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A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

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

MicroRNA-205 helps hair regrow by making hair follicle stem cells less stiff.

Higher levels of miR-203 may contribute to hair loss in alopecia areata.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

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

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

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

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Misbehaving hair follicle stem cells can cause hair loss and offer new treatment options.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Two specific genes are more active during hair growth in mice.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

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

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

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

miR-29 is a key factor that accelerates aging.

Researchers found a new mutation causing total hair loss from birth.

A new mutation in the HR gene causes hair loss in a specific family.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

Idiopathic hirsutism may be linked to increased enzyme activity.

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

The study found key factors in the cause of hidradenitis suppurativa, its link to other diseases, and identified existing drugs that could potentially treat it.

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

A specific gene mutation causes congenital hair loss.

miR-133a-3p and miR-145-5p help goat hair follicle stem cells differentiate by controlling NANOG and SOX9.

The HCR gene contributes to psoriasis risk.