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The study concludes that certain domains in Clostridium histolyticum enzymes are structurally unique, bind calcium to become more stable, and play distinct roles in breaking down collagen, with potential applications in medicine and drug delivery.

A new gene mutation causes a rare type of hair loss.

Researchers found genes for cysteine-rich proteins that form the protective layer of hair in humans and sheep.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

The research identified a gene in sheep important for wool quality, which could help improve wool traits.

TRPA1 and TRPV1 channels don't affect mechanotransduction in rat sinus hair follicles.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

A rare gene variant causes hair and nail issues in a family.

A new method was developed to detect pesticide residues on apples without damage.

Hair follicle stem cells can be turned into neuron-like cells, offering a new way for brain repair.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

ePUKs could be valuable for regenerative medicine due to their wound healing abilities.

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

MsPG3 protein gathers at root hair tips, aiding growth.

Scientists can mimic hair disorders by altering genes in lab-grown human hair follicles, but these follicles lack some features of natural ones.

EDA is vital for bone and cartilage formation and could help treat skeletal disorders.

Keratin-75 is secreted by ameloblasts in a unique way without a signal peptide.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

Disruption of glycinergic circuits increases pain sensitivity, suggesting new pain treatment options.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

The research helps in creating genetically modified animals to study hair growth.

The method effectively analyzes human hair proteins, especially nonfilamentous ones.

The new antibody, TYHF-1, specifically targets certain hair-related structures.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Researchers found two new genetic variants linked to Alzheimer's disease.

A gene mutation causes woolly hair in a Syrian patient.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.