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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.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

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

Assessing newborn scalp hair can reveal important health information.

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

Toxic Epidermal Necrolysis is a rare, serious skin condition that can affect anyone, is more common in women, and may be linked to genetics, with a 20% mortality rate mainly due to sepsis.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

MC4R gene variants not linked to female hair loss.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Cicatricial alopecia, a permanent hair loss condition, is mainly caused by damage to specific hair follicle stem cells and abnormal immune responses, with gene regulator PPAR-y and lipid metabolism disorders playing significant roles.

Skin issues can indicate immune system problems.

Accurate diagnosis of progressive supranuclear palsy requires thorough neurological assessments and MRI.

Different fish use the same genes to regrow teeth.

Selective breeding can enhance immunity in dairy cattle.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Men are more likely to have severe COVID-19 cases and fatalities than women due to factors like lifestyle, aging, and biological differences.

Postpartum depression is linked to changes in brain chemicals, inflammation, stress, and certain genes, and can potentially be identified by markers like specific steroids, serotonin levels, and vitamin D levels.

The conclusion is that PCOS is caused by ovarian sensitivity to hormones and disrupted hormone control, possibly due to ovarian factors, and more research is needed.

Female Pattern Hair Loss affects women's self-esteem and needs more research for better treatment.

The document concludes that accurate diagnosis of different types of hair loss requires careful examination of hair and scalp tissue, considering both clinical and microscopic features.

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

The document concludes that accurate diagnosis is crucial for effectively treating common scalp disorders, which often have similar symptoms.

Different types of hair loss have unique features under a microscope, but a doctor's exam is important for accurate diagnosis.

The document suggests creating a validated score to diagnose Cushing's Syndrome and considers plasma steroid profiling as a simpler diagnostic method.

The document concludes that better treatments for CCCA are needed and more research is required to understand its causes related to hairstyling and genetics.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

The document concludes that dermal papilla cells are key for hair growth and could be used in new hair loss treatments.