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3D ultrasound can detect hair follicle changes and disease phases in alopecia areata.

Hex gene plays a crucial role in starting feather development in chick embryos.

New method, hair distribution width (HDW), improves accuracy in diagnosing androgenetic alopecia (AGA).

The method effectively analyzes human hair proteins, especially nonfilamentous ones.

Scientists found a gene in mice that causes early hearing loss.

HIF-1α in fibroblasts boosts hair growth and health.

The hairline-lowering surgery was effective, safe, and left patients satisfied with few complications.

High-frequency ultrasound can effectively visualize and assess hair loss.

Mutations in the hairless protein gene cause hair loss.

Women with excessive body hair often have higher male hormones and related health issues.

The SHJH hr mice with a mutated Hr gene show signs of faster skin aging due to poor antioxidative protection.

Human hair follicles have their own thyroid hormone system.

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

Low estrogen and high testosterone may cause excessive hair growth in women.

Ovarian hyperthecosis can cause high testosterone and symptoms like hair loss, and surgery can help improve these symptoms.

Hair mass index is a precise way to measure hair loss in chemotherapy patients.

A low-glycemic diet improved hormone levels and well-being in overweight women with high androgen levels.

Ear creases might indicate heart disease risk, needing more research.

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

Ultrasonic microneedles improve hair regrowth treatment effectiveness without side effects.

Higher homocysteine levels may predict hair loss severity.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

Higher androgen levels are linked to more severe hair growth in hirsute women.

Iron deficiency causes hair loss by affecting hair differentiation and cycling.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Trichohyalin is modified by enzymes to form strong structures in hair cells.