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Activating CB1 can reduce keratin levels, potentially helping manage psoriasis and aid wound healing.

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A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

A new model helps study acne and test treatments.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

LTBP1 is a key regulator in diseases and a potential target for new treatments.

Stress hormone CRF causes hair loss and inhibits hair growth in human cells.

The hair defect is due to abnormal inner root sheath keratinization.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

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.

Forensic DNA phenotyping can help generate new leads in cold cases but faces accuracy, legal, and acceptance challenges.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

The young woman has a benign, hereditary skin condition with no signs of a more serious syndrome.

CCCA and lichen planopilaris have similar histological features, making them hard to distinguish.

Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.

A 12-year-old girl's hair loss was linked to a rare genetic condition called ALX4-related frontonasal dysplasia.

RNase L suppresses regeneration in mammals.

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

Raman spectroscopy can help identify cancerous skin tissue during surgery.

Certain blood markers can help predict and manage chemotherapy side effects in older cancer patients.

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CNGC14 is crucial for calcium entry needed for root hair growth in plants.

A young boy with a rare skin and nail condition improved significantly with simple topical treatments.

The LMNA mutation affects skin structure even in asymptomatic carriers.

Researchers identified promising inhibitors for the BRD4 protein, including finasteride and amentoflavone.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Higher levels of nidogen1 and type IV collagen are found in basal cell carcinoma compared to normal skin.