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FERONIA regulates plant growth, pollen interactions, and sugar signaling.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

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

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Blocking the Mitochondrial Pyruvate Carrier causes stress in hair follicles, which can be reduced by an ISR inhibitor.

The PP2A-B55α protein is essential for brain and skin development in embryos.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

SFRP2 and PTGDS may be key factors in female hair loss.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Nuclear Factor I-C is important for controlling hair growth by affecting the TGF-β1 pathway.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

FLRG and follistatin have different roles in wound healing.

LncRNA018392 helps goat skin cells grow by increasing CSF1R.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

The type 3 IP3 receptor is important for controlling hair loss and growth.

A new genetic variant in the EEF2K gene may contribute to polycystic ovary syndrome.

A new gene mutation causes insulin resistance in a girl and her mother.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

The TT genotype of a specific SNP in sheep is linked to better wool quality.