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

The PIP5K1A gene helps cashmere growth in goats by promoting cell proliferation, and melatonin boosts its expression.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

Lack of cystatin M/E causes thin hair and dry skin.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

LHX2, with other markers, can identify hair placodes in rats.

Keratin proteins in epithelial cells are dynamic and crucial for cell processes and disease understanding.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

Most patients with dermatomyositis had skin rash, itching, and muscle weakness, treated mainly with prednisolone and hydroxychloroquine.

Profilin1 speeds up wound healing.

Both SMS1 and SMS2 are crucial for normal hair growth and cycle in mice.

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

A PIK3CA mutation in Schwann cells causes severe nerve damage and increased glycolysis, but early treatment can help.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

Mutations in the LIPH gene cause woolly hair in a child.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

LTBP1 is a key regulator in diseases and a potential target for new treatments.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Mouse keratin 6 genes evolved independently from human ones and are regulated differently.

Acidic keratin genes are on CFA9 and basic keratin genes are on CFA27 in dogs.

The K14 promoter is more active in skin cells than the K5 promoter.

Keratin-associated proteins may have roles in various mouse tissues, not just hair.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

Fibre optic confocal imaging can visualize skin layers, blood vessels, and nerves in live mice.

LIPH mutations cause woolly hair in some Chinese people.