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The diphosphonate was the most effective at preventing calcification in rats.

The new assay can track and measure melanosome transfer between skin cells, confirming filopodia's role in this process.

TRPS1 is crucial for bone, kidney, and hair follicle development.

Placenderm® improves scalp elasticity and hair quality safely.

People with atopic dermatitis have more CD4+ T cells that respond to a certain bacterial lipid, which may play a role in the skin condition's inflammation.

K42 and K124 keratins are only found in horse hoof lamellae.

GKLF/KLF4 and Sp1 control Keratin 19 gene activity, influencing cancer-related changes.

KRTAP2 genes are crucial for hair structure and may impact hair disorders and treatments.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

A protein called MPZL3 in mitochondria slows down hair growth and could be a target for treating hair growth disorders.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

MPZL3 protein helps control the size of oil glands and the growth of oil-producing cells in both mice and humans.

Par3 protein is essential for skin cell balance and stability.

HDAC4 and HDAC7 are crucial for Th17 cell development and could be targeted to treat inflammatory diseases.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

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

Mutations in the KRT85 gene cause hair and nail problems.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

The antibody 005-C04 blocks prolactin receptors, causing reversible infertility, impaired lactation, and hair regrowth in female mice.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

MC4R gene variants not linked to female hair loss.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Desmocollin 1 helps maintain skin structure during fetal development.

Keratins are important for skin cell health and their problems can cause diseases.

AGC2-1 protein is essential for root hair growth in Arabidopsis.