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Researchers made a detailed map of gene activity for different parts of human hair follicles to help create targeted hair disorder treatments.

Early genetic testing and zinc therapy are crucial for managing acrodermatitis enteropathica in infants.

TCF/Lef1 is essential for skin barrier function by regulating lipid metabolism.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

ATP-sensitive potassium channels are important for hair growth.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

ABCD1 gene mutations cause adrenomyeloneuropathy, leading to symptoms like limb weakness and spasticity, with management focusing on rehabilitation and spasticity treatment.

Genetic variations affecting skin structure play a key role in severe acne.

The MTR gene affects wool quality and production in Chinese Merino sheep.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

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

A rabbit gene important for hair development was identified and detailed.

Certain gene variants are linked to severe acne, especially in males.

lncRNAs may regulate hair follicle development in Hu sheep.

Hoxc8 gene helps start mammary gland development by controlling specific signals.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Loss of the Y chromosome and UTY gene activity increases cancer risk in men.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Mice with the ab gene have abnormal sebaceous gland development, affecting sebum production.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

RD26 controls root hair growth during drought by repressing key genes, helping plants save energy.

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BBS7 is crucial for maintaining healthy periodontal ligaments by supporting Shh signaling.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

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