Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Julia Petschnigg"'
Autor:
Christopher J. Minnis, StJohn Townsend, Julia Petschnigg, Elisa Tinelli, Jürg Bähler, Claire Russell, Sara E. Mole
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Abstract Juvenile CLN3 disease is a recessively inherited paediatric neurodegenerative disorder, with most patients homozygous for a 1-kb intragenic deletion in CLN3. The btn1 gene is the Schizosaccharomyces pombe orthologue of CLN3. Here, we have ex
Externí odkaz:
https://doaj.org/article/6527e4bac2b54420a484033fbe621105
Autor:
Christopher J. Minnis, StJohn Townsend, Julia Petschnigg, Elisa Tinelli, Jürg Bähler, Claire Russell, Sara E. Mole
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-3 (2021)
Externí odkaz:
https://doaj.org/article/96da108b24f34e5ca18dd0cb24c426b5
Autor:
Noël Malod-Dognin, Julia Petschnigg, Sam F. L. Windels, Janez Povh, Harry Hemingway, Robin Ketteler, Nataša Pržulj
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-13 (2019)
Integration of omics data remains a challenge. Here, the authors introduce iCell, a framework to integrate tissue-specific protein–protein interaction, co-expression and genetic interaction data, enabling identification of the most rewired genes in
Externí odkaz:
https://doaj.org/article/f16ba5ea82984765ad79c0f292ce025e
Autor:
Julia Petschnigg, Robin Ketteler
Publikováno v:
Bio-Protocol, Vol 7, Iss 17 (2017)
High-content screening is a useful tool to understand complex cellular processes and to identify genes, proteins or small molecule compounds that modulate such pathways. High-content assays monitor the function of a protein or pathway by visualizing
Externí odkaz:
https://doaj.org/article/d148797adf2f4c35abdf3e5ee15ddccc
Autor:
Noël Malod-Dognin, Julia Petschnigg, Sam F. L. Windels, Janez Povh, Harry Hemingway, Robin Ketteler, Nataša Pržulj
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-1 (2019)
The original version of this Article contained an error in the spelling of the author Harry Hemingway, which was incorrectly given as Harry Hemmingway. This has been corrected in both the PDF and HTML versions of the Article.
Externí odkaz:
https://doaj.org/article/1d11223e7e4d4cb9a840512fa18fee90
Autor:
Julia Petschnigg, Jürg Bähler, Claire Russell, StJohn Townsend, Sara E. Mole, Elisa Tinelli, Christopher J. Minnis
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-3 (2021)
Autor:
Claire Russell, Jürg Bähler, Elisa Tinelli, StJohn Townsend, Sara E. Mole, Julia Petschnigg, Christopher J. Minnis
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Juvenile CLN3 disease is a recessively inherited paediatric neurodegenerative disorder, with most patients homozygous for a 1-kb intragenic deletion in CLN3. The btn1 gene is the Schizosaccharomyces pombe orthologue of CLN3. Here, we have extended th
Publikováno v:
Current Opinion in Systems Biology. 7:1-7
Precision medicine proposes to individualize the practice of medicine based on patients’ genetic backgrounds, their biomarker characteristics and other omics datasets. After outlining the key challenges in precision medicine, namely patient stratif
Autor:
Robin Ketteler, Julia Petschnigg, Nataša Pržulj, Noël Malod-Dognin, Harry Hemingway, Sam F L Windels, Janez Povh
Publikováno v:
Nature Communications
Nature Communications, Vol 10, Iss 1, Pp 1-13 (2019)
UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)
Nature Communications, Vol 10, Iss 1, Pp 1-13 (2019)
UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)
We are increasingly accumulating molecular data about a cell. The challenge is how to integrate them within a unified conceptual and computational framework enabling new discoveries. Hence, we propose a novel, data-driven concept of an integrated cel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3fffe8e93f34b2ee8eb03782dcef739
https://hdl.handle.net/2117/187766
https://hdl.handle.net/2117/187766
Publikováno v:
Nature Chemical Biology. 11:387-397
Research in signal transduction aims to identify the functions of different signaling pathways in physiological and pathological states. Traditional techniques using biochemical, genetic or cell biological approaches have made important contributions