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A new test more accurately detects citrulline in hair follicles and pilomatrixomas.

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

Deleting part of a gene in mice causes wavy hair and high pup loss.

Overexpressing COX-2 in mice skin reduces skin tumor development.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

Long-lived proteins may predict age-related diseases.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

Corneodesmosin is essential for skin and hair health, and its dysfunction can lead to skin and hair disorders.

L-PGDS has specific binding sites for its functions and could help in drug delivery system design.

A multi-drug treatment can effectively clear extensive calcinosis in juvenile dermatomyositis.

A rare case of Cushing's syndrome and pheochromocytoma requires careful re-evaluation to avoid complications.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Blocking certain pathways with kinase inhibitors may help treat cutaneous lupus erythematosus.

Linoleic acid and magnesium are key in alopecia areata progression, and tofacitinib can help by affecting their pathway.

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

JAM-A modification speeds up skin wound healing by boosting fibroblast growth.

Lysophosphatidic acid boosts stem cell growth and movement by creating reactive oxygen species.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

HLD10 can include increased body hair and Mongolian spots.

Specific immune cells and pathways contribute to hair follicle inflammation and hair loss, suggesting potential treatments for lichen planopilaris.

Two patients treated with TAC for mouth fibrosis improved but developed Cushing's Syndrome symptoms.

Astrotactin-2 is cleaved in a specific way that helps understand its maturation.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

A humanized IL-2 fusion protein boosts T regulatory cells and helps control hair loss in Alopecia Areata.

L-Carnitine-L-tartrate may help hair grow and prevent hair loss.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Laser-Assisted Exosome Delivery showed early skin improvement without side effects, but more research is needed.