Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Szymon M Kiełbasa"'
Autor:
Roberta Rovito, Hans-Jörg Warnatz, Szymon M Kiełbasa, Hailiang Mei, Vyacheslav Amstislavskiy, Ramon Arens, Marie-Laure Yaspo, Hans Lehrach, Aloys C M Kroes, Jelle J Goeman, Ann C T M Vossen
Publikováno v:
PLoS ONE, Vol 13, Iss 7, p e0200652 (2018)
Congenital Cytomegalovirus infection (cCMV) is the leading infection in determining permanent long-term impairments (LTI), and its pathogenesis is largely unknown due to the complex interplay between viral, maternal, placental, and child factors. The
Externí odkaz:
https://doaj.org/article/d0aec4e74df94aa6afe02fab2c3e2ce1
Autor:
Karsten Jürchott, Ralf-Jürgen Kuban, Till Krech, Nils Blüthgen, Ulrike Stein, Wolfgang Walther, Christian Friese, Szymon M Kiełbasa, Ute Ungethüm, Per Lund, Thomas Knösel, Wolfgang Kemmner, Markus Morkel, Johannes Fritzmann, Peter M Schlag, Walter Birchmeier, Tammo Krueger, Silke Sperling, Christine Sers, Hans-Dieter Royer, Hanspeter Herzel, Reinhold Schäfer
Publikováno v:
PLoS Genetics, Vol 6, Iss 12, p e1001231 (2010)
Transcriptional signatures are an indispensible source of correlative information on disease-related molecular alterations on a genome-wide level. Numerous candidate genes involved in disease and in factors of predictive, as well as of prognostic, va
Externí odkaz:
https://doaj.org/article/374dde0b6ad640c3b6dc0984ca6ebe07
Autor:
Szymon M Kiełbasa, Martin Vingron
Publikováno v:
PLoS ONE, Vol 3, Iss 9, p e3210 (2008)
BACKGROUND: Feedback loops are the simplest building blocks of transcriptional regulatory networks and therefore their behavior in the course of evolution is of prime interest. METHODOLOGY: We address the question of enrichment of the number of autor
Externí odkaz:
https://doaj.org/article/c5bdc62cc3024077a0d51af84f11d2ed
Autor:
Shadi Darvish Shafighi, Szymon M. Kiełbasa, Julieta Sepúlveda-Yáñez, Ramin Monajemi, Davy Cats, Hailiang Mei, Roberta Menafra, Susan Kloet, Hendrik Veelken, Cornelis A.M. van Bergen, Ewa Szczurek
Publikováno v:
Genome Medicine, Vol 13, Iss 1, Pp 1-16 (2021)
Abstract Background Drawing genotype-to-phenotype maps in tumors is of paramount importance for understanding tumor heterogeneity. Assignment of single cells to their tumor clones of origin can be approached by matching the genotypes of the clones to
Externí odkaz:
https://doaj.org/article/3d2fdb3a359f473fa50be1499b8e526d
Autor:
Maria Tió-Coma, Szymon M. Kiełbasa, Susan J.F. van den Eeden, Hailiang Mei, Johan Chandra Roy, Jacco Wallinga, Marufa Khatun, Sontosh Soren, Abu Sufian Chowdhury, Khorshed Alam, Anouk van Hooij, Jan Hendrik Richardus, Annemieke Geluk
Publikováno v:
EBioMedicine, Vol 68, Iss , Pp 103379- (2021)
Background: Leprosy, a chronic infectious disease caused by Mycobacterium leprae, is often late- or misdiagnosed leading to irreversible disabilities. Blood transcriptomic biomarkers that prospectively predict those who progress to leprosy (progresso
Externí odkaz:
https://doaj.org/article/0f9f5c8c210446449b43c08d705e8e64
Autor:
Martijn Cordes, Kirsten Canté-Barrett, Erik B. van den Akker, Federico A. Moretti, Szymon M. Kiełbasa, Sandra A. Vloemans, Laura Garcia-Perez, Cristina Teodosio, Jacques J. M. van Dongen, Karin Pike-Overzet, Marcel J. T. Reinders, Frank J. T. Staal
