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A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Dickkopf-related Protein 2 can help hair grow by activating a specific cell pathway.

PPCM microspheres can effectively release finasteride over 42 days.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

GLABRA2 represses root hair formation by inhibiting a specific gene.

DPCP may be safe for treating alopecia during pregnancy, but more research is needed.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

Severe CCCA may be biologically and clinically different from milder forms.

6.1% of patients seeking PRP for hair loss had undiagnosed cicatricial alopecia, which PRP cannot treat.

TAK-279 effectively reduces psoriasis symptoms and is safe.

Phospholipids help plant proteins move by regulating receptor interactions.

Type II porcine hair keratin supports cell growth but hinders cell differentiation.

A patient developed a blister at the injection site after hepatitis C treatment.

Sfrp2 increases during hair follicle catagen phase and slows keratinocyte growth.

PGD2 stops hair growth and is higher in bald men with AGA.

The enzyme pyruvate kinase M2 helps hair regrowth and could be a potential treatment for hair loss.

Phosphatidic acid may help hair grow by affecting cell growth pathways.

PDGF signaling is crucial for cell development, wound healing, and fluid regulation in the body.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

White lupin uses specific genes to grow root hairs and access phosphorus when it's scarce.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Activating PKCα in skin causes cell death and inflammation through different pathways.

Nociplastic type pain, common in Chronic Overlapping Pain Conditions, is a complex, heritable trait linked to 24 unique genetic factors and 127 genes, with potential shared mechanisms in cognitive, personality, and metabolic traits.

OsUEV1B protein is essential for controlling phosphate levels in rice.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

Topical calcitriol appears safe and may reduce hair loss during chemotherapy.

PAON shows skin patterns due to genetic mosaicism.

Brepocitinib effectively reduces inflammation and improves symptoms in cicatricial alopecia with good safety.