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Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

Computational techniques can improve drug development for treating certain conditions.

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

The topical inhibitor CUR61414 was not effective in treating basal cell carcinoma in human trials.

Systemic lupus erythematosus is an autoimmune disease causing diverse symptoms and major organ involvement.

Sweat gland stem cells help maintain glands, aid wound healing, and can regenerate skin structures.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

p63 controls Satb1 to help skin develop properly.

CLE14 peptide promotes root hair growth in Arabidopsis.

Ultrasound can safely produce beneficial carrageenan from red algae.

Most women with ankylosing spondylitis tested positive for HLA-B27, suggesting it's useful for diagnosis.

A boronic acid copolymer quickly forms cell clusters, useful for tissue and tumor modeling.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

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

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Early diagnosis and treatment of myositis in SLE patients lead to better outcomes.

High selenium diets in pigs cause health issues like weight loss, hair loss, and nerve damage.

Blocking SCD1 in the skin with XEN103 shrinks sebaceous glands in mice.

Suplatast tosilate successfully treated a woman's systemic sclerosis symptoms.

Early diagnosis and treatment of calcinosis cutis in lupus patients is crucial due to its rarity and potential complications.

Sweet syndrome can be the only sign of hairy cell leukemia relapse.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

A man with a rare lung-focused form of hypereosinophilic syndrome improved with steroid treatment.

Certain genetic variations in IGF2BP2 and IGFBP3 are linked to a higher risk of PCOS.

The composite sponge helps heal diabetic wounds by reducing inflammation and promoting new blood vessel growth.

A rare, non-cancerous ovarian tumor was successfully treated with surgery, improving the patient's symptoms.

Capillary microfluidic wearables are promising for non-invasive health monitoring through sweat and saliva.