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A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.

Heat shock proteins help basal cell carcinoma grow by responding to inflammation signals.

A new mouse mutation causes skin and hair defects due to a gene change.

Colorectal cancer's ability to spread is due to changes in many genes, not just one.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

Dermal fibroblasts have adjustable roles in wound healing, with specific cells promoting regeneration or scar formation.

Deleting Rac1 in the skin depletes stem cells and damages hair follicles.

Lhx2 helps retinal cells respond to signals for eye development.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

Agouti and AGRP affect pigmentation and obesity, with implications for metabolic disorders.

The gene causing hair loss and heart issues in rough coat mice is still unknown.

Hair repigmentation can indicate malignancy and should be investigated.

The study created a mouse model to mimic degenerative diseases for testing tissue repair and new therapies.

Retinoic acid causes gland formation instead of hair in mouse skin by altering epidermal and dermal interactions.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Specific keratin gene mutations can cause monilethrix.

A new protein, mK6irs, is found in specific hair layers and may help understand hair growth and diseases.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

CD8+ T cells expand significantly in alopecia areata, suggesting new treatment targets.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

MITF+ melanoma patients are more likely to have multiple melanomas and unique skin patterns.

Exosomal miR-199a-3p from dermal papilla cells helps control hair color by affecting melanocytes.

Mitochondrial Complex I reduces inflammation and increases bone breakdown by affecting certain immune cells.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Keratin 10 end domains may increase skin cancer risk by reducing cell death.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.