Search

everythinglearnresearchcommunity

for

Search:↓

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

AgK114 protein helps in hamster skin injury recovery.

Prolactin affects the production of different keratins in human hair, which could lead to new treatments for skin and hair disorders.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Androgen receptors help prostate cancer cells grow and resist drugs.

A new rat strain with a specific gene mutation causes hair loss and kidney issues.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Four new genes related to sheep wool were discovered, showing genetic diversity.

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

Thyrotropin-releasing hormone may help control skin and hair growth and could aid in treating related disorders.

Runx1 helps control the KAP5 gene in human hair follicles.

HPV8 E6 gene causes growth of certain skin stem cells.

A protein called sFRP4 can slow down hair regrowth.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

LEKTI is crucial for skin barrier and immune function, affecting conditions like Netherton syndrome and atopic dermatitis.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

Changing protein kinase levels in pituitary cells affects calcium flow and beta-endorphin release.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

H3K4me3 helps control RSPO3 to influence hair growth and development.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

A specific gene mutation causes woolly hair and hair loss.

Blue-light activation of TrkA improves hair-follicle stem cells' ability to become neurons and glial cells.

Removing the Crif1 gene in mouse skin disrupts skin balance and hair growth.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

K10 may not prevent tumors as previously thought and might increase benign tumor risk.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

TRPV3 in skin cells causes inflammation and cell death.