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Protein analysis shows aging changes in scalp cell types from women.

Using DNase enzymes to break down harmful NETs could be a new treatment for Stevens-Johnson syndrome and toxic epidermal necrolysis.

Trichohyalin, a protein from pig tongue, was purified and found to have a filamentous structure.

Two specific genes are more active during hair growth in mice.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

Clascoterone is safe for the heart, even at high doses.

A stable, active version of a growth factor was made in bacteria, showing promise for medical use.

Acne not improved by usual treatments may indicate a genetic disorder.

Controlling Tslp can improve health in AEC syndrome patients.

Natural α-hydroxyl acids cause skin exfoliation by activating TRPV3 channels.

Early involution in Hirosaki hairless rats' mammary glands is linked to a unique modification of STAT5A.

Early-stage skin cells help regenerate hair follicles, with proteins SDF1, MMP3, biglycan, and LTBP1 playing key roles.

Targeting the IL-23/IL-17 pathway effectively treats several inflammatory skin diseases.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

Fetuin A may increase collagen production and promote scarring.

Reptile skin hardens by layering beta-proteins on keratin.

The research explains how a human enzyme binds and processes its substrate, which could relate to its role in biological functions and hair loss.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Keratin-associated proteins help link filaments and affect keratin's strength.

Blocking the Wnt/β‐catenin pathway can speed up wound healing, reduce scarring, and improve cartilage repair.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Fish-derived collagen may help hair grow longer and affect hair stem cells, while bovine collagen could benefit hair stem cell maintenance, potentially aiding in hair loss conditions.

Hair follicle stem cells have significant potential for treating various disorders.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

A new AI-driven method shows promise for treating hair loss with a peptide-based drug.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.