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Obesity increases the risk of developing polycystic ovary syndrome, and weight loss can improve the condition.

Genetics and hormones play a role in male and female hair loss, but more research is needed to fully understand it.

The conclusion is that published guidelines are improving transgender medical care, but more research and education in transgender medicine are needed.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

The document concludes that while there are promising methods to control CRISPR/Cas9 gene editing, more research is needed to overcome challenges related to safety and effectiveness for clinical use.

Assessing newborn scalp hair can reveal important health information.

Lifestyle changes are the main treatment for PCOS, which is a complex condition requiring early management to reduce its health impacts.

Adrenal disorders can cause lasting brain and behavior issues in children.

Researchers created LabeledIn, a detailed list of drug uses, showing the importance of human input in making such lists.

The conclusion is that small hair follicles cause baldness in macaques, and treatments like antiandrogens and minoxidil can prevent hair loss and promote regrowth.

JAK inhibitors helped treat hair loss in two people with Down syndrome.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Loss of Fz6 disrupts hair follicle and associated structures' orientation.

Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.

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

Skin varies in thickness, color, and features due to complex genetic and cellular processes.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

Some diseases can improve the outcomes of other diseases, leading to new treatment possibilities.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Male pattern baldness may be caused by scalp pressure on hair follicles, which increases with age and leads to a cycle of hair loss. This process is not directly determined by genes.

Indian women with PCOS from Delhi and Srinagar show different symptoms, with Delhi women having higher obesity and blood sugar issues, and Srinagar women showing more hair growth and testosterone levels.

Lupus treatment requires a combination of drugs and therapies, with research needed for new options.

A rare fungal infection on a child's scalp was successfully treated with antifungal medication.

Finasteride side effects in young men may be linked to specific gene variations.

In Singapore, most skin reactions to drugs were in females and Chinese, often caused by painkillers, antibiotics, and some other drugs, with serious cases linked to genetics.

Some skin diseases and their treatments can negatively affect male fertility.

Lack of cystatin M/E causes thin hair and dry skin.

The document concludes that systemic autoimmune diseases are complex, incurable, and require ongoing treatment and research.