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Two microRNAs in stem cell exosomes help treat hair loss by targeting a specific signaling pathway.

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

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

A specific gene variant may increase the risk of developing Alopecia Areata.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A specific gene mutation causes sparse, brittle hair in a family.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

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

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

Circ 0020938 slows down hair growth in cashmere goats.

A new gene mutation causes a rare type of hair loss.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

miR-325-3p can slow down brain tumor growth by targeting FOXM1.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Mutations in the hairless protein gene cause hair loss.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

MicroRNA-22-3p hinders hair regrowth in male pattern baldness by affecting a specific protein.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

Certain blood miRNAs are linked to severe alopecia areata and could lead to new treatments.

MicroRNA-205 helps hair grow by changing the stiffness and contraction of hair follicle cells.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

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 linked to a rare hair loss condition.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

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

Blocking CXCR4 may help treat hidradenitis suppurativa.