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Three molecular subtypes of advanced skin T-cell lymphoma were identified, with potential biomarkers for predicting treatment response and disease progression.

MC1R gene variations affect skin, hair color, UV sensitivity, and melanoma risk.

Targeted cancer therapies can cause skin side effects, but activating SOS in the skin may help reduce them.

Blocking the Mitochondrial Pyruvate Carrier causes stress in hair follicles, which can be reduced by an ISR inhibitor.

Resident memory T cells and necroptosis may drive fibrosis in eosinophilic fasciitis and morphea.

Melanogenesis-related proteins may trigger immune responses in alopecia areata patients.

The spiny mouse regenerates ear tissue asymmetrically, with gene expression differences possibly explaining its unique healing abilities.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

Researchers developed a new way to measure gene activity in single hair follicles and found that a specific gene's activity changes with different amounts and times of treatment.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Skin RAGE levels are linked to inflammation and cell death.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Non-coding RNAs could help detect and treat radiation damage.

Researchers found a new mutation causing total hair loss from birth.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

PTEN was identified as a specific marker for the skin disease cutaneous lupus erythematosus, and it helps increase the expression of harmful type I interferons.

Rats can develop an immune response to prion protein peptides, but it may cause severe skin issues in older rats.

Agouti protein affects melanocortin receptors through competitive antagonism and receptor down-regulation.