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CAM practitioners in the eThekwini area are exploring ways to manage and diagnose Polycystic Ovarian Syndrome.

Standardized guidelines are needed to improve drug-loaded extracellular vesicle purification.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

The study created a skin model with realistic blood vessels that improves skin grafts and testing for drug delivery.

Combining genetic and physical data improves diagnosis and treatment for early-onset monogenic diabetes.

The exosome injections were from stem cells and plants, not umbilical cords.

Researchers created a cell model to study hair growth and test hair-growth drugs.

A man with Acrodermatitis continua did not get better with etanercept treatment, and his condition worsened, suggesting treatment effectiveness may vary by genetics and race.

A mutation in the KRTHB5 gene causes hair and nail issues.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Early diagnosis and treatment are crucial for CAPS, and Eculizumab can be effective.

Activating the hexosamine pathway can improve skin health and increase hair follicle stem cells.

High levels of androgens during early development may cause PCOS-like symptoms.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

Inclusive dermatology aims to provide personalized skin care for all by addressing diverse needs and disparities.

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

Kindler Syndrome shows diverse symptoms and needs better diagnostic tools and care in resource-limited areas.

A rare case of a transplant patient developing a skin condition linked to HPV-49.

Mutations in the KLHL24 gene cause skin blistering in epidermolysis bullosa simplex.

Early diagnosis and personalized treatment for PCOS are crucial, especially for young women in West Bengal, India.

Anti-Desmocollin 3 antibodies can cause atypical pemphigus symptoms.

The research found that the properties of solid-state Electronic Circular Dichroism (ss-ECD) are influenced by the orientation of local crystals, which could help in examining and mapping chiral materials like pharmaceutical ingredients.

DSDs are birth conditions causing unusual sex development, managed with personalized care and sometimes surgery, but still lack a standard treatment approach.

Endocrine-disrupting chemicals cause irreversible harm to children's development, increasing disease risk.

Exosomes from umbilical cord stem cells help protect hair color and health under stress.

Protein kinase C epsilon may promote skin cancer development after UV exposure by affecting nearby cells.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.