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

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

CDKN2AIP gene is less active in nevus sebaceous, affecting related RNA networks.

LIPH mutations cause woolly hair in some Chinese people.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

Researchers cloned a gene from Xinjiang fine-wool sheep, finding it very similar to other sheep and somewhat similar to goats, humans, and rabbits.

Gene expression affects fur development in rex rabbits.

Hair follicles can be used to study gene expression and understand conditions like COPD.

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

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

The method could grow hair in lab settings without using animals.

GCN reduces lung inflammation and damage from air pollution in mice.

The new delivery system could improve pain and inflammation relief in gout.

TAT-GILZ peptide promotes hair growth by boosting stem cell activity.

HSPC016 gene is important for hair growth.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

The new system makes hair transplants faster and more precise.

GPIGS peptide increases thick hair growth in balding Japanese men.

Recombinant gonadotropins improve future fertility in CHH patients.

New microneedle treatment with growth factors and a hair loss drug shows better and faster hair growth results than current treatments.

ATP6AP1‐CDG can cause hearing loss, hair loss, and protein issues, even in female carriers.

Genetic markers can help predict ear shapes for forensic use.

Multicomponent crystals in microneedles improve drug delivery for hair loss treatment.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.