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ADSC injections improve hair density, thickness, and reduce inflammation in female pattern hair loss.

Escin may help treat hair loss by boosting a specific cell growth pathway.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Beard and scalp hair cells have different gene expressions, which may affect beard growth characteristics.

Key genes linked to immune response are upregulated in hair follicles and skin tissues in chronic discoid lupus erythematosus.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

CXCR2 in skin cells promotes tumor growth.

Scientists created a new cell line from Cashmere goat hair and found that cytokeratin 13 is a unique marker for certain skin cells.

High levels of ornithine decarboxylase can cause tumors in mouse skin.

A single amino acid change in the vitamin D receptor can disrupt its function and lead to hair loss.

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

Mettl3 is essential for normal tissue development and self-renewal by regulating gene expression.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

PDGF and its receptors are crucial for stem cell growth and function.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

DPP4-positive fibroblasts play a major role in producing proteins that lead to skin fibrosis.

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

Hedgehog signaling is crucial for hair development, cadherins affect cell adhesion, neutrophils play a role in skin lesions, and BP230 autoantibodies impact skin stability.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Dauricine may help treat certain brain cancers by reducing cancer cell growth and promoting cell death.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

NEDD4 and NEDD4L help control intestinal stem cells and prevent tumors by breaking down the LGR5 receptor.

Deleting the Sox21 gene changes hair lipid composition and increases cholesterol sulfate levels.

A genetic defect in an Appenzeller Mountain Dog caused skin issues, improved with ketoconazole, showing the importance of advanced genetic testing.