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Polycystic ovary syndrome and iron overload share similar symptoms and can be potentially treated with blood removal, diet changes, and probiotics.

Fat-derived stem cells show promise for treating skin issues and improving wound healing, but more research is needed to confirm the best way to use them.

Fasting in hens affects thyroid hormones, which regulate feather and hair growth.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Plant sterols have health benefits like lowering cholesterol, but more research is needed to understand their effects and improve their extraction and sustainability.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

New treatments focusing on immune pathways show promise for stubborn hair loss.

Organoids help study and treat genetic diseases, offering personalized medicine and therapy testing.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

Scientists have improved 3D models of human skin for research and medical uses, but still face challenges in perfectly replicating real skin.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

The ABCA4 gene protects hair follicle stem cells from toxic vitamin A byproducts.

Early balding in men is linked to metabolic syndrome, so screening is important for prevention.

CO₂ laser treatment is fast and effective for some benign skin tumors with minimal side effects.

Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Lower adrenal hormone levels may cause hair loss in postmenopausal women, certain patterns help diagnose nail cancer, and a gene variant linked to higher skin cancer risk in kidney transplant patients suggests monitoring folate levels.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Blocking the FGF5 gene in sheep leads to more fine wool and active hair follicles due to changes in certain cell signaling pathways.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Follicle Stimulating Hormone is important for fertility.

The document concludes that proper diagnosis and combined treatments are key for hirsutism management, and weight loss may help overweight patients.

Advanced human skin models improve drug development and could replace animal testing.

Human hair follicle cells can be successfully transformed into different types of cells, but not more efficiently than other adult cells.

Certain inhibitors can potentially treat prostate cancer and other hormone-dependent conditions by controlling sex hormone levels in cells.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.