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A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

A gene called Taqpep affects cat coat patterns like stripes and blotches.

Overexpressing the glucocorticoid receptor in mice leads to abnormal skin development and reduced inflammation.

Nestin-expressing blood vessels help skin transplants survive and heal.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Ichthyosis serpentina may be a variant linked to bamboo hair, with a possible genetic component.

Researchers successfully grew horse skin cells that produce pigment from hair follicle samples.

The TT genotype of a specific SNP in sheep is linked to better wool quality.

Controlling transposable elements is crucial for successful tissue regeneration.

Fluphenazine and iloprost can induce hair growth.

Sporadic trichoblastic neoplasms generally don't recur or spread, with one case showing a specific genetic fusion.

A Japanese bone marrow transplant patient developed a rare skin cancer possibly linked to long-term use of the medication voriconazole.

LGR6+ stem cells may improve bone healing.

Only skin melanocytes, not other types, can color hair in mice.

Hedgehog signaling can create new hair follicles in adult skin but may increase cancer risk.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

Moles may stop growing due to cell cooperation, not just because of individual cell aging.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Inactivating both p53 and Rb genes in mice speeds up aggressive skin cancer development.

Over half of the dog skin disorders discussed have known gene variants, enabling genetic testing for diagnosis and responsible breeding.

A Holstein calf in Iran with a severe genetic skin disorder was euthanized due to incurable symptoms.

miR-5110 affects alpaca pigmentation by altering specific gene expressions.

Copper supplements during pregnancy improve survival and development in mutant mice.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.