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Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

Estrogens and androgens are crucial for male fertility.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

CTCF protein is essential for skin and hair follicle development in mice.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

The research helps improve wool quality and aids human hair research.

Controlling transposable elements is crucial for successful tissue regeneration.

Two new gene mutations cause a rare hair disorder.

TEDAR is crucial for skin cell differentiation and barrier formation.

A specific RNA modification in cashmere goats helps activate hair growth-related stem cells.

Runx1 helps control the KAP5 gene in human hair follicles.

The protein AtRXR3 limits root hair growth in Arabidopsis, affecting phosphorus uptake.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

FGF13 gene changes cause excessive hair growth in a rare condition.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Certain long non-coding RNAs are important for controlling hair growth cycles in sheep.

Msx2 deficiency in mice leads to bone growth and organ development problems.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Double stranded RNA helps skin wounds heal by coordinating specific proteins and signaling pathways.

SOX9 is crucial for cell development and repair but can cause fibrosis and cancer if misregulated.

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

A circular RNA helps cashmere goat hair cells become hair follicles by blocking a molecule to boost a gene important for hair growth.

A new mouse mutation causes skin and hair defects due to a gene change.

New biomarkers and potential treatments for skin diseases were identified.

DNA methylation controls lncRNA2919, which negatively affects hair growth.

lncRNAs influence cashmere fiber traits like diameter and color in goats.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.