Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Christian Guelly"'
Autor:
Ainur Akilzhanova, Christian Guelly, Omirbek Nuralinov, Zhannur Nurkina, Dinara Nazhat, Shalkhar Smagulov, Azat Tursunbekov, Anar Alzhanova, Gulzhaina Rashbayeva, Ayan Abdrakhmanov, Sholpan Dosmagambet, Slave Trajanoski, Zhaxybay Zhumadilov, Almaz Sharman, Mahabbat Bekbosynova
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e101059 (2014)
Channelopathies, caused by disturbed potassium or calcium ion management in cardiac myocytes are a major cause of heart failure and sudden cardiac death worldwide. The human ryanodine receptor 2 (RYR2) is one of the key players tightly regulating cal
Externí odkaz:
https://doaj.org/article/728420d056bf451e9a34ad984ada8954
Autor:
Beate Rinner, Andreas Weinhaeusel, Birgit Lohberger, Elke Verena Froehlich, Walter Pulverer, Carina Fischer, Katharina Meditz, Susanne Scheipl, Slave Trajanoski, Christian Guelly, Andreas Leithner, Bernadette Liegl
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e56609 (2013)
Chordomas are rare mesenchymal tumors occurring exclusively in the midline from clivus to sacrum. Early tumor detection is extremely important as these tumors are resistant to chemotherapy and irradiation. Despite continuous research efforts surgical
Externí odkaz:
https://doaj.org/article/4d8e2f65ad5a44068e710c9adfd562d1
Autor:
Florian R L Meyer, Heinrich Grausgruber, Claudia Binter, Georg E Mair, Christian Guelly, Claus Vogl, Ralf Steinborn
Publikováno v:
PLoS ONE, Vol 8, Iss 5, p e63125 (2013)
Reference genes (RGs) with uniform expression are used for normalization of reverse transcription quantitative PCR (RT-qPCR) data. Their optimization for a specific biological context, e.g. a specific tissue, has been increasingly considered. In this
Externí odkaz:
https://doaj.org/article/15161c99c5a94ecdaacc68e1afe60f89
Autor:
Katharina Schallmoser, Christina Bartmann, Eva Rohde, Simone Bork, Christian Guelly, Anna C. Obenauf, Andreas Reinisch, Patrick Horn, Anthony D. Ho, Dirk Strunk, Wolfgang Wagner
Publikováno v:
Haematologica, Vol 95, Iss 6 (2010)
Background Research on mesenchymal stromal cells has created high expectations for a variety of therapeutic applications. Extensive propagation to yield enough mesenchymal stromal cells for therapy may result in replicative senescence and thus hamper
Externí odkaz:
https://doaj.org/article/e2bfca2f2a674a7088eb1c661d6d1f67
Autor:
Nazanin Sareban, Peter Schlenke, Ivo Steinmetz, Tobias Niedrist, Lisa Kriegl, Sabrina Kral, Christian Guelly, Markus Herrmann, Stefanie Schiffmann, Chiara Banfi, Andrea Berghold, Christoph Zurl, Robert Krause
Publikováno v:
The Journal of Infection
Background Understanding of the true asymptomatic rate of infection of SARS-CoV-2 is currently limited, as is understanding of the population-based seroprevalence after the first wave of COVID-19 within the UK. The majority of data thus far come from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94618ada8e7f5432ccf67aab3efd9283
https://doi.org/10.1016/j.jinf.2021.08.030
https://doi.org/10.1016/j.jinf.2021.08.030
Autor:
Ulan Kozhamkulov, Ulykbek Kairov, Mahabbat Bekbosynova, Zhaxybay Zhumadilov, Saule Rakhimova, Zhannur Abilova, Ainur Akilzhanova, Ayan Abdrakhmanov, Omirbek Nuralinov, Slave Trajanoski, Christian Guelly, A. Akhmetova, S.K. Akilzhanova
Publikováno v:
The Journal of Heart and Lung Transplantation. 39:S360
Purpose Ventricular fibrillation (VF) and ventricular tachycardia (VT) are major causes of sudden cardiac death. In some cases clinical investigations fail to identify the underlying cause and the event is classified as idiopathic (iVT). Recent achie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bddfa6b347d31070978bf1be2d27e581
https://doi.org/10.1016/j.healun.2020.01.432
https://doi.org/10.1016/j.healun.2020.01.432
Autor:
Andreas R. Janecke, Jan Senderek, Slave Trajanoski, Regina Fink-Puches, Christian Windpassinger, Anton Haas, Laila El Shabrawi-Caelen, Piet Auer-Grumbach, Martin Weger, Dieter Metze, Maria Schabhüttl, Lea Papić, Eleonore Fröhlich, Thomas R. Pieber, Michaela Auer-Grumbach, Herbert Budka, Christian Guelly
Publikováno v:
Brain: A Journal of Neurology, 134
To identify the disease-causing gene responsible for an autosomal dominantly inherited Charcot–Marie–Tooth neuropathy subtype in a family excluded for mutations in the common Charcot–Marie–Tooth genes, we used array-based sequence capture to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::406c320d1b12741e170209b4dabef26e
http://doc.rero.ch/record/294441/files/awr076.pdf
http://doc.rero.ch/record/294441/files/awr076.pdf
Autor:
Thomas Kroneis, Slave Trajanoski, Peter Sedlmayr, Christian Guelly, Helmut Guttenberger, Uwe K. Simon
Publikováno v:
Molecular Biology and Evolution. 29:2231-2239
Eukaryote genomes contain multiple copies of nuclear ribosomal DNA (nrDNA) harboring both highly conserved and variable regions. This has made nrDNA the most popular genetic marker for phylogenetic studies and the region of choice for barcoding proje
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a77cfccc3afb385993850d195e61df98
https://doi.org/10.1093/molbev/mss093
https://doi.org/10.1093/molbev/mss093
Autor:
Karin Hiden, Monika M. Pichler, Werner Linkesch, Christine Beham-Schmid, Albert Wölfler, Heinz Sill, Christian Guelly, Claudia Bodner, Alexander Deutsch, Carina Fischer
Publikováno v:
British Journal of Haematology. 152:669-672
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f8eee3605db9e0a6847cd48a80bee9d
https://doi.org/10.1111/j.1365-2141.2010.08404.x
https://doi.org/10.1111/j.1365-2141.2010.08404.x
Autor:
Craig Blackstone, Mary M. Reilly, Michaela Auer-Grumbach, Andreas R. Janecke, Thomas R. Pieber, Lea Leonardis, Heimo Strohmaier, Christian Guelly, Peng Peng Zhu, Jan Willems, Jonathan Baets, Maria Schabhüttl, Lea Papić, Martina Hatz, Peter De Jonghe, Tim M. Strom, Eleonore Fröhlich, Joachim Weis, Janez Zidar, Slave Trajanoski
Publikováno v:
Am. J. Hum. Genet. 88, 99-105 (2011)
The American journal of human genetics
The American journal of human genetics
Hereditary sensory neuropathy type I (HSN I) is an axonal form of autosomal-dominant hereditary motor and sensory neuropathy distinguished by prominent sensory loss that leads to painless injuries. Unrecognized, these can result in delayed wound heal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34a83b4b0c4b26098e671b60b4b88cc6