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Personalized treatment based on detailed tumor analysis successfully managed and reduced the patient's aggressive hair follicle cancer.

TCF/Lef1 is essential for skin barrier function by regulating lipid metabolism.

A genetic change in the FGF5 gene affects hair growth in cashmere goats.

The study created a mouse model to better understand hair follicle stem cells' role in hair growth and repair.

Nod factor can trigger changes in legume root hairs with just one molecule.

Removing GRK2 in skin cells causes hair loss similar to immune-related alopecia.

A man with lung cancer had skin and eye side effects from erlotinib but continued treatment with symptom improvement.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Slug (Snai2) helps regulate hair growth timing in mice.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Sry may regulate fatty acid metabolism and shows different expression levels in rat tissues.

2′‐Fucosyllactose reduces hair loss and promotes hair growth in mice.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Imaging living plant cells shows dynamic changes in actin and endoplasmic reticulum linked to root hair growth.

A specific genetic variation affects wool quality in sheep.

Activating Nrf2 can improve wound healing by increasing hair follicle stem cells.

RUM-loaded SLN shows promise for treating acne and hair loss topically.

RG and RJ gels speed up burn wound healing better than other treatments.

Non-coding RNAs play key roles in the hair growth cycle of Angora rabbits.

Rb-bFGF improves hair transplant results and patient satisfaction with fewer complications.

Fgf9 helps create new hair follicles after injury through skin T cells.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.