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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The 4C32 gene may help in mouse skin development and differentiation.

SV40 T antigen in hair follicles causes abnormal hair and health issues in mice.

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

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

Targeting the p63 gene could help treat skin diseases.

Researchers found a gene mutation responsible for a rare hair loss condition.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

A virus protein can activate a pathway that may lead to abnormal hair follicle development.

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.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Iron deficiency causes hair loss by affecting hair differentiation and cycling.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Inactive hair follicle stem cells help prevent skin cancer.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

CCT128930 is a promising new drug that effectively targets and inhibits a cancer-related protein, showing potential for cancer treatment.

Naked-mouse hair lacks certain proteins and has less soluble fibril.

Early diagnosis of pseudopelade of Brocq in men is crucial to prevent permanent hair loss.

Mutations in hKAP1 genes may cause hereditary hair disorders.

K10 may not prevent tumors as previously thought and might increase benign tumor risk.

Aire mutation reduces alopecia areata, while Notch4 mutation prevents it in mice.

PCAT1 helps hair growth by controlling miR-329/Wnt10b.