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Hereditary hyperplastic gingivitis in silver foxes may be linked to errors in the MAPK signaling pathway, influenced by androgens.

HIF-1α is important for hair growth and could be a treatment target for hair loss.

New research has found 14 genes linked to the risk of developing alopecia areata, improving understanding and treatment options.

Genes affect cytokine production, which can influence chronic diseases, and certain interventions may help prevent related molecular damage.

Deleting the BRD4 protein in certain skin cells causes hair loss and skin inflammation.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Thyroid-related genes are active in skin cells and may affect autoimmune conditions.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

The hepatitis B vaccine did not cause hair loss in the tested mice.

Key genes and pathways in alopecia areata were identified, suggesting new treatment targets.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

New mutations in the DSG4 gene cause a rare hair condition.

Alopecia areata shares gene expression patterns with chronic skin disorders, suggesting they are linked.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

The Fas/FasL pathway may play a role in alopecia areata.

No clear link between specific gene and hair loss in Mexican brothers.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

Hsa-miR-193a-5p is important in alopecia areata by promoting inflammation and involving specific genes in hair and immune function.

VLDL could be an early warning sign for male pattern baldness.

Herbal extract may help treat certain types of hair loss.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Lack of certain fatty acids causes skin, immune, and fertility issues in mice.

Hydroxytyrosol may help treat hair loss by reducing inflammation and oxidative stress.

Hair follicle development involves specific cells and genes, crucial for understanding severe skin diseases like harlequin ichthyosis.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

PD‐L1 and PD‐L2 may not effectively control immune activation in alopecia areata.