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Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

The human K5 promoter controls specific gene expression in skin cells, with key regulatory elements near the TATA box.

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

The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

Trps1 is essential for proper hair follicle development.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Sub3 is essential for fungus adherence but not for skin invasion.

Scientists successfully created mouse hair proteins in the lab, which are stable and similar to natural hair.

Increased Stat3 activity reduces hair follicle stem cells and boosts other stem/progenitor cells.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

GPC1 is important for hair growth by helping blood vessels form around hair follicles.

The 3D structure of a key hair protein was modeled, revealing specific helical structures and stabilization features.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

HOXC13 is essential for hair and nail development by regulating Foxn1.

The B2C promoter works in sheep cells but not in mouse embryos.

The hair defect is due to abnormal inner root sheath keratinization.

The method quickly analyzes hair growth genes and shows that blocking Smo in skin cells stops hair growth.

Loss of Dnmt3a and Dnmt3b increases aggressive skin tumors by affecting PPAR-γ.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

Removing Lrig1-positive stem cells in mice causes temporary loss of sebaceous glands.

Two siblings have a rare hair condition caused by a new genetic variant.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

Sciellin is a protein that helps form protective layers in skin, hair, and nails.

The enzyme Dgat1 is essential for healthy hair and skin by controlling retinoid levels.