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Intralesional triamcinolone injections can effectively stop frontal fibrosing alopecia with minimal side effects.

Activating the GDNF-GFRα1-RET signaling pathway could potentially promote skin and limb regeneration in humans and could be used to treat hair loss and promote wound healing.

Long-lasting symptoms like fatigue and breathlessness can persist after COVID-19, requiring ongoing medical follow-up.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Some psychiatric medications can cause reversible hair loss.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Finasteride use varies among Denmark, Finland, Norway, and Sweden, with higher usage in Finland and Sweden.

More research needed to confirm finasteride as standard treatment for FFA.

The document concludes that the exact way alcohol causes harm to fetal development is unknown, but it significantly affects nutrient transport to the fetus and a safe level of alcohol during pregnancy is not determined.

Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.

Defective mitochondrial DNA replication causes aging symptoms and increased oxidative damage in mice.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Measuring reproductive hormones in brown bear hair could help identify their sex and reproductive state, but better collection methods or lab techniques are needed.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Young adults with hair loss face higher risk of stiff arteries.

A family had a rare fungal infection called white piedra, identified as Trichosporon inkin.

Both classical and L-type atypical BSE from cattle can infect goats with different incubation times, and tests can distinguish between the two strains.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

Sex steroids affect the MafB gene differently in male and female hamsters.

Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

An 87-year-old woman was diagnosed with type 3 autoimmune polyendocrine syndrome and had multiple autoimmune issues.

Convolvulus arvensis ethanolic extract can potentially promote hair growth and reduce hair loss.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Hair loss occurs due to fewer papillary cells, smaller follicles, and shorter growth phases.

Mycophenolate mofetil may improve lupus nephritis remission more than cyclophosphamide but with uncertain safety.

Different signals work together to change gene activity and guide hair follicle stem cells to become specific cell types.

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Mutations in the LSS gene cause a rare type of hereditary hair loss.