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5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Loss of OGG1 increases skin inflammation and auto-antibodies in lupus.

A gene called HDAC9 might be a new factor in male-pattern baldness.

The G(S) alpha subunit gene may help start hair follicle growth in newborn mice.

The androgen receptor gene doesn't help identify women likely to have female pattern hair loss.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Two gene areas linked to male pattern baldness found, more research needed.

The patient's hair had unique damage and a lower sulfur-to-nitrogen ratio compared to relatives, but not compared to healthy controls.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

JAK inhibitors do not increase cancer risk in severe alopecia areata compared to traditional treatments.

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

Researchers found two new genetic variants linked to Alzheimer's disease.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

No significant link was found between the studied genes and female hair loss in the Polish population.

A mutation in the KRTHB5 gene causes hair and nail issues.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Specific mutations in a receptor cause facial abnormalities and hair loss.

The protein Gnαs is found more in black mice than white mice and may influence their coat color.

A new method helps diagnose alopecia areata using specific gene markers and could guide targeted treatments.

High amphiregulin in the skin is a bad sign for acute graft-versus-host disease.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Targeting the TNFRSF1B gene may help treat hair loss.