Publications by authors named "Witt Michal"

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The lack of homozygotes with a large deletion encompassing and in primary ciliary dyskinesia patients suggests the lethal effect of the loss of POLR2K protein.
Alicja Rabiasz, Monika Drobna-Śledzińska, Patrycja Kaźmierczak, Michał Witt, Ewa Ziętkiewicz

Genes Dis· November 2025

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Analyses of 1236 genotyped primary ciliary dyskinesia individuals identify regional clusters of distinct DNA variants and significant genotype-phenotype correlations.
Johanna Raidt, Sarah Riepenhausen, Petra Pennekamp, Heike Olbrich, Israel Amirav, Michal Witt

Eur Respir J· August 2024

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Genetic data protection as an indispensable element of genomic medicine development.
Małgorzata Madej, Paweł Karpiński, Hayane Akopyan, Michał Witt, Maria M Sąsiadek

Pol Arch Intern Med· February 2023

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Multiomics to investigate the mechanisms contributing to repression of PTPRC and SOCS2 in pediatric T-ALL: Focus on miR-363-3p and promoter methylation.
Monika Drobna-Śledzińska, Natalia Maćkowska-Maślak, Roman Jaksik, Maria Kosmalska, Bronisława Szarzyńska

Genes Chromosomes Cancer· December 2022

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The hero of American and Polish nations: a molecular look at Thaddeus Kosciuszko's cause of death suggests a contribution of endocarditis caused by Cutibacterium acnes infection.
Michał Witt, Miron Tokarski, Ewa Ziętkiewicz, Arleta Lebioda, Maria Szczypek

Microb Cell Fact· November 2022

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Small RNA-Seq Reveals Similar miRNA Transcriptome in Children and Young Adults with T-ALL and Indicates miR-143-3p as Novel Candidate Tumor Suppressor in This Leukemia.
Małgorzata Dawidowska, Natalia Maćkowska-Maślak, Monika Drobna-Śledzińska, Maria Kosmalska, Roman Jaksik

Int J Mol Sci· September 2022

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CRISPRi for specific inhibition of miRNA clusters and miRNAs with high sequence homology.
Monika Drobna-Śledzińska, Natalia Maćkowska-Maślak, Roman Jaksik, Paulina Dąbek, Michał Witt

Sci Rep· April 2022

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Perspectives for Primary Ciliary Dyskinesia.
Zuzanna Bukowy-Bieryllo, Michal Witt, Ewa Zietkiewicz

Int J Mol Sci· April 2022

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Genetic testing-whether to allow complete freedom? Direct to consumer tests versus genetic tests for medical purposes.
Madej Malgorzata, Sąsiadek Maria, Witt Michał

J Appl Genet· February 2022

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In vitro differentiation of ciliated cells in ALI-cultured human airway epithelium - The framework for functional studies on airway differentiation in ciliopathies.
Zuzanna Bukowy-Bieryłło, Patrycja Daca-Roszak, Joanna Jurczak, Hanna Przystałowska-Macioła, Roman Jaksik

Eur J Cell Biol· January 2022

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Inheritance vs. infectivity as a mechanism of malady and death of Frederic Chopin.
Michał Witt, Tadeusz Dobosz

J Appl Genet· December 2021

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European context of the diversity and phylogenetic position of SARS-CoV-2 sequences from Polish COVID-19 patients.
Szymon Hryhorowicz, Adam Ustaszewski, Marta Kaczmarek-Ryś, Emilia Lis, Michał Witt

J Appl Genet· May 2021

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DNA Methylation in T-Cell Acute Lymphoblastic Leukemia: In Search for Clinical and Biological Meaning.
Natalia Maćkowska, Monika Drobna-Śledzińska, Michał Witt, Małgorzata Dawidowska

Int J Mol Sci· January 2021

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Discrimination between human populations using a small number of differentially methylated CpG sites: a preliminary study using lymphoblastoid cell lines and peripheral blood samples of European and Chinese origin.
Patrycja Daca-Roszak, Roman Jaksik, Julia Paczkowska, Michał Witt, Ewa Ziętkiewicz

BMC Genomics· October 2020

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How far musicality and perfect pitch are derived from genetic factors?
Krzysztof Szyfter, Michał P Witt

J Appl Genet· September 2020

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Access to medicines for rare diseases: beating the drum for primary ciliary dyskinesia.
Suzanne Crowley, Inês Azevedo, Mieke Boon, Andrew Bush, Ernst Eber, Michal Witt

ERJ Open Res· July 2020

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hsa-miR-20b-5p and hsa-miR-363-3p Affect Expression of and Tumor Suppressor Genes and Modulate Survival of T-ALL Cells In Vitro.
Monika Drobna, Bronisława Szarzyńska, Roman Jaksik, Łukasz Sędek, Anna Kuchmiy

Cells· May 2020

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Truncating mutations in exons 20 and 21 of can cause primary ciliary dyskinesia without associated syndromic symptoms.
Zuzanna Bukowy-Bieryllo, Alicja Rabiasz, Maciej Dabrowski, Andrzej Pogorzelski, Alina Wojda, Michal Witt

J Med Genet· November 2019

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: Mutations in Slavic Patients with Primary Ciliary Dyskinesia and a Role in Ciliary Dynein Arms Trafficking.
Ewa Zietkiewicz, Zuzanna Bukowy-Bieryllo, Alicja Rabiasz, Patrycja Daca-Roszak, Alina Wojda, Michal Witt

Am J Respir Cell Mol Biol· October 2019

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PTEN abnormalities predict poor outcome in children with T-cell acute lymphoblastic leukemia treated according to ALL IC-BFM protocols.
Bronisława Szarzyńska-Zawadzka, Joachim B Kunz, Łukasz Sędek, Maria Kosmalska, Katarzyna Zdon

Am J Hematol· April 2019

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Comprehensive Investigation of miRNome Identifies Novel Candidate miRNA-mRNA Interactions Implicated in T-Cell Acute Lymphoblastic Leukemia.
Małgorzata Dawidowska, Roman Jaksik, Monika Drobna, Bronisława Szarzyńska-Zawadzka, Maria Kosmalska

Neoplasia· March 2019

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Disease not genetic but infectious: multiple tuberculomas and fibrinous pericarditis as symptoms pathognomonic for tuberculosis of Frederic Chopin.
Michał Witt, Artur Szklener, Wojciech Marchwica, Tadeusz Dobosz

J Appl Genet· November 2018

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Identification of Endogenous Control miRNAs for RT-qPCR in T-Cell Acute Lymphoblastic Leukemia.
Monika Drobna, Bronisława Szarzyńska-Zawadzka, Patrycja Daca-Roszak, Maria Kosmalska, Roman Jaksik

Int J Mol Sci· September 2018

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A Closer Look at Frederic Chopin's Cause of Death.
Michał Witt, Artur Szklener, Jerzy Kawecki, Witold Rużyłło, Marta Negrusz-Kawecka

Am J Med· February 2018

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Cost-effective screening of DNMT3A coding sequence identifies somatic mutation in pediatric T-cell acute lymphoblastic leukemia.
Bronisława Szarzyńska-Zawadzka, Maria Kosmalska, Łukasz Sędek, Alicja Sonsala, Magdalena Twardoch

Eur J Haematol· December 2017

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