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Radiation treatment causes skin fibrosis by increasing certain fibroblast subpopulations, but using a c-Jun inhibitor or fat grafting can reduce this effect.

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

The SHJH hr mice with a mutated Hr gene show signs of faster skin aging due to poor antioxidative protection.

Daughters with affected mothers may develop frontal fibrosing alopecia early.

Excessive sun protection might contribute to frontal fibrosing alopecia.

A protein called sFRP4 can partly inhibit hair growth.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

The review suggests more research is needed to understand Frontal fibrosing alopecia, a condition causing hairline recession in postmenopausal women.

KLF4 is important for keeping hair follicle stem cells inactive.

Identifying specific hair follicle parts could lead to better hair loss treatments.

Cetaceans lost hair due to changes in the Hr and FGF5 genes.

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

Early detection of specific skin lesions can help identify Birt-Hogg-Dube syndrome and prevent serious complications.

Frontal fibrosing alopecia is increasing, especially in postmenopausal women, and treatment with finasteride can improve it.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

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

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

FFA's causes may include environmental triggers and genetic factors.

27 out of 32 candidates passed the hair restoration surgery exam.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

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

Fz3 and Fz6 can partially replace each other in tissue polarity and axon guidance.

ESR2 gene linked to female-pattern hair loss.