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Intense pulsed light treatment mainly damages pigmented hair parts but spares stem cells, allowing hair to regrow.

Both VEPA and ML-Y1 treatments are not effective enough for elderly non-Hodgkin's lymphoma patients.

The home-use IPL device effectively reduced hair and delayed its regrowth after six months of use, with users happy and no negative side effects.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

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

The type of tumor suppressor affects the form of skin cancer from hair follicle stem cells.

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

Mouse skin cancer progression involves a unique group of cells marked by ABCG2 and MTS24.

Activating PPAR-γ signalling can protect hair follicle stem cells from damage caused by chemotherapy.

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

Transcutaneous vaccination using nanoparticles can enhance immune responses and reduce basal cell carcinomas.

The research found that chickenpox virus spreads in skin through blood then to skin cells, while shingles virus moves from nerves to hair follicle areas before infecting skin cells.

A new type of pachyonychia congenita may exist, caused by a different keratin mutation.

A new one-step test can quickly identify skin cancer during surgery.

Intense pulsed light with radiofrequency showed mixed results in improving quality of life for hidradenitis suppurativa patients, with no clinical improvements.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

A girl inherited excessive body hair from her mother and grandmother.

A rare scalp tumor involving two hair follicles was successfully removed with surgery, with no recurrence after 7 months.

A rare hair follicle tumor in the hand was successfully removed with no return after four years.

A rare skin infection in a 10-year-old kidney transplant patient was successfully managed by adjusting medication.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Diseased horse foot skin shows increased keratin expression, similar to wound healing in mammals.

Antiviral medication valganciclovir may improve skin and hair in Trichodysplasia Spinulosa patients.

The photolyase-based device significantly changed the size and heat of potential skin cancer areas in patients.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

A virus protein can activate a pathway that may lead to abnormal hair follicle development.

VEGF165 helps hair follicle stem cells become blood vessel cells, aiding new blood vessel growth.

Newly found stem cells in horse hooves show promise for treating a hoof disease called laminitis.