ライフサイエンスコーパス: GM2 activator protein

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1 eramide by HexB with the assistance of mouse GM2 activator protein.

2 d by mutations in the GM2A gene encoding the GM2 activator protein.

3 be regarded as a form (truncated version) of GM2 activator protein.

4 GM2 activator cDNA and GM2A cDNA, for human GM2 activator protein.

5 o degrade GM2 ganglioside in the presence of GM2 activator protein.

6 and intron 3 of the genomic DNA sequence of GM2 activator protein.

7 only beta-hexosaminidase A together with the GM2 activator protein can degrade the natural substrate,

8 lactosidase and beta-hexosaminidases, and of GM2-activator protein, cause infantile (with tetraparesi

9 GM2 activator protein (GM2-AP) belongs to a small group

10 GM2-activator protein (GM2-AP) is a lipid transfer prote

11 The GM2-activator protein (GM2-AP) is a small lysosomal lipi

12 ding proteins, and are most similar to human GM2-activator protein (GM2-AP).

13 Like GM2 activator protein, GM2A protein also specifically re

14 The GM2 activator protein (GM2AP) is an 18 kDa nonenzymatic

15 The GM2 activator protein (GM2AP) is an accessory protein re

16 The GM2 activator protein (GM2AP) is an accessory protein th

17 GM2-activator protein (GM2AP) is a lysosomal lipid trans

18 GM2 activator protein is a protein cofactor that has bee

19 GM2 activator protein is a protein cofactor which stimul

20 blished that the NeuAc recognition domain of GM2 activator protein is located within amino acids 1-10

21 GM2 ganglioside by beta-hexosamindase A, the GM2 activator protein must participate by forming a solu

22 aining 1-109 of the 160 amino acids of human GM2 activator protein, plus a tripeptide (VST) encoded b

23 The GM2 activator protein serves as an example of a lipid tr

24 understand the reason why, in the absence of GM2 activator protein, the GalNAc and the NeuAc in GM2 (

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