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Genetic testing for cancer risk can lead to early and life-saving treatments in people without symptoms.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

Hair loss on the lower legs is common in middle-aged men, usually harmless, and doesn't need treatment.

A rare case of Cushing syndrome was successfully treated with one-sided adrenal gland removal, suggesting personalized treatment is important.

The document concludes that understanding hair follicle histology and the hair cycle is crucial for diagnosing alopecia.

Keratin 17 is linked to various diseases, including cancer and skin conditions, and may be a target for diagnosis and treatment.

Behçet's Disease may be caused by genetic and environmental factors leading to abnormal immune responses, and stress management and new treatments could improve patient outcomes.

CD8+ T cells play a key role in graft-versus-host disease in certain mice models.

Lysophospholipids like LPA and S1P are important for hair growth, immune responses, and vascular development, and could be targeted for treating diseases.

Different types of skin fibroblasts have unique roles in skin health and disease.

Skin problems are very common in people with end-stage kidney disease.

Testing hair roots with a special dye is a simple, non-invasive way to check disease progress in pemphigus vulgaris patients.

Short telomeres contribute to aging and cancer, and while telomerase can delay aging, it may also promote cancer.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

Lichen planopilaris may be an autoimmune disease causing hair loss due to immune system issues in hair follicles.

A Doberman Pinscher had a rare form of autoimmune disease causing hair loss and other severe symptoms.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Fibroblast changes in systemic sclerosis may help understand disease severity and treatment.

Skin aging is a complex process influenced by various factors, leading to wrinkles and sagging, and should be considered a disease due to its health impacts.

The document concludes that understanding how hair follicles naturally die and regenerate is important for insights into organ development and could impact health and disease treatment.

No CD44 in alopecia areata, present in normal and androgenetic alopecia.

White-tailed deer can get a hair loss condition that might make them more vulnerable to environmental threats.

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.

Shrinking of oil glands in the skin is a key sign of hair loss linked to TNF inhibitor drugs and may improve if the treatment is stopped.

Reflectance confocal microscopy is a useful, non-invasive tool for diagnosing some skin diseases, with potential for future improvements.

The dog likely has a condition similar to Canine alopecia X.

Classifying hair diseases, like alopecia, is difficult and needs more research to understand their causes.

The document concludes that using the right diagnostic methods and careful sample handling is crucial for accurately diagnosing horse skin diseases.

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

Tigers had a skin condition causing hair loss and inflammation, but the cause is unknown and treatment didn't work.