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Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

Certain proteins are significantly increased in the skin of people with hidradenitis suppurativa.

Hexi cashmere goats' hair growth varies by stage, with Hoxc13 linked to hair activity.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

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

The Spherical Skin Model improves drug and cosmetic testing by accurately mimicking human skin for efficient compound screening.

Low-penetration genes might help personalize colorectal cancer prevention.

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

KSR1 is crucial for certain skin tumor formation and could be a cancer therapy target.

Metabolic processes and key genes like FGF5, FGFR1, and RRAS significantly affect hair follicle growth in Inner Mongolian Cashmere goats.

Pig skin cells can turn into mesodermal cells but lose their ability to become neural cells.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Genomic prediction can improve breeding strategies for Korean Sapsaree dogs.

A specific gene mutation causes a severe skin disorder in a family.

Effervescent cleansing tablets with Asiatic acid were successfully developed, showing good stability and cleansing effectiveness.

Spironolactone was effective in reducing hair growth in women with hirsutism.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

High-content screening is useful for finding new treatments for rare diseases and has led to FDA-approved drugs.

Researchers created an efficient method to extract DNA from marmoset hair, reducing blood chimerism.

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

Milia, SM, and EVHC may be related conditions, not separate ones.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

Childhood hair and scalp disorders can be managed with treatments like cortisone and corticosteroids.

A rare benign scalp tumor in an infant requires surgical removal.