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

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

Researchers found 15 new genetic links to skin traits in Japanese women.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

RSPO1 could help create new diabetes treatments by increasing pancreatic β cells.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

A new genetic variant of Woodhouse-Sakati syndrome was found in two adult sisters in Russia.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

NCBP3, SDHA, and PTPRA are the best genes for normalizing goat skin experiments.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

Certain gene variations are linked to the thickness of cashmere goat hair.

Genes linked to wool fineness in sheep have been identified.

A specific gene variant may increase the risk of developing Alopecia Areata.

Certain genetic variations in the FST gene are linked to better wool quality in Chinese Merino sheep.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

A rare gene variant causes hair and nail issues in a family.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

A gene mutation causes woolly hair in a Syrian patient.

OR2AT4 helps reduce aging and cell damage in human skin cells.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

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 specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.