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PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

The GPRC6A-Duox1 axis helps control hair growth and loss by affecting hydrogen peroxide production.

JW0061 may be a new treatment for hair loss by promoting hair growth through WNT signaling.

Activating TERT in mice skin boosts hair growth by waking up hair follicle stem cells.

Tet1/2/3 enzymes affect hair follicle cell development by influencing BMP signaling.

Four new genes related to sheep wool were discovered, showing genetic diversity.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Sox6 is important in heart and kidney health, affecting diseases like diabetes, heart disease, and high blood pressure.

LGD1069 effectively prevents breast tumors in mice without toxicity.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

The treatment effectively promotes hair regrowth in androgenetic alopecia without causing skin irritation.

Outer root sheath cells consistently express certain keratins influenced by their environment.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

A missing mK6irs1 gene causes hair loss in mice.

K10 may not prevent tumors as previously thought and might increase benign tumor risk.

PTCH gene mutations contribute to basal cell carcinoma development.

CLK1 is needed for skin cells to become epidermal cells but not sebocytes.

The MtAnn3 gene affects root hair growth and is influenced by cytokinin.

miR-3606-3p reduces skin fibrosis by blocking key signaling pathways.

KAP genes are crucial for hair development and show both shared and unique traits in humans, chimpanzees, and baboons.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Vitamin D receptor binds similarly to natural and synthetic ligands, affecting gene regulation.

SVpgC2a cells show abnormal growth and keratin changes, modeling early cancer development.