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Woolly hair is a rare genetic condition with no effective treatments.

The method quickly analyzes hair growth genes and shows that blocking Smo in skin cells stops hair growth.

Fetal hair follicles have melanocytes with melanosomes at different stages, which are broken down into pigment particles in keratinocytes.

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

Hand-foot-mouth disease may cause nail loss in children.

The girl likely has Loose anagen hair syndrome, which may improve on its own or with minoxidil.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

A young boy's uncombable hair is due to a rare genetic condition that usually improves over time.

Biotin improved hair appearance in uncombable hair syndrome but didn't change hair structure.

The upper dermal sheath can regenerate hair in rats.

Prenatal retinoic acid exposure increased cell proliferation in mouse hair follicles without affecting their development.

Scientists created hair-growing skin models from stem cells, which could help treat hair loss and skin diseases.

Reduced EGFR signaling delays hair cycle and reduces fat growth, but hair development remains normal.

Different body areas in mice produce different hair types due to interactions between skin layers.

Newborn skin is uniquely prepared to adapt to new environments compared to adult skin.

Polarized microscopy helps identify hair irregularities in genetic disorders.

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

Wound-induced hair growth may help study regeneration and aging, but it's unclear if this ability decreases with age.

Two mouse mutants have defective hair cuticle cross-linking.

Mouse models help study genetic skin diseases.

The 3D skin model is better for hair growth research and testing treatments.

A young Caucasian girl had both woolly hair and alopecia areata, which is rare.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

Disrupted stem cell signals in hairpoor mice cause hair loss.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Hairless HRS/J mice resist Bacillus anthracis skin infections due to high numbers of immune cells, not because they lack hair follicles.

The boy likely has a fungal infection causing hair loss.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.