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ALRN-6924 may prevent hair loss caused by chemotherapy.

The technique effectively shows how human skin and hair cells form into ball-like structures.

Boosting HGF signaling could improve the creation of hair follicles in lab-made skin.

The gene HDC is important for the development of hair follicles in newborn mice.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

DNA methylation controls lncRNA2919, which negatively affects hair growth.

Mouse hair follicle stem cells have a flexible chromatin state that supports skin health and hair growth.

Hepatitis B vaccination can trigger HSP, and vitamin D correction and tonsillectomy can effectively manage it.

The research cloned keratin 7 genes from humans, mice, and marsupials, found similarities between human and mouse genes, and discovered new areas of K7 expression in mice.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

Hair follicle stem cells can become corneal-like cells with the help of pax6.

miR-124 helps mouse hair follicle stem cells become nerve cells by blocking Ptbp1 and Sox9.

GLPLS and LPP are variants of lichen planus.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.

Msx-2 gene removal speeds up skin wound healing in mice.

A girl had two rare hair conditions that helped understand their overlap.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

Testing basal 17-HP levels is a good way to screen for nonclassic adrenal hyperplasia in women with high androgen levels.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

The WAHRS Live Surgery Workshop and Symposium was a unique hair restoration event.

Keratin 16 delays skin maturation and affects skin and hair development in mice.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

CD98hc's role in skin health decreases with age.

BMP6 and Wnt10b control whether hair follicles are resting or growing.

High homocysteine levels in lupus may increase inflammation and cardiovascular risk.