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The DNA of ancient Koreans from the Three Kingdoms period shows a mix of northern Chinese and Japanese-Jomon ancestry, revealing two distinct genetic groups.

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

Forensic DNA phenotyping is becoming useful for predicting physical traits in criminal investigations but is limited by ethical concerns and incomplete genetic understanding.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

A genetic variant linked to hair thinning in Japanese women was found.

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

KAP8.1 protein is crucial for hair structure and interacts with keratin 85.

The research found that people's hair proteins vary by individual and body part, with some differences between ethnic groups, which could help in forensics.

SASH1 gene mutations are linked to various inherited skin pigmentation disorders.

Four genes affect hair follicle density in goats.

Genetic studies on hair traits can improve understanding of health and disease.

K6hf is a unique protein found only in a specific layer of hair follicles.

The boy's hair and skin color differences are due to a pigmentation disorder.

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

Monilethrix is a genetic hair disorder affecting hair shape, seen in two brothers.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Hairless mammals evolved quickly in both gene and non-gene areas related to skin and hair.

Common baldness is likely inherited through multiple genes, not just one.

Both HLA-B and MICA are independently linked to alopecia areata.

Male pattern hair loss may have evolved to promote younger fathers for offspring health and survival, encouraging monogamy and paternal nurturing.

The study found 65 intermediate filament genes, including new keratins, and suggested updating keratin naming.

Enzyme typing can reliably characterize human hair.

FOXN1 duplication can cause excessive hair growth.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

BioPlex-11 improves DNA profiling from telogen hair roots in forensic work.

Acute leukemias with the Philadelphia chromosome may be biphenotypic, and identifying this is important for proper treatment.