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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.

Prostaglandin D2 increases testosterone levels in skin cells through reactive oxygen species, not enzymes, which could lead to new hair loss treatments.

Dermal Papilla Cells grown in 3D and with stem cells better mimic natural hair growth conditions than cells grown in 2D.

The S-2 herbal extract significantly promotes hair growth.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Premature graying of hair is often linked with other health issues, but treatment with biotin, zinc, and calcium pantothenate is not very effective.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

Shift work disrupts the body's natural clock, leading to health problems.

Hair aging leads to color loss and reduced density, and dermatologists are key in treating it to improve quality of life.

Sonic hedgehog signaling is needed for the development of touch-receptor cells in the skin, and the loss of Polycomb repressive complex 2 can lead to more of these cells.

Riboflavin 5′-phosphate (FMN) shows potential for treating androgen-related conditions but may be limited in treating prostate cancer.

Studying rare genetic disorders can help us understand and treat common diseases better.

Activating Nrf2 can help protect against hearing loss.

Certain proteins are significantly increased in the skin of people with hidradenitis suppurativa.

Genetic manipulations that extend lifespan in mice may not work as effectively in humans.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Melatonin makes cashmere grow earlier and more by increasing certain gene activity in goats.

Mongolian gerbils heal wounds differently than mice, with unique protein levels and gene expression that affect skin repair.

Inward rectifier potassium channels are important in many body functions and diseases, and could be potential drug targets.

Understanding skin structure and development helps diagnose and treat skin disorders.

Glucosylceramides are essential for healthy skin and proper wound healing.

Different levels of microRNAs in different parts of the scalp can cause male pattern baldness.

Cepharanthine helps reduce cell aging caused by the cancer drug Doxorubicin by boosting cell cleanup processes.

The document concludes that ERBB2 mutations are common in extramammary Paget disease and may respond to systemic treatments like cancer immunotherapy.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Ethylene and auxin hormones interact in complex ways that are essential for plant growth and development.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Gene therapy in mice increased lifespan and improved health without causing cancer.

Changing the diet of mice lacking the enzyme CBS can affect symptoms related to the genetic condition.