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sPLA2-IIA increases growth in hair follicle stem cells and cancer cells, suggesting it could be targeted for hair growth and cancer treatment.

SOX2 helps reduce wound size and pressure ulcer formation by suppressing oxidative stress and increasing antioxidant activity in mice.

Urokinase, a type of protein, helps skin cells multiply faster, especially in newborn mice.

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

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

Researchers found a non-functional sheep keratin gene due to mutations.

Akt2 and SGK3 are both important for normal hair growth and development.

RNase L suppresses regeneration in mammals.

Dermal EZH2 controls skin cell growth and differentiation in mice.

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A specially designed molybdenum oxide nanozyme can treat and monitor acute kidney injury effectively.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

Procyanidins from grape seeds reduce nerve pain by blocking specific proteins and inflammation.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

QSOX enzymes help form protein bonds in cells, especially in tissues with high secretory activity.

EP 2 receptor is essential for heart repair by helping macrophages work properly.

Nephronectin is linked to worse breast cancer outcomes and helps cancer spread.

Celsr1 is crucial for skin cell alignment, while Celsr2 has little effect on this process.

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

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

JMJD3 and NF-κB activate Notch1, which is essential for skin cell movement and wound healing.

Corneodesmosin is crucial for skin and hair health, and its dysfunction can cause skin and hair disorders.

Arteannuin might work against cancer and Alzheimer's by targeting neprilysin.