Search

everythinglearnresearchcommunity

for

Search:↓

Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

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

A prostate cancer drug can lower the levels of a protein that the coronavirus uses to enter lung cells.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

BcFLA1 protein is crucial for root hair growth in response to low phosphate in Brassica carinata.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

Hex gene plays a crucial role in starting feather development in chick embryos.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

Mutations in the LIPH gene cause woolly hair in a child.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

HOTTIP and miR-10b contribute to glioma therapy resistance by affecting cell behavior, suggesting they could be targets for treatment.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

A young patient with unusual insulin resistance and high testosterone levels had a rare INSR gene mutation.

Inhibiting retinoic acid activates WNT signaling, potentially aiding hair disorder and skin cancer treatments.

Activating Wnt in skin cells controls the number of hair follicles by directing cell movement and fate.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

The hairless (hr) gene is essential for normal hair follicle function and its mutation leads to hair loss.

A feedback loop between LRH and RSL4 controls root hair growth in Arabidopsis.

The LEF-1 binding site enhances gene expression in hair follicles, with other proteins aiding specific regulation.

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

Activating TRPMLs helps human cells important for hair growth and increases hair growth in mice.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

A specific gene mutation causes Olmsted syndrome.

The TIP1 gene is crucial for normal plant cell growth in Arabidopsis.

HPV8 causes hair follicle stem cells to grow, leading to skin lesions.