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A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A specific RNA helps increase the growth of skin cells in Liaoning cashmere goats by working with a protein to boost a growth-related gene.

A 7-year-old girl was diagnosed with Netherton's Syndrome, shown by skin and hair symptoms.

The Foxn1(-/-) phenotype disrupts hair growth and affects skin stem cells.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

Mice with the naked gene have missing or abnormal hair cells.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Significant progress was made in understanding PXE, but effective treatments are still needed.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

CaM7 and CNGC14 interaction controls root hair growth in Arabidopsis.

The serum improves facial skin quality safely and effectively.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

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

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

FOXN1 duplication can cause excessive hair growth.

The LEF-1 gene in cashmere goats was successfully cloned and analyzed, showing potential for improving cashmere production.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

Certain gene variations increase the risk of alopecia areata in Koreans.

CD271 is crucial for maintaining healthy skin and preventing inflammation.

The naked mutation in mice causes hair loss and helps identify keratin genes.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

The study found key long non-coding RNAs involved in yak hair growth cycles.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

Netherton syndrome has two subtypes with shared immune traits but different allergic and immune responses, suggesting targeted treatments.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.