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Thyroid and reproductive hormones, BMI, and excess hair are linked in Iraqi women with PCOS.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Human skin cell byproducts can potentially be used to treat hair loss and promote hair growth.

Tenofovir is more effective than adefovir for resistant hepatitis B, Fibroscan is good for assessing liver damage, regulatory T cells may help hepatitis C persist, and other insights into liver health and disease were found.

An 87-year-old man showed unusual signs of Hodgkin lymphoma, primarily high calcium levels, which improved after treatment and revealed the disease.

An unusual growth of Leydig cells in a woman's ovaries caused her excessive hair growth, which was treated successfully with surgery.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

CD73 may regulate hair growth and could be targeted for hair growth treatments.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

Dlx3 is essential for hair growth and regeneration.

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

New method, hair distribution width (HDW), improves accuracy in diagnosing androgenetic alopecia (AGA).

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

SHBG binding properties are unchanged in male liver cirrhosis patients.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

Idiopathic hirsutism might not be truly idiopathic but could be an early stage of hyperandrogenic disorders.

The Hair Diameter Index (HDI) was created to help plan hair restoration surgery after finding that visual hair density is linked to hair count and thickness, not volume.

Four transcription factors can convert mouse cells into hair cell-like cells, aiding hearing loss research and treatment.

Hoxd gene regulation in mammals and birds is robust despite differences in DNA sequences, due to 3D chromatin structures.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

Type I and Type II keratin chains can form heterodimers despite sequence differences.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

A human serum-enriched medium effectively supports melanocyte growth and activity without using animal-derived supplements.

Hyperbranched polymer dots significantly boost hair regrowth better than minoxidil.

Glucocorticoids and thyroid hormones together are essential for fetal fat development.

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Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.