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A woman was diagnosed with a rare adrenal gland cancer that did not show usual hormone-related symptoms.

5-alpha reductase inhibitors may increase depression risk by 31%, but results vary based on comparison groups.

Diphencyprone (DPC) is an effective and safe long-term treatment for alopecia areata, especially with maintenance therapy.

iEdgePathDDA effectively finds new drug-disease links, outperforming other methods.

A new diagnostic model can help better diagnose and understand Alopecia Areata.

Rezpegaldesleukin shows promise for treating severe alopecia areata.

DHT enhances androgen receptor activity more than testosterone, and MAGE-11 influences this activity through specific interactions.

Ritlecitinib provides new treatment options for diverse alopecia areata patients.

Prostate cancer cells can make their own androgens to activate the androgen receptor, and treatments like abiraterone may increase this ability, suggesting new therapies should target the entire steroid-making pathway.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

CCCA is a scarring hair disorder mainly affecting people of African descent, needing better awareness and treatment.

Adipose-derived stem cells are promising for tissue and organ repair due to their easy access and versatility.

Researchers created immortal human skin cells with constant testosterone receptor activity to study hair loss and test treatments.

Trichoscopy effectively diagnoses allergic scalp contact dermatitis.

A new method helps detect androgen receptor movement in cells, aiding research on hair loss treatments.

Retinoic acid production and signaling in hair follicles are regulated by location and timing, affecting hair growth and cycling.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

The analysis shows the U.S. leads in tissue expansion research, mainly for breast reconstruction, with a slightly higher complication rate when using acellular dermal matrix.

A new gene causes hairlessness and skin cysts in rats.

We need better ways to test and understand SARMs to make safer and more effective treatments.

Dual TCR Treg cells are common in mouse tissues and vary by location.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

The model accurately detects alopecia areata with 84.3% accuracy.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.

Manipulating 5α-reductase type 2 can affect liver fat production and glucocorticoid effects.

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.