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The fuzzy gene is crucial for controlling hair growth cycles.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

A protein called COMP is part of the connective tissue in normal human hair follicles and may be important for hair health.

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

Alopecia areata patients have higher levels of certain immune receptors, suggesting new treatment possibilities.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

A 12-year-old boy had severe shingles and skin damage after a stem-cell transplant.

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

Genetic testing is crucial for diagnosing and managing non-Herlitz junctional epidermolysis bullosa.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

Alpha 6 + /MHCI - cells have stem cell traits and are similar to mouse hair follicle stem cells.

Touch dome keratinocytes in adult skin have traits of different skin cell types.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

Alopecia areata shows a unique type 1 interferon signature, suggesting potential treatment by targeting this pathway.

Profilin1 speeds up wound healing.

Trps1 plays a key role in hair follicle development and cycling.

μ-Crystallin may help hair growth by affecting thyroid hormone levels in mouse hair follicles.

Higher CRBP1 levels are linked to more severe alopecia areata.

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

Thymic transplantation normalized some T-cells but not others, maintaining immune function.

Neuronatin is found in various cells of rat tissues and has a unique location in sperm cells.

The nodule was a benign cutaneous lymphadenoma, not cancer, and was successfully removed.

A rare gene variant causes hair and nail issues in a family.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

Recombinant human TSG-6 speeds up wound healing in diabetic mice.

Monoclonal antibodies LT-1, LT-2, and LT-7 help diagnose certain blood cancers.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.