sameAs
Oncogenomic portals for the visualization and analysis of genome-wide cancer dataCopy number variation of genes involved in the hepatitis C virus-human interactomeTSC1 loss synergizes with KRAS activation in lung cancer development in the mouse and confers rapamycin sensitivity.Combined SSCP/duplex analysis by capillary electrophoresis for more efficient mutation detection.Different levels of let-7d expression modulate response of FaDu cells to irradiation and chemotherapeuticsCopy number variation of microRNA genes in the human genomeStructural basis of microRNA length variety.PCR-SSCP-HDX analysis of pooled DNA for more rapid detection of germline mutations in large genes. The BRCA1 example.The use of a two-tiered testing strategy for the simultaneous detection of small EGFR mutations and EGFR amplification in lung cancer.The role of the precursor structure in the biogenesis of microRNAStructures of trinucleotide repeats in human transcripts and their functional implications.Selection of reference genes for qPCR- and ddPCR-based analyses of gene expression in Senescing Barley leaves.Analysis of large mutations in BARD1 in patients with breast and/or ovarian cancer: the Polish population as an exampleA prospective assessment of the Y402H variant in complement factor H, genetic variants in C-reactive protein, and risk of age-related macular degenerationCopy number variation in the region harboring SOX9 gene in dogs with testicular/ovotesticular disorder of sex development (78,XX; SRY-negative)MTTE: an innovative strategy for the evaluation of targeted/exome enrichment efficiencyArabidopsis thaliana population analysis reveals high plasticity of the genomic region spanning MSH2, AT3G18530 and AT3G18535 genes and provides evidence for NAHR-driven recurrent CNV events occurring in this location.High copy number variation of cancer-related microRNA genes and frequent amplification of DICER1 and DROSHA in lung cancer.MLPA-Based Analysis of Copy Number Variation in Plant Populations.Economical protocol for combined single-strand conformation polymorphism and heteroduplex analysis on a standard capillary electrophoresis apparatus.Trinucleotide repeats in human genome and exome.Simultaneous detection of mutations and copy number variation of NPM1 in the acute myeloid leukemia using multiplex ligation-dependent probe amplification.Unpredictable changes of selected miRNA in expression profile of HNSCC.Association of common CRP gene variants with CRP levels and cardiovascular events.Cancer predisposing BARD1 mutations affect exon skipping and are associated with overexpression of specific BARD1 isoforms.Analysis of PKD1 for genomic deletion by multiplex ligation-dependent probe assay: absence of hot spots.Assessment of FSHR, AMH, and AMHRII variants in women with polycystic ovary syndrome.Comprehensive analysis of microorganisms accompanying human archaeological remains.Germline Mutations in BRCA1 and BRCA2 in Polish Families Predisposed to Breast and Ovary Cancers.Qualitative and quantitative effects of APOE genetic variation on plasma C-reactive protein, LDL-cholesterol, and apoE protein.The 30 kb deletion in the APOBEC3 cluster decreases APOBEC3A and APOBEC3B expression and creates a transcriptionally active hybrid gene but does not associate with breast cancer in the European population.A mosaic genetic structure of the human population living in the South Baltic region during the Iron Age.The preliminary association study of ADIPOQ, RBP4, and BCMO1 variants with polycystic ovary syndrome and with biochemical characteristics in a cohort of Polish women.Quantitative Methods to Monitor RNA Biomarkers in Myotonic Dystrophy.Design and generation of MLPA probe sets for combined copy number and small-mutation analysis of human genes: EGFR as an example.Novel BRCA1 mutations and more frequent intron-20 alteration found among 236 women from Western Poland.NPM1 alternative transcripts are upregulated in acute myeloid and lymphoblastic leukemia and their expression level affects patient outcomeSpectrum and Prevalence of Pathogenic Variants in Ovarian Cancer Susceptibility Genes in a Group of 333 PatientsGoth migration induced changes in the matrilineal genetic structure of the central-east European populationFaster and cheaper PCR on a standard thermocycler
P50
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P50
description
polski profesor nauk biologicznych
@pl
researcher
@en
հետազոտող
@hy
name
Piotr Kozlowski
@ast
Piotr Kozlowski
@en
Piotr Kozlowski
@es
Piotr Kozlowski
@nl
Piotr Kozłowski (biolog)
@pl
type
label
Piotr Kozlowski
@ast
Piotr Kozlowski
@en
Piotr Kozlowski
@es
Piotr Kozlowski
@nl
Piotr Kozłowski (biolog)
@pl
prefLabel
Piotr Kozlowski
@ast
Piotr Kozlowski
@en
Piotr Kozlowski
@es
Piotr Kozlowski
@nl
Piotr Kozłowski (biolog)
@pl
P106
P1153
56803390700
P21
P31
P496
0000-0003-3770-7715