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Antiandrogen therapy helps treat genetic hair loss.

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

Certain metabolites are lower in women with PCOS and could be potential markers for the condition.

Human Schwann cells can be quickly made from hair follicle stem cells for nerve repair.

Hair loss in women is genetic, diagnosed by examination and biopsy, and treated with minoxidil, finasteride, or transplantation.

Women with polycystic ovary syndrome tend to have a longer anogenital distance.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

High MUC-18/MCAM levels in blood indicate a worse outlook for melanoma patients.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

CEC levels may be a useful marker for predicting prostate cancer progression.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

High levels of 3 alpha-diol glucuronide in the blood are a marker of increased androgen action in women with excessive hair growth of unknown cause.

Keratins help protect cells, aid in cancer diagnosis, and influence cancer behavior and treatment.

Researchers successfully isolated and identified key markers of stem cell-enriched human hair follicle bulge cells.

Keratin 15 is not a reliable sole marker for identifying epidermal stem cells because it's found in various cell types.

Premature hair graying may be a sign of increased risk for heart disease, indicating biological age is more important than actual age.

Men with thinner hair from genetic hair loss may be more likely to have an enlarged prostate.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

3α, 17β-androstanediol-glucuronide is not a useful marker for androgen excess but may help monitor certain treatments.

The research found genes that change during cashmere goat hair growth and could help determine the best time to harvest cashmere.

Behçet's Disease may be caused by genetic and environmental factors leading to abnormal immune responses, and stress management and new treatments could improve patient outcomes.

Keratin 18 helps diagnose and predict cancer progression and affects cancer growth and spread.

Thiopurines help treat IBD but require genetic testing to avoid side effects.

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.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Blood tests can help understand the genetic differences in people with alopecia areata, including how severe it is and if it's inherited.

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

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

No link found between specific genes and female pattern hair loss.