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The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

New genetic mutations causing hair loss were found in a Chinese family.

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

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

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

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Cancer-associated fibroblasts promote tumor growth in skin cancer.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

CCCA affects Black men too, with a genetic link found in the PADI3 gene.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Ceramide Synthase 4 is crucial for maintaining hair follicle stem cells and preventing hair loss.

Certain compounds, especially those with a propionic substituent, could potentially be new treatments for hair loss and similar disorders.

LPA 4 helps control blood and lymph vessel development in zebrafish.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

The LMNA mutation affects skin structure even in asymptomatic carriers.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Severe CCCA may be biologically and clinically different from milder forms.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

Mutations in the DSG4 gene cause specific hair and scalp issues.

4-aminopyridine speeds up and improves skin wound healing.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Two new gene mutations cause a rare hair disorder.

Fatp4 is crucial for healthy skin development and function.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

Blocking the CXCL12–CXCR4 axis may help treat hair loss in alopecia.