Search

everythinglearnresearchcommunity

for

Search:↓

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

Cutaneous Lymphadenoma is a unique skin tumor with specific protein markers and common gene mutations that may cause continuous cell growth.

The document concludes that individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

The scalp fat tissue of men with hair loss shows changes in gene activity that may contribute to their condition.

The reconstructed skin model from hair follicles functions like human skin in processing chemicals and can be used to test ingredient safety.

Lgr5 is a marker for active, long-lasting stem cells in mouse hair follicles.

Human skin cells produce proenkephalin, which changes with environmental factors and skin diseases.

New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

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

Aging causes changes in scalp cells that can negatively affect hair health.

The conclusion is that grasping how cells determine their roles through evolution is key, with expected progress from new research models and genome editing.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

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.

Notch/CSL signaling controls hair follicle differentiation through Wnt5a and FoxN1.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

The circadian clock influences the behavior and regeneration of stem cells in the body.

Maintaining the right amount of retinoic acid is crucial for healthy hair and skin.

The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.

CD98hc's role in skin health decreases with age.

Finasteride treatment changes brain steroid levels and receptors, affecting brain function even after stopping treatment.

Treatment during development affects hormone balance and sexual behavior in male rats.

Common Black hair care products may affect hormone levels and potentially impact health, especially in reproductive and metabolic areas.

Mutations in certain receptors can cause diseases and offer new treatment options.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

High levels of male hormones in pregnant mice cause heart enlargement and poor heart function in their female babies.