CSPD, carbamyl phosphate synthetase deficiency; HHH, hyperornithinemia hyperammonemia homocitrullinuria syndrome; IVA, isovalemic acidemia; LCHADD, long chain 3-chydroxy-acyl-CoA dehydrogenase ...

Researchers studying a protein linked to a rare, severe disease have made a discovery that sheds light on how cells meet ...

Fat Transport Deficiency Unveiled as Key Factor in Rare Childhood Metabolic CrisesResearchers studying a protein linked to a ...

The Next Chapterstar Cheyenne Floyd’s oldest daughter, Ryder Wharton,is facing new health challenges after her recent EKGs. The seven-year-old was diagnosed with very long-chain acyl-CoA dehydrogenase ...

State Key Laboratory of Physical Chemistry of Solid Surfaces, Key Laboratory of Chemical Biology of Fujian Province, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, ...

In the latest study, published today in the Journal of Cell Biology, the researchers demonstrate that TANGO2 directly binds to a key fat molecule called acyl-CoA, transporting them like a shuttle ...

National Engineering Research Center for Carbohydrate Synthesis, Jiangxi Province Key Laboratory of Natural and Biomimetic Drugs Research, College of Chemistry and Materials, Jiangxi Normal University ...

研究一种与一种罕见但严重疾病有关的蛋白质的研究人员有了一项发现，揭示了细胞在代谢危机期间如何满足它们的能量需求。这一发现可能会导致新的治疗方法，并为其他涉及脂肪代谢受损的疾病的研究开辟新的途径。该研究结果与国际罕见病日（2月28日）同时发表在《Journal of Cell Biology》上。