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Glypicans help hair follicle stem cells differentiate by interacting with specific receptors, influencing hair growth.

SHPro® improved urinary symptoms and erectile function in men and is safe.

CT-707 is effective and safe for treating certain Chinese lung cancer patients.

ATR04-484 ointment shows promise for treating skin issues from cancer therapies.

Standardizing PRP therapy practices and regulations in Europe is crucial for safe and effective treatment.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

BI 2536 had limited effectiveness against several advanced cancers and caused significant side effects.

The research cloned keratin 7 genes from humans, mice, and marsupials, found similarities between human and mouse genes, and discovered new areas of K7 expression in mice.

K6hf is found in specific parts of hair follicles, nails, and tongue, and is linked to hair growth and structure.

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A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Fzd2 is important for skin and hair development through various signaling ways.

A reliable method was developed to measure dutasteride in tablets accurately and consistently.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

A single medium, PRIME AIRLIFT, supports better human hair follicle formation in grafts.

Ixekizumab is effective and safe for patients who did not improve with etanercept treatment for psoriasis.

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PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

The guidelines ensure accurate genetic testing and reporting for 21-hydroxylase deficiency.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

PEVIII is a promising treatment for Pseudomonas aeruginosa keratitis.