T cell development in the mouse thymus has been studied extensively, but less is known regarding T cell development in the human thymus. We used a combination of single-cell techniques and functional assays to perform deep immune profiling of human T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae0d836f2b2d0ce015f29018beca8bda
http://hdl.handle.net/10261/297097
http://hdl.handle.net/10261/297097
Autor:
Rayna J.S. Anijs, El Houari Laghmani, Betül Ünlü, Szymon M. Kiełbasa, Hailiang Mei, Suzanne C. Cannegieter, Frederikus A. Klok, Peter J.K. Kuppen, Henri H. Versteeg, Jeroen T. Buijs
Publikováno v:
Research and Practice in Thrombosis and Haemostasis, 6(5). WILEY
Background Colorectal cancer patients have an increased risk of developing venous thromboembolism (VTE), resulting in increased morbidity and mortality. Because the exact mechanism is yet unknown, risk prediction is still challenging; therefore, new
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0639c0bff14c69fc212551cad7286fb9
https://hdl.handle.net/1887/3494554
https://hdl.handle.net/1887/3494554
Autor:
Martijn Cordes, Kirsten Canté-Barrett, Erik B. van den Akker, Federico A. Moretti, Szymon M. Kiełbasa, Sandra Vloemans, Laura Garcia-Perez, Cristina Teodosio, Jacques J.M. van Dongen, Karin Pike-Overzet, Marcel J.T. Reinders, Frank J.T. Staal
SummaryT cell development in the mouse thymus has been studied rather extensively; in contrast, strikingly little is known regarding T cell development in the human thymus. To close this knowledge gap, we used a combination of single-cell techniques
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52b90a8ce601a29f68d371c7ce6645ac
https://doi.org/10.1101/2022.02.18.481026
https://doi.org/10.1101/2022.02.18.481026
Autor:
Laure Grand Moursel, Willeke M. C. van Roon-Mom, Szymon M. Kiełbasa, Hailiang Mei, Henk P. J. Buermans, Linda M. van der Graaf, Kristina M. Hettne, Emile J. de Meijer, Sjoerd G. van Duinen, Jeroen F. J. Laros, Mark A. van Buchem, Peter A. C. ‘t Hoen, Silvère M. van der Maarel, Louise van der Weerd
Publikováno v:
Frontiers in Aging Neuroscience
Frontiers in Aging Neuroscience, Vol 10 (2018)
Frontiers in Aging Neuroscience, 10
Frontiers in Aging Neuroscience, 10, e102. FRONTIERS MEDIA SA
Frontiers in Aging Neuroscience, Vol 10 (2018)
Frontiers in Aging Neuroscience, 10
Frontiers in Aging Neuroscience, 10, e102. FRONTIERS MEDIA SA
Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D) is an early onset hereditary form of cerebral amyloid angiopathy (CAA) caused by a point mutation resulting in an amino acid change (NP_000475.1:p.Glu693Gln) in the amyloid precurso
Autor:
Bharati Jadhav, Ramin Monajemi, Kristina K. Gagalova, Daniel Ho, Harmen H.M. Draisma, Mark A. van de Wiel, Lude Franke, Bastiaan T. Heijmans, Joyce van Meurs, Rick Jansen, GoNL Consortium, BIOS Consortium, Peter A.C. ‘t Hoen, Andrew J. Sharp, Szymon M. Kiełbasa
Combining allelic analysis of RNA-Seq data with phased genotypes in family trios provides a powerful method to detect parent-of-origin biases in gene expression. We report findings in 296 family trios from two large studies: 165 lymphoblastoid cell l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2c88f0cd61be634cd45d1b6d722b0fa