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LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

miR-218-5p helps skin and hair growth by targeting SFRP2 and activating a specific signaling pathway.

Syntaxin 9 helps in transporting and signaling of the EGF receptor in skin and stomach cells.

Sweat gland stem cells help maintain glands, aid wound healing, and can regenerate skin structures.

Variegated coat color in cats is linked to the Silver locus.

Vimentin is crucial for wound healing, cell growth, and managing immune responses.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

Food deprivation increases MST enzyme in the brain, possibly affecting energy balance.

Non-coding RNAs play key roles in the hair growth cycle of Angora rabbits.

Rabbit skin analysis showed changes in hair growth and identified miRNAs that may regulate hair follicle development.

REV7 is crucial for genome stability and cancer treatment, making it a potential target for therapy.

A gene mutation causes curly hair and hair loss in rats.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

Defective protein folding due to a mutation is key in ANE syndrome.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

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

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

ARHGEF3 is essential for proper hair follicle development in mice.

Rac1 is crucial for normal hair structure and pigmentation.

AtVPS29 is essential for proper plant growth by regulating gibberellin signaling.

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

SOX9 is essential for the development of various organs and hair follicles.

Nonpalmoplantar skin cells can be made to express keratin 9 by interacting with palmoplantar fibroblasts.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.