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Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

Certain gene variations in Jiangnan cashmere goats are linked to important traits like birth weight and fiber quality, useful for breeding.

ELIP-based CRISPR delivery improves heart disease gene editing but needs more testing.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Mutations in specific genes cause certain congenital defects in dogs, aiding in understanding similar human diseases.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

Researchers identified a new variant of the FGF5 gene in sheep that affects hair length.

Specific genes influence hair and cashmere growth in Laiwu black goats.

A rabbit gene important for hair development was identified and detailed.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Researchers created a new mouse model for studying scleroderma.

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

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

A specific gene variation in goats is linked to better growth traits.

Certain genetic markers on the Y-chromosome may influence prostate cancer risk in Iraqi males.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

The study mapped genetic variations in sheep, linking them to traits like milk production and growth.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Females are more prone to lupus and arthritis due to X chromosome factors.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

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The MTR gene affects wool quality and production in Chinese Merino sheep.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Researchers found a new mutation causing total hair loss from birth.