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Erythropoietin overexpression disrupts hair growth and fat formation in mice.

MOF controls skin development by regulating genes for mitochondria and cilia.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

Rushton's hyaline bodies form from hair keratin and blood substances.

Removing STAT5 from 3D-cultured human skin cells reduces their ability to grow hair.

The research concluded that hyaluronic acid affects the formation and growth of hair follicle-like structures in a lab setting.

PTCH gene mutations contribute to basal cell carcinoma development.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

The study created a new model to better understand human hair growth and health.

Reduced PER3 gene activity in hair follicles is linked to irregular sleep in schizophrenia.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

High levels of 3 alpha-diol glucuronide in the blood are a marker of increased androgen action in women with excessive hair growth of unknown cause.

The assay effectively detects hormonal activity of certain chemicals.

A special mix from certain skin cells can help hair grow by making hair root cells grow faster and activating growth signals.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

A unique gene mutation was found in a family with monilethrix.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

HPV8 E6 gene causes growth of certain skin stem cells.

Hox genes control hair growth patterns in mammals by regulating stem cell activity in the skin.

COL17A1 is crucial for preventing hair graying and loss by supporting hair and pigment stem cells.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Researchers developed a method to create artificial hair follicles that may help with hair loss treatment and research.

Human hair protein patterns are inherited genetically.

Suppressing ODC activity reduces tumor growth in hair follicles.

Mouse skin has special cells in the epidermis that decrease with age and are linked to keratinocyte stem cells.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

E6/E7 oncogenes in hair follicles cause continuous hair growth by skipping the resting phase.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.