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Page 1
Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome.
Genes (Basel). 2023 Mar 9;14(3):680. doi: 10.3390/genes14030680.
Genes (Basel). 2023.
PMID: 36980952
Free PMC article.
Prenatal Detection of a FOXF1 Deletion in a Fetus with ACDMPV and Hydronephrosis.
Bzdęga K, Kutkowska-Kaźmierczak A, Deutsch GH, Plaskota I, Smyk M, Niemiec M, Barczyk A, Obersztyn E, Modzelewski J, Lipska I, Stankiewicz P, Gajecka M, Rydzanicz M, Płoski R, Szczapa T, Karolak JA.
Bzdęga K, et al. Among authors: plaskota i.
Genes (Basel). 2023 Feb 23;14(3):563. doi: 10.3390/genes14030563.
Genes (Basel). 2023.
PMID: 36980834
Free PMC article.
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Prenatal Diagnosis by Array Comparative Genomic Hybridization in Fetuses with Cardiac Abnormalities.
Kowalczyk K, Bartnik-Głaska M, Smyk M, Plaskota I, Bernaciak J, Kędzior M, Wiśniowiecka-Kowalnik B, Jakubów-Durska K, Braun-Walicka N, Barczyk A, Geremek M, Castañeda J, Kutkowska-Kaźmierczak A, Własienko P, Dębska M, Kucińska-Chahwan A, Roszkowski T, Kozłowski S, Mikulska B, Issat T, Obersztyn E, Nowakowska BA.
Kowalczyk K, et al. Among authors: plaskota i.
Genes (Basel). 2021 Dec 19;12(12):2021. doi: 10.3390/genes12122021.
Genes (Basel). 2021.
PMID: 34946970
Free PMC article.
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Comparative Genomic Hybridization to Microarrays in Fetuses with High-Risk Prenatal Indications: Polish Experience with 7400 Pregnancies.
Kowalczyk K, Bartnik-Głaska M, Smyk M, Plaskota I, Bernaciak J, Kędzior M, Wiśniowiecka-Kowalnik B, Deperas M, Domaradzka J, Łuszczek A, Dutkiewicz D, Kozar A, Grad D, Niemiec M, Ziemkiewicz K, Magdziak R, Braun-Walicka N, Barczyk A, Geremek M, Castañeda J, Kutkowska-Kaźmierczak A, Własienko P, Jakubów-Durska K, Dębska M, Kucińska-Chahwan A, Kozłowski S, Mikulska B, Issat T, Roszkowski T, Nawara-Baran A, Runge A, Jakubiuk-Tomaszuk A, Kruczek A, Kostyk E, Pietras G, Limon J, Zwoliński J, Ochman K, Szajner T, Węgrzyn P, Wielgoś M, Sąsiadek M, Obersztyn E, Nowakowska BA.
Kowalczyk K, et al. Among authors: plaskota i.
Genes (Basel). 2022 Apr 14;13(4):690. doi: 10.3390/genes13040690.
Genes (Basel). 2022.
PMID: 35456496
Free PMC article.
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Application of array comparative genomic hybridization (aCGH) for identification of chromosomal aberrations in the recurrent pregnancy loss.
Kowalczyk K, Smyk M, Bartnik-Głaska M, Plaskota I, Wiśniowiecka-Kowalnik B, Bernaciak J, Chojnacka M, Paczkowska M, Niemiec M, Dutkiewicz D, Kozar A, Magdziak R, Krawczyk W, Pietras G, Michalak E, Klepacka T, Obersztyn E, Bal J, Nowakowska BA.
Kowalczyk K, et al. Among authors: plaskota i.
J Assist Reprod Genet. 2022 Feb;39(2):357-367. doi: 10.1007/s10815-022-02400-8. Epub 2022 Jan 26.
J Assist Reprod Genet. 2022.
PMID: 35079943
Free PMC article.
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Sdf-1 (CXCL12) induces CD9 expression in stem cells engaged in muscle regeneration.
Brzoska E, Kowalski K, Markowska-Zagrajek A, Kowalewska M, Archacki R, Plaskota I, Stremińska W, Jańczyk-Ilach K, Ciemerych MA.
Brzoska E, et al. Among authors: plaskota i.
Stem Cell Res Ther. 2015 Mar 24;6(1):46. doi: 10.1186/s13287-015-0041-1.
Stem Cell Res Ther. 2015.
PMID: 25890097
Free PMC article.
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