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4. Prelude to malignancy: A gene expression signature in normal mammary gland from breast cancer patients suggests pre‐tumorous alterations and is associated with adverse outcomes

5. High prevalence of somatic PIK3CA and TP53 pathogenic variants in the normal mammary gland tissue of sporadic breast cancer patients revealed by duplex sequencing

6. Personalized health risk assessment based on single-cell RNA sequencing analysis of a male with 45, X/48, XYYY karyotype

7. Tumor Predisposing Post-Zygotic Chromosomal Alterations in Bladder Cancer—Insights from Histologically Normal Urothelium

8. Tumor Predisposing Post-Zygotic Chromosomal Alterations in Bladder Cancer-Insights from Histologically Normal Urothelium

9. Immune cells lacking Y chromosome show dysregulation of autosomal gene expression

10. FRAX prognostic and intervention thresholds in the management of major bone fractures in hemodialysis patients: A two-year prospective multicenter cohort study

11. A vector-enzymatic DNA fragment amplification-expression technology for construction of artificial, concatemeric DNA, RNA and proteins for novel biomaterials, biomedical and industrial applications

12. Epigenetic inhibitor zebularine activates ear pinna wound closure in the mouse

13. Plasma protein changes reflect colorectal cancer development and associated inflammation

14. Plasma protein changes reflect colorectal cancer development and associated inflammation

15. Size matters - the impact of nucleus size on results from spatial transcriptomics

16. Additional file 3 of Size matters: the impact of nucleus size on results from spatial transcriptomics

17. Additional file 1 of Size matters: the impact of nucleus size on results from spatial transcriptomics

18. Additional file 4 of Size matters: the impact of nucleus size on results from spatial transcriptomics

19. Additional file 2 of Size matters: the impact of nucleus size on results from spatial transcriptomics

21. Immunophenotyping and transcriptional profiling of in vitro cultured human adipose tissue derived stem cells

22. Regenerative Drug Discovery Using Ear Pinna Punch Wound Model in Mice

23. Comprehensive cancer-oriented biobanking resource of human samples for studies of post-zygotic genetic variation involved in cancer predisposition

24. Comprehensive cancer-oriented biobanking resource of human samples for studies of post-zygotic genetic variation involved in cancer predisposition

25. Size matters - the impact of nucleus size on results from spatial transcriptomics

26. Targeted massively parallel sequencing of candidate regions on chromosome 22q predisposing to multiple schwannomas: An analysis of 51 individuals in a single‐center experience

28. Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas

29. Concurrent DNA Copy-Number Alterations and Mutations in Genes Related to Maintenance of Genome Stability in Uninvolved Mammary Glandular Tissue from Breast Cancer Patients

30. High prevalence of somatic PIK3CA and TP53 pathogenic variants in the normal mammary gland tissue of sporadic breast cancer patients revealed by duplex sequencing.

31. Comprehensive cancer-oriented biobanking resource of human samples for studies of post-zygotic genetic variation involved in cancer predisposition

33. PTD4 Peptide Increases Neural Viability in an In Vitro Model of Acute Ischemic Stroke

35. Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles

37. Development of a Peptide Derived from Platelet-Derived Growth Factor (PDGF-BB) into a Potential Drug Candidate for the Treatment of Wounds

40. Imunofan—RDKVYR Peptide—Stimulates Skin Cell Proliferation and Promotes Tissue Repair

41. Data regarding a new, vector-enzymatic DNA fragment amplification-expression technology for the construction of artificial, concatemeric DNA, RNA and proteins, as well as biological effects of selected polypeptides obtained using this method

42. Targeted massively parallel sequencing of candidate regions on chromosome 22q predisposing to multiple schwannomas: An analysis of 51 individuals in a single‐center experience.

44. Somatic Mosaicism for Copy Number Variation in Differentiated Human Tissues

46. Profiling of Copy Number Variations (CNVs) in Healthy Individuals From Three Ethnic Groups Using a Human Genome 32 K BA&Clone-Based Array

50. Identification of Genetic Aberrations on Chromosome 22 Outside the NF2 Locus in Schwannomatosis and Neurofibromatosis Type 2

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