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The vitamin D receptor helps control hair growth and may protect against certain skin tumors.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Cell membrane-coated nanoparticles could improve gene therapy by enhancing delivery and targeting of nucleic acids.

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

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

Removing certain hair follicle stem cells worsens skin reactions to allergens.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

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

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

The mutation causing Hutchinson-Gilford progeria syndrome leads to severe skin problems and early death in mice.

The hair follicle dermal sheath is essential for hair shedding and needs to communicate with the outer root sheath for normal hair growth cycles.

Three genes in Arabidopsis are important for plant growth and development by affecting sugar attachment to proteins.

Neural cell nanovesicles help hair growth by activating key signals.

Reducing PEDF may help treat hair loss.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

The Shh gene controls cell growth and death in cashmere goat hair follicles, affecting hair growth.

Balding scalps show different gene expressions affecting hair growth compared to non-balding scalps.

Non-thermal plasma could help hair growth by activating key cell signals.

Four genes are linked to alopecia areata, with two increasing risk and two offering protection.

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

The new ddPCR method reliably detects unwanted viruses in CAR-T cell products, ensuring their safety for patients.

A 195 bp duplication in the HOXC10 gene causes crests in domestic chickens.

BMP-2 activates the Dlx3 gene in mouse skin cells, important for hair and skin development.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

Pregnant women with PCOS have higher levels of Neurokinin B in the placenta, especially with female babies.

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

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

K6/ODC transgenic mice are effective for quickly identifying cancer-causing chemicals.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.