Publikacje

Kurkowiak M, Ziętkiewicz E, Witt M

Recent advances in primary ciliary dyskinesia genetics

J Med Genet

Ziętkiewicz E, Rutkiewicz E, Pogorzelski A, Klimek B, Voelkel K, Witt M

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

PLoS One

Geremek M, Ziętkiewicz E, Bruinenberg M, Franke L, Pogorzelski A, Wijmenga C, Witt M

Ciliary genes are down-regulated in bronchial tissue of primary ciliary dyskinesia patients

PLoS One

Kraszewska MD, Dawidowska M, Kosmalska M, Sędek Ł, Grzeszczak W, Kowalczyk JR, Szczepański T, Witt M

BCL11B, FLT3, NOTCH1 and FBXW7 mutation status in T-cell Acute Lymphoblastic Leukemia patients

Blood Cells, Molecules and Diseases

Bukowy-Bieryłło Z, Ziętkiewicz E, Loges NT, Wittmer M, Geremek M, Olbrich H, Fliegauf M, Voelkel K, Rutkiewicz E, Rutland J, Morgan L, Pogorzelski A, Martin J, Haan E, Berger W, Omran H, Witt M

RPGR mutations might cause reduced orientation of respiratory cilia

Pediatr Pulmonol.

Ziętkiewicz E, Bukowy-Bieryłło Z, Voelkel K, Klimek B, Dmeńska H, Pogorzelski A, Sulikowska-Rowińska A, Rutkiewicz E, Witt M

Mutations in radial spoke head genes and ultrastructural cilia defects in East-European cohort of primary ciliary dyskinesia patients.

PLoS One

Kraszewska MD, Dawidowska M, Kosmalska M, Sędek L, Grzeszczak W, Szczepański T, Witt M

DNA methylation pattern is altered in childhood T-cell acute lymphoblastic leukemia patients as compared with normal thymic subsets: insights into CpG island methylator phenotype in T-ALL

Leukemia

Kraszewska MD, Dawidowska M, Szczepanski T, Witt M

T-cell acute lymphoblastic leukaemia: recent molecular biology findings

Br J Haematol

Kraszewska MD, Dawidowska M, Kosmalska M, Sędek L, Grzeszczak W, Szczepański T, Witt M

Immunoglobulin/T-cell receptor gene rearrangements in the diagnostic paradigm of pediatric T-cell acute lymphoblastic leukemia patients

Leukemia & Lymphoma

Ziętkiewicz E, Witt M, Daca P, Zebracka-Gala J, Goniewicz M, Jarząb B, Witt M

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

J Appl Genet.

Bukowy Z, Ziętkiewicz E, Witt M

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

J Appl Genet

Geremek M, Bruinenberg M, Ziętkiewicz E, Pogorzelski A, Witt M, Wijmenga C

Gene expression studies in cells from primary ciliary dyskinesia patients identify 208 potential ciliary genes

Hum Genet

Ziętkiewicz E, Nitka B, Voelkel K, Skrzypczak U, Bukowy Z, Rutkiewicz E, Humińska K, Przystałowska H, Pogorzelski A, Witt M

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

Respir Res

Geremek M, Schoenmaker F, Zietkiewicz E, Pogorzelski A, Diehl S, Wijmenga C, Witt M

Sequence analysis of 21 genes located in the Kartagener syndrome linkage region on chromosome 15q

Eur J Hum Genet

Dawidowska M, Jółkowska J, Szczepański T, Derwich K, Wachowiak J, Witt M

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

Arch Immunol Ther Exp (Warsz)

Wojda A, Zietkiewicz E, Witt M

Effects of age and gender on micronucleus and chromosome nondisjunction frequencies in centenarians and younger subjects

Mutagenesis

Wojda A, Zietkiewicz E, Mossakowska M, Pawłowski W, Skrzypczak K, Witt M

Correlation between the level of cytogenetic aberrations in cultured human lymphocytes and the age and gender of donors

J Gerontol A Biol Sci Med Sci

Jólkowska J, Pieczonka A, Strabel T, Boruczkowski D, Wachowiak J, Bader P, Witt M

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

BMC Blood Disord

Geremek M, Witt M

Primary ciliary dyskinesia: genes, candidate genes and chromosomal regions

J Appl Genet

Krawczyński MR, Dmeńska H, Witt M

Apparent X-linked primary ciliary dyskinesia associated with retinitis pigmentosa and a hearing loss

J Appl Genet

Krawczyński MR, Witt M

PCD and RP: X-linked inheritance of both disorders?

Pediatr Pulmonol

Lubka M, Wojda A, Witt M

Micronuclei in human cells – formation, contents, diagnostic and prognostic application

Postępy Biol Kom

Wojda A, Witt M

Manifestations of ageing at the cytogenetic level

J Appl Genet

Wojda A, Wolnik-Brzozowska D, Lubka M, Mossakowska M, Witt M

The 102-year old woman with translocation (7;12) and infertility in anamnesis

J Appl Genet

Majka L, Goździk J, Witt M

Cystic fibrosis--a probable cause of Frédéric Chopin's suffering and death

J Appl Genet