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A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Asiasari radix extract may be a potential treatment for melanoma because it selectively triggers cell death in melanoma cells by affecting p53 regulation.

Certain genetic variants may increase the risk of developing PCOS.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

DNA analysis can help tailor alopecia treatment.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Frontal fibrosing alopecia has occurred in two related male families.

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

Researchers cloned a gene from Xinjiang fine-wool sheep, finding it very similar to other sheep and somewhat similar to goats, humans, and rabbits.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

A KRT32 gene variant causes loose anagen hair syndrome.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.