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Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Breast cancer treatments work better with AR activation, improving results and reducing side effects.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

WNT10A helps esophageal cancer cells spread and keep renewing themselves.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Tmem30b is essential for hearing by maintaining hair cell structure in the ear.

Follistatin and LIN28B together improve the ability of inner ear cells in mice to regenerate into hearing cells.

Plerixafor may help treat pigmentation disorders by promoting skin repigmentation.

WNT10A and EBF1 interaction affects hair growth in male-pattern baldness.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

New treatments for cancer and skin disorders show promise in disrupting harmful cell interactions and promoting hair growth.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

A new microneedle treatment shows promise for better hair regrowth in androgenetic alopecia.

Multiphoton microscopy can effectively detect early endometrial cancer by analyzing collagen changes.

ABCG2 protein marks stem-like skin cells in human epidermis.

LGD1069 effectively prevents breast tumors in mice without toxicity.

Adrenomedullin 2 stops cell growth and causes cell death in human hair follicles.

The Itpr3 gene causes a specific hair pattern in mice.

Non-coding RNAs help control hair growth in cashmere goats.

PRC1 influences skin stem cell development by both turning genes on and off, affecting hair growth and skin cell types.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

The combination treatment showed a higher response rate but no significant survival benefits.