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Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

Oestrogen and thyrotropin-releasing hormone affect prolactin and its receptor in human skin and hair, suggesting new treatment options for related conditions.

CRH can cause hair loss by promoting cell death in hair growth cells.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

A specific gene mutation causes congenital hair loss.

Increasing PBX1 reduces aging and cell death in hair follicle stem cells by boosting SIRT1 and lowering PARP1 activity.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

AP-2α and AP-2β proteins are essential for healthy adult skin and hair.

TRPV4 helps sense pressure in mouse skin.

Vitamin D receptor and hairless protein are essential for hair growth.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

Increasing TSPO in the brain may help improve memory problems.

Defective nuclear transport may cause gene expression changes in Progeria.

CRH causes hair loss by reducing autophagy and increasing cell death in hair cells.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

The ABI1 gene contributes to prostate cancer progression and treatment resistance.

PTHrP and its receptor can control blood vessel growth and hair development in mouse skin.

mTORC2 is crucial for healthy skin barrier by regulating lipids and filaggrin.

Trichothiodystrophy is a condition with brittle hair and various physical and mental issues due to low sulfur in proteins.

Matriptase is crucial for skin barrier, hair growth, and may contribute to skin cancer.

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

Progerin affects cell shape but not hair or skin in mice.

TPA promotes hair growth by increasing stem cell activity and activating specific cell signals.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Thymosin β4 helps with healing, inflammation, and organ protection.

Rac1 is crucial for normal hair structure and pigmentation.