Pages that link to "Q47015370"
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The following pages link to Michał Witt (Q47015370):
Displaying 50 items.
- DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm (Q24308710) (← links)
- Hematopoietic chimerism after allogeneic stem cell transplantation: a comparison of quantitative analysis by automated DNA sizing and fluorescent in situ hybridization (Q24792994) (← links)
- GLP-1/GIP chimeric peptides define the structural requirements for specific ligand-receptor interaction of GLP-1 (Q28289025) (← links)
- Feedback of Individual Genetic Results to Research Participants: Is It Feasible in Europe? (Q28601041) (← links)
- CFTR mutations spectrum and the efficiency of molecular diagnostics in Polish cystic fibrosis patients (Q28658587) (← links)
- Effects of age and gender on micronucleus and chromosome nondisjunction frequencies in centenarians and younger subjects (Q29040491) (← links)
- Aminoglycoside-stimulated readthrough of premature termination codons in selected genes involved in primary ciliary dyskinesia. (Q30820082) (← links)
- Cystic fibrosis--a probable cause of Frédéric Chopin's suffering and death (Q33186091) (← links)
- 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 (Q33588450) (← links)
- An improved, non-isotopic method of screening cells from patients with abnormalities of sexual differentiation for Y chromosomal DNA content (Q33595207) (← links)
- Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders--updated European recommendations (Q34325346) (← links)
- Population specificity of the DNAI1 gene mutation spectrum in primary ciliary dyskinesia (PCD). (Q34461593) (← links)
- Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe. (Q34508648) (← links)
- Apparent X-linked primary ciliary dyskinesia associated with retinitis pigmentosa and a hearing loss. (Q34545593) (← links)
- Recent advances in primary ciliary dyskinesia genetics. (Q34852544) (← links)
- Ciliary genes are down-regulated in bronchial tissue of primary ciliary dyskinesia patients (Q35091627) (← links)
- Manifestations of ageing at the cytogenetic level (Q35201302) (← links)
- Ullrich-Turner syndrome with a small ring X chromosome and presence of mental retardation (Q35442921) (← links)
- Current genetic methodologies in the identification of disaster victims and in forensic analysis (Q35693617) (← links)
- Mutations in radial spoke head genes and ultrastructural cilia defects in East-European cohort of primary ciliary dyskinesia patients (Q35842529) (← links)
- Impact of SNPs on methylation readouts by Illumina Infinium HumanMethylation450 BeadChip Array: implications for comparative population studies. (Q35852853) (← links)
- Primary ciliary dyskinesia: genes, candidate genes and chromosomal regions (Q35861187) (← links)
- ZMYND10--Mutation Analysis in Slavic Patients with Primary Ciliary Dyskinesia (Q35908459) (← links)
- Association of germline genetic variants in RFC, IL15 and VDR genes with minimal residual disease in pediatric B-cell precursor ALL. (Q37101299) (← links)
- Cytogenetic perspective of ageing and longevity in men and women (Q37564853) (← links)
- In vitro culturing of ciliary respiratory cells--a model for studies of genetic diseases (Q37815055) (← links)
- T-cell acute lymphoblastic leukaemia: recent molecular biology findings (Q37965247) (← links)
- Molecular assessment of post-BMT chimerism using various biologic specimens and automated DNA sizing technology (Q38465090) (← links)
- An international registry for primary ciliary dyskinesia (Q40219751) (← links)
- EurEAs_Gplex--A new SNaPshot assay for continental population discrimination and gender identification (Q40371687) (← links)
- Binding specificity and signal transduction of receptors for glucagon-like peptide-1(7-36)amide and gastric inhibitory polypeptide on RINm5F insulinoma cells (Q41549335) (← links)
- Polymerase chain reactions with alphoid-repeat primers in combination with Alu or LINEs primers, generate chromosome-specific DNA fragments (Q41677260) (← links)
- Simultaneous transplantation of two allogeneic units of cord blood in an adult patient with acute myeloblastic leukemia: a case report. (Q44129802) (← links)
- RPGR mutations might cause reduced orientation of respiratory cilia (Q44640058) (← links)
- Gene expression studies in cells from primary ciliary dyskinesia patients identify 208 potential ciliary genes. (Q45843543) (← links)
- Infant acute bilineal leukemia (Q46088310) (← links)
- Cost-effective screening of DNMT3A coding sequence identifies somatic mutation in pediatric T-cell acute lymphoblastic leukemia (Q47804935) (← links)
- PCD and RP: X-linked inheritance of both disorders? (Q49310161) (← links)
- A Closer Look at Frederic Chopin's Cause of Death (Q50068692) (← links)
- SRY gen--primary "switch" in human sex determination? (Q51002759) (← links)
- Correlation between the level of cytogenetic aberrations in cultured human lymphocytes and the age and gender of donors. (Q53605072) (← links)
- BCL11B, FLT3, NOTCH1 and FBXW7 mutation status in T-cell acute lymphoblastic leukemia patients. (Q54479492) (← links)
- Sequence analysis of 21 genes located in the Kartagener syndrome linkage region on chromosome 15q (Q56968837) (← links)
- Monika Kraszewska (Q57073220) (← links)
- Identification of Endogenous Control miRNAs for RT-qPCR in T-Cell Acute Lymphoblastic Leukemia (Q57210049) (← links)
- Transcriptomic population markers for human population discrimination (Q58797706) (← links)
- Disease not genetic but infectious: multiple tuberculomas and fibrinous pericarditis as symptoms pathognomonic for tuberculosis of Frederic Chopin (Q60296966) (← links)
- Comprehensive Investigation of miRNome Identifies Novel Candidate miRNA-mRNA Interactions Implicated in T-Cell Acute Lymphoblastic Leukemia (Q64238834) (← links)
- Bronisława Szarzyńska-Zawadzka (Q64516556) (← links)
- [A model of genetic therapy of selected disease entities] (Q68233770) (← links)