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Prostasin has two roles in skin: one for normal skin development without needing activation, and another for proper hair growth that requires activation.

The protein's size was reduced, but more work is needed to confirm its function.

The plant hormone auxin activates the TOR pathway, affecting gene expression related to growth and cell size.

Four-amino acid part makes enzyme sensitive to finasteride.

The enzyme is crucial for skin cell development and can be activated without proteolytic activation.

Thrombospondin-1 is crucial for hair follicle regression and reduced blood vessel growth during the catagen phase.

Protease Nexin-1 is found in human hair growth cells and is affected by male hormones.

PTHrP regulates various normal body functions, including bone development, skin, and muscle function.

Transglutaminases work through a ping-pong mechanism, and human plasma and platelet transglutaminases have similar catalytic subunits.

A substance called TCQA could potentially darken hair by activating certain genes and increasing melanin.

Too much parathyroid hormone-related protein in skin disrupts hair growth in mice.

Blocking mTORC1 may help prevent skin cancer by stopping the growth of certain skin stem cells.

The enzyme PA-PLA1α is important for proper hair follicle development.

DA-9401 helps protect rat testis from finasteride damage.

Paeoniflorin protects brain cells by involving a specific protein and neurosteroids.

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

TMPRSS2 affects COVID-19 severity and treatment options.

Certain tyrosine kinases may regulate hair growth and could help develop hair loss treatments.

Keratin-associated proteins may have roles in various mouse tissues, not just hair.

Neuronatin is found in specific cells within rat testis, hair follicles, tongue, and pancreas, suggesting it has various roles in tissue development and function.

New cancer treatments show promise in reducing tumor growth and improving skin regeneration in mice.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Researchers found four key proteins that affect the development of a specific hair type in Yangtze River Delta white goats.

Proteolytic enzymes damage hair follicles by detaching stem cells.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.