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

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

ZDHHC17 methylation may help treat or identify facial skin aging.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

TCDD disrupts skin stem cells, causing skin issues like chloracne.

The enzyme 17β-HSD type 2 mainly performs oxidation in human sebaceous glands, which may help protect against acne.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

The compound was successfully made and shows potential for treating prostate cancer.

Mutations in specific genes cause different types of ectodermal dysplasias.

A specific enzyme that activates the hair growth medication minoxidil when applied to the skin was identified.

A new gene mutation causes a rare type of hair loss.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Finasteride effectively inhibits the enzyme steroid 5 alpha-reductase II.

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

Consider rare forms of CAH for accurate diagnosis and treatment.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Measuring 17-hydroxyprogesterone in hair can help monitor androgen levels in people with congenital adrenal hyperplasia.

Colorectal cancer's ability to spread is due to changes in many genes, not just one.

Genetic variations may affect how well finasteride works for BPH patients.

Plerixafor may help treat pigmentation disorders by promoting skin repigmentation.

Certain gene variations may increase the risk of hair loss in Egyptians.

Longer CAG repeats in gene linked to more severe hair loss in females.