ArticleScience advances2026
Gaseous liquid nitrogen-assisted cryo-printing strategies for challenging volumetric anisotropic tissues fabrication.
Article in Science advances, 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
14 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Engineering physiologically relevant anisotropic tissues remains a major challenge due to limitations in replicating native structural cues across complex geometries. Here, we developed a cryogenic extrusion bioprinting platform by precisely guiding ice crystal growth to achieve centimeter-scale anisotropic constructs, even with ultrasoft, low-viscosity inks (2% weight/volume GelMA). This approach enables the fabrication of anatomically matched, patient-specific constructs with tunable anisotropy, including bone graft substitutes and osteoporotic disease models. To overcome the height constraints of cryo-printing, we further developed cryo-assembly and LEGO-assembly strategies that allow integration of anisotropic units while maintaining continuous internal alignment. In vivo studies across wound healing, cranial defect, and femoral defect models validated that these anisotropic cues drive spatially guided cell migration, extracellular matrix (ECM) remodeling, and tissue site-specific regeneration, as evidenced by the ECM deposition. Our platform offers a scalable, clinically adaptable solution for engineering structurally and functionally relevant tissues, redefining the boundaries of anisotropic soft tissue fabrication.
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.