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Hair transplant surgery effectively treated a specific type of hair loss and is recommended as a primary treatment option.

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

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Defective nuclear transport may cause gene expression changes in Progeria.

Acinetobacter strain A1-4-2 can safely clean water pollutants.

Researchers created a new mouse model for studying scleroderma.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

The CTLA-4 gene change studied does not affect Polycystic Ovarian Syndrome in the women tested.

Tavaborole is a safe and effective toenail fungus treatment, with the 5% solution being the best option.

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

Certain genes contribute to stronger hooves in barefoot racing horses.

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

Vitamin D receptor gene variations are not linked to alopecia areata.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

A new gene causes hairlessness and skin cysts in rats.

The model improves understanding of androgen interactions by focusing on signal intensity and system capacity.

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

KRT72 gene helps form hair.

Tofacitinib is effective and safe for treating severe alopecia areata and related conditions.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

The PP2A-B55α protein is essential for brain and skin development in embryos.

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