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The human scalp hair bulb contains different types of melanocytes with varying abilities to produce melanin.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

The research helps in creating genetically modified animals to study hair growth.

The Itpr3 gene causes a specific hair pattern in mice.

High levels of human keratin 16 in mice cause skin lesions and abnormal skin development.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

Secreted inhibitors of Wnt and IGF signaling control hair and tooth development, creating species-specific patterns.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

MC-1R is present in skin cells and may help reduce inflammation.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

Keratin 15 helps keep skin cells in a young, undifferentiated state.

Krox20 is important for cell differentiation in the brain and hair follicles.

Blocking a key energy pathway in human hair follicles can trigger stress responses that stop cell growth.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

Keratinocyte gene expression is controlled by multiple modules with specific binding sites.

Protein kinase C epsilon may increase skin cancer risk by affecting nearby cells.

Protein kinase C epsilon may promote skin cancer development after UV exposure by affecting nearby cells.

MAP-2 is crucial for the structure of hair follicles and nails.

BSSP may help skin tumors grow and could be a marker or target for skin cancer treatment.

LncRNA MSTRG.14227.1 hinders hair follicle development in cashmere goats, affecting cashmere quality.

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

CAP1/Prss8 does not activate PAR2 or inhibit PN-1.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

Protease Nexin-1 is found in human hair growth cells and is affected by male hormones.

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

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.