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New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.

Trichodysplasia spinulosa is a rare skin disease in immunocompromised patients caused by a specific virus targeting hair follicle cells.

PTHrP is higher in certain dog tumors and may act as a local growth factor.

New mutations in the hairless gene may cause hair loss and affect bone development.

Eruptive vellus hair cysts are harmless skin bumps that may go away on their own.

α-parvin is necessary for skin and hair growth and for the correct orientation of skin cells.

Psoriasis patients' immune response to a hair protein depends on their specific gene type.

A gene called HDAC9 might be a new factor in male-pattern baldness.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

Vogt–Koyanagi–Harada disease can cause rare hair growth on normally hairless thumb skin.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

A single amino acid change in the vitamin D receptor can disrupt its function and lead to hair loss.

Vitamin D receptors in hair follicles change with the hair cycle, affecting hair growth.

The gene URB is more active in human hair growth cells and responds to a hair-related hormone.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

The research found genes that may protect certain scalp cells from hair loss.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

VHL disease can cause early paragangliomas, needing lifelong monitoring.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

Immunocompromised patients can develop skin and hair issues due to a virus.

Hepatitis B virus exposure may be linked to increased risk of alopecia areata.

A DNA aptamer helps promote hair growth by enhancing a key cell growth signal in hair follicle cells.

Somatic BHD mutations are rare in Japanese renal tumors.

Hair follicle cells help protect against immune attacks by regulating T-cell activity.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

Complex basal cell carcinomas need personalized treatment due to unique genetic mutations.

Androgen receptor signaling causes early aging of cells important for hair growth by damaging their DNA.