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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Researchers found that certain miRNAs, which affect immune system regulation, are differently expressed in mice with a hair loss condition compared to healthy mice.

The Hedgehog signaling pathway is linked to cancer development, and targeting it with inhibitors shows promise but faces challenges like resistance.

The AMHR2-482A>G gene change is linked to higher PCOS risk.

A new gene mutation causes insulin resistance in a girl and her mother.

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

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Indian Hedgehog helps control skin cell growth and protects against aggressive skin cancer.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

A new DSG4 gene mutation causes hair defects in a young girl.

The gene HDC is important for the development of hair follicles in newborn mice.

Hirsute women have lower type 2 17β-HSD enzyme levels, which improve with treatment.

Ocu-miR-205 affects hair density in Rex rabbits by influencing cell processes and signaling pathways.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Shh and Dhh affect skin development and can cause tumors, while Ihh does not.

The HCR gene contributes to psoriasis risk.

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

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

miR-146b-5p may help treat hair loss by promoting hair growth and reducing inflammation.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

RNA-based treatments show promise for managing Hutchinson-Gilford Progeria Syndrome.

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

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Early involution in Hirosaki hairless rats' mammary glands is linked to a unique modification of STAT5A.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.