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A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Disrupted stem cell signals in hairpoor mice cause hair loss.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

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

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

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

A young patient with unusual insulin resistance and high testosterone levels had a rare INSR gene mutation.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

New genetic mutations causing hair loss were found in a Chinese family.

The Naked gene in mice causes abnormal sebaceous glands and disrupts hair follicle organization.

Mutations in the CYP21A2 gene are not a major factor in causing PCOS.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

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

LDE225 is a promising skin-applied treatment for basal cell carcinoma with good skin penetration and effectiveness.

A gene mutation in mice causes permanent hair loss and skin issues.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

The Naked (N) trait in mice is linked to lower glycine and tyrosine in hair proteins.

Topical minoxidil helped an 8-year-old boy with a genetic hair disorder grow hair.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.