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

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A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

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Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

The -866G/A polymorphism in the UCP2 gene is not linked to polycystic ovary syndrome.

9-cis-retinoic acid showed some effectiveness in treating AIDS-related Kaposi sarcoma but had significant side effects at higher doses.

Large language models can accurately identify monkeypox from medical records.

A specific gene change in APCDD1 increases the risk of hair loss.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

A single recessive gene causes sparse hair in certain Japanese White rabbits.

Certain genes may influence hair loss differently in men and women.

The visfatin GT genotype may increase the risk of Alopecia Areata.

GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

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The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

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Finasteride 1mg linked to diverse symptoms; other treatments improve erectile function in rats.

Wnt10b promotes hair growth, while SFRP2 inhibits it in Wanxi Angora rabbits.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

Noncoding RNAs help determine cashmere quality in goats.

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