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A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

EDA2R gene linked to hair loss.

Angiopoietin-1 helps hair follicle cells survive and grow, potentially treating hair loss.

Blocking the Mitochondrial Pyruvate Carrier causes stress in hair follicles, which can be reduced by an ISR inhibitor.

The protein ARA70/ELE1 is involved in male pattern baldness, and lower levels of its short form may lead to hair thinning.

Topical IKKα inhibitors may help prevent CCS tumours.

Fat cells help recruit healing cells and build skin structure during wound healing.

Atopic dermatitis increases the risk of some autoimmune diseases.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

Nelfb is essential for dermal fat development and survival.

Certain immune cells in atopic dermatitis skin could be targeted for treatment.

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

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Certain gene variations increase the risk of alopecia areata in Koreans.

Hair regrows faster at the front than the back of mouse skin.

ILC1-like cells can cause alopecia areata by affecting hair follicles.

CCT128930 is a promising new drug that effectively targets and inhibits a cancer-related protein, showing potential for cancer treatment.

AtZP1 protein stops root hair growth in plants by blocking certain genes.

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.

Muscarinic acetylcholine receptors in skin cells help regulate and promote hair growth.

HPV8 E6 gene causes growth of certain skin stem cells.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

The KAP 7 gene affects wool traits in Rambouillet sheep, with the BB genotype showing the best wool characteristics.

Trichohyalin is a versatile protein involved in hair and skin structure.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

CD8A and FOXD2-AS1 may be key for diagnosing and treating alopecia areata.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

People with alopecia areata have higher levels of RBP4 protein and antibodies against it.