Butyrylcholinesterase Protein Ends in the Pathogenesis of Alzheimer’s Disease—Could BCHE Genotyping Be Helpful in Alzheimer’s Therapy?

Por Jasiecki, Jacek, Wasąg, Bartosz
Publicado no Biomolecules (2019)

Genetic Mosaicism in a Group of Patients With Cornelia de Lange Syndrome

Por Krawczynska, Natalia, Wierzba, Jolanta, Wasag, Bartosz
Publicado no Front Pediatr (2019)

The Role of Butyrylcholinesterase and Iron in the Regulation of Cholinergic Network and Cognitive Dysfunction in Alzheimer’s Disease Pathogenesis

Por Jasiecki, Jacek, Targońska, Monika, Wasąg, Bartosz
Publicado no Int J Mol Sci (2021)

Molecular characterization of two novel intronic variants of NIPBL gene detected in unrelated Cornelia de Lange syndrome patients

Por Krawczynska, Natalia, Wierzba, Jolanta, Jasiecki, Jacek, Wasag, Bartosz
Publicado no BMC Med Genet (2019)

The kinase inhibitor TKI258 is active against the novel CUX1-FGFR1 fusion detected in a patient with T-lymphoblastic leukemia/lymphoma and t(7;8)(q22;p11)

Por Wasag, Bartosz, Lierman, Els, Meeus, Peter, Cools, Jan, Vandenberghe, Peter
Publicado em 2011

The genome of Dasychira pudibunda nucleopolyhedrovirus (DapuNPV) reveals novel genetic connection between baculoviruses infecting moths of the Lymantriidae family

Por Krejmer, Martyna, Skrzecz, Iwona, Wasag, Bartosz, Szewczyk, Boguslaw, Rabalski, Lukasz
Publicado no BMC Genomics (2015)

Improved Detection of KIT Exon 11 Duplications in Formalin-Fixed, Paraffin-Embedded Gastrointestinal Stromal Tumors

Por Lasota, Jerzy, Wasag, Bartosz, Steigen, Sonja E., Limon, Janusz, Miettinen, Markku
Publicado em 2007

Mosaic Intronic NIPBL Variant in a Family With Cornelia de Lange Syndrome

Por Krawczynska, Natalia, Kuzniacka, Alina, Wierzba, Jolanta, Parenti, Ilaria, Kaiser, Frank J., Wasag, Bartosz
Publicado no Front Genet (2018)

FUMARASE DEFICIENT UTERINE LEIOMYOMAS – AN IMMUNOHISTO-CHEMICAL, MOLECULAR GENETIC, AND CLINICOPATHOLOGIC STUDY OF 86 CASES

Por Miettinen, Markku, Felisiak-Golabek, Anna, Wasag, Bartosz, Chmara, Magdalena, Wang, Zengfeng, Butzow, Ralf, Lasota, Jerzy
Publicado no Am J Surg Pathol (2016)

Synergy between the alteration in the N-terminal region of butyrylcholinesterase K variant and apolipoprotein E4 in late-onset Alzheimer’s disease

Por Jasiecki, Jacek, Limon-Sztencel, Anna, Żuk, Monika, Chmara, Magdalena, Cysewski, Dominik, Limon, Janusz, Wasąg, Bartosz
Publicado no Sci Rep (2019)

Detection of somatic BRCA1/2 mutations in ovarian cancer – next‐generation sequencing analysis of 100 cases

Por Koczkowska, Magdalena, Zuk, Monika, Gorczynski, Adam, Ratajska, Magdalena, Lewandowska, Marzena, Biernat, Wojciech, Limon, Janusz, Wasag, Bartosz
Publicado no Cancer Med (2016)

Severe acute toxicity following gemcitabine administration: A report of four cases with cytidine deaminase polymorphisms evaluation

Por Hryciuk, Beata, Szymanowski, Bartosz, Romanowska, Anna, Salt, Ewa, Wasąg, Bartosz, Grala, Bartłomiej, Jassem, Jacek, Duchnowska, Renata
Publicado no Oncol Lett (2018)

