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01 Reduced HLA diversity and impaired immune surveillance in very early-onset ovarian cancer patients

by admin | Sep 2, 2026 | Publications

Soukupova, J. et al. (2026) “01 Reduced HLA diversity and impaired immune surveillance in very early-onset ovarian cancer patients,” Journal for Immunotherapy of Cancer, 14(Suppl 1), p. A19. Available at: https://doi.org/10.1136/JITC-2026-ITOC.34.

Thin glomerular basement membrane phenotypes with no identified pathogenic COL4A3/A4/A5 variant

by admin | Sep 2, 2026 | Publications

Riella, C. V et al. (2026) “Thin glomerular basement membrane phenotypes with no identified pathogenic COL4A3/A4/A5 variant,” Kidney International Reports, p. 106548. Available at: https://doi.org/10.1016/j.ekir.2026.106548.

ORMDL Proteins Turnover via Proteasome and Autophagy Is Cell-Type Dependent and Tied to Ceramide Homeostasis

by admin | Sep 2, 2026 | Publications

Mrkacek, M. et al. (2026) “ORMDL Proteins Turnover via Proteasome and Autophagy Is Cell-Type Dependent and Tied to Ceramide Homeostasis.,” FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 40(6), p. e71655....

Online Deglycosylation of Monomeric Intact Proteins Using the PNGase Rc Immobilized-Enzyme Reactor

by admin | Sep 2, 2026 | Publications

Molnárová, K. et al. (2026) “Online Deglycosylation of Monomeric Intact Proteins Using the PNGase Rc Immobilized-Enzyme Reactor,” ACS Omega, 11(17), pp. 25724–25729. Available at: https://doi.org/10.1021/acsomega.6c00577.

A missense mutation in the SAA1 protein causing hereditary amyloid A amyloidosis

by admin | Sep 2, 2026 | Publications

Leung, N. et al. (2026) “A missense mutation in the SAA1 protein causing hereditary amyloid A amyloidosis,” Kidney International [Preprint]. Available at: https://doi.org/10.1016/j.kint.2026.01.035.
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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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