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Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

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

The document concludes that identifying the cause of amenorrhea is crucial for proper treatment.

The document concludes that lifestyle changes and medical treatments can significantly reduce symptoms of Hidradenitis Suppurativa, a chronic skin condition.

The document concludes that more research is needed to fully understand the causes of PCOS.

Hormone therapy may increase migraines in transgender women and decrease them in transgender men; more research is needed on migraine management in transgender individuals.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

The review concludes that more research is needed to better improve the health outcomes for people with Polycystic Ovarian Syndrome.

A man with testotoxicosis was fertile despite low FSH levels, suggesting high testosterone may allow sperm production without FSH.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Chemotherapy patients don't all lose their hair due to factors like hair growth rates, age, genetics, and the type of drugs used.

Early treatment of PCOS in teens is crucial to prevent long-term health issues like diabetes and heart disease.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

The conclusion is that more research is needed to understand if the drug finasteride causes Post-Finasteride Syndrome or if it's due to individual genetic makeup.

Women with PCOS are more than twice as likely to develop nonalcoholic fatty liver disease.

Lichen Planopilaris and Frontal Fibrosing Alopecia may help us understand hair follicle stem cell disorders and suggest new treatments.

Fat cells are important for healthy skin, hair growth, and healing, and changes in these cells can affect skin conditions and aging.

Hormone imbalances can cause specific skin changes, which may help in early detection of endocrine disorders.

Metformin taken during pregnancy increases SHBG in newborns but doesn't change other hormone levels in mothers or babies.

Androgens affect bone and fat cell development differently based on the cells' embryonic origin.

Vitamin D deficiency is common in women with PCOS and linked to some metabolic problems, but not the main cause of their metabolic issues.

The enzyme type 1 5α-reductase is more active in the hair follicle's lower part than in the skin's outer layer.

Chesapeake Bay retrievers' hair loss is likely a breed-specific, hereditary condition linked to abnormal steroid levels and distinct skin changes.

Chicken feather gene mutation helps understand human hair disorders.

Eyelashes are important for looks and eye protection, and more people are treating sparse eyelashes; more research is needed to understand eyelash biology and improve treatments.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

Hair loss in men treated best with early medication or transplant, new treatments researched.

Regular use of sunscreen may be linked to frontal fibrosing alopecia.