Search

everythinglearnresearchcommunity

for

Search:↓

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

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

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

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

Tongue cancer cells show more plectin-1 than non-cancer cells, but both have similar levels of trichohyalin.

Neutrophils quickly respond to skin injury.

The research suggests that p63 and TGF-β1 may help determine tumor type and malignancy in hair follicle and sebaceous tumors.

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

AGD1's PH domain is essential for its role in root hair growth and polarity.

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

Hair proteins in preschool children and their mothers could indicate developmental changes and health status.

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

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.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

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

The WNT signaling pathway is important in many diseases and targeting it could offer new treatments.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Found different proteins in balding and non-balding cells, giving insight into hair loss causes.

Collagen XVII is important for skin aging and wound healing.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

Many people diagnosed with androgenic alopecia might actually have hidden scarring or inflammation.

Terbinafine can cause hair loss.

Cyclosporin doesn't stop hair loss.

Stem cells are crucial for skin repair and new treatments for chronic wounds.

Hair follicle stem cells are key for hair and skin regeneration, can be reprogrammed, and have potential therapeutic uses, but also carry a risk of cancer.

Keratinocytes help heal skin wounds by interacting with immune cells and producing substances that kill pathogens.

K6hf is a unique protein found only in a specific layer of hair follicles.

Animals that change color with the seasons mainly do so in response to daylight changes, but climate change is causing camouflage problems that may require evolutionary changes.