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Different cells affect hair follicle blood vessels, endothelial cells react differently to inflammation and oxidized fats, and prasugrel better protects heart vessels during a procedure than clopidogrel.

The method can effectively extract biomedical information without needing expert annotation, performing better than previous models.

Shorter CAG repeats may cause hair and skin issues, while longer ones may link to acne.

Sex hormones affect brain injury differently in males and females.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Hair loss involves immune responses, inflammation, and disrupted signaling pathways.

Male hormones cause different growth in identical human hair follicles due to their unique epigenetic characteristics.

No clear link between androgen receptor variation and hair loss, but more research needed.

Longer CAG repeats in gene linked to more severe hair loss in females.

Mercury allergy linked to specific genes may contribute to burning mouth syndrome, and silicon might play a role in maintaining healthy hair.

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.

Intralesional chemotherapy with 5-fluorouracil and methotrexate may worsen keratoacanthoma-type skin cancer in transplant patients.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

Skin problems are common in Bangladesh due to arsenic, prompt treatment of diabetic foot ulcers is crucial, maternal transmission causes most neonatal herpes, treatments for pediatric vasculitis are effective, the chickenpox vaccine works, more frequent UVB therapy helps psoriasis, certain jobs increase hand dermatitis risk, monoclonal antibodies treat psoriasis well, lifestyle affects psoriasis, alefacept improves psoriasis, imiquimod cream partially clears basal cell carcinoma, and iron may not help chronic hair loss.

The document concludes that various treatments for skin conditions are effective, but some require further research, and certain factors like gender and lifestyle can influence disease outcomes.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.

Finasteride improves hair growth and reduces hirsutism in women, but side effects and optimal dosages need further research.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

The document concludes that stem cells and their environments are crucial for skin and hair health and have potential for medical treatments.

Higher levels of nidogen1 and type IV collagen are found in basal cell carcinoma compared to normal skin.

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

The document concludes that various medications and treatments can have significant, sometimes adverse, effects on health outcomes.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

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

Mutation in hairless gene may increase hair loss risk.

Mutation in hairless gene may increase hair loss risk.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.