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The FTO gene hinders stem cells in hair follicles from becoming pigment cells.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

A new gene mutation causes a rare type of hair loss.

Removing the p75 gene in mouse skin cells didn't affect their skin or hair growth.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Neuropilin 2 may be a biomarker for melanoma and affects melanocyte behavior.

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

CDKN2AIP gene is less active in nevus sebaceous, affecting related RNA networks.

Hairless protein is key for hair growth, cell differences cause gene expression variation, and the N-end rule pathway senses nitric oxide for protein breakdown.

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

Targeting NCoR1 can help treat heart enlargement and dysfunction.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

The Foxn1 gene is essential for normal nail and hair development.

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

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Noggin promotes skin tumors by activating certain cell signaling pathways.

FOXN1 duplication can cause excessive hair growth.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

The LEF-1 binding site enhances gene expression in hair follicles, with other proteins aiding specific regulation.

Sea cucumbers have unique genes that help them regenerate their intestines.

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

FOXN1 is crucial for thymus development and immune response in Xenopus laevis.

BLMP-1 is important for regular molting and gene expression cycles in worms.

The Celsr1 gene is crucial for normal hair patterning in mice.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

MOF controls skin development by regulating genes for mitochondria and cilia.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.