Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Grazyna Kostrzewa"'
Autor:
Agnieszka, Stembalska, Małgorzata, Rydzanicz, Agnieszka, Pollak, Grazyna, Kostrzewa, Piotr, Stawinski, Mateusz, Biela, Rafal, Ploski, Robert, Smigiel
Publikováno v:
Genes
Renal cystic diseases are characterized by genetic and phenotypic heterogeneity. Congenital renal cysts can be classified as developmental disorders and are commonly diagnosed prenatally using ultrasonography and magnetic resonance imaging. Progress
Akademický článek
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Autor:
Mateusz, Spiewak, Łukasz A, Małek, Grazyna, Kostrzewa, Bartłomiej, Kisiel, Agnieszka, Serafin, Krzysztof J, Filipiak, Rafał, Płoski, Grzegorz, Opolski
Publikováno v:
Kardiologia polska. 67(8)
Genetic C3435T polymorphism of the multidrug resistance gene-1 (MDR-1) limits oral bioavailability of clopidogrel and influences prognosis in patients with myocardial infarction.To assess the effects of C3435T polymorphism on platelet reactivity and
Autor:
Renata Glowczynska, Lukasz A. Malek, Mateusz Spiewak, Krzysztof J. Filipiak, Marcin Grabowski, Bartlomiej Kisiel, Janusz Kochman, Grazyna Kostrzewa, Rafal Ploski, Grzegorz Opolski
Publikováno v:
International Journal of Cardiology. 116:134-135
Autor:
Małgorzata Rydzanicz, Pawel Olszewski, Darek Kedra, Hanna Davies, Natalia Filipowicz, Bozena Bruhn‐Olszewska, Marco Cavalli, Krzysztof Szczałuba, Marlena Młynek, Marcin M. Machnicki, Piotr Stawiński, Grażyna Kostrzewa, Paweł Krajewski, Dariusz Śladowski, Krystyna Chrzanowska, Jan P. Dumanski, Rafał Płoski
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 1, Pp n/a-n/a (2021)
Abstract Background Phenotypically discordant monozygotic twins (PDMZTs) offer a unique opportunity to study post‐zygotic genetic variation and provide insights into the linkage between genotype and phenotype. We report a comprehensive analysis of
Externí odkaz:
https://doaj.org/article/853c2803d00245c78a246f0a79689b02
Autor:
Agnieszka Kalińska-Bienias, Grażyna Kostrzewa, Magdalena Malejczyk, Rafał Płoski, Sławomir Majewski
Publikováno v:
Przegląd Dermatologiczny, Vol 103, Iss 2, Pp 102-108 (2016)
Introduction . Polymorphisms of EVER genes are related to increased risk of actinic keratosis (AK), squamous skin cancers (SCC) and cervical cancer. Objective . The aim of this study was to analyze the haplotypes of the EVER 2 gene in 65 subjects wit
Externí odkaz:
https://doaj.org/article/4d366f8edf174c2c9bbd761ca60ed3da
Autor:
Joanna Kinga Ponińska, Bolesław Samoliński, Aneta Tomaszewska, Filip Raciborski, Piotr Samel-Kowalik, Artur Walkiewicz, Agnieszka Lipiec, Barbara Piekarska, Edyta Krzych-Fałta, Andrzej Namysłowski, Grażyna Kostrzewa, Andrzej Pawlik, Monika Jasek, Andrzej Wiśniewski, Piotr Kuśnierczyk, Sławomir Majewski, Rafał Płoski
Publikováno v:
PLoS ONE, Vol 12, Iss 9, p e0183922 (2017)
The T allele of rs7927894 (at 11q13.5) was associated with atopic dermatitis and other allergic diseases. Our purpose was to replicate the association with allergic phenotypes and explore the role of rs7927894 in predisposing to persistent allergic r
Externí odkaz:
https://doaj.org/article/26bbb5d34ce94090b124867f9d8703bb
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e68155 (2013)
Genetic variants of Y chromosome predispose to hypertension in rodents, whereas in humans the evidence is conflicting. Our purpose was to study the distribution of a panel of Y chromosome markers in a cohort from a cross-sectional population-based st
Externí odkaz:
https://doaj.org/article/535043517dd74670b3962d1b746fa363
Autor:
Joanna Ponińska, Bolesław Samoliński, Aneta Tomaszewska, Filip Raciborski, Piotr Samel-Kowalik, Artur Walkiewicz, Agnieszka Lipiec, Barbara Piekarska, Jarosław Komorowski, Edyta Krzych-Fałta, Andrzej Namysłowski, Jacek Borowicz, Grażyna Kostrzewa, Sławomir Majewski, Rafał Płoski
Publikováno v:
PLoS ONE, Vol 6, Iss 2, p e16933 (2011)
BACKGROUND: FLG null variants of which 2282del4 and R501X are the most frequent in Caucasians are established risk factors for atopic dermatitis (AD) with an effect probably mediated through impairment of epidermal barrier. Among subjects with AD FLG
Externí odkaz:
https://doaj.org/article/f0fd4691f32947a5bdf623626a1a3977