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ISCK03 stops melanin production in human melanoma cells and lightens skin color in mice and guinea pigs.

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Esrp1 is important for skin health by helping form and maintain the skin barrier.

Tofacitinib helps improve skin conditions in people with Down syndrome, especially alopecia areata.

SB414 may be an effective treatment for atopic dermatitis by reducing swelling and bacterial infection.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

Robertsonian translocation can cause recurrent miscarriages.

SIG-1451 could be a promising new treatment for atopic dermatitis.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A specific gene mutation causes a severe skin disorder in a family.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

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

CDPDFM can improve acne symptoms in rabbit ears.

Krt15+ cells in the mouse intestine resist radiation and can start tumors.

A new mouse mutation causes skin and hair defects due to a gene change.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

A 30 Gy radiation dose effectively causes severe radiodermatitis in rabbits.

RTA 408 cream protects mice from radiation skin damage.

cDermo-1 causes dense skin, feathers, and scales in chickens.

MC4R gene variants not linked to female hair loss.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

IL-17C is important in inflammatory skin diseases and could be a target for treatment.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

Fractional radiofrequency effectively and safely improves rosacea symptoms.

The CTLA-4 gene change studied does not affect Polycystic Ovarian Syndrome in the women tested.

rwSALT accurately measures hair regrowth in alopecia areata using scalp photos.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.