MYH11 Gene - GeneCards | MYH11 Protein | MYH11 Antibody
2024年12月25日 · MYH11 (Myosin Heavy Chain 11) is a Protein Coding gene. Diseases associated with MYH11 include Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 2 …
Myosin-11 - Wikipedia
Myosin-11 is a smooth muscle myosin belonging to the myosin heavy chain family. Myosin-11 is a subunit of a hexameric protein that consists of two heavy chain subunits and two pairs of non …
MYH11 gene: MedlinePlus Genetics
The MYH11 gene provides instructions for making a protein called smooth muscle myosin heavy chain 11. It belongs to a group of proteins called myosins, which are involved in cell movement …
肌球蛋白重链 11（MYH11）基因 | MCE - MCE-生物活性分子大师
该基因编码的蛋白质是属于肌球蛋白重链家族的平滑肌肌球蛋白。 该基因产物是六聚体蛋白的一个亚基，由两个重链亚基和两对不同的轻链亚基组成。 它作为一种主要的收缩蛋白发挥作用， …
MYH11 myosin heavy chain 11 [ Homo sapiens (human) ]
2025年2月8日 · A stable-isotope labeling by amino acids in cell culture coupled with mass spectrometry-based proteomics identifies upregulation of myosin, heavy chain 11 (MYH11, …
弗吉尼亚大学发现全新Myh11-CreERT2-RAD小鼠可作为平滑肌细 …
Myh11-CreERT2-Off小鼠品系 被认为是SMC研究中的金标准，目前已广泛用于条件突变或谱系追踪实验。 这个品系在血管和内脏SMC中发生特异性重组，表明编码平滑肌肌球蛋白重链 …
MYH11 myosin heavy chain 11 [ (human)] - National Center for ...
MYH11 gene mutation is associated with family history of thoracic aortic aneurysm dissection. MYH11 mutations are rare and are identified in patients with thoracic aortic …
MYH11 myosin heavy chain 11 - NIH Genetic Testing Registry …
2015年11月12日 · Protein-elongating mutations in MYH11 are implicated in a dominantly inherited smooth muscle dysmotility syndrome with severe esophageal, gastric, and intestinal disease.
Myh11小鼠基因|Myh11基因功能|Myh11小鼠模型-RDDC官网
这个基因的人类同源物与动脉导管未闭和胸主动脉瘤有关。 与人类MYH11 (肌球蛋白重链11)正交。 [由基因组资源联盟，2022年4月提供] 该基因暂未发现相关的转录本和蛋白质序列信息。 该 …
MYH11人源基因|MYH11基因突变_致病性_靶点-RDDC官网
Protein-elongating mutations in MYH11 are implicated in a dominantly inherited smooth muscle dysmotility syndrome with severe esophageal, gastric, and intestinal disease. Variants in …