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Certain herbal compounds, especially from bitter melon, can inhibit cancer growth and promote hair growth by blocking PAK1.

Mirex seems to promote a unique group of skin cells different from those affected by another tumor promoter, TPA.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

Certain mice without specific receptors or mast cells don't lose hair from stress.

Lysophosphatidic acid is important for skin health and disease, and could be a target for new skin disorder treatments.

SK2 channels help control sensory signals in rat muscle spindles and hair follicles.

MC4R gene variants not linked to female hair loss.

Scarring alopecia involves increased immune cells and specific gene changes near damaged hair follicles.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Increasing PBX1 reduces aging and cell death in hair follicle stem cells by boosting SIRT1 and lowering PARP1 activity.

Interleukin-1 increases keratin K6 production in skin cells.

Melatonin may help whisker growth in mice.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

Monilethrix involves multiple genes affecting hair structure, including DSG4 mutations.

ACBP is crucial for healthy skin in mice.

A protein called PLC2 is important for the growth and development of plant roots influenced by auxin.

Wnt signaling affects the development and growth of Langerhans cells in mice.

ILC1-like cells can cause alopecia areata by themselves.

New therapies and trials are needed for Merkel cell carcinoma, a tough skin cancer.

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

Melatonin helps improve Cashmere goat hair quality by promoting hair follicle growth through a specific cell signaling pathway.

SGK1 is important in cancer growth and treatment resistance, and targeting it could improve therapies.

Removing Mediator 1 from certain mouse cells causes teeth to grow hair instead of enamel.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Mouse skin cells can become sperm-like cells in the lab.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.