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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.

Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

Constant-release melatonin reduces SOX21 gene expression in goats during the hair follicle resting phase.

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

BBS7 is crucial for maintaining healthy periodontal ligaments by supporting Shh signaling.

A peptide from hair follicle stem cells can boost hair growth.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

Melatonin receptor genes likely play an important role in the development of goose feather follicles.

CDKN2AIP gene is less active in nevus sebaceous, affecting related RNA networks.

Epiprofin helps cells grow in developing teeth, hair, and limbs.

Trps1 plays a key role in hair follicle development and cycling.

Polyamines are important in deciding hair follicle stem cell behavior, affecting hair growth and loss.

PTEN helps control the number and health of skin stem cells by working with the protein BMAL1.

A gene mutation causes monilethrix in a Chinese family.

Sox9 is crucial for hair follicle stem cells to become melanocytes instead of glial cells.

Defects in certain proteins cause major heart abnormalities during early development.

The ZIP13 variant is linked to abnormal hair quality.

SPRY1 deficiency in skin cells causes stem cells to move to the skin surface, leading to increased pigmentation.

A specific RNA in cashmere goats helps improve hair growth by interacting with certain molecules.

The UHS promoter is specific to mouse hair follicles.

Prostasin has two roles in skin: one for normal skin development without needing activation, and another for proper hair growth that requires activation.

CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

miR-29a-5p prevents the formation of early hair structures by targeting a gene important for hair growth and is regulated by a complex network involving lncRNA627.1.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

A rabbit gene important for hair development was identified and detailed.

The goat hair keratin gene is very similar to sheep's and is strongly expressed in goat hair follicles.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

The enzyme sEH is important for hair growth and its inhibition could help treat hair loss.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.