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MCHR2 gene duplications may be linked to alopecia areata.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Self-amplifying RNA could be a better option for protein replacement therapy with lower doses and lasting effects, but delivering it into cells is still challenging.

New nonsteroidal molecules can potentially increase dihydrotestosterone in neurons by blocking certain enzymes, without affecting prostate and seminal vesicle weight.

Newer retinoid drugs are effective for skin conditions but have significant side effects.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

A newly found RNA in Cashmere goats may play a role in hair growth and development.

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

A brominated phenoxy compound effectively inhibits a human enzyme and shows potential for clinical use.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

5α-reductase inhibitors can interfere with doping tests by masking banned substances.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Retinoic acid production and signaling in hair follicles are regulated by location and timing, affecting hair growth and cycling.

A gene mutation causes curly hair and hair loss in rats.

The enzyme 5α-reductase type 1 is important for blood vessel development and fertility in the uterus.

Too much AKR1C3 enzyme causes resistance to finasteride by increasing testosterone.

Loss of Rap1 protein speeds up heart aging in mice.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

A unique gene mutation was found in a family with monilethrix.

A new small peptide may help hair growth by activating a specific receptor and should be tested in humans.

5α-reductase enzyme affects hormone levels, influencing conditions like acne and hair loss.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Foxn1 is essential for hair pigmentation by directing pigment transfer to hair cells.

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

Basonuclin may help control ribosomal RNA gene activity in skin cells.

Agouti and AGRP affect pigmentation and obesity, with implications for metabolic disorders.

Double-stranded RNA causes inflammation in hair follicle cells, which may help understand and treat alopecia areata.