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A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Vδ1+ T-cells in the skin contribute to hair loss in alopecia areata and could be targeted for treatment.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Combining specific proteins and cell-derived particles may help treat hair loss.

Polyomavirus A2 infection in newborn mice caused hair follicle tumors.

Identical p53 gene mutations in different cancers suggest the need for careful treatment.

Overexpressing thrombospondin-1 in mice skin prevents UVB-induced skin damage.

SLVs help maintain muscle stretch sensitivity and could aid in treating hypertension and muscle spasticity.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Surgical grafting may fix nail issues caused by valproic acid.

AP collagen peptides help hair grow and improve hair health.

Vimentin, desmin, and laminin help maintain rat skin structure.

Mutations in the LIPH gene cause woolly hair in a child.

Sdr16c5 and Sdr16c6 genes regulate a key point in lipid production that affects eye and skin gland function.

RALF22 is essential for root hair growth in response to fungal emissions in Arabidopsis.

cgVEGF164 boosts hair follicle growth in mice.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

Vitamin D receptor helps control skin cell growth and hair development.

Chinese fine-wool sheep have genetic variations linked to traits like milk and health, with some genes under strong selection.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Vitamin D receptor helps prevent skin tumors.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.