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A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

A woman with lupus also developed a severe skin condition linked to a genetic factor.

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.

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

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

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

The conclusion is that differentiating wound types in RDEB patients is important for clinical trials and understanding the disease.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Genetic testing is crucial for diagnosing and managing non-Herlitz junctional epidermolysis bullosa.

Antiviral drugs, especially daclatasvir, may be a new treatment for a rare skin disease, improving survival and reducing symptoms in mice.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Skin grafts from related donors significantly healed chronic wounds in patients with a severe skin condition over a year.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Neutrophils quickly respond to skin injury.

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

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

Genetic variations affecting skin structure play a key role in severe acne.

Thymosin β4 helps improve skin healing and reduce scarring.

The study created hair-bearing skin models that lack a key protein for skin layer attachment, limiting their use for certain skin disease research.

Hair loss in autoimmune blistering skin diseases varies and may regrow with disease control.

When skin blisters, healing the wound is more important than growing hair, and certain stem cells mainly fix the blisters without helping hair growth.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

Cannabinoids may help some skin conditions but more research is needed.

Mesenchymal stem cells show promise for treating various skin conditions and may help regenerate hair.

A woman developed a severe skin reaction after getting a birth control implant.

The document concludes that stem cells and their environments are crucial for skin and hair health and have potential for medical treatments.