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Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

A rabbit gene important for hair development was identified and detailed.

Genetic defects in the Wnt/PCP pathway may cause congenital yellow nail syndrome.

IL-19 and IL-24 help cells respond to DNA damage and could be targeted for cancer and age-related disease treatments.

NXC736 significantly reduced hair loss in mice with alopecia areata.

Phospholipase C-δ1 is crucial for normal hair development.

PolyQ repeats in neural proteins evolve together, affecting brain function and disease.

Taking photos of your own skin can lead to fewer skin biopsies for mole monitoring.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

Long non-coding RNAs affect feather growth in chickens in ways that don't follow traditional genetic rules.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

The G(S) alpha subunit gene may help start hair follicle growth in newborn mice.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Transplanted whisker follicles caused hair growth on the spine of mice.

lncRNAs may regulate hair follicle development in Hu sheep.

A single recessive gene causes sparse hair in certain Japanese White rabbits.

Certain gene variations may increase the risk of PCOS in South Indian women.

White lupin uses specific genes to grow root hairs and access phosphorus when it's scarce.

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

SeV-Tp speeds up healing of drug-resistant infections by targeting wounds and killing bacteria with light activation.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

The patient's hair improved after treatment, but the genetic link is unclear.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

SKPs are similar to adult skin stem cells and could help in skin repair and hair growth.

A rare gene variant causes hair and nail issues in a family.

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

Using polymeric micelles to deliver spironolactone topically could improve wound healing in skin affected by glucocorticoids.

Type II porcine hair keratin supports cell growth but hinders cell differentiation.