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Single-nucleus transcriptome analysis provides new insights into B chromosome elimination in sorghum

by admin | Oct 7, 2025 | News

B chromosomes (Bs) are supernumerary entities found in many plant species, with some exhibiting tissue-specific elimination. In Sorghum purpureosericeum, extensive level of the B chromosome elimination occurs during embryogenesis. It progresses quickly and affects...

De novo heterozygous variants in EHMT2 genocopy Kleefstra syndrome via loss of G9a methyltransferase activity

by admin | Sep 25, 2025 | News

EHMT1 and EHMT2 genes encode human euchromatin histone lysine methyltransferase 1 and 2 (EHMT1 alias GLP; EHMT2 alias G9a) that form heteromeric GLP/G9a complexes with essential roles in epigenetic regulation of gene expression. While EHMT1 haploinsufficiency was...

Novel structure motif for the selective inhibition of TET1 protein based on perimidines

by admin | Aug 20, 2025 | News

The targeting of epigenetic factors, particularly TET proteins (ten-eleven translocation methylcytosine dioxygenases), has emerged as a significant focus in medicinal and biological research. Recent findings indicate that iron chelators possess substantial potential...

Mechanistic Modelling of Recessive Disease through Allelic Integration of Variant Effects

by admin | Aug 16, 2025 | News

Interpreting the effects of genetic variants remains a major challenge in recessive diseases, where clinical outcomes often depend on interactions between alleles. Multiplex assays of variant effects (MAVEs) measure variant function at scale, but nonlinear...

PU.1-driven enrichment enables microglia profiling from frozen brain tissue using the high-throughput Smart-seq3xpress method

by admin | Aug 15, 2025 | News

Single-cell transcriptomics has revealed the central role of microglia in brain development, homeostasis, and disease, particularly in the context of neuroinflammation. While single-cell RNA-sequencing enables targeted microglial analysis from fresh tissue, studying...
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Recent Posts

  • The list of recent publications supported by CZ.02.01.01/00/23_020/0008540 has been updated. – 27.2.2026
  • Long-Read Sequencing of the MUC1 VNTR: Genomic Variation, Mutational Landscape, and Its Impact on ADTKD Diagnosis and Progression
  • An Observational Study of SGLT2 Inhibitors and Their Use in Autosomal Dominant  Tubulointerstitial Kidney Disease
  • DDX3X syndrome: a multicenter genotype-phenotype study
  • Physiological cell culture media alter nucleotide metabolism in T lymphocytes and increase their sensitivity to methotrexate

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The MULTIOMICS_CZ project is supported by programme Johannes Amos Comenius, Ministry of Education, Youth and Sports of the Czech Republic,
ID Project CZ.02.01.01/00/23_020/0008540 – Co-funded by the European Union.

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