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

FOXC1 is essential for keeping hair follicle stem cells inactive and maintaining their environment for healthy hair growth.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

Isoxazole 9 (ISX9) may help regrow hair by activating certain cell signals.

The study created a mouse model to better understand hair follicle stem cells' role in hair growth and repair.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

A specific RNA modification in cashmere goats helps activate hair growth-related stem cells.

ocu-miR-205 affects hair density in Rex rabbits by altering hair follicle growth and signaling pathways.

Certain long non-coding RNAs are important for the growth of hair follicles in Inner Mongolian cashmere goats.

Cronkhite-Canada syndrome is rare, with high mortality and cancer risk, needing more research for treatment guidelines.

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.

New genetic mutations causing hair loss were found in a Chinese family.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

ocu-miR-205 affects hair density in Rex rabbits by promoting cell changes that lead to more hair follicles entering resting phases.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

Rac1 is essential for proper hair structure and color.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

Local positive feedback helps shape root hair cells by stabilizing growth sites.

Blocking the JAK/STAT pathway may help reduce skin sensitivity in Xeroderma pigmentosum.

A specific gene mutation causes a severe skin disorder in a family.

Seven genes are highly expressed in both germ-line and hematopoietic stem cells.

MEX3A is crucial for maintaining intestinal stem cells in mice.

TRPA1 and TRPV1 channels don't affect mechanotransduction in rat sinus hair follicles.