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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 defective gene causes hair loss and taste insensitivity in BTBR mice.

TRM21 helps control flavonoid production and root hair growth in Arabidopsis thaliana.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

A unique gene mutation was found in a family with monilethrix.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

A gene mutation causes monilethrix in a Chinese family.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

TRH stimulates human hair growth and extends the hair growth phase.

Trichohyalin is modified by enzymes to form strong structures in hair cells.

CTHRC1 helps hair grow back, and plantar dermis mixture boosts it.

The hr gene is linked to hair loss in Valle del Belice sheep.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Artemis phosphorylation at Ser516 may help regulate skin and hair structures.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.