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The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

EGF–FGF2 helps mouse stem cells grow and become more like nerve cells.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

New mutations in the DSG4 gene cause a rare hair condition.

The p75 neurotrophin receptor is important for hair follicle regression by controlling cell death.

Involucrin gene expression is controlled by specific proteins and signaling pathways.

The human K5 promoter controls specific gene expression in skin cells, with key regulatory elements near the TATA box.

The study found nine new hair protein genes in human hair follicles.

Targeting specific cell interactions may help treat skin fibrosis.

ARHGEF3 is essential for proper hair follicle development.

LRIG1 is linked to better survival in Merkel cell carcinoma.

MicroRNA-302 helps improve the conversion of body cells into stem cells by blocking NR2F2.

Two main types of fibroblasts with unique functions and additional subtypes were identified in human skin.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

Delta1 is crucial for controlling skin cell growth and preventing tumors in mice.

Blocking the FGF5 gene in sheep leads to more fine wool and active hair follicles due to changes in certain cell signaling pathways.

A specific molecular switch, driven by MAPK/ERK signaling, helps spiny mice heal wounds by regenerating skin instead of forming scars.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

Researchers found specific genes in the part of hair follicles that could help treat hair disorders.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

Stem cell factor and certain proteins help melanocytes from hair follicles move and attach better, aiding vitiligo repigmentation.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Lef1 helps adult skin cells maintain their ability to heal wounds and regenerate hair, but the study's methods and conclusions have been questioned.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

SFRP-4 might be an early indicator of diabetes and hypertension in men with androgenic alopecia.

EGFR helps control how hair grows and forms without needing p53 protein.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.