Search

everythinglearnresearchcommunity

for

Search:↓

The document concludes that ERBB2 mutations are common in extramammary Paget disease and may respond to systemic treatments like cancer immunotherapy.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Different hair growth problems are caused by genetic issues or changes in hair growth cycles, and new treatments are being developed.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

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

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Ayurveda's descriptions of genetic disorders align with modern genetic understanding.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

Different types of stem cells exist within individual skin layers, and they can adapt to damage, transplantation, or tumor growth. These cells are regulated by their environment and genetic factors. Tumor growth is driven by expanding, genetically altered cells, not long-lived mutant stem cells. There's evidence of cancer stem cells in skin tumors. Other cells, bacteria, and genetic factors help maintain balance and contribute to disease progression. A method for growing mini organs from single cells has been developed.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

Scarring alopecias are complex hair loss disorders that require early treatment to prevent permanent hair loss.

The document concludes that identifying the specific cells where skin cancers begin is important for creating better prevention, detection, and treatment methods.

Genetic testing is crucial for diagnosing rare hair loss disorders.

People with atopic dermatitis are more likely to develop other skin conditions due to shared genetics and immune pathways.

Skin aging is caused by stem cell damage and can potentially be delayed with treatments like antioxidants and stem cell therapy.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

Twins had rare skin cysts likely due to genetics.

Coloring shampoos for gray hair may cause gene mutation, reproductive issues, and skin damage, needing stricter regulation and expert consultation.

The document concludes that early recognition and treatment of PCOS in adolescents is crucial for managing symptoms and long-term health risks.

New genetic discoveries may lead to better treatments for alopecia areata.

Psoriasis involves immune and genetic factors, and understanding these can improve treatments.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

Hair pattern in androgenetic alopecia overlaps with scalp and bone demarcations, with distinct gene profiles affecting susceptibility.

Skin's epithelial stem cells are crucial for repair and maintenance, and understanding them could improve treatments for skin problems.

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

Genes and hormones cause hair loss, with four genes contributing equally.