Search

everythinglearnresearchcommunity

for

Search:↓

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Enhanced stem cells from the placenta can help treat Graves' eye disease by stopping fat cell growth.

Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

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

Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

CLE40 and CRN/CLV2 pathways have opposite effects on root growth in Arabidopsis.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

Hemoglobin α acts as an antioxidant in skin cells, especially protecting hair follicle stem cells from UV damage.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

Neuregulin3 affects cell development in the skin and mammary glands.

A substance called compound-1 could help increase hair growth by maintaining prostaglandin levels in hair follicles.

Activating TLR9 helps heal large wounds and regrow hair by involving a specific type of immune cell.

Blocking the HEDGEHOG-GLI1 pathway can reduce keloid growth and may be a potential treatment.

HSPC016 gene is important for hair growth.

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

The hHa7 gene is regulated by androgens in certain body hair, not scalp hair.

Mutations in β1 integrins cause embryonic death but have milder effects on skin.

Rats can develop an immune response to prion protein peptides, but it may cause severe skin issues in older rats.

A specific DNA region controls skin cell gene expression by working with certain proteins.

IGFBP-rP1 could be a new treatment for a common type of hair loss.

Platelet-rich plasma may help hair follicle cells grow by affecting certain genes and pathways.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

Hair growth-related cells need the enzyme SCD1 to help maintain the area that supports hair growth.

Toll-like receptor 3 helps repair the skin barrier after UV damage.