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Uterine leiomyomas don't significantly change gene expression in the scalp of people with Central Centrifugal Cicatricial Alopecia.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

A litter of cats had a hair condition similar to a mouse mutation, leading to hair loss and abnormal hair and skin.

Alkaline phosphatase activity in Beagle dog hair follicles is weakest in anagen and strongest in telogen.

ILC1-like cells can independently cause alopecia areata.

Rare genetic variants in 125 genes are linked to male-pattern hair loss.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

Decreased CD200 in hair follicles may cause immune issues in some alopecia areata cases.

Chemotherapy-induced hair loss is partly due to decreased laminin-511 and increased laminin-332.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

A KRT32 gene variant causes loose anagen hair syndrome.

The LEF-1 binding site enhances gene expression in hair follicles, with other proteins aiding specific regulation.

Hairless gene not strongly linked to baldness.

Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

Targeting IL-15 may help treat Alopecia Areata.

In alopecia areata, certain immune cells increase and express a protein linked to immune activation.

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

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

Mutations in the AR gene cause hair thinning and loss.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

Björnstad syndrome can cause hair loss similar to androgenetic alopecia, and treatment with baricitinib and minoxidil may help.

CARASIL can cause different symptoms even with the same genetic mutation.

Hedgehog signaling is crucial for hair development, cadherins affect cell adhesion, neutrophils play a role in skin lesions, and BP230 autoantibodies impact skin stability.

Colorectal cancer's ability to spread is due to changes in many genes, not just one.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

Nilotinib can cause keratosis pilaris, a skin condition.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

The document suggests a rare skin condition might be caused by a genetic phenomenon.