AMP deaminase

Chức năng

Điều hòa

Bệnh lý

Tham khảo

1. ^ “Human PubMed Reference:”.
2. ^ Mahnke-Zizelman DK, Sabina RL (tháng 10 năm 1992). “Cloning of human AMP deaminase isoform E cDNAs. Evidence for a third AMPD gene exhibiting alternatively spliced 5'-exons”. J. Biol. Chem. 267 (29): 20866–77. PMID 1400401.
3. ^ ^{a b} Bản mẫu:EntrezGene
4. ^ Ouyang J, Parakhia RA, Ochs RS (tháng 1 năm 2011). “Metformin activates AMP kinase through inhibition of AMP deaminase”. J. Biol. Chem. 286 (1): 1–11. doi:10.1074/jbc.M110.121806. PMC 3012963. PMID 21059655.^{[nguồn y khoa không đáng tin cậy?]}
5. ^ Skladanowski, Andrzej (1979). “Potassium-dependent regulation by ATP and ADP of AMP-deaminase from beef heart”. International Journal of Biochemistry. 10 (2): 177–181. doi:10.1016/0020-711X(79)90114-9.

Đọc thêm

• Fishbein WN, Armbrustmacher VW, Griffin JL (1978). “Myoadenylate deaminase deficiency: a new disease of muscle”. Science. 200 (4341): 545–8. doi:10.1126/science.644316. PMID 644316.
• Sabina RL, Fishbein WN, Pezeshkpour G, và đồng nghiệp (1992). “Molecular analysis of the myoadenylate deaminase deficiencies”. Neurology. 42 (1): 170–9. doi:10.1212/wnl.42.1.170. PMID 1370861.
• Morisaki T, Gross M, Morisaki H, và đồng nghiệp (1992). “Molecular basis of AMP deaminase deficiency in skeletal muscle”. Proc. Natl. Acad. Sci. U.S.A. 89 (14): 6457–61. doi:10.1073/pnas.89.14.6457. PMC 49520. PMID 1631143.
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• van Laarhoven JP, de Gast GC, Spierenburg GT, de Bruyn CH (1983). “Enzymological studies in chronic lymphocytic leukemia”. Leuk. Res. 7 (2): 261–7. doi:10.1016/0145-2126(83)90016-4. PMID 6406772.
• Kelemen J, Rice DR, Bradley WG, và đồng nghiệp (1982). “Familial myoadenylate deaminase deficiency and exertional myalgia”. Neurology. 32 (8): 857–63. doi:10.1212/wnl.32.8.857. PMID 7201581.
• Baumeister FA, Gross M, Wagner DR, và đồng nghiệp (1993). “Myoadenylate deaminase deficiency with severe rhabdomyolysis”. Eur. J. Pediatr. 152 (6): 513–5. doi:10.1007/BF01955062. PMID 8335021.
• Morisaki T, Holmes EW (1993). “Functionally distinct elements are required for expression of the AMPD1 gene in myocytes”. Mol. Cell. Biol. 13 (9): 5854–60. doi:10.1128/MCB.13.9.5854. PMC 360332. PMID 8355716.
• Bruno C, Minetti C, Shanske S, và đồng nghiệp (1998). “Combined defects of muscle phosphofructokinase and AMP deaminase in a child with myoglobinuria”. Neurology. 50 (1): 296–8. doi:10.1212/wnl.50.1.296. PMID 9443500.
• Hisatome I, Morisaki T, Kamma H, và đồng nghiệp (1998). “Control of AMP deaminase 1 binding to myosin heavy chain”. Am. J. Physiol. 275 (3 Pt 1): C870–81. doi:10.1152/ajpcell.1998.275.3.C870. PMID 9730972.
• Sims B, Powers RE, Sabina RL, Theibert AB (1999). “Elevated adenosine monophosphate deaminase activity in Alzheimer's disease brain”. Neurobiol. Aging. 19 (5): 385–91. doi:10.1016/S0197-4580(98)00083-9. PMID 9880040.
• Loh E, Rebbeck TR, Mahoney PD, và đồng nghiệp (1999). “Common variant in AMPD1 gene predicts improved clinical outcome in patients with heart failure”. Circulation. 99 (11): 1422–5. doi:10.1161/01.cir.99.11.1422. PMID 10086964.
• Abe M, Higuchi I, Morisaki H, và đồng nghiệp (2000). “Myoadenylate deaminase deficiency with progressive muscle weakness and atrophy caused by new missense mutations in AMPD1 gene: case report in a Japanese patient”. Neuromuscul. Disord. 10 (7): 472–7. doi:10.1016/S0960-8966(00)00127-9. PMID 10996775.
• Morisaki H, Higuchi I, Abe M, và đồng nghiệp (2001). “First missense mutations (R388W and R425H) of AMPD1 accompanied with myopathy found in a Japanese patient”. Hum. Mutat. 16 (6): 467–72. doi:10.1002/1098-1004(200012)16:6<467::AID-HUMU3>3.0.CO;2-V. PMID 11102975.
• Gross M, Rötzer E, Kölle P, và đồng nghiệp (2002). “A G468-T AMPD1 mutant allele contributes to the high incidence of myoadenylate deaminase deficiency in the Caucasian population”. Neuromuscul. Disord. 12 (6): 558–65. doi:10.1016/S0960-8966(02)00008-1. PMID 12117480.
• Mahnke-Zizelman DK, Sabina RL (2003). “N-terminal sequence and distal histidine residues are responsible for pH-regulated cytoplasmic membrane binding of human AMP deaminase isoform E.”. J. Biol. Chem. 277 (45): 42654–62. doi:10.1074/jbc.M203473200. PMID 12213808.

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