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A young woman's symptoms suggested PCOS, but tests and surgery confirmed and treated a rare ovarian tumor, resolving her condition.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

Akt2 protein is essential for normal cell division in early mouse embryos.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

The conclusion is that accurately identifying folliculosebaceous tumors requires understanding their clinical signs and microscopic features.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A man with multiple autoimmune diseases developed liver injury from azathioprine, but his liver improved after stopping the drug.

Two mouse mutations cause similar hair loss despite different skin changes.

Overexpression of R-spondin 3 leads to sparse hair and impaired hair regeneration.

SOX9 helps determine stem cell roles by interacting with DNA and proteins that control gene activity.

Dermal EZH2 controls skin cell development and hair growth in mice.

Women with hair loss have more androgen receptors in certain hair follicles.

Mice genetically modified to produce more Del1 protein had faster hair regrowth.

Lower zinc levels may predict less effective hair loss treatment.

Narrowband UVB treatment increases certain gene expressions in psoriasis skin and improves symptoms.

Women with nonclassic 21-hydroxylase deficiency can have successful pregnancies through IVF, with certain factors affecting their chances.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

Besnoitiosis, a parasitic disease, has been found in donkeys in Italy and may be more common in Europe than previously thought.

OsUEV1B protein is essential for controlling phosphate levels in rice.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

Men with less sun-sensitive skin have lower PSA levels, while men with more sun-sensitive skin have higher PSA levels.

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

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

Genetic differences within ethnic groups may affect prostate cancer treatment effectiveness.

The HIF-2α/ARNT complex is important for hair follicle development by controlling cell growth.