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The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

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

A new DSG4 gene mutation causes hair defects in a young girl.

MED1 affects skin wound healing differently in young and old mice.

Proteomic analysis can identify genetic differences in mouse hair, helping understand hair defects and variations.

MsPG3 protein gathers at root hair tips, aiding growth.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

Keratin 17 is crucial for early hair strength and cell survival.

miR-124 helps mouse hair follicle stem cells become nerve cells by blocking Ptbp1 and Sox9.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

THH and PAD type III appear together early in hair growth, but deiminated THH appears later, suggesting another factor is involved.

FGFR2 signaling controls Merkel cell formation in different skin regions.

Artemis phosphorylation at Ser516 may help regulate skin and hair structures.

A mouse gene mutation increases the risk of skin cancer.

The N gene affects the protein makeup of mouse hair.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

NuMA-microtubule interactions are vital for proper skin structure formation and function.

Elastic Net DNA methylation clocks are inaccurate for predicting age and health status; a "noise barometer" may better indicate aging and disease.

KAP8.1 protein is crucial for hair structure and interacts with keratin 85.

MEGA PROTAC improves prediction and ranking of protein complexes better than existing methods.

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

Progesterone and its metabolites affect myelin protein expression differently in male and female rat Schwann cells.

The improved genome of the African spiny mouse helps study its tissue regeneration.

Somatic BHD mutations are rare in Japanese renal tumors.

Hyper-keratinisation in Meibomian glands contributes to gland dysfunction.

HOTTIP and miR-10b contribute to glioma therapy resistance by affecting cell behavior, suggesting they could be targets for treatment.

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

Hoxc13 gene is essential for hair, nail, and papilla development.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.