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Meis2 is essential for touch sensation and proper nerve connection to touch receptors in certain skin areas of mice.

Bioassays help find useful compounds in nature for making medicines, supplements, and cosmetics.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

Curcumin supplements increase adiponectin and decrease leptin in adults.

New liposome treatment successfully delivers CRISPR to deactivate a key enzyme in androgen-related disorders.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Gender-affirming hormone therapy improves physical performance in trans men to the level of cisgender men, while in trans women, it increases fat mass and decreases muscle mass, with no advantage in physical performance after 2 years.

A 36-year-old woman with low potassium levels was found to have Cushing disease, and after treatment, her potassium levels normalized.

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

New tools show that in fish, NPY increases feeding and somatostatin decreases it.

Low zinc levels may contribute to hair loss due to increased oxidative DNA damage.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.

Fibroblast growth factors are crucial for hair follicle development and regeneration.

Skin stem cells in hair follicles are important for touch sensation.

Hair follicle stem cells are crucial for touch sensation and proper nerve structure in mice.

FKBP10 and FBN2 are key proteins for hair growth in cashmere goats.

The C3H/HeJ mouse model is useful for studying and testing treatments for alopecia areata.

People with common hair loss conditions may have a higher risk of heart disease and related health issues.

More personalized and effective treatments for androgenetic alopecia are needed.

Hair conditions can be linked to diabetes and affect psychological health.

JAM-A helps hair regrowth in alopecia areata by protecting VCAN in skin cells.

The WNT signaling pathway is important in many diseases and targeting it could offer new treatments.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Understanding how androgens work is key for creating new treatments for prostate issues and hair/skin conditions.

Genetic mutations can affect female sexual development, requiring personalized medical care.