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Different types of fibroblasts play various roles in diseases and healing, and more research on them could improve treatments.

Researchers used a laser to create advanced skin models with hair-like structures.

Retinoic acid helps change skin cells and is important for skin development and hair growth.

Acyclovir can prevent rejection of skin grafts in herpes-related lip leucoderma.

Lichen simplex chronicus on the scalp can be diagnosed by specific hair and skin signs and treated with corticosteroids and therapy.

Zinc sulphate solution was not effective in reducing the number, duration, or severity of recurrent herpes simplex infections.

RANKL improves the immune response against herpes simplex virus by enhancing T cell activation and could help develop better treatments or vaccines.

The study found different absorbance values for simplex and complex homoeopathic hair oils when analyzed with a UV-visible spectrophotometer.

Injecting anti-herpes antibodies locally can prevent skin lesions and sweating problems caused by herpes simplex virus in mice.

Herpes simplex virus infections should be considered in pemphigus patients to avoid unnecessary changes in treatment.

Chronic bacterial infections of hair follicles can cause ongoing skin inflammation.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

The document's conclusion cannot be provided because the document is not available or cannot be understood.

A patient with a rare hair condition and skin disorder showed hair improvement after treatment.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Isotretinoin may effectively treat hereditary hypotrichosis simplex, a rare hair loss condition.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

A 15-year-old girl has a skin condition causing blisters on her feet, likely inherited from her family.

Combining PRP injections with minoxidil 2% effectively promotes hair growth in hereditary hair loss.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

A woman lost her hair after taking acyclovir, but it grew back when she stopped the medication.