Search

everythinglearnresearchcommunity

for

Search:↓

Understanding how Regulatory T Cells work could help create treatments for certain skin diseases and cancers.

Modified β-catenin can cause different effects in mouse skin cells, leading to cysts or tumors depending on the cell type.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

The type of tumor suppressor affects the form of skin cancer from hair follicle stem cells.

TGFβ-2 may cause hair loss in androgenetic alopecia.

The enzymes Tet1, Tet2, and Tet3 are important for the development of hair follicles and determining hair shape by controlling hair keratin genes.

T cell subsets are crucial in kidney cancer, and a new model predicts patient outcomes using key genes.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

Activated LEF/TCF complexes are crucial for hair development and cycling.

Thyroid-related genes are active in skin cells and may affect autoimmune conditions.

The technology can create transgenic cashmere goats with improved wool quality.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

TCHHL1 is a protein important for hair growth, found in hair follicles.

Small molecules KY19382 and KY19334 may help treat skin cancer by reducing CDK1 levels and blocking harmful cell signals.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

The new method found new shared genetic areas linked to both Type 2 Diabetes and Prostate Cancer.

Researchers used CRISPR/Cas9 to create a goat with a gene that increased cashmere production by 74.5% without affecting quality.

TMPRSS2 is crucial for COVID-19 infection and is a potential target for treatment.

Lower TGFß1 levels help stem cells become beige fat cells.

AtCSLD3 and GhCSLD3 genes enhance root growth and cell elongation in plants.

A protein called lfTSLP is important in causing allergic and other skin diseases and could be a target for treatment.

Low-penetration genes might help personalize colorectal cancer prevention.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.