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The potential of exosomes in regenerative medicine and in the diagnosis and therapies of neurodegenerative diseases and cancer

by admin | Oct 16, 2025 | Publications

Odehnalová N, Šandriková V, Hromadka R, et al (2025) Front Med 12 https://doi.org/10.3389/fmed.2025.1539714

Integrated omics reveals disease-associated radial glia-like cells with epigenetically dysregulated interferon response in multiple sclerosis

by admin | Oct 16, 2025 | Publications

Park B, Nicaise AM, Tsitsipatis D, et al (2025) Neuron https://doi.org/10.1016/j.neuron.2025.09.022

Genetic Testing in Adults over 50 Years with Chronic Kidney Disease: Diagnostic Yield and Clinical Implications in a Specialized Kidney Genetics Clinic

by admin | Oct 16, 2025 | Publications

Schott C, Alajmi M, Bukhari M, et al (2025) Genes (Basel) 16 https://doi.org/10.3390/genes16040408

Interaction of Selected Anthracycline and Tetracycline Chemotherapeutics with Poly(I:C) Molecules

by admin | Oct 16, 2025 | Publications

Skaličková M, Abramenko N, Charnavets T, et al (2025) ACS Omega 10:15935–15946. https://doi.org/10.1021/acsomega.4c05483

Recent Advances in Understanding the Pathophysiology of Fabry Disease

by admin | Oct 16, 2025 | Publications

Warnock DG, Linhart A, Bleyer AJ, Kmoch S (2025) Nephron 569–571 https://doi.org/10.1159/000546085

Phosphoribosylformylglycinamidine Synthase (PFAS) Deficiency: Clinical, Genetic and Metabolic Characterisation of a Novel Defect in Purine de Novo Synthesis

by admin | Oct 16, 2025 | Publications

Zikanova M, Skopova V, Stuurman KE, et al (2025) J Inherit Metab Dis 48:1–8 https://doi.org/10.1002/jimd.70041
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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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