Tina Beyer
Elfriede Aulhorn Str. 7
Tuebingen, BW 72076, Germany
Tuebingen, BW 72076, Germany
Last Updated: 09/26/2026
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Found 30 publications
Identification of novel blood-borne soluble binding partners of factor H-related proteins.
Journal: Scientific reports
Published: September 23, 2025
Loss of INPP5E affects photoreceptor outer segment membrane biogenesis in iPSC-derived human retinal organoids.
Journal: Journal of cell science
Published: September 05, 2025
The EH Binding protein EHBP1 operates in a ciliary functional module affected by INPP5E dysfunction.
The EH Binding protein EHBP1 operates in a ciliary functional module affected by INPP5E dysfunction.
Journal: Journal of cell science
Published: April 16, 2025
The EH-binding protein EHBP1 operates in a ciliary functional module affected by INPP5E dysfunction.
The EH-binding protein EHBP1 operates in a ciliary functional module affected by INPP5E dysfunction.
Journal: Journal of cell science
Published: April 16, 2025
Ciliopathy-Associated Missense Mutations in IFT140 are Tolerated by the Inherent Resilience of the IFT Machinery.
Journal: Molecular & cellular proteomics : MCP
Published: April 25, 2024
WeSA: a web server for improving analysis of affinity proteomics data.
Journal: Nucleic acids research
Published: March 24, 2024
Mutant dominant-negative rhodopsin∆I256 causes protein aggregates degraded via ERAD and prevents normal rhodopsin from proper membrane trafficking.
Journal: Frontiers in molecular biosciences
Published: January 11, 2024
Affinity Purification of Intraflagellar Transport (IFT) Proteins in Mice Using Endogenous Streptavidin/FLAG Tags.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: October 19, 2023
Human CRB1 and CRB2 form homo- and heteromeric protein complexes in the retina.
Journal: Life science alliance
Published: October 17, 2023
Paralog-specific TTC30 regulation of Sonic hedgehog signaling.
Journal: Frontiers in molecular biosciences
Published: July 28, 2023
Defective airway intraflagellar transport underlies a combined motile and primary ciliopathy syndrome caused by IFT74 mutations.
Journal: Human molecular genetics
Published: June 23, 2023
Last Updated: 09/26/2026