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Prenatal diagnosis of trichothiodystrophy is possible in the second trimester using fetal eyebrow biopsy, with sulfur content analysis being more reliable.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

The Chinese version of the PCOS quality of life questionnaire is reliable and valid for Chinese-speaking women with PCOS.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Researchers found a good way to isolate hair follicle stem cells from newborn goats for further study.

USB videodermatoscopes are a practical and affordable alternative for diagnosing skin conditions.

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A new therapy for a skin blistering condition has not been developed yet.

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

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

A reliable method was developed to detect hair growth compounds in products, ensuring safety and compliance.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

Different body parts have varying levels of certain hair follicle markers.

A specific gene mutation causes long hair in Angora rabbits.

A 73-year-old woman with Hypopigmented Mycosis Fungoides, a rare skin lymphoma, experienced disease progression despite treatment, emphasizing the need for ongoing monitoring.

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Mutations in β1 integrins cause embryonic death but have milder effects on skin.

A gene mutation in mice causes skin defects and early death.

Mouse keratin 6 isoforms have different expression patterns in various tissues.

Targeting impaired Nrf2 signaling might help treat hidradenitis suppurativa early on.

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