Bone, joint, and mobility is the main area connected here, and any felt benefit should be read together with the human evidence base.
The 81.5 score includes research signals from patient or disease contexts. General supplement evidence is not repeated enough, so the B tier remains conservative.
Representative tier calculated from paper evidence that passed the collection audit.
The representative ingredient tier is calculated from these target-level evidence groups.
Potential benefit studied in Bone and joint health. These findings come from a defined study population, so everyday effects may differ.
This score reflects the strength of this benefit group. The ingredient tier also considers paper count, repetition, population, and study context.
Potential benefit studied in Skin, hair, and nails. These findings come from a defined study population, so everyday effects may differ.
This score reflects the strength of this benefit group. The ingredient tier also considers paper count, repetition, population, and study context.
Potential benefit studied in Exercise performance and recovery. These findings come from a defined study population, so everyday effects may differ.
This score reflects the strength of this benefit group. The ingredient tier also considers paper count, repetition, population, and study context.
This range includes studies in specific patient groups. It is not a general dose or recommendation.
Standalone side-effect signals and combination cautions are listed separately.
Paper IDs and full lists are private. Only study types and summaries are shown.
The existence of several hot spots for ligand interactions on type I collagen and the existence of mutations associated with osteogenesis imperfecta and other disorders show apparently nonrandom distribution patterns within both the monomer and fibril, implyin
Type and source of extraction are the main factors that affect HC properties, such as molecular weight of the peptide chain, solubility, and functional activity.
It is demonstrated that disseminated tumor cells remodel the extracellular matrix by secreting collagen III and generate a stromal architecture that favors dormancy through DDR1 and STAT1 signaling, which support the idea that the manipulation of these mechani
The aim was to investigate the effect of oral supplementation with specific collagen peptides on skin hydration and the dermal collagen network in a clinical setting.
The data demonstrate that compared with placebo, collagen peptide supplementation in combination with resistance training further improved body composition by increasing FFM, muscle strength and the loss in FM.
The utility of a supervised learning protocol for streamlining the analysis of collagen alignment with respect to tumor stromal boundaries is demonstrated and TACS positive fibers are more well-aligned with each other, are of generally lower density, and termi