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Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

Wnt3a activates certain genes in hair follicle cells, including a newly discovered one, EP2, which may affect hair growth.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

The LMNA mutation affects skin structure even in asymptomatic carriers.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

The arrector pili muscle plays a key role in hair loss in androgenetic alopecia.

Anorexia nervosa may cause a hair defect called pili torti due to malnutrition and high vitamin A levels.

KRT72 gene helps form hair.

Mycophenolic acid may help treat hair loss by promoting hair growth and cell proliferation.

Overexpressing SSAT enzyme reduces prostate tumor growth in mice.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Nestin-positive cells are important for hair follicle regeneration in alopecia areata.

Sgk3 is essential for normal hair follicle growth and maintenance.

Androgen receptor signaling causes early aging of cells important for hair growth by damaging their DNA.

High amphiregulin in the skin is a bad sign for acute graft-versus-host disease.

Nestin helps identify certain melanoma cells in nodular melanoma.

Total glucosides of paeony may help treat alopecia areata by reducing inflammation and hair loss.

ALRN-6924 can protect hair follicles from chemotherapy damage by temporarily stopping cell division.

WNT10B affects hair growth by altering gene activity in hair cells.

The microenvironment affects the behavior and survival of melanocytes with the GNAQ oncogene in melanoma.

Keratinocytes can reverse the effects of the GNAQ oncogene, inhibiting melanoma cell growth.

Trps1 is essential for proper hair follicle development.

Changing protein kinase levels in pituitary cells affects calcium flow and beta-endorphin release.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

CircAGK affects cell death in hair cells by controlling the miR-3180-5p/BAX pathway, which can lead to hair loss.

The PI's development is closely linked to skin and hair pigmentation in macaques.

The upper hair follicle is stable, while the lower part allows movement during hair growth.

Excessive putrescine causes hair loss in transgenic mice by disrupting hair follicle development.