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Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

A specific mutation in PA-PLA1α causes abnormal hair growth.

Ac-GFFY-IGF peptide is a promising, safe, and effective treatment for hair loss, better than current options.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

A protein made in a plant stopped hair growth in mice.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Overexpressing Tβ4 in cashmere goats improves hair fiber traits and increases cashmere yield.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Changing the 6-position on benzopyran molecules affects insulin release, with some compounds showing strong inhibitory effects.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

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

A gene variation is linked to hair thickness in Asians.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

rPanglaoDB helps study rare cell types by merging RNA data, confirming fibrocytes' role in healing.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

FERONIA is crucial for plant growth, pollen tube reception, and sugar signaling.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

The fer-ts mutation in plants prevents root hair growth at high temperatures.

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

Fatty acid transport protein 4 is essential for skin and hair development.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A new peptide, FOL-005, may help treat excessive hair growth by reducing a hair growth promoter, FGF7.

LIPH mutations cause woolly hair in some Chinese people.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.