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Collagen XVIII affects wound healing, hair growth, and bone development, with its absence speeding up processes and overexpression causing delays and abnormalities.

A specific RNA helps increase the growth of skin cells in Liaoning cashmere goats by working with a protein to boost a growth-related gene.

TRPS1 is crucial for bone, kidney, and hair follicle development.

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

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Nestin is found in hair follicle progenitor cells, linking them to neural stem cells.

p120-catenin helps control skin inflammation by regulating cadherin levels.

TCHHL1 is a protein important for hair growth, found in hair follicles.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

Collagen XVII and CD151 affect cell movement, with CD151 inhibiting migration when bound to integrins.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

Hair stem cells produce a protein called COL17A1 that plays a key role in their development and is linked to hair thinning and baldness.

Intermediate filaments are crucial for cell structure and function, regulated by specific genes and proteins.

TRPA1 is crucial for mechanical sensitivity in skin sensory neurons.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.

Deleting the CDSN gene causes severe skin and hair problems, leading to death.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

Lack of TrkC receptor delays hair follicle development.

Neprilysin is important for hair growth regulation.

Keratin 17 is crucial for cell growth in wound healing by aiding protein synthesis.

Stem cell niche exit in C. elegans is influenced by Sh1 cell membrane protrusions.

XMU-MP-1 stops cell growth in a human mini-organ and reduces the effectiveness of the chemotherapy drug paclitaxel.

SOX11 and SOX4 help skin cells act like embryonic cells to heal wounds in mice.

Certain skin proteins can form anchoring structures without the protein AMACO.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.