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SR-ECDi helps better understand and map the chiroptical properties of solid chiral materials.

The new X-ray technique allows for precise and non-destructive measurement of elements in hair, creating the first database of its kind for a specific ethnic group.

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

Human hair has different protein structures in its cuticle and cortex.

Scientists created a detailed map of gene activity in different parts of human hair follicles.

Most people have similar hair protein patterns, but a rare variant was found in two women.

A new gene mutation is linked to monilethrix in the studied family.

The B2 genes are crucial for hair growth in rats.

The research found that the properties of solid-state Electronic Circular Dichroism (ss-ECD) are influenced by the orientation of local crystals, which could help in examining and mapping chiral materials like pharmaceutical ingredients.

The SHJH hr mice with a mutated Hr gene show signs of faster skin aging due to poor antioxidative protection.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

Elemental composition of hair affects its x-ray diffraction patterns.

Both HPSAM and PLS methods accurately measure minoxidil and tretinoin concentrations.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

A new method helps find proteins in hair to identify fetal growth issues.

Neurospectrum effectively analyzes neural signals to predict and identify brain activity patterns better than traditional methods.

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

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

A genetic hair protein variant is more common in Japanese people and is inherited.

The system helps monitor hair properties using RGB video microscopy.

A new method improves protein analysis in hair, aiding health and disease research.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

The study improved understanding of keratin fiber structure by showing consistent microfibril diameter but varying distances and electron density profiles.