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Early recognition and management of gastrointestinal tuberculosis in lupus patients are crucial to prevent complications.

Increasing zinc intake improved skin and hair symptoms in a rare genetic disorder.

Birth control pills increase certain receptor activities in female gerbil prostate glands and can lead to prostate changes.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Albendazole treatment for echinococcosis can cause serious side effects and requires close monitoring.

Gender-affirming hormone therapy affects metabolism differently based on treatment type.

RXRα is crucial for proper immune response and links diet to immune function.

RNase L suppresses regeneration in mammals.

GERD symptoms are linked to acid exposure time and daytime sleepiness, influenced by ghrelin levels.

Immature blackbuck pancreas has underdeveloped goblet cells and similar Langerhans islets in both sexes.

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Pediatric patients with dystrophic epidermolysis bullosa face more hospital admissions, procedures, and complications than others.

Sub3 is essential for fungus adherence but not for skin invasion.

Injecting platelet-rich plasma into the muscle layer improves intestinal healing and reduces adhesions.

A new compound from Royoporus badius activates immune cells and induces inflammatory responses.

Different miRNAs in Rex rabbit skin affect cell processes and hair growth.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

Turning food waste into useful products is key for a sustainable economy.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

Androgen self-administration might be controlled by membrane receptors, not nuclear ones.

Calprotectin starves Pseudomonas aeruginosa of essential metals, affecting its growth and resistance.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Analyzing bear poop helps measure their stress without harming them.