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TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

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

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

PTCH gene mutations contribute to basal cell carcinoma development.

TBX3 gene affects pigmentation and marking formation in Dun Mongolian horses.

Krox20 (Egr2) is important for the function of epithelial stem cells.

cDermo-1 causes dense skin, feathers, and scales in chickens.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

Isoxazole 9 (ISX9) may help regrow hair by activating certain cell signals.

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

MEX3A is crucial for maintaining intestinal stem cells in mice.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Human basal cell carcinomas and squamous cell carcinomas have unique gene expression patterns not fully mirrored in mouse models.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Foxp1 helps control hair stem cell growth and response to stress during hair growth cycles.

Too much keratin 16 in mice skin causes abnormal skin thickening and structure.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

TET enzymes are important for skin and hair development by controlling gene activity in specific areas.

PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

A specific genetic deletion in goats affects cashmere yield and thickness.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Phospholipase C-δ1 is crucial for normal hair development.

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

HSPC016 gene is important for hair growth.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Type XIX Collagen is present in specific skin and hair cells during development.