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Glioblastoma cells can make androgens, which might help the tumor grow.

Targeting glycolysis may help treat PCOS by improving insulin sensitivity and ovarian function.

Puerariae Lobatae Radix can reduce sebaceous gland size and secretion, potentially treating related skin conditions.

The conclusion is that analyzing RNA from skin oils is a promising way to understand skin diseases.

Ursolic acid from Ochrosia elliptica leaves may help manage PCOS symptoms.

Genetic factors, skin barrier, immune function, and obesity influence risk of fungal skin infections.

Lack of certain cells causes abnormal nipple development and nursing failure.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

African American women have a higher risk of preterm delivery than Caucasian women, and inflammatory stimuli affect gene expression in cells related to PCOS, showing a heightened inflammatory state in women with PCOS.

Activating the Eda/Edar pathway improves wound healing by enhancing hair follicle growth.

AKR1C3 could be a treatment target for metabolic issues in PCOS.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

Certain inhibitors can potentially treat prostate cancer and other hormone-dependent conditions by controlling sex hormone levels in cells.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Accurate diagnosis and early specialist referral are crucial for managing 46,XY Disorders of Sex Development.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Human adrenals and gonads have a unique enzyme for steroid hormone production.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

This enzyme helps metabolize fatty acids and isoleucine, and could be key in treating neurological diseases and certain cancers.

Somatic BHD mutations are rare in Japanese renal tumors.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

CDH3-related disease causes worsening eye and hair issues.

Inhibitors of 11β-HSD1 show potential for treating type 2 diabetes but require more testing for safety and effectiveness.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Consider rare forms of CAH for accurate diagnosis and treatment.

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

A woman's hair loss and other symptoms were due to a rare hormone deficiency treatable with steroids.