New Insights into Butyrylcholinesterase Activity Assay: Serum Dilution Factor as a Crucial Parameter

Por Jońca, Joanna, Żuk, Monika, Wasąg, Bartosz, Janaszak-Jasiecka, Anna, Lewandowski, Krzysztof, Wielgomas, Bartosz, Waleron, Krzysztof, Jasiecki, Jacek
Publicado no PLoS One (2015)

The algorithm for Alzheimer risk assessment based on APOE promoter polymorphisms

Por Limon-Sztencel, Anna, Lipska-Ziętkiewicz, Beata S., Chmara, Magdalena, Wasag, Bartosz, Bidzan, Leszek, Godlewska, Beata R., Limon, Janusz
Publicado no Alzheimers Res Ther (2016)

Detection of BRCA1/2 mutations in circulating tumor DNA from patients with ovarian cancer

Por Ratajska, Magdalena, Koczkowska, Magdalena, Żuk, Monika, Gorczyński, Adam, Kuźniacka, Alina, Stukan, Maciej, Biernat, Wojciech, Limon, Janusz, Wasąg, Bartosz
Publicado no Oncotarget (2017)

Aortic valve calcium score in hypercholesterolemic patients with and without low-density lipoprotein receptor gene mutation

Por Gałąska, Rafal, Kulawiak-Gałąska, Dorota, Chmara, Magdalena, Chlebus, Krzysztof, Studniarek, Michał, Fijałkowski, Marcin, Wasąg, Bartosz, Rynkiewicz, Andrzej, Gruchała, Marcin
Publicado no PLoS One (2018)

Carotid intima–media thickness (IMT) in patients with severe familial and non-familial hypercholesterolemia: The effect of measurement site on the IMT correlation with traditional...

Por Gałąska, Rafał, Kulawiak-Gałąska, Dorota, Chmara, Magdalena, Chlebus, Krzysztof, Mickiewicz, Agnieszka, Rynkiewicz, Andrzej, Wasąg, Bartosz, Studniarek, Michał, Fijałkowski, Marcin, Gruchała, Marcin
Publicado no Cardiol J (2021)

Higher Responsiveness to Rosuvastatin in Polygenic versus Monogenic Hypercholesterolemia: A Propensity Score Analysis

Por Mickiewicz, Agnieszka, Futema, Marta, Ćwiklinska, Agnieszka, Kuchta, Agnieszka, Jankowski, Maciej, Kaszubowski, Mariusz, Chmara, Magdalena, Wasąg, Bartosz, Fijałkowski, Marcin, Jaguszewski, Miłosz, Humphries, Steve E., Gruchała, Marcin
Publicado no Life (Basel) (2020)

Long-term lipoprotein apheresis in the treatment of severe familial hypercholesterolemia refractory to high intensity statin therapy: Three year experience at a lipoprotein apheres...

Por Mickiewicz, Agnieszka, Borowiec-Wolna, Justyna, Bachorski, Witold, Gilis-Malinowska, Natasza, Gałąska, Rafał, Raczak, Grzegorz, Chmara, Magdalena, Wasąg, Bartosz, Jaguszewski, Miłosz J., Fijałkowski, Marcin, Gruchała, Marcin
Publicado no Cardiol J (2020)

Spectrum and Prevalence of Pathogenic Variants in Ovarian Cancer Susceptibility Genes in a Group of 333 Patients

Por Koczkowska, Magdalena, Krawczynska, Natalia, Stukan, Maciej, Kuzniacka, Alina, Brozek, Izabela, Sniadecki, Marcin, Debniak, Jaroslaw, Wydra, Dariusz, Biernat, Wojciech, Kozlowski, Piotr, Limon, Janusz, Wasag, Bartosz, Ratajska, Magdalena
Publicado no Cancers (Basel) (2018)