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The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.

FoxN1 gene is crucial for proper thymus structure and normal skin appearance.

An automated method accurately assesses melanoma risk using 3D body images to analyze skin traits.

FoxN1 gene is essential for proper thymus structure and preventing hair loss.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Patients with acute and subacute skin lupus respond faster to belimumab than those with chronic skin lupus.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

The type of PCOS a woman has doesn't strongly predict her skin or metabolic symptoms; obesity is a more important factor.

K16 can partially replace K14 but causes hair loss and skin issues.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

A mouse gene mutation increases the risk of skin cancer.

MPZL3 is crucial for seborrheic dermatitis development.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Shh and Dhh affect skin development and can cause tumors, while Ihh does not.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

Glucosylceramides are essential for healthy skin and proper wound healing.

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

Small molecule DMF improves psoriasis and multiple sclerosis, adult skin cells can be made to grow new hair, certain skin cells initiate hair growth, IL-17C controls gut health and can cause skin inflammation, and skin cells produce IL-17 that can lead to psoriasis.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

The fuzzy gene is crucial for controlling hair growth cycles.

A gene mutation in Lama3 is linked to a common type of hair loss.

The HR protein's role as a repressor is essential for controlling hair growth.

Lead and selenium levels don't cause premature graying.

Blocking SCD1 in the skin with XEN103 shrinks sebaceous glands in mice.

Blocking DGAT1 reduces oil gland size in mice and dogs, but only mice experience hair loss.

Fatty acid transport protein 4 is essential for skin and hair development.

Mice with human skin protein K8 had more skin problems and cancer.

Pangolins have lost some skin-related genes, but kept others, leading to their unique scales and skin features.

Tight junctions are key for skin protection and controlling what gets absorbed or passes through the skin.