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The study developed a 3D model that closely imitates remaining ovarian cancer after treatment and identified a potential drug targeting resistant cancer cells.

Male-pattern hair loss is largely influenced by genetics, with key genes identified.

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

More research is needed to understand the genetic causes of Alopecia areata to develop better treatments.

Vitiligo is often found with other autoimmune diseases, which is important to know to help patients.

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.

MicroRNA-148a is crucial for maintaining healthy skin and hair growth by affecting stem cell functions.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

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

Adrenal disorders can cause lasting brain and behavior issues in children.

Different genes cause Female Pattern Hair Loss compared to male hair loss, and treatments vary, but more research is needed to understand it fully.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Using protein degradation to fight cancer drug resistance shows promise but needs more precise targeting and fewer side effects.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

Lupus is a complex disease that requires personalized treatment because it varies greatly between individuals.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

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

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Oral contraceptives lower testosterone levels in women, especially those with certain genetic traits, and may be linked to increased breast cancer risk.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Different skin stem cells help heal wounds, with hair follicle cells becoming more important over time.

There is no causal relationship between androgenetic alopecia and serum uric acid.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

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.