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A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Alkaline Ceramidase 1 prevents early hair loss in mice by keeping hair follicle stem cells balanced.

Human skin xenografting could improve our understanding of skin development, renewal, and healing.

Researchers used CRISPR/Cas9 to create a goat with a gene that increased cashmere production by 74.5% without affecting quality.

Deleting the Sox21 gene changes hair lipid composition and increases cholesterol sulfate levels.

Different fish use the same genes to regrow teeth.

Sdr16c5 and Sdr16c6 genes regulate a key point in lipid production that affects eye and skin gland function.

TRPA1 is crucial for mechanical sensitivity in skin sensory neurons.

CTHRC1 helps hair grow back, and plantar dermis mixture boosts it.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

Acid can block TRPV3 from outside the cell but boost its function from inside.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

The T-Fast multi-implanter makes hair transplant surgeries quicker and cheaper.

PrPC is important for neural differentiation in cattle and mouse embryonic stem cells.

Mouse and human skin development share similar fibroblast timelines.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

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

Grasp protein helps maintain skin health after UVB exposure.

A natural compound called VB-1 can help promote hair growth by boosting a specific cell signal in human skin cells.

Laminin-511 is essential for proper melanocyte movement and development in mice.

Scientists turned rat thymus cells into stem cells that can help repair skin and hair.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

Lhx2 helps retinal cells respond to signals for eye development.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

TNFα helps grow and maintain liver cells in 3D culture for a long time.