Zobrazeno 1 - 10
of 86
pro vyhledávání: '"Stefan Wieczorek"'
Autor:
Anne D. D. Joseph, Nirmala D. Sirisena, Thirunavukarasu Kumanan, Vathualan Sujanitha, Veronika Strelow, Raina Yamamoto, Stefan Wieczorek, Vajira H. W. Dissanayake
Publikováno v:
BMC Endocrine Disorders, Vol 19, Iss 1, Pp 1-8 (2019)
Abstract Background Barakat syndrome is an autosomal dominant rare genetic disease caused by haploinsufficiency of the GATA binding protein 3 (GATA3) gene. It is also known as HDR syndrome, and is characterized by varying degrees of hypoparathyroidis
Externí odkaz:
https://doaj.org/article/869a786f925a43978aad12dee33c2d3a
Autor:
Sourabh Chand, Julia U Holle, Marc Hilhorst, Matthew J Simmonds, Stuart Smith, Lavanya Kamesh, Peter Hewins, Amy Jayne McKnight, Alexander P Maxwell, Jan Willem Cohen Tervaert, Stefan Wieczorek, Lorraine Harper, Richard Borrows
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e69022 (2013)
Immunosuppression is cornerstone treatment of antineutrophil cytoplasmic antibody associated vasculitis (AAV) but is later complicated by infection, cancer, cardiovascular and chronic kidney disease. Caveolin-1 is an essential structural protein for
Externí odkaz:
https://doaj.org/article/22ec0a87d3b5496085a6b00e830a4d44
Publikováno v:
PPAR Research, Vol 2009 (2009)
Externí odkaz:
https://doaj.org/article/ac35bc6350fc4a829b791604ae3f4822
Publikováno v:
PPAR Research, Vol 2009 (2009)
A major genomic region involved in Wegener's granulomatosis includes the gene for retinoid receptor beta (RXRB) which forms heterodimers with peroxisome proliferator-activated receptors (PPARs). It is unclear whether this association directly arises
Externí odkaz:
https://doaj.org/article/068063f163134316819dea5dc1e1498f
Autor:
Marco Tembrink, Wanda Maria Gerding, Stefan Wieczorek, Thomas Mika, Roland Schroers, Huu Phuc Nguyen, Deepak Ben Vangala, Verena Nilius-Eliliwi
Publikováno v:
Cancers; Volume 15; Issue 11; Pages: 2942
Optical genome mapping (OGM) recently has demonstrated the potential to improve genetic diagnostics in acute myeloid leukemia (AML). In this study, OGM was utilized as a tool for the detection of genome-wide structural variants and disease monitoring
Autor:
Veronika Strelow, Stefan Wieczorek, Anne D. D. Joseph, Vajira H. W. Dissanayake, Vathualan Sujanitha, Thirunavukarasu Kumanan, Raina Yamamoto, Nirmala D. Sirisena
Publikováno v:
BMC Endocrine Disorders
BMC Endocrine Disorders, Vol 19, Iss 1, Pp 1-8 (2019)
BMC Endocrine Disorders, Vol 19, Iss 1, Pp 1-8 (2019)
Background Barakat syndrome is an autosomal dominant rare genetic disease caused by haploinsufficiency of the GATA binding protein 3 (GATA3) gene. It is also known as HDR syndrome, and is characterized by varying degrees of hypoparathyroidism, sensor
Autor:
Kenneth G. C. Smith, Augusto Vaglio, Zdenka Hruskova, Neda Farahi, Maria C. Cid, Annette Bruchfeld, Andrew J. Rees, Peter Lamprecht, Chen Au Peh, Stephen Leslie, Barbara Rewerska, Mårten Segelmark, Richard A. Watts, Jochen Zwerina, Federica Mescia, Richard M.R. Coulson, Miriam J. Ball, Coen A. Stegeman, Conleth Feighery, Wolfgang L. Gross, Iva Gunnarsson, Thomas Neumann, Caroline O. S. Savage, Jan Willem Cohen Tervaert, Roser Solans, Limy Wong, Davide Martorana, Stefan Wieczorek, Giuseppe A. Ramirez, Bo Baslund, Lorraine Harper, Alan D. Salama, Julia U Holle, Benjamin Terrier, Charles D. Pusey, Stefanie Quickert, David Jayne, Vladimir Tesar, Federico Alberici, Benjamin Wilde, Sophie Ohlsson, Loïc Guillevin, Jan-Stephan F. Sanders, Paul Brenchley, Wojciech Szczeklik, Mark A. Little, Paul A. Lyons
Publikováno v:
Rheumatology. 58
Publikováno v:
International Journal of Immunogenetics. 42:106-110
Summary Variations in two genes of the tumour necrosis factor (TNF) alpha pathway have been implicated in the pathogenesis of autoimmune diseases: polymorphisms in the TNFRSF1A gene, encoding TNF receptor 1, showed significant association with MS in
Autor:
Gina Gregorini, Julia U Holle, Kenneth G. C. Smith, Augusto Vaglio, Stefan Wieczorek, David Jayne, Thomas Neumann, Maria C. Cid, Bo Baslund, Vladimir Tesar, Rona M Smith, Federico Alberici, Annette Bruchfeld, Renato Alberto Sinico, Zdenka Hruskova, Sophie Ohlsson, Iva Gunnarsson, Lisa C. Willcocks, Mariana Fonseca, Davide Martorana, Rachel B Jones, Paul A. Lyons
This study was supported by the National Institute of Health Research Cambridge Biomedical Research Centre (http://www.cambridge-brc.org.uk). F.A. has been supported by a European Renal Association-European Dialysis and Transplant Association long-te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44b2d9b63c7820d058c0bea20c89783b
http://hdl.handle.net/10281/139116
http://hdl.handle.net/10281/139116
Autor:
Frank Jacobsen, Andrea Tannapfel, Sandeep Nambiar, Stefan Wieczorek, Lars Steinstraesser, Ingo Stricker, A. Rittig, Daniel J. Tilkorn, Mustafa Becerikli, Wiebke Köhne, Joerg T. Epplen, Alireza Mirmohammadsadegh
Publikováno v:
Experimental Cell Research. 319:1724-1731
Soft tissue sarcomas (STS) are characterized by co-participation of several epigenetic and genetic events during tumorigenesis. Having bypassed cellular senescence barriers during oncogenic transformation, the factors further affecting growth rate of