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Eribulin-based chemotherapy is more effective and has fewer side effects for advanced triple-negative breast cancer.

Anti-Desmocollin 3 antibodies can cause atypical pemphigus symptoms.

Activating Nrf2 in skin cells causes skin disease similar to chloracne in mice.

PP2Acα is essential for proper hair and skin development.

BMAL1 controls skin cell growth and UV damage risk, peaking at night.

A new method can detect mutations in mice by observing changes in hair follicle cells.

Boswellia may improve skin inflammation symptoms and positively influence hair growth in mice.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Tmem50b and 2610305D13Rik genes play key roles in early mouse embryo development.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Clq deficiency is linked to systemic lupus erythematosus symptoms.

MEF2C is crucial for normal hair cycle progression.

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

The -866G/A polymorphism in the UCP2 gene is not linked to polycystic ovary syndrome.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

Fgfr2b helps maintain healthy skin and prevent cancer.

NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

SKH1 hairless mice have identifiable epidermal stem cells with specific markers.

Protein kinase C epsilon may promote skin cancer development after UV exposure by affecting nearby cells.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Alopecia areata is influenced by genetics and immune system factors, and better understanding could improve treatments.

OCIAD2 and DCN genes affect hair growth in goats by having opposite effects on a growth signaling pathway and inhibiting each other.

Parental uveitis increases offspring's risk and severity of autoimmune eye disease.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

A patient with Birt-Hogg-Dubé Syndrome also had choroidal melanoma, suggesting the need for careful eyelid exams in such patients.

Adjusting estradiol-ANGPT2 levels can promote hair growth in female pattern hair loss.

Claudin expression changes help the skin respond to injury.

The Naked (N) trait in mice is linked to lower glycine and tyrosine in hair proteins.