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

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Lgr5 and the vitamin D receptor are key in controlling skin inflammation and tumor risk in mice.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

PrrH sRNA controls pyochelin production in *Pseudomonas aeruginosa*.

HDAC4 and HDAC7 are crucial for Th17 cell development and could be targeted to treat inflammatory diseases.

Some people have a genetic variation that makes them less effective at breaking down drugs.

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

PROTACs offer a new, precise way to treat cancer by breaking down harmful proteins.

Epithelial-derived Pop-Up Keratinocytes (ePUKs) may enhance wound healing in regenerative medicine.

Mirex seems to promote a unique group of skin cells different from those affected by another tumor promoter, TPA.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

HPV16 oncogenes disrupt the normal activity of hair follicle stem cells.

The enzyme PA-PLA1α is important for proper hair follicle development.

Type XVII collagen may help prevent skin aging.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Plakophilin 1 helps control skin cell immune responses to prevent excessive inflammation.

Researchers developed a method to label and study human hair follicle stem cells using a fluorescent protein.

KAP7.1 and KAP8.2 genes are crucial for cashmere quality in goats.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

Keratin-associated proteins are crucial for hair strength and structure.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

Keratin K6irs is a marker for the inner root sheath of hair follicles in mice and humans.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.