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Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

Six key genes can predict bladder cancer outcomes and may serve as prognostic biomarkers.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

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

Changes in KRT17 gene activity linked to wool production in Angora rabbits.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

The improved genome of the African spiny mouse will help understand its tissue regeneration abilities.

Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

FOXN1 gene variants cause low T cells and immune issues from birth.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Researchers cloned a gene from Xinjiang fine-wool sheep, finding it very similar to other sheep and somewhat similar to goats, humans, and rabbits.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

Topical IKKα inhibitors may help prevent CCS tumours.

A gene mutation in mice causes permanent hair loss and skin issues.

The CORT, FGF5, and CD36 genes are crucial for the cold weather adaptation of Yanbian cattle.

CTHRC1 is essential for healing and preventing heart rupture after a heart attack.

A new DSG4 gene mutation causes hair defects in a young girl.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

BTNL proteins help control inflammatory bowel disease by maintaining specific immune cells.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

AMPK activation may reduce melanoma risk in red-haired individuals.

The TRPV3 channel structure changes linked to severe itch and hyperkeratosis were identified using cryo-EM.

Inherited color dilution in rabbits is linked to DNA methylation changes.

The study found 65 intermediate filament genes, including new keratins, and suggested updating keratin naming.