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A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Mutations in the Whn gene affect hair keratin gene expression differently.

The hr gene is linked to hair loss in Valle del Belice sheep.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

Damaging mitochondrial DNA in mice speeds up aging due to increased reactive oxygen species, not through the p53/p21 pathway.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

Lgr5 and the vitamin D receptor are key in controlling skin inflammation and tumor risk in mice.

Folate receptor β helps suppress the immune system in macrophages and affects cancer growth and hair health.

Hair follicles protect melanocytes from sun damage, helping them replenish skin.

A gene variant causes a skin and hair disorder by disrupting protein balance.

A new DSG4 gene mutation causes hair defects in a young girl.

Genetically modified rats help reveal how vitamin D affects bone and skin health.

The androgen receptor's shape-changing ability helps it function but can lead to cancer treatment resistance.

Keratin 10 end domains may increase skin cancer risk by reducing cell death.

Lack of functional CYLD in mice leads to early aging and cancer.

The same gene mutation can cause different symptoms in family members.

Removing β-catenin in certain stem cells causes hair whitening and pigmentation issues.

Msx2-deficient mice experience irregular hair growth and loss due to disrupted hair cycle phases.

Hirosaki hairless rats have sparse, twisted hair due to missing hair keratin genes.

Krox20 is important for maintaining stem cells in the skin and affects hair growth and color.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

Thymic transplantation normalized some T-cells but not others, maintaining immune function.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

Thioredoxin reductase 1 does not affect glucocorticoid receptor activity in hair follicle cells.