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Researchers found four key proteins that affect the development of a specific hair type in Yangtze River Delta white goats.

HOXC13 is essential for hair and nail development by regulating Foxn1.

A stable, active version of a growth factor was made in bacteria, showing promise for medical use.

Ku80 is a key receptor for Thymosin β4, affecting cell migration and wound healing.

Prdm1 is necessary for early whisker development in mice but not for other hair, and its absence changes nerve and brain patterns related to whiskers.

A new gene mutation causes a rare type of hair loss.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Mutations in β1 integrins cause embryonic death but have milder effects on skin.

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Targeting METTL1 may help slow papillary thyroid cancer growth and spread.

Researchers found genes and microRNAs that control curly fleece in Chinese Tan sheep.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

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

Mutations in the KRT16 gene can cause skin and nail disorders.

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

The STRIPAK complex is crucial for skin cell organization and creating a functional skin barrier.

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

FLRG and follistatin have different roles in wound healing.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

The N gene affects the protein makeup of mouse hair.