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1 McArdle disease and mitochondrial myopathy impair muscle
2 McArdle disease is a nonlysosomal glycogenosis that clas
3 McArdle rat hepatoma cells (McA-RH7777), which secrete V
4 fied the editing activity from extracts of a McArdle cell line overexpressing His6-hemagglutinin-tagg
5 secretion of apoB-containing lipoproteins by McArdle hepatoma cells may be coordinately linked throug
7 abdomyolysis in myophosphorylase deficiency (McArdle's disease [MD]) may lead patients to shun exerci
8 t patients with myophosphorylase deficiency (McArdle's disease) who cannot metabolize intramuscular g
10 in a model of VLDL metabolism, rat hepatoma McArdle cells, were either decreased by a mimetic of sup
13 on (CM)-retinyl esters (RE) by rat hepatoma (McArdle-RH7777) cells stably transfected with a rat CEL
16 tion, additional studies were carried out in McArdle RH-7777 rat hepatoma cells, in which the second
17 xpressed wild-type (WT) and variant PCSK9 in McArdle-7777 rat hepatoma cells and shown by confocal mi
19 bit elevated lactate and reduced uridine; in McArdle disease purine nucleotide metabolites, including
20 uoles and stress the importance of including McArdle disease in the differential diagnosis of axial m
23 This is a highly atypical presentation of McArdle disease with severe paraspinal wasting and weakn
25 ion of apoB100 across the ER, we transfected McArdle RH7777, HepG2, or Chinese hamster ovary cells wi
26 n, as determined by transiently transfecting McArdle-RH7777 cells with constructs of wild-type PEMT o
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