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A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Two new gene mutations cause a rare hair disorder.

Using special RNA to target a mutant gene fixed hair problems in mice.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

The study created a mouse model to better understand hair follicle stem cells' role in hair growth and repair.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

GTL1 is needed to control root hair growth and prevent problems when there are too many nutrients.

Overactivating Hedgehog signaling makes hair follicle cells in mice grow hair faster and create more follicles.

Transgenic sheep cells with spider silk gene were successfully created for future sheep hair expression.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

A new DSG4 gene mutation causes hair defects in a young girl.

Researchers created a new mouse model for studying scleroderma.

New genetic mutations causing hair loss were found in a Chinese family.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Transgenic sheep embryos with a specific promoter were successfully created, but more research is needed for gene expression in hair follicles.

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

Homozygous K5Cre transgenic mice have wavy hair and faster cancer progression.