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The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

Three genes linked to the development of trichilemmal cysts were found.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

TSC2 is crucial for proper hair follicle development and patterning.

Researchers created a new mouse model for studying scleroderma.

Pax9 is crucial for proper tongue surface development and preventing skin-like changes.

GLI1 might protect against the start of skin cancer and is not linked to cancer severity.

TB and BCC tumors show similar follicular differentiation patterns.

New biological pathways and potential treatment targets for male pattern baldness were identified.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

Monoclonal antibodies LT-1, LT-2, and LT-7 help diagnose certain blood cancers.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

The study found key long non-coding RNAs involved in yak hair growth cycles.

Proper niche formation in Drosophila requires Slit-Robo signaling for cell migration.

Hair follicle stem cells use specific chromatin changes to control their growth and differentiation.

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

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

Killing specific cells in hair follicles can lead to hair growth problems in mice.

The research identified specific genes that are active in the cells crucial for hair growth.

Trichoscopy can reveal specific hair and scalp changes in linear morphea.

The LMNA mutation affects skin structure even in asymptomatic carriers.

Trps1 plays a key role in hair follicle development and cycling.

LGR6+ stem cells may improve bone healing.

A mutation in mice causes hair loss and immune problems.

Sporadic trichoblastic neoplasms generally don't recur or spread, with one case showing a specific genetic fusion.

S100A4 and S100A6 proteins may activate stem cells for hair follicle regeneration and could be potential targets for hair loss treatments.

Pig skin cells can turn into mesodermal cells but lose their ability to become neural cells.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.