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NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

Properly formulated large molecules can reach active levels at the hair bulb.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

ABCG2 protein marks stem-like skin cells in human epidermis.

Overexpression of E2F1 can lead to skin tumors and disrupt hair growth.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

Newly born mesenchymal cells quickly spread out in response to tissue tension during early development.

β1 integrin is essential for the survival, growth, and movement of human epithelial progenitor cells.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

Transcutaneous vaccination using nanoparticles can enhance immune responses and reduce basal cell carcinomas.

A unique type of complex cyst was found on a man's scrotum.

Inherited color dilution in rabbits is linked to DNA methylation changes.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A mutation in the Sgkl gene causes defective hair growth in mice.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

New mutations in the hairless gene may cause hair loss and affect bone development.

HLD10 can include increased body hair and Mongolian spots.

HPV8 causes skin cancer by expanding specific skin stem cells.

Special gut cells help stem cells move to and fix injured areas by activating a specific signaling pathway.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Ectomesenchyme is a key source of skin stem cells.

MsPG3 protein gathers at root hair tips, aiding growth.

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

Dermal EZH2 controls skin cell development and hair growth in mice.

A protein in plants needs to bind two lipids to help with root hair growth, and this process is similar across different plant species.