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The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

Fibroblast changes in systemic sclerosis may help understand disease severity and treatment.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Two new reliable Arabic questionnaires for measuring quality of life in women with PCOS were created, one for married and one for unmarried women.

Pregnant women with PCOS have higher levels of Neurokinin B in the placenta, especially with female babies.

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

Understanding how acne develops in different diseases could lead to new treatments.

Clinical signs of hyperandrogenism are related to female pattern hair loss severity, but biochemical markers are not.

Epithelial stem cells can adapt and help in tissue repair and regeneration.

Intestinal intraepithelial lymphocytes are crucial for gut immunity and maintaining the mucosal barrier.

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

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Stress in hair follicle stem cells causes inflammation in a chronic skin condition through a specific immune response pathway.

Unconventional lymphocytes are important for quick immune responses and healing of skin and mucosal barriers.

High triglyceride levels are a key factor affecting testosterone levels in women with PCOS.

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

Lung and liver macrophages protect our tissues and their dysfunction can cause various diseases.

The research showed how melanocytes develop, move, and respond to UV light, and their stem cells' role in hair color and skin cancer risk.

Early recognition and treatment of tinea capitis are crucial to prevent severe scalp issues and prolonged therapy.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

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.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

Certain fungi protect skin health, but changes can allow harmful fungi to cause serious infections, needing more research for treatment and control.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

The document concludes that better targeted treatments are needed for wound healing, and single-cell technologies may improve cell-based therapies.

The document concludes that stem cell inactivity is actively controlled and important for tissue repair and balance.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Improving insulin sensitivity and weight loss can help manage polycystic ovary syndrome (PCOS).