Matthew C. Micsenyi - Publications

2013 Neuroscience Yeshiva University, New York, NY, United States 

13 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2017 Sikora J, Dworski S, Jones EE, Kamani MA, Micsenyi MC, Sawada T, Le Faouder P, Bertrand-Michel J, Dupuy A, Dunn CK, Xuan IC, Casas J, Fabrias G, Hampson DR, Levade T, et al. Acid Ceramidase Deficiency in Mice Results in a Broad Range of Central Nervous System Abnormalities. The American Journal of Pathology. 187: 864-883. PMID 28342444 DOI: 10.1016/J.Ajpath.2016.12.005  0.593
2015 Dworski S, Jones EE, Sikora J, Micsenyi M, Sawada T, Le Faouder P, Bertrand-Michel J, Dupuy A, Kamani M, Dunn CK, Xuan I, Hampson DR, Carpentier S, Casas J, Fabrias G, et al. Spatial distribution of brain ceramides in an acid ceramidase deficient murine model: Subsequent histological manifestations and functional deficits Molecular Genetics and Metabolism. 114: S38-S39. DOI: 10.1016/J.Ymgme.2014.12.070  0.528
2014 Sawada T, Dworski S, Sikora J, Micsenyi M, Medin JA, Walkley SU, Hampson DR. Farber disease: characterization of behavior and brain pathology in a new murine model Molecular Genetics and Metabolism. 111: S93. DOI: 10.1016/J.Ymgme.2013.12.227  0.485
2013 Micsenyi MC, Sikora J, Stephney G, Dobrenis K, Walkley SU. Lysosomal membrane permeability stimulates protein aggregate formation in neurons of a lysosomal disease. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 10815-27. PMID 23804102 DOI: 10.1523/Jneurosci.0987-13.2013  0.575
2012 Micsenyi MC, Walkley SU. The Lysosomal System: Physiology and Pathology Lysosomal Storage Disorders: a Practical Guide. 1-12. DOI: 10.1002/9781118514672.ch1  0.485
2011 Strømme P, Dobrenis K, Sillitoe RV, Gulinello M, Ali NF, Davidson C, Micsenyi MC, Stephney G, Ellevog L, Klungland A, Walkley SU. X-linked Angelman-like syndrome caused by Slc9a6 knockout in mice exhibits evidence of endosomal-lysosomal dysfunction. Brain : a Journal of Neurology. 134: 3369-83. PMID 21964919 DOI: 10.1093/Brain/Awr250  0.726
2010 Walkley SU, Sikora J, Micsenyi M, Davidson C, Dobrenis K. Lysosomal compromise and brain dysfunction: examining the role of neuroaxonal dystrophy. Biochemical Society Transactions. 38: 1436-41. PMID 21118103 DOI: 10.1042/Bst0381436  0.716
2010 Curcio-Morelli C, Charles FA, Micsenyi MC, Cao Y, Venugopal B, Browning MF, Dobrenis K, Cotman SL, Walkley SU, Slaugenhaupt SA. Macroautophagy is defective in mucolipin-1-deficient mouse neurons. Neurobiology of Disease. 40: 370-7. PMID 20600908 DOI: 10.1016/J.Nbd.2010.06.010  0.571
2010 Curcio-Morelli C, Charles FA, Micsenyi MC, Cao Y, Venugopal B, Browning MF, Dobrenis K, Cotman SL, Walkley SU, Slaugenhaupt SA. 34. Macroautophagy is defective in mucolipin 1-deficient mouse neurons Molecular Genetics and Metabolism. 99: S15. DOI: 10.1016/J.Ymgme.2009.10.051  0.485
2009 Davidson CD, Ali NF, Micsenyi MC, Stephney G, Renault S, Dobrenis K, Ory DS, Vanier MT, Walkley SU. Chronic cyclodextrin treatment of murine Niemann-Pick C disease ameliorates neuronal cholesterol and glycosphingolipid storage and disease progression. Plos One. 4: e6951. PMID 19750228 DOI: 10.1371/Journal.Pone.0006951  0.696
2009 Micsenyi MC, Dobrenis K, Stephney G, Pickel J, Vanier MT, Slaugenhaupt SA, Walkley SU. Neuropathology of the Mcoln1(-/-) knockout mouse model of mucolipidosis type IV. Journal of Neuropathology and Experimental Neurology. 68: 125-35. PMID 19151629 DOI: 10.1097/Nen.0B013E3181942Cf0  0.594
2009 Walkley S, Walkley SU, Dobrenis K, Micsenyi M, Cristin D. 145. The greater lysosomal system and lysosomal disease Molecular Genetics and Metabolism. 96: S44. DOI: 10.1016/J.Ymgme.2008.11.146  0.485
2009 Micsenyi M, Dobrenis K, Stephney G, Walkley S. 91. P62/Sequestosome 1 accumulates in the CNS of lysosomal diseases Molecular Genetics and Metabolism. 96: S32. DOI: 10.1016/J.Ymgme.2008.11.092  0.485
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