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Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

A certain smell receptor in hair follicles can affect hair growth when activated by a synthetic sandalwood scent.

High levels of ornithine decarboxylase can cause tumors in mouse skin.

miR-133a-3p and miR-145-5p help goat hair follicle stem cells differentiate by controlling NANOG and SOX9.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

Higher androgen levels and site-specific AR expression cause sex-related skeletal differences, and certain steroids can boost AR expression and androgen effects in bone cells.

miR-200a reduces goose fibroblast growth by targeting PITX2 in the Wnt pathway.

RORA may help regulate hair growth by affecting hair follicle stem cells.

Certain miRNAs are linked to Cashmere goat hair quality.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

Overexpression of a specific receptor in mice skin causes skin thinning, early skin barrier formation, eye issues, and hair loss.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

Higher levels of miR-1199-5p may reduce the effectiveness of certain prostate treatments.

Oxytocin receptors are found in skin cells near touch and pain neurons.

PRX01, PRX44, and PRX73 are essential for root hair growth in Arabidopsis thaliana.

miR-144 affects hair growth by interacting with Lhx2.

Ptprq has multiple forms that change during inner ear development.

MicroRNA-181a slows sheep hair growth by targeting GNAI2 and affecting a key growth pathway.

New probes were created to effectively measure specific enzymes involved in fat metabolism, which could help develop new drugs.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Antizyme slows skin tumor growth by reducing cell growth in mice.

Pvalb8 is essential for zebrafish hearing and hair cell development, and its mutation causes hearing loss.

Targeting ornithine decarboxylase can help prevent skin cancer.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.