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Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

Two genes, ERBB4 and ROR1, may cause the unique pigmentation in Lanping black-boned sheep.

Different enzymes are active in different parts of developing mouse organs.

IL-1 promotes fat cell growth in skin, while WNT inhibits it and encourages scar formation.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

A new gene mutation is linked to monilethrix in the studied family.

lncRNAs are important for understanding and treating skin diseases.

miR‑339‑5p can slow down hair follicle stem cell differentiation by targeting DLX5.

A protein called lfTSLP is important in causing allergic and other skin diseases and could be a target for treatment.

Fetal skin has unique immune cells different from adult skin.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

Hulunbuir lambs adapt better to cold than Hu lambs, showing more wool growth and thicker skin.

NLRP3 helps control inflammation and repair in wound healing, making it a potential target for treatment.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Type 3 Innate Lymphoid Cells help maintain skin health and balance, and are involved in skin diseases and healing.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

The research updated the skin cell profile, finding new skin cell markers and showing fibroblasts' key role in skin health.

A substance called poly(I:C) increases a protein called carbonic anhydrase II in skin cells, which might help with skin defense and healing.

Alarmin cytokines are key in controlling skin immunity and inflammation.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

Certain IL-18 gene variations may increase the risk of alopecia areata.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

CRAC channels are crucial for the development and function of specialized immune cells, preventing severe inflammation and autoimmune diseases.

ceRNA networks offer potential treatments for skin aging and wound healing.

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

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.