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TYK2 inhibition may help treat alopecia areata by promoting hair growth and reducing immune response.

Introducing the OTC gene improved symptoms in mice with OTC deficiency.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

New compounds show promise for treating benign prostate hyperplasia with fewer side effects.

Stopping shaving or removing hair follicles usually resolves Pseudofolliculitis barbae.

The newborn was diagnosed with a rare skin disorder causing blisters, which requires careful wound care and family support.

Mutations in Far2 mice cause hair loss due to sebaceous gland issues.

Pimozide treatment resolved cysts and partially restored cheek fat in a man with Barraquer–Simons syndrome.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

The LMNA mutation affects skin structure even in asymptomatic carriers.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Pygo2 is important for early growth and progression of intestinal tumors, and could be a target for treating cancers with certain mutations.

KRTAP2-3 could help predict cancer recurrence by identifying specific cancer cells.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

A new enzyme, BSSP, is found in high amounts in the hair follicles of nude mice.

The BASP classification is a detailed and accurate way to categorize hair loss in both men and women.

C/EBPalpha and C/EBPbeta are crucial for normal skin and oil gland cell development in adult mice.

Gremlin proteins help regulate hair growth by balancing signals in hair follicles.

Blocking a key energy pathway in human hair follicles can trigger stress responses that stop cell growth.

Sex steroids affect the MafB gene differently in male and female hamsters.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

ErbB2 signaling is crucial for skin cell growth and cancer development in mice.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

PSAT1 is key for hair growth and stem cell function in cashmere goats.

Astrotactin-2 is cleaved in a specific way that helps understand its maturation.

Activating brown fat may help manage PCOS symptoms.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.

Charnoly bodies could be a marker for cell damage, and certain nutrients and proteins might prevent them, potentially helping with brain diseases and cancer.