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Small proline-rich proteins and trichohyalin help make epithelial tissues tougher and more flexible.

Multiphoton microscopy can effectively distinguish between scarring and non-scarring alopecia.

CIP/KIP proteins help stop cell division and support hair growth.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

A new vaccine using a porous scaffold boosts immunity and protects against the flu better than traditional methods.

A rare skin tumor with bone formation was successfully removed without recurrence.

The G allele of IFITM3 rs12252 is linked to more severe COVID-19.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

Hair follicle cells and intestinal tissue can create strong, functional blood vessel replacements.

A new protein, mK6irs, is found in specific hair layers and may help understand hair growth and diseases.

A new gene mutation is linked to monilethrix in the studied family.

Monilethrix Syndrome causes fragile, beaded hair that breaks easily and needs early diagnosis for better care.

NFIC helps rat dental cells grow and turn into bone-like cells.

PIKFyve is essential for normal platelet function and its deficiency causes organ issues and macrophage infiltration.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

The hydrogel helps skin heal by encouraging new blood vessel growth.

Pili torti hair is fragile due to loose keratin filaments and weak disulfide bonds.

Using Wharton's jelly stem cells and scaffolds can help regenerate skin and hair.

Hair shaft malformation contributes to Central Centrifugal Cicatricial Alopecia.

Alopecia can be caused by multicentric reticulohistiocytosis.

The research provided a detailed view of the non-keratinous parts of human hair fibers.

Mechanical tension worsens keloid scars by activating inflammation and fibrosis pathways.

MX1 and AR genes are linked to milder COVID-19, while TMPRSS2 increases severe risk, especially in women.

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

TNC+ fibroblasts play a key role in skin inflammation by interacting with T cells.

Multiphoton excitation microscopy is a promising tool for deep tissue imaging and clinical applications.

Fibroblasts can be mistaken for neural cells, so functional validation is needed.

The study suggests that the arrector pili muscle is important for hair health and its damage might contribute to hair loss.