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Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

Researchers found a non-functional sheep keratin gene due to mutations.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

A gene variation is linked to hair thickness in Asians.

Early genetic testing and zinc therapy are crucial for managing acrodermatitis enteropathica in infants.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

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

The study found that p63 needs signals from morphogens to help skin cells differentiate properly.

A new gene mutation linked to a skin condition was found in a Spanish family.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

A genetic variant linked to hair thinning in Japanese women was found.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

TLR3 signaling enhances the immunosuppressive properties of human periodontal ligament stem cells.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

A new genetic mutation was found causing hair and eye issues in a boy.

The polyG fragment in Hoxc13 protein helps evolve mammalian skin and hair by enhancing gene interactions.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

PTEN was identified as a specific marker for the skin disease cutaneous lupus erythematosus, and it helps increase the expression of harmful type I interferons.

Hoxc13 is essential for hair growth and follicle development.

Sheep cells were successfully modified to include a spider silk protein gene.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

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

Defects in certain proteins cause major heart abnormalities during early development.

A gene mutation in mice causes skin defects and early death.

AtCSLD3 and GhCSLD3 genes enhance root growth and cell elongation in plants.