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Scientists made new substances that can block an enzyme linked to prostate issues and hair loss, with potential for creating a new treatment.

Plasmalogens activate a channel in cells that may stimulate hair growth.

Removing β-catenin in certain stem cells causes hair whitening and pigmentation issues.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

MPA increases cancer spread by boosting Eph A2 activity.

The Journal of Cutaneous and Aesthetic Surgery is now included in PubMed.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

A man with Cronkhite-Canada syndrome improved significantly with immunosuppressive therapy.

CD200 is not a reliable marker for identifying stem cells in all skin types.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

CD2 might be a new treatment target for patchy alopecia areata.

Microparticles help caffeic acid stay longer in hair follicles for better treatment of folliculitis.

ETS2 drives cancer progression in squamous cell carcinoma and is linked to poor patient outcomes.

Energy healing treatment improved L-cysteine's stability, solubility, bioavailability, and shelf-life.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Kaposi's sarcoma lesions might originate from benign tissue changes.

The peptide GHK-Cu helps heal and remodel tissue, improves skin and hair health, and has potential for treating age-related inflammatory diseases.

The CORT, FGF5, and CD36 genes are crucial for the cold weather adaptation of Yanbian cattle.

XEDAR triggers a specific signaling pathway in cells.

Trichilemmal carcinoma shares genetic traits with other skin cancers, suggesting similar treatment options.

Trichilemmal carcinoma shares genetic traits with other skin cancers, suggesting similar treatment options.

SCD1 is crucial for skin health and overall energy balance.

Calcium hydroxylapatite can be successfully integrated into healing skin and stimulates collagen.

Mutations in specific genes cause certain congenital defects in dogs, aiding in understanding similar human diseases.

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

Women with non-classic congenital adrenal hyperplasia have higher risk for heart and metabolic problems.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.