178 results on '"Limon, Janusz"'
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2. Legend for supplementary Figure S1 from Tumor Genotype Is an Independent Prognostic Factor in Primary Gastrointestinal Stromal Tumors of Gastric Origin: A European Multicenter Analysis Based on ConticaGIST
3. Figure S1 from Tumor Genotype Is an Independent Prognostic Factor in Primary Gastrointestinal Stromal Tumors of Gastric Origin: A European Multicenter Analysis Based on ConticaGIST
4. Comparative Genomic Hybridization to Microarrays in Fetuses with High-Risk Prenatal Indications: Polish Experience with 7400 Pregnancies
5. Albert de la Chapelle—pro memoriam
6. Monitoring the Effects of Hypolipidemic Treatment in Children with Familial Hypercholesterolemia in Poland
7. Association of Genes Related to Oxidative Stress with the Extent of Coronary Atherosclerosis
8. NADPH Oxidase Gene Polymorphism is Associated with Mortality and Cardiovascular Events in 7-Year Follow-Up
9. Cell-free DNA BRAF V600E measurements during BRAF inhibitor therapy of metastatic melanoma: long-term analysis
10. Bayesian multilevel model of micro RNA levels in ovarian-cancer and healthy subjects
11. Folate/homocysteine metabolism and lung cancer risk among smokers
12. Synergy between the alteration in the N-terminal region of butyrylcholinesterase K variant and apolipoprotein E4 in late-onset Alzheimer’s disease
13. A study in a Polish ataxia cohort indicates genetic heterogeneity and points to MTCL1 as a novel candidate gene
14. Spectrum and Prevalence of Pathogenic Variants in Ovarian Cancer Susceptibility Genes in a Group of 333 Patients
15. Detection of BRCA1/2 mutations in circulating tumor DNA from patients with ovarian cancer
16. Skuteczna chemioterapia indukująco-konsolidująca u 20-letniej chorej na ostrą białaczkę promielocytową niewyrażającej zgody na przetoczenia preparatów krwiopochodnych z powodu przekonań religijnych
17. Mitochondrial DNA levels in Huntington disease leukocytes and dermal fibroblasts
18. Application of high-resolution genomic profiling in the differential diagnosis of liposarcoma
19. Antagonizing functions of BARD1 and its alternatively spliced variant BARD1δ in telomere stability
20. An open label phase II study evaluating first-line EGFR tyrosine kinase inhibitor erlotinib in non-small cell lung cancer patients with tumors showing high EGFR gene copy number
21. Genomic findings in patients with clinical suspicion of 22q11.2 deletion syndrome
22. Coincidence of PTPN22 c.1858CC and FCRL3 -169CC genotypes as a biomarker of preserved residual β-cell function in children with type 1 diabetes
23. B26 Differential mitochondrial DNA levels in HD patients depending on the cell type
24. Efficacy of clinical diagnostic criteria for familial hypercholesterolemia genetic testing in Poland
25. The algorithm for Alzheimer risk assessment based on APOE promoter polymorphisms
26. Detection of somaticBRCA 1/2mutations in ovarian cancer – next‐generation sequencing analysis of 100 cases
27. A simple modification to improve the accuracy of methylation-sensitive restriction enzyme quantitative polymerase chain reaction
28. Transcriptomic Effects of Estrogen Starvation and Induction in the MCF7 Cells. The Meta-analysis of Microarray Results
29. A novel splicing mutation in the SLC9A3R1 gene in tumors from ovarian cancer patients
30. EGFR mutation diagnostic program for NSCLC patients in Poland between 2011-2014
31. Cancer predisposing BARD1 mutations affect exon skipping and are associated with overexpression of specific BARD1 isoforms
32. Concurrent DNA Copy-Number Alterations and Mutations in Genes Related to Maintenance of Genome Stability in Uninvolved Mammary Glandular Tissue from Breast Cancer Patients
33. NOD2 gene variant rs2066844 and association with postoperative respiratory failure phenotype in 517 elective adult cardiac surgical patients
34. Analysis of large mutations in BARD1 in patients with breast and/or ovarian cancer: the Polish population as an example
35. Tumor Genotype Is an Independent Prognostic Factor in Primary Gastrointestinal Stromal Tumors of Gastric Origin: A European Multicenter Analysis Based on ConticaGIST
36. Chromosome 18q deletion syndrome with autoimmune diabetes mellitus: putative genomic loci for autoimmunity and immunodeficiency
37. Mutational analysis of BRCA1/2 in a group of 134 consecutive ovarian cancer patients. Novel and recurrent BRCA1/2 alterations detected by next generation sequencing
38. Mild phenotype of a large partial 13q trisomy
39. Noninvasive assessment of endothelial function and vascular parameters in patients with familial and nonfamilial hypercholesterolemia
40. Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe
41. The efficacy of EGFR gene mutation testing in various samples from non-small cell lung cancer patients: a multicenter retrospective study
42. Rare cancers
43. Management of familial hypercholesterolemia in children and adolescents. Position paper of the Polish Lipid Expert Forum
44. Original article Proliferation index revisited in neuroblastic tumors
45. The Outcome of Targeted Therapy in Advanced Gastrointestinal Stromal Tumors (Gist) with Non-Exon 11 Kit Mutations
46. What are the current outcomes of advanced gastrointestinal stromal tumors: who are the long-term survivors treated initially with imatinib?
47. Stanowisko dotyczące postępowania w rodzinnej hipercholesterolemii u dzieci i młodzieży. Stanowisko Forum Ekspertów Lipidowych
48. Management in familial hypercholesterolaemia in children and adolescents. Position of the Lipid Expert Forum
49. Polymorphisms of the Histamine Receptor (H1HR) Gene Are Not Associated With Olanzapine-Induced Weight Gain
50. High Resolution Melting analysis as a rapid and efficient method of screening for small mutations in the STK11gene in patients with Peutz-Jeghers syndrome
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