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Prostaglandin E2 helps prevent hair loss from radiotherapy by protecting hair growth cells and aiding self-repair.

Collagen XVIII is crucial for maintaining tissue structure and function in the brain, kidneys, and hair.

We know less about human hair pigmentation than mouse coat color, but pH and cysteine levels are key factors.

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

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

The HCR gene contributes to psoriasis risk.

The assay effectively detects hormonal activity of certain chemicals.

Thallium is highly toxic, causing severe health issues, and Prussian blue is the best antidote.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Aspergillus niger culture creates two finasteride derivatives with enzyme-inhibiting effects.

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

The availability of certain hormones and specific stimulation patterns affect long-term synaptic changes in the male rat brain.

Introducing the OTC gene improved symptoms in mice with OTC deficiency.

The study created a new method to test drugs that affect hormone processing in skin.

The peptide GPIGS helps hair cells grow and speeds up hair regrowth in mice.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

Certain gene variations are found in people with polycystic ovary syndrome.

Reduced neurosteroids and growth issues can harm fetal brain development, especially in males.

New mutations in the DSG4 gene cause a rare hair condition.

Finasteride may treat baldness but less effective for those with 5α-reductase deficiency.

SGK3 is essential for proper hair growth and health.

Monilethrix is linked to a gene cluster on chromosome 12.

Low ERCC3 gene activity is linked to non-pigmented hair growth.

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

No significant link was found between the studied genes and female hair loss in the Polish population.

Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

Phloroglucinol may help improve hair loss by promoting hair growth and reducing oxidative stress.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.