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

Monitoring TGF-β and linc-PINT expression may help identify and treat high-risk heart arrhythmia patients.

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

New biomarkers and potential treatments for skin diseases were identified.

LncRNAs play a crucial role in muscle regulation and could help develop treatments for Duchenne muscular dystrophy.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

lncRNA MRPS28 regulates hair follicle development in cashmere goats, affecting cashmere quality.

Mouse and human skin development share similar fibroblast timelines.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

Naked-mouse hair lacks certain proteins and has less soluble fibril.

Certain genes are linked to the risk of developing Alopecia Areata.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

sPLA2-X is crucial for normal hair growth and follicle health.

Mutations in the DSG4 gene cause specific hair and scalp issues.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

HLD10 can include increased body hair and Mongolian spots.

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

The Gsdma3 gene is essential for normal hair development in mice.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

Four new genes related to sheep wool were discovered, showing genetic diversity.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

A newly found RNA in Cashmere goats may play a role in hair growth and development.

Scarred skin in lichen planopilaris loses immune cells due to a decrease in a specific protein in skin cells.

Two new gene mutations cause a rare hair disorder.

Pvalb8 is essential for zebrafish hearing and hair cell development, and its mutation causes hearing loss.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

A specific gene mutation causes congenital hair loss.