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TIP39 and PTH2R help control calcium levels and skin cell development.

Mutations in the Sgk3 gene cause fuzzy hair in mice.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

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

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

KAP6 genes are conserved across species and active in hair follicles.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

The Celsr1 gene is crucial for normal hair patterning in mice.

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

ARL15 is important for fat cell development and the release of the hormone adiponectin.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

PrPC is important for neural differentiation in cattle and mouse embryonic stem cells.

NFIB and STAT5 work together to control specific genetic programs in cells.

A peptide from hair follicle stem cells promotes hair growth by activating specific skin cells.

UC.145 may be a new biomarker for predicting gastric cancer.

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.

MYB30 and EIN3 work against each other to control root hair growth and phosphorus uptake in plants when phosphate is low.

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

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

Neuregulin3 affects cell development in the skin and mammary glands.

A specific gene mutation causes severe skin and nail issues and hair loss.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Mutations in specific genes cause different types of ectodermal dysplasias.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

Intu gene is crucial for hair follicle formation by helping keratinocytes differentiate through primary cilia.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.