Zobrazeno 1 - 10
of 2 001
pro vyhledávání: '"Sulek, A."'
Autor:
Hoffman-Zacharska, Dorota1,2 (AUTHOR) anna.sulek@lazarski.pl, Sulek, Anna2,3 (AUTHOR)
Publikováno v:
International Journal of Molecular Sciences. Aug2024, Vol. 25 Issue 15, p8190. 11p.
Autor:
Hansen, Torben, Mann, Matthias, Matthijnssens, Jelle, Krag, Aleksander, Bork, Peer, Arumugam, Manimozhiyan, Trebicka, Jonel, Karsdal, Morten, Anastasiadou, Ema, Israelsen, Hans, Melberg, Hans Olav, Legido-Quigley, Cristina, Thiele, Maja, Villesen, Ida Falk, Niu, Lili, Johansen, Stine, Sulek, Karolina, Nishijima, Suguru, Espen, Lore Van, Keller, Marisa, Israelsen, Mads, Suvitaival, Tommi, Zawadzki, Andressa de, Juel, Helene Bæk, Brol, Maximilian Joseph, Stinson, Sara Elizabeth, Huang, Yun, Silva, Maria Camilla Alvarez, Kuhn, Michael, Leeming, Diana Julie, Dalgaard, Louise Torp, Jensen, Lars Juhl
Publikováno v:
In Journal of Hepatology August 2024 81(2):345-359
Autor:
Peter Rossing, Simone Theilade, Christian Stevns Hansen, Marie Frimodt-Moller, Viktor Rotbain Curovic, Tine W Hansen, Cristina Legido-Quigley, Nete Tofte, Tarunveer S Ahluwalia, Ismo Matias Mattila, Brede A Sørland, Siddhi Y Jain, Karolina Sulek, Kajetan Trost, Signe Abitz Winther
Publikováno v:
BMJ Open Diabetes Research & Care, Vol 12, Iss 2 (2024)
Introduction Diabetic retinopathy (DR), diabetic kidney disease (DKD) and distal symmetric polyneuropathy (DSPN) share common pathophysiology and pose an additive risk of early mortality.Research design and methods In adults with type 1 diabetes, 49
Externí odkaz:
https://doaj.org/article/1af062286c6c4c5eac1dbe7151d7f537
Computer Aided Engineering in the application of rotational forming of axially asymmetric geometries
Publikováno v:
In Journal of Manufacturing Processes 15 April 2024 115:275-288
Autor:
Bjørn Kromann, Lili Niu, Line B. P. Møller, Julie Sølberg, Karolina Sulek, Mette Gyldenløve, Beatrice Dyring-Andersen, Lone Skov, Marianne B. Løvendorf
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 16, p 8791 (2024)
Knowledge about the molecular mechanisms underlying the systemic inflammation observed in psoriasis remains incomplete. In this study, we applied mass spectrometry-based proteomics to compare the plasma protein levels between patients with psoriasis
Externí odkaz:
https://doaj.org/article/38571d061c914bea8c9d1b2400d81300
Autor:
Dorota Hoffman-Zacharska, Anna Sulek
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 15, p 8190 (2024)
Since 1991, several genetic disorders caused by unstable trinucleotide repeats (TNRs) have been identified, collectively referred to as triplet repeat diseases (TREDs). They share a common mutation mechanism: the expansion of repeats (dynamic mutatio
Externí odkaz:
https://doaj.org/article/fece605fb2d04e9ea6e5abaff0e6c5dd
Autor:
Kamiński, Robert, Wibig, Tadeusz, Castillo, David Alvarez, Cheminant, Kevin Almeida, Ćwikła, Aleksander, Duffy, Alan R., Góra, Dariusz, Homola, Piotr, Jagoda, Paweł, Kasztelan, Marcin, Knap, Marek, Kopański, Konrad, Kovacs, Peter, Krupiński, Michał, Magryś, Marek, Nazari, Vahabeddin, Niedźwiecki, Michał, Noga, Wojciech, Rosas, Matias, Ryszkowski, Szymon, Smelcerz, Katarzyna, Smolek, Karel, Stasielak, Jarosław, Stuglik, Sławomir, Sułek, Mateusz, Sushchov, Oleksandr, Woźniak, Krzysztof
Publikováno v:
Acta Phys.Polon.B 50 (2019) 2001-2010, Erratum Acta Phys. Pol. B 51, 903 (2020)
The Cosmic-Ray Extremely Distributed Observatory (CREDO) is a project created a few years ago in the Institute of Nuclear Physics PAS in Krak\'ow and dedicated is to global studies of extremely extended cosmic-ray phenomena. The main reason for creat
Externí odkaz:
http://arxiv.org/abs/2009.12314
Akademický článek
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Autor:
Kordaczuk, Jakub, Sułek, Michał, Mak, Paweł, Śmiałek-Bartyzel, Justyna, Hułas-Stasiak, Monika, Wojda, Iwona
Publikováno v:
In Developmental and Comparative Immunology October 2023 147
Autor:
Ewelina Elert-Dobkowska, Iwona Stepniak, Wiktoria Radziwonik-Fraczyk, Amir Jahic, Christian Beetz, Anna Sulek
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 9, p 5008 (2024)
The most common form of hereditary spastic paraplegia (HSP), SPG4 is caused by single nucleotide variants and microrearrangements in the SPAST gene. The high percentage of multi-exonic deletions or duplications observed in SPG4 patients is predispose
Externí odkaz:
https://doaj.org/article/6c94afd21f844714b653cf9f9d0e74b8