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A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Specific keratin gene mutations can cause monilethrix.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

The model can effectively test gene functions and drug responses in human skin.

Histamine and its enzyme may help start hair regrowth.

Whn is essential for hair growth, and its malfunction causes hair loss.

Growth hormone-releasing hormone (GHRH) boosts hair growth and human scalp hair follicles have their own growth hormone system.

Ishophloroglucin A from Ishige okamurae may be a natural alternative for treating hair loss by inhibiting 5α-reductase and promoting hair growth.

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

Exosomes from certain stem cells can fight hair loss by promoting hair growth and maintaining the growth phase of hair.

IL-15 helps maintain hair growth and protects the immune status of hair follicles.

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

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

Hair transplant surgeons in the British Association of Hair Restoration Surgery must follow specific behavior and performance rules.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

Combining genetic models helps improve heat tolerance in beef cattle.

Stress in hair follicle stem cells causes inflammation in a chronic skin condition through a specific immune response pathway.

BMP signaling affects hair color by interacting with the MC-1R pathway.

miR-200c-3p could help diagnose and treat alopecia areata.

The research helps in creating genetically modified animals to study hair growth.

The E2 protein affects gene activity in hair follicles of mice.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

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.

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

The GH-IGF-I axis is likely involved in the hormonal imbalances seen in non-obese women with functional hyperandrogenism.

BBS7 is crucial for maintaining healthy periodontal ligaments by supporting Shh signaling.