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The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

TGF-β1 increases androgen receptor activity in hair loss, but Hic-5/ARA55 can counter this effect.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

The research found that the molecule lncRNA-H19 helps hair follicle cells grow by affecting certain cell pathways in cashmere goats.

PRO-C22 can help diagnose and monitor the severity of hidradenitis suppurativa.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

The hairless protein is important for skin, hair, and may influence cancer development.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

The RNA AL136131.3 slows down hair growth and speeds up hair loss by affecting sugar breakdown in hair follicles.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

A specific RNA can help hair growth in baldness by boosting stem cell activity.

DNMT1 may help treat hypospadias by improving cell function and preventing unwanted cell changes.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Blocking miR-27a increases sheep hair follicle stem cell growth and decreases cell death, which could help improve wool quality and treat hair loss.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Patients with hidradenitis suppurativa have higher levels of cell-free DNA in their blood.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

miR-140-y helps control feather growth in geese by affecting the Wnt signaling pathway.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.