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A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

The EDAR gene greatly affects hair thickness in Asian populations.

Versican, a protein, is less present in thinning hair follicles and this decrease might contribute to common hair loss in men.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

FOXO1 is important for wound healing, but its dysfunction in diabetes can slow the healing process.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

Mutant mice help researchers understand hair growth and related genetic factors.

Mannosylerythritol lipids are good for skin and hair care products.

Phospholipase A2 is necessary for the correct placement of PIN proteins in plant roots, affecting root growth.

Certain types of T cells are essential for healthy skin and play a role in skin diseases, but more research is needed to improve treatments.

The TGF-β family helps control how cells change and move, affecting skin, hair, and organ development.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

Minoxidil boosts hair growth by activating PGHS-1.

White lupin uses specific genes to grow root hairs and access phosphorus when it's scarce.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Muscles and nerves that cause goosebumps also help control hair growth.

Human skin cells produce proenkephalin, which changes with environmental factors and skin diseases.

The three estrogen receptor genes are highly expressed in zebrafish neuromasts during development.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

The circadian clock influences the behavior and regeneration of stem cells in the body.

Cells in hair follicles help create fat cells in the skin by releasing a protein called Sonic Hedgehog.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Restoring mitochondrial function in mice reversed their skin wrinkling and hair loss.

The HR protein's role as a repressor is essential for controlling hair growth.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

S100A4 and S100A6 proteins may activate stem cells for hair follicle regeneration and could be potential targets for hair loss treatments.

mTOR signaling helps activate hair stem cells by balancing out the suppression caused by BMP during hair growth.