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A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Human placenta hydrogel helps restore cells needed for hair growth.

Human hair follicle cells can be turned into stem cells similar to embryonic stem cells.

FGF signaling is crucial for starting feather development in chicken embryos.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

Seven genes are highly expressed in both germ-line and hematopoietic stem cells.

Trichohyalin is a versatile protein involved in hair and skin structure.

Histone H4, released by cells exposed to colchicine, can cause hair loss by inhibiting cell growth and enzyme activity.

Two new gene mutations cause a rare hair disorder.

PTHrP regulates various normal body functions, including bone development, skin, and muscle function.

LEF-1 boosts cell growth in goat hair follicles, aiding cashmere production.

Mutations in the Whn gene affect hair keratin gene expression differently.

PLIN2 affects hair growth in cashmere goats, potentially improving cashmere quality.

Blimp1 is crucial for hair follicle growth and skin health.

The assay effectively identifies compounds that affect immune cell activation.

Hoxc13 is essential for hair growth and follicle development.

Newly designed proteins can effectively degrade specific proteins in cells, offering a promising alternative for targeted protein degradation.

Hepatitis B virus alters steroid hormones in male mice, reducing dihydrotestosterone to inhibit viral replication.

Mice without certain skin proteins had abnormal skin and hair development.

Higher PHGDH levels cause unusual melanin buildup in hair follicles.

Pegylated interferon-alpha 2a can cause a rare nerve disorder, but early treatment can lead to full recovery.

Rat hair-follicle stem cells can become heart cells with specific supplements.

HAP stem cells can repair nerves and spinal cords by becoming Schwann cells.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

CD8+ T cells play a key role in graft-versus-host disease in certain mice models.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.