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Zinc supplements improved symptoms in a Uyghur infant with a rare genetic disorder affecting zinc absorption.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

A woman's severe skin reaction was caused by an allergy to a skin treatment.

Safusidenib erbumine shows promise as a treatment for certain brain tumors, but mild side effects like hair loss need attention.

The new delivery system could improve pain and inflammation relief in gout.

Optimizing the structure of a specific compound greatly improved its effectiveness and precision for treating diabetic complications.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

miR-182 may help treat hallux valgus by targeting FGF9.

3D culture better preserves sweat gland cell identity than 2D culture.

Targeting ACE2 and TMPRSS2 may help prevent or treat COVID-19 in cancer patients.

The study created a mouse model to mimic degenerative diseases for testing tissue repair and new therapies.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Sodium valproate can cause serious high blood pressure in children.

SLHA can be hard to diagnose and needs teamwork between specialists.

Stilbamidine and hydroxystilbamidine inhibit enzyme release from lysosomes and have effects similar to cortisol and chloroquine.

Scientists made a sensor that can detect a specific type of RNA related to androgen receptors quickly and accurately.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

The document reviews 20 U.S. patents from July and August 2004 about new drug forms, cancer treatments, aroma chemicals, statin drugs, and various chemical production methods.

A woman had a rare skin condition with recurring painful nodules that heal in 6 weeks, often without needing treatment.

Lithium for bipolar disorder can cause skin problems like rashes, which go away when the medication is stopped.

The new composite material is safe and has anticoagulant properties.

Early diagnosis and management of congenital heart block in mothers with autoimmune conditions are crucial for improving neonatal outcomes.

KLHL24-mutant stem cells help understand skin and heart disease.

LHX2, with other markers, can identify hair placodes in rats.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

Nanocarriers with spironolactone and 2-deoxy-D-ribose may improve hair loss treatment by targeting hair follicles directly.

The study mapped genetic variations in sheep, linking them to traits like milk production and growth.

Low-penetration genes might help personalize colorectal cancer prevention.