Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Lavinia Gordon"'
Autor:
Natalie J. Hannan, Owen Stock, Rebecca Spencer, Clare Whitehead, Anna L. David, Katie Groom, Scott Petersen, Amanda Henry, Joanne M. Said, Sean Seeho, Stefan C. Kane, Lavinia Gordon, Sally Beard, Kantaraja Chindera, Smita Karegodar, Richard Hiscock, Natasha Pritchard, Tu’uhevaha J. Kaitu’u-Lino, Susan P. Walker, Stephen Tong
Publikováno v:
BMC Medicine, Vol 18, Iss 1, Pp 1-16 (2020)
Abstract Background Fetuses affected by placental insufficiency do not receive adequate nutrients and oxygenation, become growth restricted and acidemic, and can demise. Preterm fetal growth restriction is a severe form of placental insufficiency wit
Externí odkaz:
https://doaj.org/article/5038f8b3592448bf89b3883d5313043b
Autor:
Roger Huerlimann, Jeff A Cowley, Nicholas M Wade, Yinan Wang, Naga Kasinadhuni, Chon-Kit Kenneth Chan, Jafar S Jabbari, Kirby Siemering, Lavinia Gordon, Matthew Tinning, Juan D Montenegro, Gregory E Maes, Melony J Sellars, Greg J Coman, Sean McWilliam, Kyall R Zenger, Mehar S Khatkar, Herman W Raadsma, Dallas Donovan, Gopala Krishna, Dean R Jerry
Publikováno v:
G3: Genes, Genomes, Genetics (2022)
AbstractShrimp are a valuable aquaculture species globally; however, disease remains a major hindrance to shrimp aquaculture sustainability and growth. Mechanisms mediated by endogenous viral elements have been proposed as a means by which shrimp tha
Externí odkaz:
https://doaj.org/article/7dba95ad77444360bd23699adb0e10f5
Autor:
Roger Huerlimann, Nicholas M. Wade, Lavinia Gordon, Juan D. Montenegro, Jake Goodall, Sean McWilliam, Matthew Tinning, Kirby Siemering, Erika Giardina, Dallas Donovan, Melony J. Sellars, Jeff A. Cowley, Kelly Condon, Greg J. Coman, Mehar S. Khatkar, Herman W. Raadsma, Gregory E. Maes, Kyall R. Zenger, Dean R. Jerry
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-2 (2022)
Externí odkaz:
https://doaj.org/article/ebbda40fbe4b4da39f6d7baad75f8405
Autor:
Bhupinder Pal, Yunshun Chen, François Vaillant, Paul Jamieson, Lavinia Gordon, Anne C. Rios, Stephen Wilcox, Naiyang Fu, Kevin He Liu, Felicity C. Jackling, Melissa J. Davis, Geoffrey J. Lindeman, Gordon K. Smyth, Jane E. Visvader
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-14 (2017)
The mammary epithelium comprises two cell lineages but the heterogeneity amongst these during development is unclear. Here, the authors report single-cell RNA sequencing of the mouse mammary epithelium at four developmental stages, revealing diversit
Externí odkaz:
https://doaj.org/article/dca0603f7480455abce0a865cd2cb6d0
Autor:
Kai-Leng Tan, King-Hwa Ling, Chelsee A. Hewitt, Pike-See Cheah, Ken Simpson, Lavinia Gordon, Melanie A. Pritchard, Gordon K. Smyth, Tim Thomas, Hamish S. Scott
Publikováno v:
Genomics Data, Vol 2, Iss C, Pp 314-317 (2014)
The Ts1Cje mouse model of Down syndrome (DS) has partial trisomy of mouse chromosome 16 (MMU16), which is syntenic to human chromosome 21 (HSA21). It develops various neuropathological features demonstrated by DS patients such as reduced cerebellar v
Externí odkaz:
https://doaj.org/article/9212847e836c422097926b54962cdfd3
Autor:
Simon Ghaly, Nadeem O. Kaakoush, Frances Lloyd, Lavinia Gordon, Cynthia Forest, Ian C. Lawrance, Prue H. Hart
Publikováno v:
Nutrients, Vol 10, Iss 8, p 1069 (2018)
Reduced sunlight exposure has been associated with an increased incidence of Crohn’s disease and ulcerative colitis. The effect of ultraviolet radiation (UVR) on the faecal microbiome and susceptibility to colitis has not been explored. C57Bl/6 fem
Externí odkaz:
https://doaj.org/article/d9a2eb30e5854687811bf7dde85063e0
Autor:
Anissa M Jabbour, Lavinia Gordon, Carmel P Daunt, Benjamin D Green, Chung H Kok, Richard D'Andrea, Paul G Ekert
Publikováno v:
PLoS ONE, Vol 7, Iss 2, p e31428 (2012)
p53 is critical in the normal response to a variety of cellular stresses including DNA damage and loss of p53 function is a common feature of many cancers. In hematological malignancies, p53 deletion is less common than in solid malignancies but is a
Externí odkaz:
https://doaj.org/article/a750fb97acc74931ad4395ca8d2afb30
Copy number variation in patients with disorders of sex development due to 46,XY gonadal dysgenesis.
