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Nestin-expressing cells turn into a specific type of skin cell in hair follicles during development and in adults.

EGFR helps mouse hair follicles stop growing by reducing certain growth regulators.

Sox13 is a new marker for early hair follicle development and differentiation.

NLRP3 helps control inflammation and repair in wound healing, making it a potential target for treatment.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

miR-195-5p reduces hair growth ability in cells by blocking a specific growth signal.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

Ritlecitinib effectively regrows hair in severe alopecia areata and is well tolerated.

Ritlecitinib helps regrow hair in alopecia areata and is safe for long-term use.

Changes in KRT17 gene activity linked to wool production in Angora rabbits.

lncRNA MTC helps goat skin cells grow and may aid hair growth by controlling proteins linked to cell growth.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

A specific gene mutation causes complete hair loss without other health issues.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Peficitinib can turn human fibroblasts into cells that help grow hair.

Ritlecitinib effectively reduces severe hair loss in alopecia areata over 24 months.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

RIPK1 inhibitors might help prevent alopecia areata.

Researchers created rat liver stem cells that could help repair liver failure in rats and may be useful for studying human liver diseases.

Hair follicles can be kept in RNAlater® at cool or room temperature for a week without harming RNA quality.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

New genetic mutations linked to rare skin disorders were found in three newborns.

Activating Nrf2 can help protect against hearing loss.

ELL is crucial for gene transcription related to skin cell growth.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

Two new gene mutations cause a rare hair disorder.

BMP receptor IA is essential for proper hair cell differentiation in mice.

Ritlecitinib is effective for long-term hair regrowth in alopecia areata, especially in females and early treatment.