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PRC1 influences skin stem cell development by both turning genes on and off, affecting hair growth and skin cell types.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Activated erbB-2 in mice skin causes severe skin and hair abnormalities.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Genetic variants in specific genes cause a type of hair loss.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Mutations in the KRT85 gene cause hair and nail problems.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Phospholipids help plant proteins move by regulating receptor interactions.

POUF51 and HES3 are key in controlling stem cell numbers in psoriasis.

Protein kinase C epsilon may promote skin cancer development after UV exposure by affecting nearby cells.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

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

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Ezh2 controls skin development by balancing signals for dermal and epidermal growth.

PAD type III enzyme is specific to rat skin and hair follicles.

Researchers created a new mouse model for studying scleroderma.

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

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

A specific gene mutation causes woolly hair and hair loss.

PmtHEE is a better model for studying pigmented skin because it includes melanocytes and shows improved cell differentiation.

MPZL3 protein helps control the size of oil glands and the growth of oil-producing cells in both mice and humans.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

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

The protein aPKCλ is crucial for keeping hair follicle stem cells inactive and for hair growth and regeneration.