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A Japanese bone marrow transplant patient developed a rare skin cancer possibly linked to long-term use of the medication voriconazole.

Etanercept effectively treated a severe skin condition when other treatments failed.

Early and accurate diagnosis of primary vitreoretinal lymphoma is crucial to prevent serious complications.

VDR regulation varies by tissue and is crucial for its biological functions.

New genetic mutations linked to rare skin disorders were found in three newborns.

Vitamin D receptor helps control hair growth genes in skin cells.

The MtAnn3 gene affects root hair growth and is influenced by cytokinin.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

Natural α-hydroxyl acids cause skin exfoliation by activating TRPV3 channels.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

Aromatase gene variation may increase female hair loss risk.

A genetic change in the FGF5 gene affects hair growth in cashmere goats.

CRISPR/Cas systems show promise for cancer treatment by targeting miRNAs, but delivery and specificity challenges remain.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

Sphingosine 1-phosphate affects inflammation and gene expression in different aorta cells.

The improved genome of the African spiny mouse will help understand its tissue regeneration abilities.

Astressin-B can reverse and prevent hair loss in stressed mice.

A specific mutation in PA-PLA1α causes abnormal hair growth.

A genetic variant in the KRT25 gene causes tightly curled hair.

CaV1.2 helps activate hair follicle stem cells without calcium flux.

The treatment was not recommended due to limited effectiveness and significant side effects.

Upadacitinib improved both Crohn's ileitis and alopecia universalis in a patient.

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.