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A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Lack of cystatin M/E causes thin hair and dry skin.

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

Keratins are crucial for cell structure, growth, and disease risk.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

Cysteines in wool fibers are accessible and form important disulfide bonds.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

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

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Mesenchymal MEIS2 is essential for whisker development without needing sensory nerves.

Sesn2 protects inner ear hair cells from damage by regulating certain cell survival pathways.

Both SMS1 and SMS2 are crucial for normal hair growth and cycle in mice.

Mouse hair keratins mHa1 and mHb4 can't form a strong network on their own in cells.

The 3D structure of a key hair protein was modeled, revealing specific helical structures and stabilization features.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

COX2 and ATP synthase control the size of hedgehog spines.

A new imaging method helps see and study touch nerve endings in mouse skin.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

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

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

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

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.