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iPSC-derived stem cells on a special membrane can help repair full-thickness skin defects.

Researchers made stem cells from human hair follicle cells with better efficiency than from skin cells.

The review concludes that innovations in regenerative medicine, tissue engineering, and developmental biology are essential for effective tissue repair and organ transplants.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

A new ethical skin model using stem cells offers a reliable alternative for dermatological research.

Hair loss in male pattern baldness is linked to changes in specific genes and proteins that affect hair growth and scalp health.

The document concludes that regenerating functional ectodermal organs like teeth and hair is promising for future therapies.

Keratin 15 is not a reliable sole marker for identifying epidermal stem cells because it's found in various cell types.

Mesenchymal stem cells show potential for skin healing and anti-aging, but more research is needed for safe use, especially regarding stem cells from induced pluripotent sources.

Hair follicle stem cells need all reprogramming factors to become pluripotent.

Stem cell niches are crucial for regulating stem cell behavior and tissue health, and their decline can impact aging and cancer.

Skin problems can be caused or worsened by physical forces and pressure on the skin.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

People with Epidermolysis bullosa have many health problems including poor oral health, which is often neglected due to other medical issues.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

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.

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

Mutations in keratin genes cause cell fragility and various skin disorders.

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

Scientists created a functional 3D skin system from stem cells that can be transplanted into wounds.

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.

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

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Scientists improved how to make skin-like structures from stem cells using special gels and a device that controls growth signals, leading to better hair and skin features.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Microneedle arrays deliver botulinum toxin effectively for sweat suppression, similar to injections.

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

Estrogen therapy helped regrow hair in a bald man.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.