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Low Vitamin D receptor levels in breast cancer are linked to worse outcomes and more bone metastases, and could be a marker for prognosis.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

LRIG1 is linked to better survival in Merkel cell carcinoma.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The LMNA mutation affects skin structure even in asymptomatic carriers.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

A woman with HIV had a severe skin condition that improved with antiretroviral therapy.

Vitamin D receptor and hairless protein are essential for hair growth.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

Higher RBP4 levels are linked to severe alopecia areata, but genetic variant rs3758539 doesn't affect baricitinib response.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

The SHJH hr mice with a mutated Hr gene show signs of faster skin aging due to poor antioxidative protection.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Mutations in the hairless gene cause a rare form of permanent hair loss.

These gene variations are not linked to alopecia areata in Egyptians.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

PLAU and SerpinB2 affect cell death differently in various forms of leprosy and could be targets for new treatments.

A gene mutation in mice causes permanent hair loss and skin issues.

EBV infection increases a specific keratin variant in carcinoma cells, possibly affecting cell structure and cancer progression.

CD8+ T cells expand significantly in alopecia areata, suggesting new treatment targets.

Nucleic acid polymers can enhance antiviral responses and improve treatment outcomes for chronic hepatitis B.

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

Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.