安裝中文字典英文字典辭典工具!
安裝中文字典英文字典辭典工具!
|
- ATP1A1 Gene - GeneCards | AT1A1 Protein | AT1A1 Antibody
ATP1A1 (ATPase Na+ K+ Transporting Subunit Alpha 1) is a Protein Coding gene Diseases associated with ATP1A1 include Charcot-Marie-Tooth Disease, Axonal, Type 2Dd and Hypomagnesemia, Seizures, And Impaired Intellectual Development 2 Among its related pathways are Cardiac conduction and Infectious disease
- ATP1A1 gene: MedlinePlus Genetics
The ATP1A1 gene provides instructions for making one part (the alpha-1 subunit) of a protein pump known as a Na + K + ATPase This protein uses energy from a molecule called adenosine triphosphate (ATP) to transport charged atoms (ions) into and out of cells
- ATP1A1 ATPase Na+ K+ transporting subunit alpha 1 [Homo sapiens (human . . .
Homophilic ATP1A1 binding induces activin A secretion to promote EMT of tumor cells and myofibroblast activation
- ATPase, Na+ K+ TRANSPORTING, ALPHA-1 POLYPEPTIDE; ATP1A1 - OMIM
The ATP1A1 gene encodes the alpha-1 isoform of the Na (+),K (+)-ATPase (EC 3 6 1 9), an integral membrane protein responsible for establishing and maintaining the electrochemical gradients of Na and K ions across the plasma membrane
- ATP1A1 Gene: Function, Mutations, and Disease Associations
Learn about the ATP1A1 gene, its role in the sodium-potassium pump, common mutations, and associated diseases Explore research, testing, and resources
- ATP1A1 gene - MedlinePlus
The ATP1A1 gene provides instructions for making one part (the alpha-1 subunit) of a protein pump known as a Na+ K+ ATPase This protein uses energy from a molecule called adenosine triphosphate (ATP) to transport charged atoms (ions) into and out of cells
- Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2
In this way—by combining data from seven countries on four continents—we were able to define mutations in ATP1A1, which encodes the alpha1 subunit of the Na +,K + -ATPase, as a cause of autosomal-dominant CMT2
|
|
|