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DDX3X syndrome: a multicenter genotype-phenotype study

by admin | Mar 10, 2026 | Publications

Unpublished preprint Coci EG, Gertzen CGW, Millan PC, et al (2025) DOI:10.21203/rs.3.rs-7842722/v1 (preprint) Available here

Physiological cell culture media alter nucleotide metabolism in T lymphocytes and increase their sensitivity to methotrexate

by admin | Mar 10, 2026 | Publications

Unpublished preprint Cano-Estrada, C. et al. (2026) (preprint – available here)

Targeting tumors and inflammation: A quinoline–chalcone ruthenium complex with therapeutic promise

by admin | Mar 10, 2026 | Publications

Veselá K, Tatar A, Kejík Z, et al (2026) Biomed Pharmacother 194:118930. https://doi.org/https://doi.org/10.1016/j.biopha.2025.118930

 Ruthenium-enhanced curcumin derivatives target tumor growth and cancer-related  inflammation in head and neck cancer models

by admin | Mar 10, 2026 | Publications

Veselá K, Tatar A, Kejík Z, et al (2025) Front Oncol 15:1708944. https://doi.org/10.3389/fonc.2025.1708944

Plasma Metabolites Associated with CKD Stage in Autosomal Dominant Tubulointerstitial Kidney Disease

by admin | Mar 10, 2026 | Publications

Mušálková, D. et al. (2026) Kidney360, 7(2). Available at: https://journals.lww.com/kidney360/fulltext/2026/02000/plasma_metabolites_associated_with_ckd_stage_in.14.aspx

Regulation of Embryonic Wound Healing by Matrix Metalloproteinases in Xenopus  laevis Tailbud Stage

by admin | Mar 10, 2026 | Publications

Kraus, D. et al. (2026) Wound repair and regeneration : official publication of the Wound Healing Society  [and] the European Tissue Repair Society, 34(1), p. e70134. Available at: https://doi.org/10.1111/wrr.70134.
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Recent Posts

  • Single-Molecule Real-Time Sequencing for MUC1 Variable Number of Tandem Repeat Variation to Improve Autosomal Dominant Tubulointerstitial Kidney Disease Diagnosis
  • Recurrent Single-Nucleotide Insertions in the Mitochondrial Second Light-Strand Promoter Cause Tubulointerstitial Kidney Disease
  • A role for EHMT2 in a novel autosomal recessive neurodevelopmental syndrome? A case report
  • paRDal: Bioinformatics Framework for a Parallel RNA and DNA NGS Analysis in Hereditary Cancer Diagnostics
  • Tri‐Parametric Assessment of α‐Galactosidase A Activity, lysoGb3 and X‐Inactivation Aids Genotype‐Phenotype Categorization of Fabry Disease Female Patients

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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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