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Blue-light activation of TrkA improves hair-follicle stem cells' ability to become neurons and glial cells.

A boy's hair turned red because of genetic mutations, not lack of zinc.

Old drugs are often used for new, different medical purposes in endocrine pharmacology.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Newly designed proteins can effectively degrade specific proteins in cells, offering a potential new therapy method.

GmMAX3b gene in soybeans boosts nodulation and affects hormone levels.

The document confirms the structures of major metabolites of the CRTh2 antagonist Setipiprant and identifies minor metabolites.

FOXN1 duplication can cause excessive hair growth.

The hr gene is linked to hair loss in Valle del Belice sheep.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

The nature of the side chain in RU 58841 derivatives greatly affects its AR affinity, with the N-(iodopropenyl) derivative 13 showing the highest AR binding affinity, suggesting its potential for developing high-affinity radioiodinated AR radioligands.

Reducing Tyrosinase prevents mature color pigment cells from forming in mouse hair.

Five different TPO gene mutations were found in PCOS patients with thyroid hormone issues.

Metabolic disorders can cause hair structure defects and growth issues, but amino acid levels in hair remain normal.

The model helps test drugs for clubfoot fibrosis by mimicking cell environments and shows minoxidil reduces harmful collagen links.

Organoid technology is improving personalized medicine by better predicting drug responses and treatments.

Mouse touch-sensitive nerve cells adjust their connections based on competition with other similar cells.

Small molecule treatments improve the ability of human amniotic fluid stem cells to become different cell types.

Methylene blue staining effectively highlights detailed nerve structures in rat fur.

Desmoglein 3 organization in cell connections changes without calcium, affecting cell adhesion.

The mystacial pad's innervation in adult rats is more complex than previously thought.

Human hair has a new region with ordered filaments and the cuticle contains β-keratin sheets.

Hair follicles significantly enhance electroosmotic transport during iontophoresis.

Low testosterone can cause a heart rhythm problem in men, but fixing it can prevent the issue.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

Solid-state NMR can effectively study keratin structure and treatment effects in fur.

The EDA pathway plays a key role in bone development by interacting with other signaling pathways.

Runx1 is crucial for proper hair structure and development.

Human sexuality involves complex mental processes unique to humans.