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A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

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

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

Mosaic Klinefelter syndrome can affect male fertility and may be missed in routine tests.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

A new keratin gene was found in mice, explaining hair growth.

BI 2536 had limited effectiveness against several advanced cancers and caused significant side effects.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

Asiasari radix extract may be a potential treatment for melanoma because it selectively triggers cell death in melanoma cells by affecting p53 regulation.

The man has a genetic skin condition called pachyonychia congenita.

Two gene variants cause white spots in cattle.

The research identified two types of keratinocytes in chicken scales: one for hard scales and another for soft skin, with similarities to human skin differentiation.

Two rice strains showed stable high yield and Zinc content in different climates.

Researchers identified genes linked to coat color, body size, cashmere production, and high altitude adaptation in goats.

A new gene mutation is linked to monilethrix in the studied family.

Feather diversity is due to different keratin gene combinations, and chickens can help study human keratin diseases.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

Symmetrical Acrokeratoderma (SAK) may be a unique skin condition in China, lacking specific treatment and needing long-term monitoring.

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

Four new genes related to sheep wool were discovered, showing genetic diversity.

Roots adapt to uneven environments by changing growth and gene expression.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

Stem cells from elderly skin can become neurons, offering potential for brain therapy.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.