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

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

Lrig1 could be a marker for advanced sebaceous carcinoma.

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

HLA can be linked to autoimmune hepatitis.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

LONRF1 is important for oxidative damage response and tissue remodeling during wound healing.

LHX2, with other markers, can identify hair placodes in rats.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

The new antibody, TYHF-1, specifically targets certain hair-related structures.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

The LTF gene may help predict and manage nonspecific orbital inflammation.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

Human hair follicles have their own thyroid hormone system.

A specific gene mutation causes congenital hair loss.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

The HR protein helps hair grow by blocking a hair growth inhibitor, aiding in hair follicle regeneration.

TRASER effectively targets blood vessels and hair follicles for potential use in vascular and hair removal treatments.

Activating TRPMLs helps human cells important for hair growth and increases hair growth in mice.

PTHrP regulates various normal body functions, including bone development, skin, and muscle function.

CARASIL can cause different symptoms even with the same genetic mutation.

A specific gene mutation causes different hair defects in Indian monilethrix families.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

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

TLR2 is important for hair growth and can be targeted to treat hair loss.