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Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

The boy's hair loss was caused by the tuberculosis drug isoniazid but grew back after stopping the medication.

Some skin conditions are associated with other serious diseases, and office microscopy may miss many fungal infections.

The Rotterdam Study aims to understand various diseases in older adults.

Thymus transplantation successfully restored immune function in infants with FOXN1 deficiency.

Blocking 11β-HSD1 can lessen the harmful effects of glucocorticoids on hair growth cells.

The document is a detailed guide on skin conditions and treatments for dermatologists.

Intermediate filaments are crucial for cell differentiation and stem cell function.

Early treatment of Lupus Erythematosus Alopecia can prevent permanent hair loss, and various medications are effective.

High-dose finasteride may help treat glioblastoma but needs localized delivery for effectiveness.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

Scientists found out the structure of a human enzyme linked to prostate cancer and hair loss, which could help in designing drugs.

Progranulin overexpression leads to shorter, thinner hair and increased cell death in mouse hair follicles.

Desolvation of finasteride depends on environment and technique.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Young women with diffuse hair loss may have low SHBG levels, which could lead to more active testosterone and contribute to their hair loss.

Researchers found potential urine markers for polycystic ovary syndrome, including testosterone-glucuronide and 11α-hydroxyprogesterone, which may help diagnose the condition.

Three new finasteride solvates found, change forms under different drying conditions.

Some newly made compounds can block an enzyme linked to hair loss and prostate growth, with one in particular being very selective.

Three finasteride forms exist; "form X" doesn't.

Lecithin organogels could be good for applying drugs to the skin because they are stable, safe, and can improve drug absorption.

Low SHBG and high FAI, FT, and DHEAS levels are effective in identifying PCOS.

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.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Nested PCR can reliably identify fungal infections when traditional methods fail.