In vitro culturing of ciliary respiratory cells—a model for studies of genetic diseases

Por Bukowy, Zuzanna, Ziętkiewicz, Ewa, Witt, Michał
Publicado em 2010

Molecular aspects of hematologic malignancies diagnostic tools and clinical applications /

Por Witt, Michal., Dawidowska, Malgorzata., Szczepanski, Tomasz.
Publicado em 2012

Recent advances in primary ciliary dyskinesia genetics

Por Kurkowiak, Małgorzata, Ziętkiewicz, Ewa, Witt, Michał
Publicado no J Med Genet (2015)

Privacy and confidentiality measures in genetic testing and counselling: arguing on genetic exceptionalism again?

Por Witt, Magdalena M., Witt, Michał P.
Publicado no J Appl Genet (2016)

Aminoglycoside-stimulated readthrough of premature termination codons in selected genes involved in primary ciliary dyskinesia

Por Bukowy-Bieryllo, Zuzanna, Dabrowski, Maciej, Witt, Michał, Zietkiewicz, Ewa
Publicado no RNA Biol (2016)

Implementation of the standard strategy for identification of Ig/TCR targets for minimal residual disease diagnostics in B-cell precursor ALL pediatric patients: Polish experience

Por Dawidowska, Małgorzata, Jółkowska, Justyna, Szczepański, Tomasz, Derwich, Katarzyna, Wachowiak, Jacek, Witt, Michał
Publicado em 2008

CFTR Mutations Spectrum and the Efficiency of Molecular Diagnostics in Polish Cystic Fibrosis Patients

Por Ziętkiewicz, Ewa, Rutkiewicz, Ewa, Pogorzelski, Andrzej, Klimek, Barbara, Voelkel, Katarzyna, Witt, Michał
Publicado em 2014

Hematopoietic chimerism after allogeneic stem cell transplantation: a comparison of quantitative analysis by automated DNA sizing and fluorescent in situ hybridization

Por Jółkowska, Justyna, Pieczonka, Anna, Strabel, Tomasz, Boruczkowski, Dariusz, Wachowiak, Jacek, Bader, Peter, Witt, Michał
Publicado em 2005

Ciliary Genes Are Down-Regulated in Bronchial Tissue of Primary Ciliary Dyskinesia Patients

Por Geremek, Maciej, Ziętkiewicz, Ewa, Bruinenberg, Marcel, Franke, Lude, Pogorzelski, Andrzej, Wijmenga, Cisca, Witt, Michał
Publicado em 2014

ZMYND10 - Mutation Analysis in Slavic Patients with Primary Ciliary Dyskinesia

Por Kurkowiak, Małgorzata, Ziętkiewicz, Ewa, Greber, Agnieszka, Voelkel, Katarzyna, Wojda, Alina, Pogorzelski, Andrzej, Witt, Michał
Publicado no PLoS One (2016)

Current genetic methodologies in the identification of disaster victims and in forensic analysis

Por Ziętkiewicz, Ewa, Witt, Magdalena, Daca, Patrycja, Żebracka-Gala, Jadwiga, Goniewicz, Mariusz, Jarząb, Barbara, Witt, Michał
Publicado em 2011

Impact of SNPs on methylation readouts by Illumina Infinium HumanMethylation450 BeadChip Array: implications for comparative population studies

Por Daca-Roszak, Patrycja, Pfeifer, Aleksandra, Żebracka-Gala, Jadwiga, Rusinek, Dagmara, Szybińska, Aleksandra, Jarząb, Barbara, Witt, Michał, Ziętkiewicz, Ewa
Publicado no BMC Genomics (2015)

Population specificity of the DNAI1 gene mutation spectrum in primary ciliary dyskinesia (PCD)

Por Ziętkiewicz, Ewa, Nitka, Barbara, Voelkel, Katarzyna, Skrzypczak, Urszula, Bukowy, Zuzanna, Rutkiewicz, Ewa, Humińska, Kinga, Przystałowska, Hanna, Pogorzelski, Andrzej, Witt, Michał
Publicado em 2010

Mutations in Radial Spoke Head Genes and Ultrastructural Cilia Defects in East-European Cohort of Primary Ciliary Dyskinesia Patients

Por Ziętkiewicz, Ewa, Bukowy-Bieryłło, Zuzanna, Voelkel, Katarzyna, Klimek, Barbara, Dmeńska, Hanna, Pogorzelski, Andrzej, Sulikowska-Rowińska, Anna, Rutkiewicz, Ewa, Witt, Michał
Publicado em 2012

Feedback of Individual Genetic Results to Research Participants: Is It Feasible in Europe?

Por Budin-Ljøsne, Isabelle, Mascalzoni, Deborah, Soini, Sirpa, Machado, Helena, Kaye, Jane, Bentzen, Heidi Beate, Rial-Sebbag, Emmanuelle, D'Abramo, Flavio, Witt, Michał, Schamps, Geneviève, Katić, Višnja, Krajnovic, Dusanca, Harris, Jennifer R.
Publicado no Biopreserv Biobank (2016)

Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders – updated European recommendations

Por Dequeker, Els, Stuhrmann, Manfred, Morris, Michael A, Casals, Teresa, Castellani, Carlo, Claustres, Mireille, Cuppens, Harry, des Georges, Marie, Ferec, Claude, Macek, Milan, Pignatti, Pier-Franco, Scheffer, Hans, Schwartz, Marianne, Witt, Michal, Schwarz, Martin, Girodon, Emmanuelle
Publicado em 2009

Association of germline genetic variants in RFC, IL15 and VDR genes with minimal residual disease in pediatric B-cell precursor ALL

Por Dawidowska, Małgorzata, Kosmalska, Maria, Sędek, Łukasz, Szczepankiewicz, Aleksandra, Twardoch, Magdalena, Sonsala, Alicja, Szarzyńska-Zawadzka, Bronisława, Derwich, Katarzyna, Lejman, Monika, Pawelec, Katarzyna, Obitko-Płudowska, Agnieszka, Pawińska-Wąsikowska, Katarzyna, Kwiecińska, Kinga, Kołtan, Andrzej, Dyla, Agnieszka, Grzeszczak, Władysław, Kowalczyk, Jerzy R., Szczepański, Tomasz, Ziętkiewicz, Ewa, Witt, Michał
Publicado no Sci Rep (2016)

DNAI2 Mutations Cause Primary Ciliary Dyskinesia with Defects in the Outer Dynein Arm

Por Loges, Niki Tomas, Olbrich, Heike, Fenske, Lale, Mussaffi, Huda, Horvath, Judit, Fliegauf, Manfred, Kuhl, Heiner, Baktai, Gyorgy, Peterffy, Erzsebet, Chodhari, Rahul, Chung, Eddie M.K., Rutman, Andrew, O'Callaghan, Christopher, Blau, Hannah, Tiszlavicz, Laszlo, Voelkel, Katarzyna, Witt, Michal, Ziętkiewicz, Ewa, Neesen, Juergen, Reinhardt, Richard, Mitchison, Hannah M., Omran, Heymut
Publicado em 2008