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PRAME helps distinguish between benign and malignant skin cells in most cases.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Home-use treatment for severe alopecia areata is as effective as office-use but costs half as much.

VDAC2 promotes cell death in cashmere goat hair follicles through the P53 pathway.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

C4BPA protein may link acne severity and insulin resistance.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

Specific immune cells and pathways contribute to hair follicle inflammation and hair loss, suggesting potential treatments for lichen planopilaris.

Potential therapeutic targets for scarring hair loss are identified.

A new treatment using nanoparticles can effectively prevent and reduce hair loss caused by chemotherapy.

The arrector pili muscle attaches to the extracellular matrix using α5β1 integrin and connects muscle cells using α1β1 integrin.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

RAPK is a rare skin disorder with pigmented spots, mainly on hands and feet, starting in youth.

Alopecia is common in severe cases of autosomal recessive congenital ichthyosis.

CircAGK affects cell death in hair cells by controlling the miR-3180-5p/BAX pathway, which can lead to hair loss.

A protein called ectodysplasin-A2 increases a hair growth inhibitor in balding cells, which could be a target for hair loss treatment.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

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

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

KAP8.1 gene variations affect cashmere weight in Inner Mongolian goats.

Early genetic testing and zinc therapy are crucial for managing acrodermatitis enteropathica effectively.

A new type of pachyonychia congenita may exist, caused by a different keratin mutation.

DNCB is highly effective for treating alopecia areata with minimal long-term side effects.

Deucravacitinib helped a man regrow hair and improve psoriasis.

Tofacitinib effectively improved severe skin symptoms in a patient with Hypohidrotic Ectodermal Dysplasia.

A woman's cyclic Cushing syndrome was caused by a tumor in her adrenal gland that produced ACTH.

Fibrosing alopecia can be diagnosed without typical signs of lichen planopilaris.

Fatp4 is crucial for healthy skin development and function.