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

Multiomics is revolutionizing biology by enabling breakthroughs in research and disease diagnosis.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Anti-CD19 therapy may help treat SLE and NMOSD.

EH-MSCs may help treat hair loss by boosting regeneration and reducing inflammation.

Old C57BL/6 mice with unsynchronized hair cycles show less melanin in their spleens.

MSM reduces hair loss and promotes hair growth in male mice.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

The 14-3-3σ gene is essential for preventing hair loss.

Sulfated polysaccharides from Microcosmus exasperatus may help treat cancer without causing blood thinning.

A new mouse model helps understand and find treatments for alopecia areata.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

Slug (Snai2) helps regulate hair growth timing in mice.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

Defective mitochondrial DNA replication causes aging symptoms and increased oxidative damage in mice.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

The Gsdma3 gene is essential for normal hair development in mice.

MPA increases cancer spread by boosting Eph A2 activity.

Different keratins have unique expression patterns in mouse skin cells.

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

Removing SIX1 in fat cells reduces skin fibrosis.

Copper supplements during pregnancy improve survival and development in mutant mice.

FOL-005, a hair growth promoter, acts locally on mouse skin where injected and could be a promising hair loss treatment.

Obese mice with a leptin gene mutation have a longer resting phase in their hair cycle, which may help understand certain hair loss conditions.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.