Research indicates that microbes and their metabolites are essential for regulating human metabolism and immunity [2], as they can produce vital vitamins and gene products [3] while also shielding the host from pathogenic invasions [4]. Therefore, maintaining a healthy balance of the microbiome can...
Ensembl Gene ID ENSG00000136110.13 Ensembl mRNA ID CNMD-201 包装清单: 产品编号 产品名称 包装 QH07817S Human CNMD qPCR Primer Pair 1nmol each — 说明书 1份 保存条件: -20℃保存。建议复溶后进行适当分装,避免反复冻融。 注意事项: PCR扩增产物的长度可能会因基因转录后存在多种剪接形式而有所差异。
The future is evolving toward a major involvement of the pharmaceutical industry with new drugs and gene-delivered therapy, the use of biomarkers and robotics as well as of artificial intelligence, both for interpreting morphology, DNA, and imaging diagnostic, and such developments w...
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An exciting paper on gene therapy for one of the limb girdle muscular dystrophies raises the prospect of meaningful treatment for these disorders in the relatively near future. Similarly, treatments of neuromuscular junction disorders are discussed as are treatments for inflammatory myopathies. There ...
novel mutation of CAPN3More than 300 mutations were identified in Calpainopathy (CAPN3) gene in limb-girdle muscular dystrophy type 2A (LGMD2A) patients. LGMD2A type is also known as Calpainopathy, which is characterized by selective atrophy and weakness of proximal limb muscles. We report...
Congenital myasthenic syndromes are clinically and genetically heterogeneous disorders characterized by a neuromuscular transmission defect. Mutations in novel genes have been described in recent years. Among these, MUSK gene mutations are extremely rare, with onl...
Although the cloning of the dystrophin gene has led to major advances in the knowledge of the genetic, molecular basis of Duchenne Muscular Dystrophy (DMD), Becker Muscular Dystrophy (BMD), and other muscular dystrophies, with mutations of genes encoding the dystrophin-associated glycoprotein complex...