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A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

Old C57BL/6 mice with unsynchronized hair cycles show less melanin in their spleens.

Plerixafor may help treat pigmentation disorders by promoting skin repigmentation.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

The virus linked to a rare disease was found in a patient's blood and urine before skin symptoms appeared.

Quiescent cells have increased mitochondrial activity and ECM gene expression, but reduced glycolysis.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

A new DSG4 gene mutation causes hair defects in a young girl.

Recognizing RSCC is crucial due to its aggressive nature and high risk of poor outcomes.

The monkey's hair loss was due to an autoimmune disease, not genetics.

The study found specific skin and cell changes in patients with monkeypox, helping diagnose and understand the disease.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

A rare type of skin cancer with mucosal involvement was partially treated but eventually relapsed.

Careful monitoring is crucial to prevent JC virus reactivation in lupus patients treated with rituximab.

Keratinocyte gene expression is controlled by multiple modules with specific binding sites.

Gene expression, especially Dkk4, is key to cat color patterns.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

SQSTM1 is linked to increased risk of alopecia areata.

Majocchi's granuloma can occur in kidney transplant patients on tacrolimus and can be treated with antifungal medication.

Injury boosts normal skin cell growth, reducing cancer cell advantage.

Retinoic acid affects male and female muscle energy use and function differently.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Giving immune serum from vaccinated mice to mice without T cells prevents infection and tumor growth.

Acitretin improved monilethrix symptoms temporarily, but they returned after stopping treatment.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.