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The document concludes that pregnancy and cancer share immune evasion tactics, but more research is needed before using checkpoint blockade immunotherapy in pregnant cancer patients to avoid harm to the placenta.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Hormone imbalances can cause skin diseases, and understanding these links is important for diagnosis and treatment.

Hormones and genes affect hair growth and male baldness.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

Indian Hedgehog helps control skin cell growth and protects against aggressive skin cancer.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

Alopecia areata causes hair loss due to an immune attack on hair follicles, influenced by genetics and environment.

Hairless gene not strongly linked to baldness.

Tamoxifen caused hair loss in a 52-year-old woman.

SARS-CoV-2, the virus causing COVID-19, can affect all endocrine organs and systems, altering their function and potentially leading to disorders. Factors like diabetes and obesity increase infection risk and severity. Understanding these effects is key for effective treatment.

CBG may help with various medical conditions but needs more human research to confirm safety and effectiveness.

The conclusion is that a thorough approach is needed to diagnose and manage hyperandrogenism in teenage girls, recognizing its major psychological and health effects.

Hair and skin can regenerate without bulge stem cells due to other compensating cells.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

A gene mutation causes woolly hair in a Syrian patient.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

The study found that a specific signaling pathway helps skin wounds heal faster but may lead to larger scars.

Stem cells compete for space using cell adhesion, and mutations can affect their competitive success, with implications for tissue health and disease.

Understanding hair biology is key to developing better treatments for hair and scalp issues.

The PP2A-B55α protein is essential for brain and skin development in embryos.

Targeting immune tolerance issues in Alopecia Areata could restore hair growth and maintain remission.

Alcohol in teen years leads to more adult drinking, finasteride doesn't help.

New hair loss treatments may include topical medications, injections, and improved transplant methods.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Genetic factors affect hair loss, and molecular testing may help predict, diagnose, and treat it.