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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.

The Itpr3 gene causes a specific hair pattern in mice.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

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

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

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

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

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

TTD patients don't have a higher skin cancer risk because their main issue is with transcription, not DNA repair.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

CTHRC1 is essential for healing and preventing heart rupture after a heart attack.

Trps1 is essential for proper hair follicle development.

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.

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

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

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

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

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

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

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

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

A mutation in the KRTHB5 gene causes hair and nail issues.

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

Thyrotropin-releasing hormone may help control skin and hair growth and could aid in treating related disorders.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

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

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

The HCR gene contributes to psoriasis risk.