Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Aneta Zdral"'
Autor:
Edita Poluzioroviene, Joanna Chorostowska-Wynimko, Sigita Petraitiene, Arunas Strumila, Adriana Rozy, Aneta Zdral, Arunas Valiulis
Publikováno v:
Advances in Respiratory Medicine, Vol 92, Iss 4, Pp 291-299 (2024)
Severe inherited alpha-1 antitrypsin deficiency (AATD) is an autosomal genetic condition linked to chronic obstructive pulmonary disease (COPD). The significance of heterozygous, milder deficiency variants (PiSZ, PiMZ, PiMS) is less clear. We studied
Externí odkaz:
https://doaj.org/article/8859bf38c0a74bd6b83656c53b036ad7
Autor:
Mateusz Florczuk, Piotr Rudzinski, Joanna Chorostowska-Wynimko, Katarzyna Duk, Adam Szpechcinski, Renata Langfort, Aneta Zdral, Stefan Rudzinski, Dorota Giedronowicz, Tadeusz Orłowski, Wlodzimierz Kupis, Maciej Bryl, Grzegorz Czyzewicz, Emil Wojda, Aleksander Barinow-Wojewodzki
Publikováno v:
Cellular and Molecular Life Sciences
MicroRNAs (miRNAs), key regulators of gene expression at the post-transcriptional level, are grossly misregulated in some human cancers, including non-small-cell lung carcinoma (NSCLC). The aberrant expression of specific miRNAs results in the abnorm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4e8c05993685ec04de6370a9ff22987
http://europepmc.org/articles/PMC6697756
http://europepmc.org/articles/PMC6697756
Autor:
Wlodzimierz Kupis, Stefan Rudzinski, Adam Szpechcinski, Aneta Zdral, Tadeusz Orłowski, Joanna Chorostowska-Wynimko, Ewa Szczepulska-Wójcik, Urszula Lechowicz, Katarzyna Duk, Joanna Moes-Sosnowska, Renata Langfort, Piotr Rudzinski
Publikováno v:
Molecular pathology and funct. genomics.
Introduction: Molecular diagnosis of non-small-cell lung cancer (NSCLC) is commonly based on qPCR which provides sufficient sensitivity and specificity but has low sample throughput and allows parallel analysis of few amplicons only. NGS offers highe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42094d252ff07e04deea3a73c8a57940
https://doi.org/10.1183/13993003.congress-2019.pa4059
https://doi.org/10.1183/13993003.congress-2019.pa4059
Autor:
Malgorzata, Hadzik-Blaszczyk, Aneta, Zdral, Tadeusz M, Zielonka, Ada, Rozy, Renata, Krupa, Andrzej, Falkowski, Kazimierz A, Wardyn, Joanna, Chorostowska-Wynimko, Katarzyna, Zycinska
Publikováno v:
Advances in experimental medicine and biology. 1070
Alpha-1 antitrypsin (A1AT) deficiency is one of the most common genetic disorders in Caucasian population. There is a link between granulomatosis with polyangiitis (GPA) and most frequent variants of SERPINA1 gene encoding severe alpha-1 antitripsin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bfb03ed947850edf3f68ec6f5c31cb84
https://pubmed.ncbi.nlm.nih.gov/29460271
https://pubmed.ncbi.nlm.nih.gov/29460271
Autor:
Tadeusz M Zielonka, Andrzej Falkowski, Joanna Chorostowska-Wynimko, Aneta Zdral, Kazimierz Wardyn, Małgorzata Hadzik-Błaszczyk, Renata Krupa, Katarzyna Zycinska, Ada Rozy
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9783319896649
Alpha-1 antitrypsin (A1AT) deficiency is one of the most common genetic disorders in Caucasian population. There is a link between granulomatosis with polyangiitis (GPA) and most frequent variants of SERPINA1 gene encoding severe alpha-1 antitripsin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67eb55fae11d01d41cb159a12f8c9007
https://doi.org/10.1007/5584_2018_156
https://doi.org/10.1007/5584_2018_156
Publikováno v:
Molecular Pathology and Functional Genomics.
Epidermal growth factor receptor (EGFR) mutation assessment is essential for targeted therapy of non-small cell lung cancer (NSCLC) as predictive biomarker of the response to EGFR tyrosine kinase inhibitors (TKI). There is a number of well-known muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5903d021054c324bf342c3a979769e85
https://doi.org/10.1183/1393003.congress-2017.pa4952
https://doi.org/10.1183/1393003.congress-2017.pa4952
Autor:
Kazimierz Roszkowski-Sliz, Wlodzimierz Kupis, Mateusz Florczuk, Renata Langfort, Piotr Rudzinski, Katarzyna Duk, Aneta Zdral, Adam Szpechcinski, Jolanta Zaleska, Michal Komorowski, Joanna Chorostowska-Wynimko, Tadeusz Orłowski, Emilia Debek
Publikováno v:
Molecular Pathology and Functional Genomics.
Background: Alpha-1 antitrypsin (AAT) is encoded by the highly polymorphic SERPINA1 gene. Mutations in this gene cause AAT deficiency (AATD) - a risk factor for a number of chronic lung diseases. The causative link between AATD and non-small cell lun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b12366d14e82d032ee0a7110f71f85c
https://doi.org/10.1183/1393003.congress-2017.pa4953
https://doi.org/10.1183/1393003.congress-2017.pa4953
Autor:
Renata Langfort, Dariusz M. Kowalski, P. Rudzinski, Joanna Chorostowska-Wynimko, M. Skroński, P. Skrońska, Aneta Zdral, Katarzyna Duk, T. Orlowski
Publikováno v:
Journal of Thoracic Oncology. 13:S810-S811
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::398584f728c950e925439f0e873d8e5e
https://doi.org/10.1016/j.jtho.2018.08.1426
https://doi.org/10.1016/j.jtho.2018.08.1426
Autor:
Radoslaw Struniawski, Beata Szumna, Aneta Zdral, Katarzyna Duk, Joanna Chorostowska-Wynimko, Adriana Rozy
Publikováno v:
3.1 Molecular Pathology and Functional Genomics.
SERPINA1 gene encoding the alpha-1 antitrypsin (A1AT) protein is highly polymorphic. Apart from the most prevalent PI*S and PI*Z deficiency alleles, other so-called rare variants also predispose individuals to severe chronic respiratory disorders (CR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e06e6032fb35e8147defd9caeb4cf09
https://doi.org/10.1183/13993003.congress-2016.pa880
https://doi.org/10.1183/13993003.congress-2016.pa880
Frequency of Rare Alpha-1 Antitrypsin Variants in Polish Patients with Chronic Respiratory Disorders
Publikováno v:
Respiratory Medicine and Science ISBN: 9783319306582
The SERPINA1 gene encoding the alpha-1 antitrypsin (A1AT) protein is highly polymorphic. It is known that, apart from the most prevalent PI*S and PI*Z A1AT deficiency variants, other so-called rare variants also predispose individuals to severe chron
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::261c4cc2aca161b3323adeb7a1c948cf
https://doi.org/10.1007/5584_2016_213
https://doi.org/10.1007/5584_2016_213