Autor:
Stefan White, Thomas Ohnesorg, Amanda Notini, Kelly Roeszler, Jacqueline Hewitt, Hinda Daggag, Craig Smith, Erin Turbitt, Sonja Gustin, Jocelyn van den Bergen, Denise Miles, Patrick Western, Valerie Arboleda, Valerie Schumacher, Lavinia Gordon, Katrina Bell, Henrik Bengtsson, Terry Speed, John Hutson, Garry Warne, Vincent Harley, Peter Koopman, Eric Vilain, Andrew Sinclair
Publikováno v:
PLoS ONE, Vol 6, Iss 3, p e17793 (2011)
Disorders of sex development (DSD), ranging in severity from mild genital abnormalities to complete sex reversal, represent a major concern for patients and their families. DSD are often due to disruption of the genetic programs that regulate gonad d
Externí odkaz:
https://doaj.org/article/8c96c6570dbc4f25bd07b98733f2c64e
Autor:
Novita Puspasari, Simone M Rowley, Lavinia Gordon, Paul J Lockhart, Panos A Ioannou, Martin B Delatycki, Joseph P Sarsero
Publikováno v:
PLoS ONE, Vol 6, Iss 7, p e22001 (2011)
BACKGROUND: Friedreich ataxia (FRDA) is the most common form of hereditary ataxia characterized by the presence of a GAA trinucleotide repeat expansion within the first intron of the FXN gene. The expansion inhibits FXN gene expression resulting in a
Externí odkaz:
https://doaj.org/article/7e18d190ce6f465fa8bda9c0ff9b9657
Autor:
Elena Savva, Ivan Macciocca, Tiong Yang Tan, Victor S Lin, Ivone U.S. Leong, Mark J. Caulfield, Richard H. Scott, Ana Lisa Taylor Tavares, Crystle Lee, Kevin Savage, Kathryn N. North, Olivia Niblock, Christopher Boustred, Sarah Leigh, Arina Puzriakova, Ellen M. McDonagh, Alison Yeung, William Bellamy, Catherine E. Snow, Ellen R.A. Thomas, Antonio Rueda-Martin, Paul De Fazio, Bryony A. Thompson, Louise C. Daugherty, Helen K. Brittain, Eleanor Williams, Chirag Patel, Oliver Hofmann, Ain Roesley, Zornitza Stark, Jane Deller, Zandra C. Deans, Susan M. White, Rebecca E. Foulger, Lilian Downie, Sue Hill, Augusto Rendon, Sebastian Lunke, Meriel McEntagart, Oleg Gerasimenko, Lavinia Gordon, Roman Valls
Publikováno v:
Am J Hum Genet
Clinical validity assessments of gene-disease associations underpin analysis and reporting in diagnostic genomics, and yet wide variability exists in practice, particularly in use of these assessments for virtual gene panel design and maintenance. Ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0a7bb1d7c13503703eaacf84893bd36
https://doi.org/10.1016/j.ajhg.2021.06.020
https://doi.org/10.1016/j.ajhg.2021.06.020