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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.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

RNA aptamers can specifically block FGF5-related cell growth, potentially treating related diseases or hair disorders.

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

Phospholipids help plant proteins move by regulating receptor interactions.

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

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

Eflornithine improved symptoms in Bachmann–Bupp Syndrome patients.

Sheep cells were successfully modified to include a spider silk protein gene.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

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

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

A gene mutation in mice causes severe skin disorder similar to a human condition.

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

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

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

A mutation in the VDR gene affects hair cycling without needing ligand binding.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Hypaphorine from a fungus changes the internal structure of Eucalyptus root hairs, stopping their growth.

Researchers identified promising inhibitors for the BRD4 protein, including finasteride and amentoflavone.

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

The fuzzy gene is crucial for controlling hair growth cycles.

Two new gene mutations cause a rare hair disorder.

New findings suggest the protein linked to Birt–Hogg–Dubé syndrome is important in cell signaling and could affect treatment understanding.

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

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.

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

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