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Whole hair strands can reliably measure gamma ray exposure using ESR techniques, but samples should be analyzed quickly or stored in liquid nitrogen.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

Csdc2 helps hair growth in cashmere goats by regulating specific genes.

Certain gene variations are found in people with polycystic ovary syndrome.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

VEGFR-2 is active in hair follicles, sebaceous glands, sweat glands, and skin on the human scalp.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

A specific mutation known for causing cancer is also found to cause a skin condition in a young girl.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Certain immune system genes are linked to a higher risk of psoriasis and psoriatic arthritis, while others may offer protection.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

SLC24A5 shows a clear selective sweep, but no link to UV radiation intensity.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

The protein ER71/ETV2 helps regrow hair after chemotherapy by improving the growth of new blood vessels.

A gene mutation causes curly hair and hair loss in rats.

EDA and EDAR are important for hair follicle development in cashmere goats and affect other related genes.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

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

Removing UBE2N from skin cells causes inflammation and immune response, which can be lessened with specific inhibitors.

A specific genetic mutation may increase male pattern baldness risk, especially in Europeans.

SQSTM1 is linked to increased risk of alopecia areata.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.