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Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

The new drug delivery system improves exemestane's absorption and effectiveness.

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A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

Researchers developed new compounds that target the androgen receptor effectively with fewer side effects.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

The KAP 7 gene affects wool traits in Rambouillet sheep, with the BB genotype showing the best wool characteristics.

DVI provides detailed 3D imaging of hair and shows how various products protect and enhance hair.

DHEA is the main sex steroid in cerebrospinal fluid, and testosterone in the fluid comes from the blood.

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

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Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

A new genetic mutation was found causing hair and eye issues in a boy.

The method effectively measures drug impact on DHT levels in prostate treatments.

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

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

High DHEA and short cervical length in women with PCOS and recurrent miscarriages may harm pregnancy outcomes.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Nanoporous silica entrapped lipid-drug complexes significantly improve the solubility and absorption of drugs that don't dissolve well in water.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.