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A quick method was developed to detect banned substances in urine for doping control.

The research found specific genes that are more active in balding cells, which could be causing hair loss.

The research updated the skin cell profile, finding new skin cell markers and showing fibroblasts' key role in skin health.

The Indus River dolphin has low genetic diversity due to a past bottleneck and human impact.

The protocol allows easy imaging of dividing cells in C. elegans and can be used for other organisms.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

A new method effectively measures nicotine and cotinine in blood and urine for forensic analysis.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Dupilumab helped improve skin and prevent new lesions in a child with a rare immune disorder and severe eczema.

MCHR2 gene duplications may be linked to alopecia areata.

A specific genetic deletion in goats affects cashmere yield and thickness.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

Adding a second method to PROTACs could improve cancer treatment.

Multiphoton microscopy can effectively assess breast cancer treatment responses without labels.

The technology can create transgenic cashmere goats with improved wool quality.

A nonviral method was developed to label and culture human hair follicle stem cells.

A deep learning model was developed to help diagnose trichothiodystrophy by analyzing hair patterns.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Uncombable hair is inherited dominantly with complete penetrance.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

Dysplastic nevi have unique gene expressions, making them distinct from common melanocytic nevi.