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Products should be called 'sperm-safe' only after thorough, well-designed tests.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Hair follicle hyperplasia is common in both benign and malignant skin lymphoproliferative disorders, with a proposed new term "pseudolymphomatous adnexitis."

Melatonin stimulates the skin components of ram's scrotum during their non-breeding season.

A woman's masculine symptoms were caused by an ovarian tumor, which improved after surgery.

Human hair varies widely and should be classified by curl type rather than race.

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

Deep learning helps detect skin conditions and is advancing dermatology diagnosis and treatment.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

The document discusses various nail and hair disorders and their treatments.

Mast cells play a significant role in hair loss conditions like male pattern hair loss and alopecia areata.

Ovarian steroid cell tumors should be considered in adults with hirsutism and high testosterone, with surgery as the main treatment.

Deep learning can accurately automate hair density measurement, with YOLOv4 performing best.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

A 69-year-old man with sinus infection and fainting spells was diagnosed with a rare kidney disease, treated with steroids and a specific drug, which improved his condition.

A patch with curcumin-zinc can improve hair growth and health by delivering beneficial particles to the skin, increasing hair follicles, and reversing effects of a hair loss hormone.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

Sox21 is crucial for tooth development and enamel formation by preventing cells from changing into a different type.

3D bioprinting in plastic surgery could lead to personalized grafts and fewer complications.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

Two-photon microscopy helps observe hair follicle stem cell behaviors in mice.

Photothermal hydrogels are promising for infection control and tissue repair, and combining them with other treatments could improve results and lower costs.

MSC-protein helps regenerate gum tissue and bone.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.

Nanomaterials in biomedicine can improve treatments but may have risks like toxicity, needing more safety research.

Long COVID causes a wide range of long-lasting symptoms that change over time and are hard to diagnose and treat.

Optical imaging and light therapy show promise for diagnosing and treating liver injury caused by surgery.

Research on the human skin microbiome has grown, focusing on skin health and diseases, with more studies needed on antibiotic resistance and AI applications.