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Thrombospondin-1 is crucial for hair follicle regression and reduced blood vessel growth during the catagen phase.

Turning off a specific gene in stem cells speeds up skin healing by helping cells move better.

GLPLS is a rare skin condition with specific hair loss and skin symptoms.

The transgene likely activated an oncogene or interrupted a tumor suppressor gene, causing melanoma in mice.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

Further testing of paclitaxel poliglumex for this cancer treatment is not justified.

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

Low-level laser therapy is a safe and effective long-term treatment for hair loss, improving hair density and thickness.

Androgen-deprivation therapies increase the risk of certain heart conditions, but testosterone treatment may help.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

A new method helps grow skin stem cells better, which could improve skin grafts for burn victims.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Low-level laser therapy helps male and female hair loss alone or with other treatments.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Higher expression of the keratin-associated protein 8.1 gene in Liaoning cashmere goats is linked to finer cashmere fibers.

Targeting 5α-reductase type 1 may help manage Tourette-like symptoms.

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

TLR3 activation helps improve skin and hair follicle healing in mice.

A 3-year-old boy was diagnosed with a rare, non-scarring hair loss condition called temporal triangular alopecia.

The SLICK1 allele in Holstein heifers affects hair and immune traits without altering prolactin signaling.

A genetic variant in the KRT25 gene causes tightly curled hair.

Increased LC3 gene expression may be linked to premature graying of hair.

A rare EGFR mutation in newborns leads to severe health issues and early death.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

TGF-β1 from dermal papilla cells suppresses hair growth, and targeting it may help treat androgenetic alopecia.