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A new DSG4 gene mutation causes hair defects in a young girl.

The study found 65 intermediate filament genes, including new keratins, and suggested updating keratin naming.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

EISA uses enzymes to create precise nanostructures in cells, offering new ways to design adaptive materials and therapies.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

The 14-3-3σ gene is essential for preventing hair loss.

FA2H is essential for normal fur and sebum production in mice.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

Overexpressing a specific enzyme in mice causes hair loss and female infertility.

Sebaceous glands help study fatty acid transporters and binding proteins.

Type II keratin genes are crucial for hair follicle differentiation and have a conserved structure and expression pattern.

Arabidopsis Formin 2 stabilizes actin filaments, affecting cell-to-cell movement and virus susceptibility.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

A mutation in the Sgkl gene causes defective hair growth in mice.

Altering SSAT affects fat metabolism and body fat in mice.

A genetic hair protein variant is more common in Japanese people and is inherited.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

The method successfully created stable transfection donor cells for goat hair follicle research.

The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Oxidized trichocyte keratin has a helical dislocation in its structure.