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Different Myc family proteins are located in various parts of the hair follicle and may affect stem cell behavior.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Keratinocyte stem cells are crucial for skin renewal and have potential in wound healing and tissue regeneration.

Different materials affect the growth of brain cells and fibroblasts, with matrigel being best for brain cell growth.

The Gsdma3 gene is essential for normal hair development in mice.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

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

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

DcR3 helps heal wounds and regrow hair by changing macrophages to a repair-focused type.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

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

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

Using an anti-ICAM-1 antibody with rapamycin improves hair transplant survival in monkeys.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A gene mutation in Lama3 is linked to a common type of hair loss.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Gasdermin A3 causes hair follicle stem cells to activate too early, leading to hair loss.

CDH3-related disease causes worsening eye and hair issues.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Mettl3 is essential for normal tissue development and self-renewal by regulating gene expression.

DNA methylation of miR-365-1 causes hair follicle stem cell death by affecting DAP3.

Overexpressing Dsg3 in mice skin causes excessive cell growth and abnormal skin development.

Mice with a mutated Dsg3 gene showed severe symptoms but not the typical blistering of pemphigus vulgaris.

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

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.