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Some hair proteins are specific to hair, while others are also found in skin cells.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

Increased 14-3-3 proteins may block hair cycle regression, causing hair loss.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Chemical treatments weaken hair's thermal stability and structure.

Cis-UCA can form new compounds without enzymes, and sulphide donors reduce its UVB-induced toxicity in skin cells.

Human hair can effectively absorb arsenic from water.

Hair follicle development involves specific cells and genes, crucial for understanding severe skin diseases like harlequin ichthyosis.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

Brazilian keratin treatment can cause severe skin reactions.

Human hair keratin helps repair nerve damage in rats.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

The research identified two types of keratinocytes in chicken scales: one for hard scales and another for soft skin, with similarities to human skin differentiation.

Loose anagen hair syndrome may be caused by keratin gene mutations.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

Increasing SSAT makes skin more prone to cancer.

Protein kinase C epsilon may increase skin cancer risk by affecting nearby cells.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

The observed "toughening" in keratin was actually due to water evaporation, not a real change in keratin.

A hair cyst can become cancerous, showing specific keratins from the hair sheath.

GRK2 is essential for healthy hair follicle function, and its absence can lead to hair loss and cysts.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Haircare products with a pH between 5 and 7 are best for maintaining healthy hair.

Electrophoresis can effectively analyze hair proteins for forensic use, even after cosmetic treatments and up to 2 years of weathering.

Dermal EZH2 controls skin cell development and hair growth in mice.

Pathologic tissues have more soluble proteins than normal tissues.

Two distinct caspases in human skin help with cell death and skin formation.

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.