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Desmocollin 1 and 3 have distinct patterns in human tissues, with Dsc1 in specific skin and hair layers and Dsc3 in various epithelial layers.

AL136131.3 slows hair growth by affecting energy processes in hair loss.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

α3β1 integrin is essential for skin stability and proper wound healing.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

A protein called desmoglein 3 is important for keeping hair follicle stem cells inactive and helps in their regeneration.

Gsdma3 affects hair growth by controlling Wnt5a, which influences hair cell development.

TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.

Type 3 5α-reductase is more common and finasteride and dutasteride strongly inhibit it.

The TRPV3 channel structure changes linked to severe itch and hyperkeratosis were identified using cryo-EM.

A protein called MPZL3 in mitochondria slows down hair growth and could be a target for treating hair growth disorders.

The new 3D imaging method accurately measures hair surface details quickly.

Activating TLR3 improves the healing and immune properties of periodontal ligament stem cells.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Basonuclin may help control ribosomal RNA gene activity in skin cells.

Trichothiodystrophy causes abnormal protein deposits and distortion in hair follicles.

Activating TLR3 may help produce retinoic acid, important for tissue regeneration.

Claudin-1 and Claudin-3 are crucial for keeping hair follicle structure and preventing a type of hair loss called telogen effluvium.

The mTurq2-Col4a1 mouse model shows that cells can divide while attached to stable basement membranes during development.

Variation in the TCHH gene affects wool curliness in sheep.

C.I. Acid Orange 3 caused cancer in female rats but not in male rats or mice.

Overexpression of R-spondin 3 leads to sparse hair and impaired hair regeneration.

TBX3 gene affects pigmentation and marking formation in Dun Mongolian horses.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.