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Toxic epidermal necrolysis is a severe skin condition often caused by drugs, with complex treatment and a high risk of death, but survivors usually heal without scars.

Nanoparticles can deliver vaccines through hair follicles, triggering immune responses and providing protection.

Cathepsin L is essential for normal hair growth and development.

Injectable platelet-rich fibrin has improved healing and regeneration in various medical fields and can be more effective than previous treatments.

3D bioprinting improves wound healing by precisely creating scaffolds with living cells and biomaterials, but faces challenges like resolution and speed.

Planarian regeneration begins with a specific gene activation caused by injury, essential for healing and tissue regrowth.

Hyperprolactinemia should be treated before confirming a PCOS diagnosis.

The document concludes that transplantology has evolved with improved techniques and materials, making transplants more successful and expanding the types of transplants possible.

The document concludes that Catalyst software is effective for drug design, identifying potent compounds for various medical conditions.

SIRT7 protein is crucial for starting hair growth in mice.

Platelet Rich Plasma (PRP) shows promise for tissue repair and immune response, but more research is needed to fully understand it and optimize its use.

Glutathione helps Arabidopsis roots adapt to low phosphate by regulating a specific growth pathway.

Cavity macrophages gather on organ surfaces but don't really invade or help repair the organs after injury.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

KLF4 is important for maintaining skin stem cells and helps heal wounds.

PDGF signaling is crucial for maintaining and renewing hair follicle stem cells, which could help treat hair loss.

Mice lacking fibromodulin have disrupted healing patterns, leading to abnormal skin repair and scarring.

Women with hair loss have more androgen receptors in certain hair follicles.

Overexpression of sPLA2-IIA in mouse skin reduces hair stem cells and increases cell differentiation through JNK/c-Jun pathway activation.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

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

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A specific gene mutation causes a severe skin disorder in a family.