Serum miRNA Profile in Diabetic Patients With Ischemic Heart Disease as a Promising Non-Invasive Biomarker

Autor: Agnieszka Bielska, Magdalena Niemira, Witold Bauer, Iwona Sidorkiewicz, Anna Szałkowska, Anna Skwarska, Justyna Raczkowska, Damian Ostrowski, Kamil Gugała, Sławomir Dobrzycki, Adam Krętowski

Publikováno v: Frontiers in Endocrinology, Vol 13 (2022)

The increasing morbidity and mortality of type 2 diabetic mellitus (T2DM) patients with ischemic heart disease (IHD) highlight an urgent need to identify early biomarkers, which would help to predict individual risk of development of IHD. Here, we po

Externí odkaz: https://doaj.org/article/0dd5592e23a04446ace3e339339d63ac

Abstract P2-23-06: Estrogen receptor-negative progesterone receptor-positive breast cancer is a molecularly distinct group characterized by the down-regulation of genes controlled by ESR1 and SUZ12

Autor: Michał Kunc, Marta Popęda, Michał Bieńkowski, Marcin Braun, Aleksandra Łacko, Barbara Radecka, Joanna Pikiel, Maria Litwiniuk, Katarzyna Pogoda, Magdalena Niemira, Anna Szałkowska, Ewa Iżycka-Świeszewska, Gabor Cserni, Wojciech Biernat, Elżbieta Senkus

Publikováno v: Cancer Research. 83:P2-23

Background: Single hormone receptor-positive breast cancers (BCs) display two distinct phenotypes: ER+/PgR– and ER–/PgR+ further stratified by their HER2 status. Their molecular features are not well defined. Our study aimed to identify different

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3f25249027d630e4b02dc6ad47452a87
https://doi.org/10.1158/1538-7445.sabcs22-p2-23-06

Evaluation of Transcriptomic Regulations behind Metabolic Syndrome in Obese and Lean Subjects

Autor: Magdalena Paczkowska-Abdulsalam, Magdalena Niemira, Agnieszka Bielska, Anna Szałkowska, Beata Anna Raczkowska, Sini Junttila, Attila Gyenesei, Edyta Adamska-Patruno, Katarzyna Maliszewska, Anna Citko, Łukasz Szczerbiński, Adam Krętowski

Publikováno v: International Journal of Molecular Sciences, Vol 21, Iss 4, p 1455 (2020)

Multiple mechanisms have been suggested to confer to the pathophysiology of metabolic syndrome (MetS), however despite great interest from the scientific community, the exact contribution of each of MetS risk factors still remains unclear. The presen

Externí odkaz: https://doaj.org/article/aa3b48c944604a11a93a6ed720aa6936

Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity

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Mazzei, Susanna, Guerrini, Edoardo, Conticini, Luca, Cantarini, Bruno, Frediani, Danilo, Tacconi, Chiara Spertilli Raffaelli, Marco, Feri, Alice, Donati, Raffaele, Scala, Luca, Guidelli, Genni, Spargi, Marta, Corridi, Cesira, Nencioni, Leonardo, Croci, Gian Piero Caldarelli, Maurizio, Spagnesi, Davide, Romani, Paolo, Piacentini, Maria, Bandini, Elena, Desanctis, Silvia, Cappelli, Anna, Canaccini, Agnese, Verzuri, Valentina, Anemoli, Manola, Pisani, Agostino, Ognibene, Alessandro, Pancrazzi, Maria, Lorubbio, Massimo, Vaghi, Antonella, D 'Arminio Monforte, Federica Gaia Miraglia, Mario, U Mondelli, Massimo, Girardis, Sophie, Venturelli, Stefano, Busani, Andrea, Cossarizza, Andrea, Antinori, Alessandra, Vergori, Arianna, Emiliozzi, Stefano, Rusconi, Matteo, Siano, Arianna, Gabrieli, Agostino, Riva, Daniela, Francisci, Elisabetta, Schiaroli, Francesco, Paciosi, Andrea, Tommasi, Pier Giorgio Scotton, Francesca, Andretta, Sandro, Panese, Stefano, Baratti, Renzo, Scaggiante, Francesca, Gatti, 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Publikováno v: Human genetics 141 (2021): 147–173. doi:10.1007/s00439-021-02397-7
info:cnr-pdr/source/autori:Fallerini, Chiara; Picchiotti, Nicola; Baldassarri, Margherita; Zguro, Kristina; Daga, Sergio; Fava, Francesca; Benetti, Elisa; Amitrano, Sara; Bruttini, Mirella; Palmieril, Maria; Croci, Susanna; Lista, Mirjam; Beligni, Giada; Valentino, Floriana; Meloni, Ilaria; Tanfoni, Marco; Minnai, Francesca; Colombo, Francesca; Cabri, Enrico; Fratelli, Maddalena; Gabbi, Chiara; Mantovani, Stefania; Frullanti, Elisa; Gori, Marco; Crawley, Francis P.; Butler-Laporte, Guillaume; Richards, Brent; Zeberg, Hugo; Lipcsey, Miklos; Hultstrom, Michael; Ludwig, Kerstin U.; Schulte, Eva C.; Pairo-Castineira, Erola; Baillie, John Kenneth; Schmidt, Axel; Frithiof, Robert; Mari, Francesca; Renieri, Alessandra; Furini, Simone; GEN-COVID Multicenter Study (which includes Alessandra Stella and Filippo Biscarini)/titolo:Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity/doi:10.1007%2Fs00439-021-02397-7/rivista:Human genetics/anno:2021/pagina_da:147/pagina_a:173/intervallo_pagine:147–173/volume:141
Human genetics
Hum. Genet. 141, 147-173 (2022)
Human Genetics
2021, ' Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity ', Human Genetics . https://doi.org/10.1007/s00439-021-02397-7

The combined impact of common and rare exonic variants in COVID-19 host genetics is currently insufficiently understood. Here, common and rare variants from whole-exome sequencing data of about 4000 SARS-CoV-2-positive individuals were used to define

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4836dbe8027e2289c8e8ff11bfe68cc
https://doi.org/10.1101/2021.09.03.21262611