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Characterization of Wild-Type Human Medium-Chain Acyl-CoA Dehydrogenase (MCAD) and Mutant Enzymes Present in MCAD-Deficient Patients by Two-Dimensional Gel Electrophoresis: Evidence for Posttranslational Modification of the Enzyme

机译：MCAD缺陷患者的野生型人脑酰基辅酶脱氢酶（MCAD）和突变酶的表征通过二维凝胶电泳：酶意外改性的证据

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P. Bross; T.G. Jensen; B.S. Andresen; M. Kjeldsen; A. Nandy; S. Kolvraa; S. Ghisla; I. Rasched; L. Bolund; N. Gregersen;
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1. Thermodynamics of ligand binding and catalysis in human liver medium-chain acyl-CoA dehydrogenase: Comparative studies involving normal and 3 '-dephosphorylated C-8-CoAs and wild-type and Asn191 -> Ala(N191A) mutant enzymes [J] . Peterson KL., Srivastava DK., Peterson KM. Biochemistry . 1998,第36期

机译：人肝中链酰基辅酶A脱氢酶中配体结合和催化的热力学：涉及正常和3'-去磷酸化的C-8-CoA与野生型和Asn191-> Ala（N191A）突变酶的比较研究
2. Neonatal screening for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in The Netherlands: the importance of enzyme analysis to ascertain true MCAD deficiency. [J] . Derks TG, Boer TS, van-Assen A, Journal of inherited metabolic disease . 2008,第1期

机译：荷兰新生儿中链酰基辅酶A脱氢酶（MCAD）缺乏症的筛查：酶分析对确定真正MCAD缺乏症的重要性。
3. Neonatal screening for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in The Netherlands: The importance of enzyme analysis to ascertain true MCAD deficiency [J] . T. G. J. Derks, T. S. Boer, A. van Assen, Journal of Inherited Metabolic Disease . 2008,第1期

机译：荷兰新生儿中链酰基辅酶A脱氢酶（MCAD）缺乏症的筛查：酶分析对确定真正的MCAD缺乏症的重要性
4. Structural characterization of human UDP-glucose dehydrogenase reveals novel insights into regulatory modes of the enzyme [D] . Hyde, Annastasia S. 2014

机译：人类UDP-葡萄糖脱氢酶的结构表征揭示了对该酶调节模式的新见解
5. Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Mutations Identified by MS/MS-Based Prospective Screening of Newborns Differ from Those Observed in Patients with Clinical Symptoms: Identification and Characterization of a New Prevalent Mutation That Results in Mild MCAD Deficiency [O] . Brage Storstein Andresen, Steve F. Dobrowolski, Linda OReilly, 2001

机译：中链酰基辅酶A脱氢酶（MCAD）突变通过基于MS / MS的新生儿前瞻性筛查与临床症状患者中观察到的新生儿不同而鉴定：新的普遍突变导致轻度MCAD缺乏症的鉴定和表征
6. Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms:identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency [O] . Andresen, B S, Dobrowolski, S F, O'Reilly, L, 2001

机译：通过基于MS / MS的新生儿前瞻性筛查确定的中链酰基辅酶A脱氢酶（MCAD）突变与临床症状患者中观察到的突变不同：鉴定和表征导致轻度MCAD缺乏的新的普遍突变
7. The Application of Polyacrylamide Gel Electrophoresis to the Characterization of Cholinesterase Enzymes Used in Detector Kits. [R] . goodman,alan mccormack,lawrence m. 1977

机译：聚丙烯酰胺凝胶电泳在检测试剂盒中胆碱酯酶酶表征中的应用。

Characterization of Wild-Type Human Medium-Chain Acyl-CoA Dehydrogenase (MCAD) and Mutant Enzymes Present in MCAD-Deficient Patients by Two-Dimensional Gel Electrophoresis: Evidence for Posttranslational Modification of the Enzyme

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