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Expanded View of the Pathophysiology of Fabry Disease

by admin | Mar 10, 2026 | Publications

Kmoch S, Živná M, Dvela-Levitt M, et al (2025) Nephron 149:620–624. https://doi.org/10.1159/000546555

Integrated multi-omics profiling uncovers miRNA-guided regulatory networks after spinal cord injury in rats.

by admin | Mar 10, 2026 | Publications

Klassen RA, Chytilova S, Arzhanov I, et al (2025) Mol Ther Nucleic Acids 36:. https://doi.org/10.1016/j.omtn.2025.102746

Severe Prenatal Presentation of Adenylosuccinate Lyase Deficiency Caused by a Synonymous ADSL Variant Inducing Aberrant Splicing.

by admin | Mar 10, 2026 | Publications

Klapperich, A. et al. (2026) Prenatal diagnosis [Preprint]. Available at: https://doi.org/10.1002/pd.70087.

Characterization of Monogenic Kidney Disease in Older Patients With CKD

by admin | Mar 10, 2026 | Publications

Elhassan, E.A.E. et al. (2025) Kidney International Reports, 10(7), pp. 2140–2152. Available at: https://doi.org/https://doi.org/10.1016/j.ekir.2025.04.017.

Extracellular vesicles as precision therapeutics for psychiatric conditions: targeting interactions among neuronal, glial, and immune networks

by admin | Oct 16, 2025 | Publications

Kawiková I, Špička V, Lai JCK, et al (2025) Front Immunol 16:1–19 https://doi.org/10.3389/fimmu.2025.1454306

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

by admin | Oct 16, 2025 | Publications

Kejík Z, Kaplánek R, Abramenko N, et al (2026) J Mol Struct 1349 https://doi.org/10.1016/j.molstruc.2025.143720
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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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