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BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.

AgK114 protein helps in hamster skin injury recovery.

Astraglus polysaccharide may help hair growth by boosting follicle stem cell activity.

A specific RNA molecule blocks hair growth by affecting a protein related to hair loss conditions.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

ECM changes may play a role in hair loss, with differences between males and females.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

Editing the FGF5 gene in sheep increases wool length, confirming its role in hair growth.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

Tenascin-C and tenascin-W help control stem cell movement and growth in whisker follicles.

A synthetic octapeptide may help promote hair growth and counteract hair loss.

Sirolimus and propranolol may reduce abnormal cell growth and improve lymphatic malformations in children.

HAT-L4 is crucial for preventing body fluid loss by maintaining skin barrier integrity.

Desmosomal adhesion is essential for healthy skin structure and function.

Biglycan helps regulate hair growth and regeneration.

Activating Tgr5 may help treat hair loss and bone loss.

The hydrogel helps skin heal by encouraging new blood vessel growth.

Cathepsin L deficiency causes hair and skin issues in mice.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

Mutations in the LIPH gene cause woolly hair in a child.

ULBP3 could be a marker for diagnosing alopecia areata incognita and may be linked to its cause and development.

Long non-coding RNAs help regulate wool fineness in Gansu alpine fine-wool sheep.