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Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

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

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

A protein called CBP is found in prostate cancer and can increase the effectiveness of certain prostate cancer treatments.

Overexpression of LRIG3 in skin causes hair loss.

Trps1 is essential for proper hair follicle development.

Matriptase is crucial for skin barrier, hair growth, and may contribute to skin cancer.

Sphingosine 1-phosphate affects inflammation and gene expression in different aorta cells.

20(S)-Protopanaxadiol-aglycone may help prevent and treat prostate cancer by reducing androgen receptor activity.

Protein Kinase Cε increases skin sensitivity to UV damage and skin cancer risk.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

S100A6 protein is linked to disease progression, especially in cancers.

TMPRSS2 is crucial for COVID-19 infection and is a potential target for treatment.

Spt4 and Spt6 are essential for fat cell development.

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

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

Microneedle-delivered polyglutamate effectively and safely improves hair growth in androgenetic alopecia.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

PGA-4HGF may help treat hair loss by activating hair growth pathways and extending the hair growth phase.

Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

TGM3 is important for skin and hair structure and may help diagnose cancer.

p2y5, now called LPA6, is a receptor important for human hair growth.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Enhanced stem cells from the placenta can reduce fat cell formation in eye disease.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

Mutations in the SNRPE gene cause hereditary hair loss.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

Desmoglein 3 is important for keeping hair follicle stem cells inactive and maintaining their special properties.