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Topical latanoprost and bimatoprost ophthalmic solutions don't help eyelash growth in patients with alopecia areata.

Correct diagnosis is crucial for treating overlapping conditions like NMOSD and SLE effectively.

Enhanced stem cells from the placenta can help treat Graves' eye disease by stopping fat cell growth.

LHX2 is crucial for development, tissue repair, and preventing diseases.

Decreased CD200 in hair follicles may cause immune issues in some alopecia areata cases.

Skin changes like hair loss, white patches, and nail changes are common in children after bone marrow transplants, often linked to chronic rejection.

A kidney transplant patient developed leprosy, likely due to immunosuppression and genetic factors, and improved with treatment.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

Recognizing and treating oral lichen sclerosus is important, but treatment guidelines are lacking.

Biotin supplements improved skin and hair problems in a girl with biotinidase deficiency.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Deleting Rac1 in the skin depletes stem cells and damages hair follicles.

SLE and DM can coexist but are rare and need careful evaluation.

SPRY1 deficiency in skin cells causes stem cells to move to the skin surface, leading to increased pigmentation.

Alpha 6 + /MHCI - cells have stem cell traits and are similar to mouse hair follicle stem cells.

Visual field defects in lupus nephritis can be caused by hypertensive retinopathy, not glaucoma or medication toxicity.

About 8% of people with systemic lupus erythematosus have chronic scarring alopecia, with certain symptoms and positive antibodies increasing the risk, while immunosuppressants may lower it.

Mice with human fetal thymic tissue and stem cells developed symptoms similar to chronic graft-versus-host disease.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

LC-OCT helps accurately diagnose different types of infant hair loss without invasive methods.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

The protein aPKCλ is crucial for keeping hair follicle stem cells inactive and for hair growth and regeneration.

Deleting the BRD4 protein in certain skin cells causes hair loss and skin inflammation.

ILC1-like cells can cause alopecia areata by themselves.

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

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

A woman's sudden hair loss three years after a bone marrow transplant was a sign of chronic graft-versus-host disease but improved with treatment.

BST2 is a key marker for hair loss disease alopecia areata.

Hair follicle stem cell transplants can reverse liver cirrhosis by blocking harmful cell activation.