All Stories

  1. Pharmacological rescue of cilia trafficking defects in IFT140 retinal organoid and RPE models of retinal dystrophy

    Article • May 2026, openRxiv

    Marian Seda

  2. Ciliopathy-Associated Missense Mutations in IFT140 are Tolerated by the Inherent Resilience of the IFT Machinery

    Article • Molecular & Cellular Proteomics, March 2025, Elsevier

    Marian Seda

  3. Structure and tethering mechanism of dynein-2 intermediate chains in intraflagellar transport

    Article • The EMBO Journal, March 2024, Springer Science + Business Media

    Marian Seda

  4. De-Suppression of Mesenchymal Cell Identities and Variable Phenotypic Outcomes Associated with Knockout of Bbs1

    Article • Cells, November 2023, MDPI AG

    Marian Seda

  5. Affinity Purification of Intraflagellar Transport (IFT) Proteins in Mice Using Endogenous Streptavidin/FLAG Tags

    Article • October 2023, Springer Science + Business Media

    Marian Seda

  6. A CRISPR/Cas9-generated mutation in the zebrafish orthologue of PPP2R3B causes idiopathic scoliosis

    Article • Scientific Reports, April 2023, Springer Science + Business Media

    Marian Seda

  7. Ciliopathy-associated missense mutations in IFT140 are hypomorphic and have edgetic effects on protein interaction networks

    Article • January 2023, Cold Spring Harbor Laboratory Press

    Marian Seda

  8. A CRISPR/Cas9-generated mutation in the zebrafish orthologue of PPP2R3B causes idiopathic scoliosis

    Article • December 2022, Research Square

    Marian Seda

  9. Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutations

    Article • Scientific Reports, August 2020, Springer Science + Business Media

    Marian Seda

  10. Diverse Species-Specific Phenotypic Consequences of Loss of Function Sorting Nexin 14 Mutations

    Article • November 2019, Cold Spring Harbor Laboratory Press

    Marian Seda

  11. Generating Mutant Renal Cell Lines Using CRISPR Technologies

    Article • November 2019, Springer Science + Business Media

    David Long, Marian Seda

  12. Analysis of transgenic zebrafish expressing the Lenz-Majewski syndrome gene PTDSS1 in skeletal cell lineages

    Article • F1000Research, March 2019, Faculty of 1000, Ltd.

    Marian Seda

  13. A CRISPR/Cas9-generated zebrafish mutant implicates PPP2R3B loss in idiopathic scoliosis pathogenesis in Turner syndrome.

    Article • September 2018, Cold Spring Harbor Laboratory Press

    Marian Seda

  14. An FDA-Approved Drug Screen for Compounds Influencing Craniofacial Skeletal Development and Craniosynostosis

    Article • Molecular Syndromology, July 2018, Karger Publishers

    Marian Seda

  15. SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20

    Article • Human Molecular Genetics, April 2018, Oxford University Press (OUP)

    Marian Seda

  16. Dissecting the Transcriptional Regulatory Properties of Human Chromosome 16 Highly Conserved Non-Coding Regions

    Article • PLOS One, September 2011, PLOS

    Altuna A, Marian Seda

  17. Functional and Molecular Characterization of Voltage-Gated Sodium Channels in Uteri from Nonpregnant Rats1

    Article • Biology of Reproduction, November 2007, Oxford University Press (OUP)

    Marian Seda

  18. A role for tachykinins in the regulation of human sperm motility

    Article • Human Reproduction, April 2007, Oxford University Press (OUP)

    Marian Seda

  19. Molecular diversity of voltage-gated sodium channel α and β subunit mRNAs in human tissues

    Article • European Journal of Pharmacology, July 2006, Elsevier

    Marian Seda