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The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Researchers found a gene mutation responsible for a rare hair loss condition.

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

Gene differences affect finasteride side effects in men with hair loss.

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

A specific RNA modification in cashmere goats helps activate hair growth-related stem cells.

The Fas/FasL pathway may play a role in alopecia areata.

Taking 5-alpha reductase inhibitors might be linked to breast cancer in men.

The LMNA mutation affects skin structure even in asymptomatic carriers.

Nerve growth factor helps cashmere goat hair cells grow and is more active during the hair growth phase.

Blocking CCR5 can prevent and improve hair loss in alopecia areata.

Differences in androgen receptor expression and tissue properties may lead to higher cryptorchidism risk in certain rats.

Scientists discovered two versions of a new human hair keratin gene.

A soluble factor in developing mouse whisker pads boosts nerve growth factor mRNA production.

The TG5 gene affects beef cattle weight, and the CC genotype leads to higher weights.

Androgens help motor neurons grow by increasing neuritin.

DNA analysis can help tailor alopecia treatment.

Specific RNA patterns are linked to alopecia areata.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

The protein Gnαs is found more in black mice than white mice and may influence their coat color.

The Engrailed-1 gene plays a key role in the development of sweat glands in mice.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

Hairless protein is key for hair growth, cell differences cause gene expression variation, and the N-end rule pathway senses nitric oxide for protein breakdown.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

The study improved understanding of gene roles in cashmere goat hair growth, aiding future cashmere production.

The G allele of IFITM3 rs12252 is linked to more severe COVID-19.