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New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Vitamin D receptor FokI gene variation is not linked to alopecia areata.

A new fluorescent material can detect dextran sulfate sodium, turning green when present, useful for forensic and environmental monitoring.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

A gene mutation in mice causes severe skin disorder similar to a human condition.

CD8A and FOXD2-AS1 may be key for diagnosing and treating alopecia areata.

Lgr5 and the vitamin D receptor are key in controlling skin inflammation and tumor risk in mice.

New genetic mutations causing hair loss were found in a Chinese family.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

MITF and WNT3A are key in Dun Mongolian horse pigmentation.

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

MARCKSL1 is important for wound healing and could be a target to reduce scarring.

A single amino acid change in the vitamin D receptor can disrupt its function and lead to hair loss.

A new method can almost perfectly distinguish adenomyosis from similar conditions using blood tests.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

CT60 polymorphism might increase the risk of Alopecia Areata.

There is no significant link between the MMP-1 rs1799750 polymorphism and androgenetic alopecia in the Indonesian population.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

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

SOX18 helps sheep hair cells grow by activating a specific cell growth pathway.