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The research suggests that immune cells and a specific type of cell death called ferroptosis are involved in Frontal fibrosis alopecia.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

The method successfully created stable transfection donor cells for goat hair follicle research.

The fuzzy gene is crucial for controlling hair growth cycles.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

Scientists successfully made a human growth factor in a plant, which could help with hair growth and bone development.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Renaming frontal fibrosing alopecia to a syndrome could improve diagnosis and treatment.

A new gene mutation causes insulin resistance in a girl and her mother.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

Phospholipids help plant proteins move by regulating receptor interactions.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

Eflornithine improved symptoms in Bachmann–Bupp Syndrome patients.

Pro-Ile could be used in cosmetics to improve skin, hair growth, and healing.

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

Compound 6 is a promising candidate for better wound healing.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

New lipid/fiber microplexes improve mRNA therapy for degenerative diseases by enhancing cell function and treatment effectiveness.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

The FGF5 gene determines hair length in dogs.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Sugar molecule helps hair growth, less in balding, returns with treatment.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.