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FERONIA and LRX proteins help control cell growth in plants by regulating vacuole expansion.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

Mexican patients had a lower incidence of skin reactions to drugs and no significant link between these reactions and the TNF2 gene variant.

Removing UBE2N from skin cells causes inflammation and immune response, which can be lessened with specific inhibitors.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Mutations at Val-889 and Arg-752 disrupt key interactions in androgen receptor dimerization.

A specific genetic variation affects wool quality in sheep.

Genetic variations in FTO and MC4R may contribute to PCOS by affecting obesity.

The OVOL1 gene, controlled by β-catenin, is crucial for creating hair follicles.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

A new protein was made to detect specific skin cell growth receptors and worked in normal skin but not in skin cancer cells.

Erythropoietin overexpression disrupts hair growth and fat formation in mice.

Gene variation affects prostate issues and hair loss.

Stress increases a factor in mice that leads to hair loss, and blocking this factor may prevent it.

Nucleic acids trigger chemokine production in skin cells, affecting skin inflammation.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Noncoding RNAs help determine cashmere quality in goats.

The research found that the molecule lncRNA-H19 helps hair follicle cells grow by affecting certain cell pathways in cashmere goats.

K6hf is found in specific parts of hair follicles, nails, and tongue, and is linked to hair growth and structure.