Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Maciej, Sykulski"'
Autor:
Bartłomiej Kisiel, Katarzyna Kisiel, Konrad Szymański, Wojciech Mackiewicz, Ewelina Biało-Wójcicka, Sebastian Uczniak, Anna Fogtman, Roksana Iwanicka-Nowicka, Marta Koblowska, Helena Kossowska, Grzegorz Placha, Maciej Sykulski, Artur Bachta, Witold Tłustochowicz, Rafał Płoski, Andrzej Kaszuba
Publikováno v:
PLoS ONE, Vol 12, Iss 6, p e0179348 (2017)
To confirm the association of previously discovered psoriasis (Ps) risk loci with the disease in a Polish population and to create predictive models based on the combination of these single nucleotide polymorphisms (SNPs).Thirty-eight SNPs were genot
Externí odkaz:
https://doaj.org/article/b1d441dc5dd846e7a51c1c161aad8cc0
Publikováno v:
Journal of Computational Biology. 26:782-793
The development of single cell RNA sequencing (scRNA-seq) has enabled innovative approaches to investigating mRNA abundances. In our study, we are interested in extracting the systematic patterns of scRNA-seq data in an unsupervised manner, thus we h
Autor:
Agata Skórka, Victor Murcia Pienkowski, Agnieszka Koppolu, Anna Walczak, Jennifer Castaneda, Robert Śmigiel, Anna Gambin, Małgorzata Rydzanicz, Anna Biernacka, Marlena Młynek, Ewa Obersztyn, Joanna Kosińska, Maciej Sykulski, Paweł Krajewski, Marzena Kucharczyk, Małgorzata Krajewska-Walasek, Barbara Poszewiecka, Elżbieta Jurkiewicz, Rafał Płoski, Renata Posmyk, Krzysztof Szczałuba, Krystyna H. Chrzanowska
Publikováno v:
Journal of Medical Genetics. 56:104-112
BackgroundMapping the breakpoints in de novo balanced chromosomal translocations (BCT) in symptomatic individuals provides a unique opportunity to identify in an unbiased way the likely causative genetic defect and thus find novel human disease candi
Autor:
Łukasz Krych, Maciej Sykulski, Laura M. Forero-Junco, Morten Arendt Rasmussen, Morten B. Mikkelsen, Josué L. Castro-Mejía, Dennis Sandris Nielsen, Daniel N. Moesby
Publikováno v:
Krych, L, Castro-Mejía, J L, Forero-Junco, L M, Moesby, D N, Mikkelsen, M B, Rasmussen, M A, Sykulski, M & Nielsen, D S 2019, ' DNA enrichment and tagmentation method for species-level identification and strain-level differentiation using ON-rep-seq ', Communications Biology, vol. 2, 369 . https://doi.org/10.1038/s42003-019-0617-x
Communications Biology, Vol 2, Iss 1, Pp 1-10 (2019)
Communications Biology
Communications Biology, Vol 2, Iss 1, Pp 1-10 (2019)
Communications Biology
Despite the massive developments within culture-independent methods for detection of microorganisms during the last decade, culture-based methods remain a cornerstone in microbiology. Yet, the problem of rapid, accurate and inexpensive identification
Autor:
Shizhen Zhang, David J. McConkey, Woonyoung Choi, Weronika Wronowska, Vipulkumar Dadhania, Tadeusz Majewski, Maciej Sykulski, Enrique Fuentes-Mattei, Ashish M. Kamat, Colin P.N. Dinney, Li Zhang, Arlene O. Siefker-Radtke, Yan Wang, Keith A. Baggerly, John N. Weinstein, Bogdan Czerniak, Charles C. Guo, Jolanta Bondaruk, Anna Gambin
Publikováno v:
European Urology. 70:611-620
Background Progression of conventional urothelial carcinoma of the bladder to a tumor with unique microscopic features referred to as micropapillary carcinoma is coupled with aggressive clinical behavior signified by a high propensity for metastasis
Autor:
Josué L. Castro-Mejía, Daniel N. Moesby, Łukasz Krych, Maciej Sykulski, Dennis Sandris Nielsen, Morten B. Mikkelsen, Morten Arendt Rasmussen
Despite the massive developments within culture-independent methods for detection and quantification of microorganisms during the last decade, culture-based methods remain a cornerstone in microbiology. We have developed a new method for bacterial DN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30a67dbc614dc1cd6a3b85ec7bda4b79
Autor:
Victor, Murcia Pienkowski, Marzena, Kucharczyk, Marlena, Młynek, Krzysztof, Szczałuba, Małgorzata, Rydzanicz, Barbara, Poszewiecka, Agata, Skórka, Maciej, Sykulski, Anna, Biernacka, Agnieszka Anna, Koppolu, Renata, Posmyk, Anna, Walczak, Joanna, Kosińska, Paweł, Krajewski, Jennifer, Castaneda, Ewa, Obersztyn, Elżbieta, Jurkiewicz, Robert, Śmigiel, Anna, Gambin, Krystyna, Chrzanowska, Małgorzata, Krajewska-Walasek, Rafał, Płoski
Publikováno v:
Journal of medical genetics. 56(2)
Mapping the breakpoints in de novo balanced chromosomal translocations (BCT) in symptomatic individuals provides a unique opportunity to identify in an unbiased way the likely causative genetic defect and thus find novel human disease candidate genes
Autor:
Maciej Sykulski, Maria M. Sasiadek, Magdalena Bartnik-Głaska, Małgorzata Rydzanicz, Beata Nowakowska, Joanna Kosińska, Victor Murcia Pienkowski, Bogusława Krzykwa, Piotr Gasperowicz, Rafał Płoski, Karolina Pesz, Agnieszka Pollak, Magdalena Kiszko
Publikováno v:
European journal of medical genetics. 61(10)
Mapping of de novo balanced chromosomal translocations (BCTs) in patients with sporadic poorly characterized disease(s) is an unbiased method of finding candidate gene(s) responsible for the observed symptoms. We present a paediatric patient sufferin
Publikováno v:
Bioinformatics Research and Applications ISBN: 9783319949673
ISBRA
ISBRA
The development of single cell RNA sequencing (scRNA-seq) has enabled innovative approaches to investigating mRNA abundances. In our study, we are interested in extracting the systematic patterns of scRNA-seq data in an unsupervised manner, thus we h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07e8fcaaf1599e7e68b6c079b84756fb
https://doi.org/10.1007/978-3-319-94968-0_32
https://doi.org/10.1007/978-3-319-94968-0_32
Autor:
Pawel Stankiewicz, Anna Kutkowska-Kaźmierczak, Kamila Ziemkiewicz, Marta Kędzior, Maciej Sykulski, Anna Gambin, Magdalena Bartnik, Tadeusz Mazurczak, Tomasz Gambin, Ewa Bocian, Natalia Bezniakow, Ewa Obersztyn, Katarzyna Derwińska, Barbara Wiśniowiecka-Kowalnik, Jakub Klapecki, Beata Nowakowska, Lech Korniszewski, Krzysztof Szczałuba, Chad A. Shaw, Joanna Bernaciak
Publikováno v:
Journal of Applied Genetics
We used whole-genome exon-targeted oligonucleotide array comparative genomic hybridization (array CGH) in a cohort of 256 patients with developmental delay (DD)/intellectual disability (ID) with or without dysmorphic features, additional neurodevelop