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Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

Fz3 and Fz6 can partially replace each other in tissue polarity and axon guidance.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

UV exposure reduces Lgr6+ stem cells in mouse skin and they don't significantly contribute to skin cancer development.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

CAP1 decreases the expression of a hair-related protein in young Tan sheep's skin.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Mutations in the hairless protein gene cause hair loss.

Increasing SSAT makes skin more prone to cancer.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

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.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

α-parvin is necessary for skin and hair growth and for the correct orientation of skin cells.

Keratin 17 is important for skin's response to radiation, affecting many genes and cell division.

Pannexin 3 helps skin and hair growth by controlling a protein called Epiprofin.

Infants with severe KID syndrome may be more prone to serious infections and need close monitoring.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Increased ODC expression makes normally tumor-resistant mice more prone to tumor development.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

A genetic variant in goats is linked to cashmere growth.

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

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

SLC45A2 and GPNMB genes help control chicken feather color by promoting melanin.

Akt2 protein is essential for normal cell division in early mouse embryos.