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Researchers found a new mite species causing severe hair loss and skin problems in yellow-bellied marmots.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

Knocking out the FGF5 gene in sheep increased wool production and hair-follicle density.

A girl had rickets due to a gene mutation affecting vitamin D response.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

Too much IKZF1 and Ikaros protein may cause alopecia areata.

A young woman with a rare skin cancer was diagnosed late because her symptoms were unusual for the disease.

M-CSF-stimulated myeloid cells can cause alopecia areata in mice.

Monilethrix Syndrome causes fragile, beaded hair that breaks easily and needs early diagnosis for better care.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Zinc made mice's coarse hair turn into fine hair without affecting skin structure.

Dimethylarsinic acid speeds up skin tumor growth in certain mice.

Two genes, Tabby and Ticked, determine cat coat patterns.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

The IRF2BP2 gene affects sheep fleece quality by influencing fiber traits.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Zinc supplements improved the girl's skin and hair condition.

Certain chemicals cause hair graying in black mice but not yellow mice.

Certain microRNAs are linked to various skin diseases and could be used to diagnose and treat these conditions.

5% topical minoxidil can significantly improve hair growth in children with Marie Unna hereditary hypotrichosis.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

A new protein, mK6irs, is found in specific hair layers and may help understand hair growth and diseases.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.