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A new genetic tool improves the study of hair growth and potential hair disorder treatments.

A specific group of slow-growing stem cells marked by Thy1 is crucial for skin maintenance and healing in mice.

Keratin 10 end domains may increase skin cancer risk by reducing cell death.

Tongue cancer cells show more plectin-1 than non-cancer cells, but both have similar levels of trichohyalin.

A gene mutation in mice causes permanent hair loss and skin issues.

Matrical tumors share a common growth mechanism involving the Wnt pathway and consistent PHLDA1 expression.

Thy-1 protein helps improve blood flow and wound healing in the skin.

The E2 protein affects gene activity in hair follicles of mice.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

ETC-159 was safe up to 30 mg, but no tumor shrinkage was seen.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

PTEN helps control the number and health of skin stem cells by working with the protein BMAL1.

Tebentafusp-tebn improves survival rates in uveal melanoma patients but has common side effects like rash and fatigue.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

DMBT1 and galectin-3 may help suppress epithelial skin cancer.

CCC1 is essential for pH balance and normal cell function in plants.

TCDD reduces EGF receptors in the liver, affecting growth and development.

Thymic transplantation normalized some T-cells but not others, maintaining immune function.

Nitrate helps plants manage phosphate uptake and starvation responses through NIGT1 proteins.

Deleting MED1 in skin cells causes hair loss and skin changes.

Truncated LTBP-1 disrupts TGF-beta signaling, affecting hair growth.

The ABI1 gene contributes to prostate cancer progression and treatment resistance.

Matriptase imbalance contributes to cancer development and spread.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Mitf plays a key role in melanoma progression and is linked to disease stage.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Intu gene is crucial for hair follicle formation by helping keratinocytes differentiate through primary cilia.

TCF/Lef1 activity is essential for proper skin cell development and renewal.