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A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

A new gene mutation is linked to monilethrix in the studied family.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Rats can develop an immune response to prion protein peptides, but it may cause severe skin issues in older rats.

GhPLDα1 helps thicken cotton fiber walls by boosting cellulose production.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Activating TLR3 may help produce retinoic acid, important for tissue regeneration.

VEGF165 influences hair follicle cell growth and movement through VEGFR-2 activation.

PRF lysates reduce inflammation in cancer cells and boost immune response in healthy oral cells.

A mutation in the KRT75 gene causes frizzle feathers in chickens.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Specific keratin gene mutations can cause monilethrix.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

RORA may help regulate hair growth by affecting hair follicle stem cells.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

HLD10 can include increased body hair and Mongolian spots.

Enhanced stem cells can reduce fat buildup in eye tissue for Graves' disease.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

LH and hCG reduce certain protein levels in women's skin.

Researchers found a way to make rat hair follicle cells start turning into motor neuron-like cells, but couldn't fully turn them into working motor neurons.

High lactate dehydrogenase activity is not necessary for the growth of squamous cell carcinoma.

A new gene mutation causes insulin resistance in a girl and her mother.

RNase L suppresses regeneration in mammals.

A gene variation is linked to hair thickness in Asians.

GMG-43AC may help reduce unwanted hair growth and treat certain hair loss conditions.

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.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

Cyclohexyl salicylate promotes human hair growth and increases certain hair follicle stem cell progeny.