Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Steven Monger"'
Autor:
Ingrid Tarr, Stephanie Hesselson, Siiri E. Iismaa, Emma Rath, Steven Monger, Michael Troup, Ketan Mishra, Claire M.Y. Wong, Pei-Chen Hsu, Keerat Junday, David T. Humphreys, David Adlam, Tom R. Webb, Anna A. Baranowska-Clarke, Stephen E. Hamby, Keren J. Carss, Nilesh J. Samani, Monique Bax, Lucy McGrath-Cadell, Jason C. Kovacic, Sally L. Dunwoodie, Diane Fatkin, David W.M. Muller, Robert M. Graham, Eleni Giannoulatou
Publikováno v:
Circulation. Genomic and precision medicine. 15(4)
Background: Spontaneous coronary artery dissection (SCAD) is a cause of acute coronary syndrome that predominantly affects women. Its pathophysiology remains unclear but connective tissue disorders (CTD) and other vasculopathies have been observed in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa986447b04b2df8b621df51938acdb2
https://pubmed.ncbi.nlm.nih.gov/35980654
https://pubmed.ncbi.nlm.nih.gov/35980654
Autor:
Matthew S. Edwards, David S. Winlaw, Dimuthu Alankarage, Kavitha R Iyer, Bernadette C Hanna, Steven Monger, Gavin Chapman, Victoria C. O'Reilly, Justin O. Szot, Michelle Yam, Annabelle Enriquez, Julie L. M. Moreau, Ella M M A Martin, Sally L. Dunwoodie, Duncan B. Sparrow, Helen E. Ritchie, Joelene A Greasby, Eleni Giannoulatou, Hongjun Shi, Gillian M. Blue, Eddie I P, Stuart M. Grieve
Publikováno v:
Hum Mol Genet
Congenital heart disease (CHD) is the most common birth defect and brings with it significant mortality and morbidity. The application of exome and genome sequencing has greatly improved the rate of genetic diagnosis for CHD but the cause in the majo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0f4aedb11c92ae713b9b813716d7b59
https://doi.org/10.1093/hmg/ddz270
https://doi.org/10.1093/hmg/ddz270
Autor:
Martin Chivers, Jana Kralovicova, Igor Vorechovsky, Ivana Borovska, Steven Monger, Eleni Giannoulatou, Maria Alvarez
Publikováno v:
RNA Biology
article-version (VoR) Version of Record
article-version (VoR) Version of Record
Transposed elements (TEs) have dramatically shaped evolution of the exon-intron structure and significantly contributed to morbidity, but how recent TE invasions into older TEs cooperate in generating new coding sequences is poorly understood. Employ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86f5080b66e37e7a0e2a24de4660136e
https://eprints.soton.ac.uk/444241/
https://eprints.soton.ac.uk/444241/
Publikováno v:
Bioinformatics. 35:4405-4407
Motivation In silico prediction tools are essential for identifying variants which create or disrupt cis-splicing motifs. However, there are limited options for genome-scale discovery of splice-altering variants. Results We have developed Spliceogen,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2c5ed05233f12677e53f09b2884ce20
https://doi.org/10.1093/bioinformatics/btz263
https://doi.org/10.1093/bioinformatics/btz263