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Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

The plant pathogen in Australia evolves through existing genetic variation, not new genotypes.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

Some prostate cancers have gene changes that may affect treatment with certain drugs.

Dynamet Technology won an award for its advanced titanium technology.

A genetic marker linked to a type of hair loss was found in most patients studied.

Mutations at Val-889 and Arg-752 disrupt key interactions in androgen receptor dimerization.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

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

High levels of TNF-α may contribute to obesity and insulin resistance in PCOS, but not due to the C850T genetic variation.

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

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

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

Certain gene combinations improve cashmere quality and production in Liaoning goats.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

A new, efficient method was developed to synthesize a specific compound and its derivatives.

Krt15+ cells in mice can resist radiation, regenerate tissue, and start tumors, suggesting new cancer treatment targets.

The KRTAP13-3 gene affects wool fibre diameter variability in Chinese Tan sheep.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

HOXC13 is essential for hair and nail development by regulating Foxn1.

A new therapy for a skin blistering condition has not been developed yet.

The CTLA-4 gene polymorphism does not affect polycystic ovarian syndrome.

Certain genes affect udder shape in Holstein cows, important for health and milk production.

Haplogroup X found in Altaian population supports Amerindian origin.

WNT10A gene mutations cause short anagen hair syndrome.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

The combination of TACE and Donafenib is effective and tolerable for treating unresectable liver cancer.