Citations for
1MLYCD
A novel frameshift mutation of malonyl-CoA decarboxylase deficiency: clinical signs and therapy response of a late-diagnosed case.
Ersoy M, Akyol MB, Ceylaner S, Çakır Biçer N.
Clin Case Rep. Jun 28;5(8):1284-1288. doi: 10.1002/ccr3.1013. eCollection 2017 Aug. 2017
2MLYCD
A new case of malonyl-CoA decarboxylase deficiency with mild clinical features.
Liu H, Tan D, Han L, Ye J, Qiu W, Gu X, Zhang H.
Am J Med Genet A. May;170A(5):1347-51. doi: 10.1002/ajmg.a.37590. Epub 2016 Feb 9 2016
3MLYCD
Identification of the active site of human mitochondrial malonyl-coenzyme a decarboxylase: A combined computational study
Ling B, Liu Y, Li X, Wang Z, Bi S
Proteins Jun;84(6):792-802. doi: 10.1002/prot.25029. Epub 2016 Mar 25 2016
4MLYCD
Malonyl-CoA decarboxylase deficiency: long-term follow-up of a patient new clinical features and novel mutations.
Polinati PP, Valanne L, Tyni T.
Brain Dev. Jan;37(1):107-13. doi: 10.1016/j.braindev.2014.02.001. Epub 2014 Mar 7 2015
5MLYCD, SIRT4
SIRT4 coordinates the balance between lipid synthesis and catabolism by repressing malonyl CoA decarboxylase.
Laurent G, German NJ, Saha AK, de Boer VC, Davies M, Koves TR, Dephoure N, Fischer F, Boanca G, Vaitheesvaran B, Lovitch SB, Sharpe AH, Kurland IJ, Steegborn C, Gygi SP, Muoio DM, Ruderman NB, Haigis MC.
Mol Cell 50(5):686-98. doi: 10.1016/j.molcel.2013.05.012. 2013
6MLYCD
Malonyl coenzyme A decarboxylase deficiency: early dietary restriction and time course of cardiomyopathy.
Prada CE, Jefferies JL, Grenier MA, Huth CM, Page KI, Spicer RL, Towbin JA, Leslie ND.
Pediatrics 130(2):e456-60. doi: 10.1542/peds.2011-2927. Epub 2012 Jul 9. 2012
7MLYCD, STARD4
The mammalian START domain protein family in lipid transport in health and disease.
Clark BJ.
J Endocrinol 212(3):257-75. doi: 10.1530/JOE-11-0313. Epub 2011 Sep 30. Review. 2012
8MLYCD
Fatty acid oxidation and malonyl-CoA decarboxylase in the vascular remodeling of pulmonary hypertension.
Sutendra G, Bonnet S, Rochefort G, Haromy A, Folmes KD, Lopaschuk GD, Dyck JR, Michelakis ED.
Sci Transl Med 2(44):44ra58. doi: 10.1126/scitranslmed.3001327. 2010
9ACACA, MLYCD, PRKAB1
Myocardial hypertrophy and the maturation of fatty acid oxidation in the newborn human heart.
Yatscoff MA, Jaswal JS, Grant MR, Greenwood R, Lukat T, Beker DL, Rebeyka IM, Lopaschuk GD.
Pediatr Res 64(6):643-7. doi: 10.1203/PDR.0b013e318184d281. 2008
10MLYCD
Malonyl CoenzymeA decarboxylase regulates lipid and glucose metabolism in human skeletal muscle.
Bouzakri K, Austin R, Rune A, Lassman ME, Garcia-Roves PM, Berger JP, Krook A, Chibalin AV, Zhang BB, Zierath JR.
Diabetes 57(6):1508-16. doi: 10.2337/db07-0583. Epub 2008 Feb 26. 2008
11MLYCD
Clinical, enzymatic and molecular characterization of nine new patients with malonyl-coenzyme A decarboxylase deficiency.
Salomons GS, Jakobs C, Pope LL, Errami A, Potter M, Nowaczyk M, Olpin S, Manning N, Raiman JA, Slade T, Champion MP, Peck D, Gavrilov D, Hillman R, Hoganson GE, Donaldson K, Shield JP, Ketteridge D, Wasserstein M, Gibson KM.
J Inherit Metab Dis 30(1):23-8. Epub 2006 Dec 20. 2007
12MLYCD
Malonyl-CoA decarboxylase is present in the cytosolic, mitochondrial and peroxisomal compartments of rat hepatocytes.
Joly E, Bendayan M, Roduit R, Saha AK, Ruderman NB, Prentki M.
FEBS Lett 579(29):6581-6. Epub 2005 Nov 9. 2005
13MLYCD
Expression, purification, and characterization of human malonyl-CoA decarboxylase.
Zhou D, Yuen P, Chu D, Thon V, McConnell S, Brown S, Tsang A, Pena M, Russell A, Cheng JF, Nadzan AM, Barbosa MS, Dyck JR, Lopaschuk GD, Yang G.
Protein Expr Purif 34(2):261-9. 2004
14MLYCD
MLYCD mutation analysis: evidence for protein mistargeting as a cause of MLYCD deficiency.
Wightman PJ, Santer R, Ribes A, Dougherty F, McGill N, Thorburn DR, FitzPatrick DR.
Hum Mutat 22(4):288-300. 2003
15MLYCD
MCD encodes peroxisomal and cytoplasmic forms of malonyl-CoA decarboxylase and is mutated in malonyl-CoA decarboxylase deficiency.
Sacksteder KA, Morrell JC, Wanders RJ, Matalon R, Gould SJ.
J Biol Chem 274(35):24461-8. 1999
16MLYCD
The molecular basis of malonyl-CoA decarboxylase deficiency.
FitzPatrick DR, Hill A, Tolmie JL, Thorburn DR, Christodoulou J.
Am J Hum Genet 65(2):318-26. 1999
17MLYCD
Cloning and mutational analysis of human malonyl-coenzyme A decarboxylase.
Gao J, Waber L, Bennett MJ, Gibson KM, Cohen JC.
J Lipid Res 40(1):178-82. 1999
18MLYCD
A new case of malonyl coenzyme A decarboxylase deficiency presenting with cardiomyopathy.
Yano S, Sweetman L, Thorburn DR, Mofidi S, Williams JC.
Eur J Pediatr 156(5):382-3. 1997
19MLYCD
Malonyl coenzyme A decarboxylase deficiency.
Brown GK, Scholem RD, Bankier A, Danks DM.
J Inherit Metab Dis 7(1):21-6. 1984