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Human head hair proteins can be typed into eight distinct patterns, useful for genetic and forensic investigations.

A new method quickly detects alcohol use from hair in under an hour.

Bhringaraj plant may help in wastewater treatment and improving drinking water quality.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

A patient with Rhupus was diagnosed with Rowell syndrome and treated with various medications.

The hairless protein is important for skin, hair, and may influence cancer development.

Sry may regulate fatty acid metabolism and shows different expression levels in rat tissues.

Two new gene clusters important for hair formation were found on human chromosome 11.

Mammoth hair from different ages shows distinct surface textures and elemental compositions.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

S-Methylmethionine sulfonium can protect skin from UVB damage.

Red light increases hair follicles and ATP in mouse skin.

HFMs can help study hair growth and test potential hair growth drugs.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

The hair keratin variant is mostly found in Caucasians.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

Age-related hair curvature increases due to internal structural changes from grooming.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Hair properties change under electromagnetic fields and are influenced by individual characteristics and the environment.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Two genetic variations in Moa buffalo help them adapt to heat.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

A new method accurately measures long-term steroid levels in human hair.

The study found genetic diversity in coat color dilution among Czech pointers in Slovakia.

POUF51 and HES3 are key in controlling stem cell numbers in psoriasis.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Human hair medulla doesn't break down hydrogen peroxide, which may affect hair color formation.

THCCOOH levels in hair decrease from root to tip and don't match well with self-reported cannabis use.