yun Zhao, Raymond Luo, Stuart K Archer, Thomas Preiss, Vivek Tanavde, Leah A Vardy
Publikováno v:
PLoS ONE, Vol 11, Iss 1, p e0143235 (2016)
The presence of multiple variants for many mRNAs is a major contributor to protein diversity. The processing of these variants is tightly controlled in a cell-type specific manner and has a significant impact on gene expression control. Here we inves
Externí odkaz:
https://doaj.org/article/195e17d0725547809eef156eb1085c0b
Publikováno v:
Cell Death Differ
Splicing introns from precursor-messenger RNA (pre-mRNA) transcripts is essential for translating functional proteins. Here, we report that the previously uncharacterized Caenorhabditis elegans protein MOG-7, acts as a pre-mRNA splicing factor. Deple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1b079fe45ab9fcf0386935e12a4dca5
https://doi.org/10.1101/2021.06.04.447173
https://doi.org/10.1101/2021.06.04.447173
Autor:
Shuo Li, Hideaki Morita, Damian F. J. Purcell, Cezmi A. Akdis, Kirstin Jansen, Tadech Boonpiyathad, Stuart K. Archer, Keisuke Orimo, Mimi L.K. Tang, Ge Tan, Magdalena Plebanski, Milena Sokolowska, Lennart Opitz
Publikováno v:
Journal of Allergy and Clinical Immunology. 143:2321-2325
Autor:
Nadia Rosenthal, Milena B. Furtado, Vivek M. Philip, Stuart K. Archer, Jan M. Schilling, Anjana Chandran, Raghav Pandey, Hemal H. Patel, Julia C. Wilmanns, Gael Cagnone, Qizhu Wu, James T. Pearson, Joerg Heineke, Olivia J Hon, Preeti Bais, Mauro W. Costa, Heidi Kocalis, Mirana Ramialison, Elvira Forte, David Coleman
Publikováno v:
Molecular Metabolism, Vol 20, Iss, Pp 102-114 (2019)
Molecular Metabolism
Molecular Metabolism
Objective Congenital heart disease (CHD) is the most frequent birth defect worldwide. The number of adult patients with CHD, now referred to as ACHD, is increasing with improved surgical and treatment interventions. However the mechanisms whereby ACH
Autor:
Hieu T. Nim, Louis Dang, Harshini Thiyagarajah, Daniel Bakopoulos, Michael See, Natalie Charitakis, Tennille Sibbritt, Michael P. Eichenlaub, Stuart K. Archer, Nicolas Fossat, Richard E. Burke, Patrick P. L. Tam, Coral G. Warr, Travis K. Johnson, Mirana Ramialison
Publikováno v:
Genome Biology
Genome Biology, Vol 22, Iss 1, Pp 1-21 (2021)
Genome Biology, Vol 22, Iss 1, Pp 1-21 (2021)
Background Congenital heart diseases are the major cause of death in newborns, but the genetic etiology of this developmental disorder is not fully known. The conventional approach to identify the disease-causing genes focuses on screening genes that