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Deleting the Far2 gene in mice causes sebaceous gland issues and patchy hair loss.

About half the patients treated with capecitabine and docetaxel developed severe hand-foot syndrome.

Patients with severe alopecia areata have higher levels of MIF, which decrease after successful treatment.

Loose Anagen Syndrome is more common in females and may be inherited, often confused with other hair disorders, and lacks evidence for biotin treatment effectiveness.

Bacteria in our hair can affect its health and growth, and studying these bacteria could help us understand hair diseases better.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

Injecting CHIR-99021 into goose embryos improves feather growth by changing gene activity and energy processes.

Researchers identified genes and proteins that may influence wool thickness in sheep.

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

We need better treatments for hair loss, and while test-tube methods are helpful, they can't fully replace animal tests for evaluating new hair growth treatments.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

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

The study concluded that changing the culture conditions can cause sika deer skin cells to switch from a flat to a 3D pattern, which is important for creating hair follicles.

Swiss Holstein cattle with curly, short hair carry genes from the Simmental breed.

Mutations in specific llama genes may affect fiber quality for textiles.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Older hair follicle stem cells have a reduced ability to renew themselves, leading to more hair loss.

Triptolide effectively and safely reduces actinic keratosis lesions in mice.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

Blood tests for tumor cells could improve prostate cancer diagnosis and treatment; hair loss severity linked to a gene affecting prostate conditions.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

Prostate cancer cells can make their own androgens to activate the androgen receptor, and treatments like abiraterone may increase this ability, suggesting new therapies should target the entire steroid-making pathway.

Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

Keratin mutations cause skin diseases and could lead to new treatments.