Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Santosh S Atanur"'
Autor:
Michelle D Johnson, Michael Mueller, Martyna Adamowicz-Brice, Melissa J Collins, Pascal Gellert, Klio Maratou, Prashant K Srivastava, Maxime Rotival, Shahena Butt, Laurence Game, Santosh S Atanur, Nicholas Silver, Penny J Norsworthy, Sarah R Langley, Enrico Petretto, Michal Pravenec, Timothy J Aitman
Publikováno v:
PLoS Genetics, Vol 10, Iss 12, p e1004813 (2014)
Epigenetic marks such as cytosine methylation are important determinants of cellular and whole-body phenotypes. However, the extent of, and reasons for inter-individual differences in cytosine methylation, and their association with phenotypic variat
Externí odkaz:
https://doaj.org/article/05edfc5efe3442ebbf5bdb0c4e3f8e9f
Autor:
Samuel A. Watson, James Duff, Ifigeneia Bardi, Magdalena Zabielska, Santosh S. Atanur, Richard J. Jabbour, André Simon, Alejandra Tomas, Ryszard T. Smolenski, Sian E. Harding, Filippo Perbellini, Cesare M. Terracciano
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-15 (2019)
Cultured adult cardiac tissue undergoes rapid dedifferentiation, which hinders chronic in vitro studies. Here the authors investigate biomimetic electromechanical stimulation of adult myocardial slices applying different preload conditions, identifyi
Externí odkaz:
https://doaj.org/article/3121859689094ac79bf739761e7891fe
Autor:
Alistair T. Pagnamenta, Jing Yu, Tracey A. Willis, Mona Hashim, Eleanor G. Seaby, Susan Walker, Jiaqi Xian, Emily W. Y. Cheng, Ana Lisa Taylor Tavares, Francesca Forzano, Helen Cox, Tabib Dabir, Angela F. Brady, Neeti Ghali, Santosh S. Atanur, Sarah Ennis, Diana Baralle, Jenny C. Taylor
Publikováno v:
Human Mutation.
SRRM2 encodes a splicing factor recently implicated in developmental disorders due to a statistical enrichment of de novo mutations. Using data from the 100,000 Genomes Project, four unrelated individuals with intellectual disability (ID) were identi
Autor:
Jane A. Mitchell, Ricky Vaja, Blerina Ahmetaj-Shala, Nicholas S. Kirkby, Peter M. George, Santosh S. Atanur
Publikováno v:
JACC: Basic to Translational Science
Objectives: To obtain mechanistic insight into COVID-19 within a cardiovascular setting. Background: Thrombosis and vascular dysfunction are part of the complex pathology seen in severe COVID-19 and advancing age is the most significant risk factor.
Autor:
Špela Mikec, Martin Šimon, Nicholas M. Morton, Santosh S. Atanur, Janez Konc, Peter Dovč, Simon Horvat, Tanja Kunej
Publikováno v:
Molecular biology reports. 49(6)
Adipose tissue hypoxia and members of the hypoxia-inducible factor alpha (HIFA) are involved in development of obesity. However, the mechanism and functions of HIF3A, one of three HIFA paralogs, in fat deposition have not been sufficiently studied.In
Autor:
Sonal Dahale, Sebastiaan van Heesch, Jorge Ruiz-Orera, Michal Pravenec, Norbert Hubner, Jan Silhavy, Santosh S. Atanur
The role of alternative promoter usage in tissue specific gene expression has been well established, however, its role in complex diseases is poorly understood. We performed cap analysis of gene expression (CAGE) tag sequencing from the left ventricl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d0f7cd53ae4715fee8857d733f4d111
https://doi.org/10.1101/2021.08.28.458014
https://doi.org/10.1101/2021.08.28.458014
Autor:
Ricky-Kumar Vaja, Peter M. George, Santosh S. Atanur, Jane A. Mitchell, Nicholas S. Kirkby, Blerina Ahmetaj-Shala
COVID-19, caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has rapidly spread throughout the world with unprecedented global healthcare and socio-economic consequences. There is now an established secondary syndrome of COVID-19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb5dc683ac123a23738098e7e81e2381
https://doi.org/10.1101/2020.06.23.165324
https://doi.org/10.1101/2020.06.23.165324
Autor:
Timothy J. Aitman, Margarita Moreno, Oliver Staehlin, Bianca Jupp, Stephanie Taylor, Silvia Pitzoi, Wolfgang H. Sommer, Santosh S. Atanur, Jeffrey W. Dalley, Emma S J Robinson, Rainer Spanagel, Prashant K. Srivastava, Enrico Petretto, Gunter Schumann, Norbert Hubner, Adam C. Mar, Trevor W. Robbins, Barry J. Everitt, YP Oliver, Emily R Jordan, Kathrin Saar
Publikováno v:
Jupp, B, Pitzoi, S, Petretto, E, Mar, A C, Oliver, Y P, Jordan, E R, Taylor, S, Atanur, S, Srivastava, P K, Saar, K, Hübner, N, Sommer, W, Staehlin, O, Spanagel, R, Robinson, E S, Schumann, G, Moreno, M, Everitt, B J, Robbins, T W, Aitman, T J & Dalley, J W 2020, ' Impulsivity is a heritable trait in rodents and associated with a novel quantitative trait locus on chromosome 1 ', Scientific Reports . https://doi.org/10.1038/s41598-020-63646-9
Scientific Reports, Vol 10, Iss 1, Pp 1-13 (2020)
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-13 (2020)
Scientific Reports
Impulsivity describes the tendency to act prematurely without appropriate foresight and is symptomatic of a number of neuropsychiatric disorders. Although a number of genes for impulsivity have been identified, no study to date has carried out an unb
Autor:
Sonal Dahale, Jorge Ruiz-Orera, Jan Silhavy, Norbert Hübner, Sebastiaan van Heesch, Michal Pravenec, Santosh S Atanur
Publikováno v:
Life Science Alliance
Cap analysis of gene expression (CAGE) tag sequencing from left ventricles of a rat model of hypertension identifies genes that use alternative promoters in a disease condition.
The role of alternative promoter usage in tissue-specific gene expr
The role of alternative promoter usage in tissue-specific gene expr
Autor:
Cesare M. Terracciano, Ryszard T. Smolenski, James Duff, Richard J. Jabbour, Santosh S. Atanur, Magdalena A. Zabielska, Samuel A. Watson, Filippo Perbellini, Ifigeneia Bardi, Sian E. Harding
Publikováno v:
European Heart Journal. 39