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Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

Cold waving solutions quickly reduce cystine to cysteine in hair.

Two specific genes are more active during hair growth in mice.

A gene mutation in mice causes skin defects and early death.

Mast cells and the CB1 receptor may be key in causing IgA vasculitis.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

There is no standard treatment for the rare Cronkhite–Canada syndrome, which can be fatal and lead to cancer.

Certain gene variations are linked to severe acne in Egyptian patients and could guide treatment choices.

The study found stem cells in minor salivary glands that can differentiate and are involved in tumor formation when exposed to tobacco.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

Catalytic antibodies are early indicators and active participants in the development of systemic lupus erythematosus.

Cathepsin L is essential for normal hair growth and development.

The cuneate nucleus has two main neuron types: relay neurons and interneurons.

Newly designed proteins can effectively degrade specific proteins in cells, offering a potential new therapy method.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.

Certain amino acids in 5AR1 and 5AR2 are crucial for binding and resistance to Finasteride.

Arteannuin might work against cancer and Alzheimer's by targeting neprilysin.

Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

Ritlecitinib provides new treatment options for diverse alopecia areata patients.

Trichohyalin in sheep hair follicles may help with structure and calcium binding.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

pCLCA2 protein may help maintain skin structure and function.