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Hispanic patients in the USA have lower survival rates for melanoma compared to non-Hispanic Whites.

Skin side effects from melanoma immunotherapy are common and may indicate better survival.

Hedgehog pathway inhibitors could be effective in treating melanoma.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

Targeting MIG and MCP-1 may help treat inflammation in alopecia areata.

A new method can detect mutations in mice by observing changes in hair follicle cells.

Researchers discovered potential origins and new treatments for skin cancer, including biomarkers for melanoma and therapies that reduce tumor growth.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

Topical melatonin may reduce skin aging by inhibiting certain cellular pathways.

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

Low-penetration genes might help personalize colorectal cancer prevention.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

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

A new gene mutation causes insulin resistance in a girl and her mother.

RAR-gamma 1 is important for normal skin maintenance and differentiation.

The new assay can track and measure melanosome transfer between skin cells, confirming filopodia's role in this process.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

The FTO gene hinders stem cells in hair follicles from becoming pigment cells.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Immune cells boost stem cell activity in hairy moles, causing more hair growth.

Genetic variations affecting skin structure play a key role in severe acne.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

Alopecia areata is linked to immune system differences, with specific biomarkers like CXCL9 and CXCL10 being key for diagnosis and potential treatment targets.

Synthetic hormone treatment reduces melanin and hair growth in rats.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Glucocorticoid receptors help regulate genes important for skin health and hair growth.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

Mouse melanocyte structure and function are influenced by genetics, hormones, and environmental factors.