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Coloring shampoos for gray hair may cause gene mutation, reproductive issues, and skin damage, needing stricter regulation and expert consultation.

PT-20 did not significantly improve gray hair repigmentation.

Correcting EDA fibronectin organization and YAP translocation can improve wound healing in fibrotic conditions.

CRISPR gene editing reduces harmful molecules in cells from Emery–Dreifuss Muscular Dystrophy patients.

Nephronectin helps attach muscle cells to hair follicles.

Goat neck skin has a complex network of collagen, elastic, and reticular fibers.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

A dark-haired Chinese girl had hair that looked banded under certain light but was normal under a microscope.

Actin filaments help stabilize and integrate cell membranes during transfer.

Male yak hair growth is influenced by DHT synthesis, which is promoted by 5α-red1 and AR during growth phases, while E2 may inhibit growth through ERα.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

3D images of skin show collagen is evenly spread, but elastic fibers are fewer near hair follicles.

Danon disease can be hard to diagnose due to non-specific symptoms.

Keratins are crucial for hair strength, and mutations in certain keratin genes cause hair disorders.

Monilethrix is not caused by a metabolic defect.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

New techniques helped identify rare wool proteins by reducing dominant ones.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Actin and alpha-smooth muscle actin help skin heal in mouse fetuses.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Neuromyotonia and morphoea can occur together in the same body areas.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Familial dyskeratotic comedones are a rare, inherited skin condition that is hard to treat but may improve slightly with topical retinoids and urea cream.

Changes in keratin make hair follicles stiffer.

Pili torti hair is fragile due to loose keratin filaments and weak disulfide bonds.