Immunologic distinction of human muscle adenylate deaminase from the isozyme(s) in human peripheral blood cells: Implications for myoadenylate deaminase deficiency
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Biochemistry,Biophysics
Reference23 articles.
1. Myoadenylate Deaminase Deficiency: A New Disease of Muscle
2. Abstr. IV Int. Congr. Neuromusc. Dis;Hogan,1978
3. Myoadenylate deaminase deficiency
4. 70 MYOADEHYIATE DEAMINASE DEFICIENCY
Cited by 17 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. A competitive allele-specific oligomers polymerase chain reaction assay for the cis double mutation in AMPD1 that is the major cause of myo-adenylate deaminase deficiency*, **;Molecular Diagnosis;1997-06
2. Immunolocalization of AMP-deaminase isozymes in human skeletal muscle and cultured muscle cells: concentration of isoform M at the neuromuscular junction.;Journal of Histochemistry & Cytochemistry;1994-07
3. Immunologic evidence for three isoforms of AMP deaminase (AMPD) in mature skeletal muscle;Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology;1993-04
4. Molecular basis of AMP deaminase deficiency in skeletal muscle.;Proceedings of the National Academy of Sciences;1992-07-15
5. Expression of different isoenzymes of adenylate deaminase in cultured human muscle cells. Relation to myoadenylate deaminase deficiency;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;1992-06
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