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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.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

PLAU and SerpinB2 affect cell death differently in various forms of leprosy and could be targets for new treatments.

LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

Keratin is crucial for skin barrier formation and affects mitochondrial function.

AIMP1 can boost hair growth by increasing stem cell activity.

Certain peptides can prevent hair loss in young rats caused by a cancer drug.

Enzymes that change arginine to citrulline are important for skin barrier and hair formation, and their malfunction can lead to skin conditions and hair disorders.

The PIRL laser cuts tissue with less damage and scarring than traditional methods.

Mutations in the LIPH gene cause woolly hair in a child.

ILC1-like cells can cause alopecia areata by themselves.

Epimorphin helps shape and develop epithelial cells, like those in hair follicles.

Phospholipases help maintain and restore skin and hair health, potentially leading to new treatments for related conditions.

A protein called PLC2 is important for the growth and development of plant roots influenced by auxin.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

The drug IPI-926 is safe at 160 mg daily and may help treat certain tumors, especially basal cell carcinoma.

ALKBH5 helps wounds heal faster by stabilizing PELI2 mRNA.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

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

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

SIPHL1 from tomato enhances plants' response to low phosphate levels.

TCF/Lef1 is essential for skin barrier function by regulating lipid metabolism.

Normal human melanocytes can avoid cell death through multiple pathways.

β1 integrin is essential for the survival, growth, and movement of human epithelial progenitor cells.

Targeting PTEN can improve healing in venous leg ulcers.

A genetic mutation in the LIPH gene causes hair loss and growth defects.

PADI4 enzyme slows down cell growth in developing hair follicles.

Alkaline Ceramidase 1 prevents early hair loss in mice by keeping hair follicle stem cells balanced.

Laminin 332 is essential for normal skin cell behavior and structure.