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

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

Cubosomes enhance antimicrobial peptide stability and effectiveness.

Trichohyalin is modified by enzymes to form strong structures in hair cells.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

The nanofiber membranes effectively promote wound healing and have strong antibacterial properties.

The protein CCN2 controls hair growth by affecting hair follicle formation and stem cell activity in mice.

The research shows how certain drug molecules form stable structures with polymers, which could help create new drug forms.

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

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

New genetic mutations linked to rare skin disorders were found in three newborns.

Dlx3 is essential for hair growth and regeneration.

The conclusion is that substances can penetrate hair fibers through multiple pathways, including both the cell membrane complex and the non-keratinous parts.

Trichothiodystrophy involves brittle hair due to low sulfur amino acids, not a transport defect.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

Adding fetal calf serum helps Merkel cells survive and change shape.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Trichocyte filaments have a low-density core and may include proteins for hair structure.

Alpha 6 + /MHCI - cells have stem cell traits and are similar to mouse hair follicle stem cells.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

Ca²⁺-mediated protein citrullination controls cell growth in the CNS and may help treat brain tumors.

RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.

Cysteine formation on hair indicates damage, best detected at pH 4.5.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Mast cell and nerve fiber interactions in mouse skin change with the hair cycle.

CD34 is a marker for isolating stem-like cells in mouse hair follicles.

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

QLT0267 stops hair follicle cell growth and movement.