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Jatropha dioica may have antiviral, antifungal, and other medicinal properties, but more research is needed.

Most medicinal plants in Mexican folklore have safe element levels, but arsenic exceeds safe limits in almost all.

The document concludes that non-scarring alopecias can be reversed, but scarring alopecias cause permanent hair loss.

The review found that the way Platelet-Rich Plasma is made varies a lot, which can change the results of medical treatments.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

Social media data can help track and predict COVID-19 symptoms and trends.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

PRP helps skin heal, possibly through special cells called telocytes.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Diagnosing both systemic lupus and hemoglobinopathy is challenging due to overlapping symptoms.

Environmental factors like diet and vitamin levels, especially Vitamin D, can affect autoimmune diseases differently, with lifestyle changes potentially improving outcomes.

The document concludes that careful surgical methods and choosing the right materials are key for successful scalp, skull, and frontal sinus reconstruction.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

Minoxidil helps prevent hair loss from chemotherapy in rats.

The mTurq2-Col4a1 mouse model shows that cells can divide while attached to stable basement membranes during development.

Blocking IL-17 can reduce skin inflammation in a mouse model of pityriasis rubra pilaris.

New genetic locations explain much of hair color variation in Europeans.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Treating non-classic congenital adrenal hyperplasia is complex because the benefits of hormone treatment must be weighed against potential health risks.

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.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

Dutasteride does not seem to change rat spermatogenesis or oxidative stress.

Male pattern baldness is not a risk factor for heart disease based on cholesterol levels alone.

Dutasteride did not change rat spermatogenesis or oxidative stress but needs more research.