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

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The study suggests that changes in immune system receptors and their interaction with a cell component may be important in the development of a type of hair loss condition.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Mutations in the Sgk3 gene cause fuzzy hair in mice.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

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

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Lichen planopilaris may have a genetic link.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

RACB in barley is crucial for cell polarity and nucleus positioning, aiding fungal infection.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

Differences in androgen receptor expression and tissue properties may lead to higher cryptorchidism risk in certain rats.

Frontal fibrosing alopecia may be linked to genital Lichen sclerosus through an autoimmune process.

Lef1 helps stem cells become hair cells by interacting with specific signaling pathways.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

GLPLS and LPP are variants of lichen planus.

Lichen Planus in siblings may be influenced by genetics and environment.

A mutant FERONIA gene affects root hair growth at high temperatures.

Basonuclin may help control ribosomal RNA gene activity in skin cells.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.