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MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

MOF controls skin development by regulating genes for mitochondria and cilia.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

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

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

Hair loss in men might be linked to changes in cell energy factories.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

COX2 and ATP synthase control the size of hedgehog spines.

The document concludes that alopecia has significant social and psychological effects, leading to a market for hair loss treatments.

The document concludes that understanding health requires considering evolutionary perspectives on reproductive fitness, and recognizing the complexity of factors like diet, testosterone, and sexual orientation.

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

Antioxidants may help improve mitochondrial health and could be used to treat diseases related to cell damage.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Mitochondrial reactive oxygen species are essential for skin and hair development.

Mitochondrial Complex I reduces inflammation and increases bone breakdown by affecting certain immune cells.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Certain genes are linked to the quality of cashmere in goats.

Tetrathiomolybdate reduces hair growth marker in skin cells by boosting harmful oxygen molecules, but effects can be reversed.

Mitochondrial dysfunction is linked to various skin conditions and could be a target for treatments.

Androgens and androgen receptors are important for metabolic health, affecting how the body uses glucose and fats through mitochondrial function.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Skin cell types develop when specific genes are turned on by removing certain chemical tags from DNA.

Quercitrin may help treat hair loss by promoting hair growth and improving cell health.