Fully exploiting SNP arrays: a systematic review on the tools to extract underlying genomic structure

L Balagué-Dobón, A Cáceres… - Briefings in …, 2022 - academic.oup.com
Single nucleotide polymorphisms (SNPs) are the most abundant type of genomic variation
and the most accessible to genotype in large cohorts. However, they individually explain a …

Downregulation of ACE, AGTR1, and ACE2 genes mediating SARS-CoV-2 pathogenesis by gut microbiota members and their postbiotics on Caco-2 cells

SA Badi, A Malek, A Paolini, MR Masoumi… - Microbial …, 2022 - Elsevier
Abstract Introduction Coronavirus disease-2019 (COVID-19) is a complex infection caused
by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that can cause also …

[HTML][HTML] Pathogenic and likely pathogenic germline variation in patients with myeloid malignancies and their unrelated HLA-matched hematopoietic stem cell donors

A Clay-Gilmour, J Cooper, J Wang, Q Zhu… - Journal of …, 2024 - oaepublish.com
Aims: The revised 2022 World Health Organization classification recognizes myeloid
neoplasms with associated germline predisposition as a defined subcategory, underscoring …

The Evolving Role of Allogeneic Stem Cell Transplant in the Era of Molecularly Targeted Agents

F Kinsella, C Craddock - The Cancer Journal, 2022 - journals.lww.com
Allogeneic stem cell transplantation (allo-SCT) is an increasingly important treatment
strategy in fit adults with acute myeloid leukemia (AML). Increased donor availability and a …

[ОПИСАНИЕ][C] Myeloperoxidase‐positive bilineal mixed phenotype acute leukemia (B/T) with chromosome copy neutral loss of heterozygosity exhibits simultaneous …

K Huang, Y Du, M Wu, Y Li, D Nie… - Pediatric Blood & …, 2023 - Wiley Online Library
To the Editor: A 28-year-old female was admitted with multiple arthralgias. Complete blood
count revealed: white blood cell 4.57× 109/L, hemoglobin 96 g/L, platelet 75× 109/L …