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Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Significant progress was made in understanding PXE, but effective treatments are still needed.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

Genetic differences affect COVID-19 severity and treatment effectiveness.

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

Genetically repaired stem cells may treat certain genetic diseases, Th17 cells are key in fighting systemic fungal infections, hair loss in AGA is due to progenitor cell loss, and α-synuclein transfer might contribute to Parkinson's disease progression.

Stat3 influences keratinocyte stem cell behavior, affecting differentiation and migration.

Type XVII collagen helps control skin cell growth and may have anti-aging effects.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

K6hf is found in specific parts of hair follicles, nails, and tongue, and is linked to hair growth and structure.

Human cathepsin V can replace mouse cathepsin L to maintain normal skin and hair in mice.

The technology can create transgenic cashmere goats with improved wool quality.

Gorab deficiency speeds up skin aging by disrupting protein regulation and reducing collagen.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

The biofilm enhances skin healing by promoting cell growth and blood vessel formation.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

An allele of the KRTAP13-2 gene may improve wool quality in sheep.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

UVB exposure increases appetite by activating p53 in skin cells.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Mutations in the Whn gene affect hair keratin gene expression differently.

Type XVII collagen helps control skin cell growth and rejuvenates skin.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.