ArticleBiochemistry and biophysics reports2026
Oxysterol-binding protein-related protein 6 regulates neuronal morphology and migration of cerebellar granule cells during cerebellar development
Article in Biochemistry and biophysics reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Oxysterol-binding protein (OSBP)-related protein (ORP) 6, a member of subfamily III of the ORP family, localizes at endoplasmic reticulum-plasma membrane contact sites and is involved in regulating the turnover of the lipid composition of the plasma membrane through the counter-transport of phosphatidylinositol-4-phosphate and phosphatidylserine in neurons. However, the physiological functions of ORP6-mediated lipid counter-transport remain poorly understood. In the present study, we investigated the developmental expression of ORP6 protein in the mouse cerebellum and the role of ORP6 in neuronal differentiation and migration using Neuro-2A cells and primary cultured cerebellar granule cells (CGCs). The expression of the ORP6 protein increased from P7 to P21, coinciding with a key period of granule cell progenitor proliferation and immature CGC migration. Both ORP6 RNAi knockdown and overexpression of two different types of dominant-negative ORP6 constructs significantly increased the number and length of neurites in retinoic acid-induced differentiated Neuro-2A cells. Similarly, ORP6 knockdown in primary cultured CGCs increased neurite number and length and disrupted their migration
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.