Search

everythinglearnresearchcommunity

for

Search:↓

New treatments for hair growth and psoriasis may be possible, and gene differences could affect baldness and the severity of skin conditions.

R-spondin2 may help treat hair loss, gene differences could explain baldness, a peptide's regulation is linked to psoriasis, B-defensin gene copies may affect a skin condition's risk and severity, and potential markers and targets for alopecia areata were identified.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

Hormone treatments for transgender individuals generally improve mental health and physical transition, with some health risks that require medical supervision.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Feather patterns form through genetic and epigenetic controls, with cells self-organizing into periodic patterns.

EGFR is essential for normal hair development and follicle differentiation.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

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

Androgenetic alopecia involves genetics, hormones, and can be treated with medications or surgery.

FFA's causes may include environmental triggers and genetic factors.

Acne is caused by genetics, diet, hormones, and bacteria, with treatments not yet curative.

Generalized vitiligo in Chinese patients is linked to other autoimmune diseases, especially in familial cases.

Researchers found genes for cysteine-rich proteins that form the protective layer of hair in humans and sheep.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

The document concludes that targeting 5α-reductase, the androgen receptor, and hair growth genes, along with using compounds with anti-androgenic properties, could lead to more effective hair loss treatments.

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

MicroRNAs are crucial for controlling skin development and healing by regulating genes.

Artesunate is generally safe for severe malaria, but patients should be monitored for delayed anemia after treatment.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

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

Female pattern hair loss involves hormonal factors, genetics, and may be linked to low ferritin levels.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

Researchers found genes that control hair color and growth change before the visible coat color changes in snowshoe hares.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

The study found that Central Centrifugal Cicatricial Alopecia mainly affects middle-aged African descent women, is linked to certain hair care practices and genetics, and often goes undiagnosed for years.

Genetic changes in mice help understand skin and hair disorders, aiding treatment development for acne and hair loss.

Genetic factors alone might not cause pemphigus vulgaris; other factors like birth complications and puberty may trigger it.