| Year |
Citation |
Score |
| 2020 |
Viana GM, Gonzalez EA, Alvarez MMP, Cavalheiro RP, do Nascimento CC, Baldo G, D'Almeida V, de Lima MA, Pshezhetsky AV, Nader HB. Cathepsin B-associated Activation of Amyloidogenic Pathway in Murine Mucopolysaccharidosis Type I Brain Cortex. International Journal of Molecular Sciences. 21. PMID 32093427 DOI: 10.3390/Ijms21041459 |
0.375 |
|
| 2020 |
Viana GM, Priestman DA, Platt FM, Khan S, Tomatsu S, Pshezhetsky AV. Brain Pathology in Mucopolysaccharidoses (MPS) Patients with Neurological Forms. Journal of Clinical Medicine. 9. PMID 32024172 DOI: 10.3390/Jcm9020396 |
0.323 |
|
| 2020 |
Heon-Roberts R, Nguyen ALA, Pshezhetsky AV. Molecular Bases of Neurodegeneration and Cognitive Decline, the Major Burden of Sanfilippo Disease. Journal of Clinical Medicine. 9. PMID 32012694 DOI: 10.3390/Jcm9020344 |
0.331 |
|
| 2019 |
Nagel L, Oliveira R, Pshezhetsky AV, Morales CR. HGSNAT enzyme deficiency results in accumulation of heparan sulfate in podocytes and basement membranes. Histology and Histopathology. 18131. PMID 31157913 DOI: 10.14670/Hh-18-131 |
0.379 |
|
| 2018 |
Wen XY, Tarailo-Graovac M, Brand-Arzamendi K, Willems A, Rakic B, Huijben K, Da Silva A, Pan X, El-Rass S, Ng R, Selby K, Philip AM, Yun J, Ye XC, Ross CJ, ... ... Pshezhetsky AV, et al. Sialic acid catabolism by N-acetylneuraminate pyruvate lyase is essential for muscle function. Jci Insight. 3. PMID 30568043 DOI: 10.1172/Jci.Insight.122373 |
0.342 |
|
| 2018 |
Oliveira R, Hermo L, Pshezhetsky AV, Morales CR. Presence of aberrant epididymal tubules revealing undifferentiated epithelial cells and absence of spermatozoa in a combined neuraminidase-3 and -4 deficient adult mouse model. Plos One. 13: e0206173. PMID 30359429 DOI: 10.1371/Journal.Pone.0206173 |
0.336 |
|
| 2018 |
Bigger BW, Begley DJ, Virgintino D, Pshezhetsky AV. Anatomical changes and pathophysiology of the brain in mucopolysaccharidosis disorders. Molecular Genetics and Metabolism. PMID 30145178 DOI: 10.1016/J.Ymgme.2018.08.003 |
0.319 |
|
| 2018 |
Pshezhetsky AV, Ashmarina M. Keeping it trim: roles of neuraminidases in CNS function. Glycoconjugate Journal. PMID 30088207 DOI: 10.1007/S10719-018-9837-4 |
0.342 |
|
| 2018 |
Tordo J, O'Leary C, Antunes ASLM, Palomar N, Aldrin-Kirk P, Basche M, Bennett A, D'Souza Z, Gleitz H, Godwin A, Holley RJ, Parker H, Liao AY, Rouse P, Youshani AS, ... ... Pshezhetsky A, et al. A novel adeno-associated virus capsid with enhanced neurotropism corrects a lysosomal transmembrane enzyme deficiency. Brain : a Journal of Neurology. PMID 29788236 DOI: 10.1093/Brain/Awy126 |
0.344 |
|
| 2018 |
Pshezhetsky AV, Martins C, Ashmarina M. Sanfilippo type C disease: pathogenic mechanism and potential therapeutic applications Expert Opinion On Orphan Drugs. 6: 635-646. DOI: 10.1080/21678707.2018.1534585 |
0.41 |
|
| 2017 |
Pan X, De Aragão CBP, Velasco-Martin JP, Priestman DA, Wu HY, Takahashi K, Yamaguchi K, Sturiale L, Garozzo D, Platt FM, Lamarche-Vane N, Morales CR, Miyagi T, Pshezhetsky AV. Neuraminidases 3 and 4 regulate neuronal function by catabolizing brain gangliosides. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. PMID 28442549 DOI: 10.1096/Fj.201601299R |
0.324 |
|
| 2017 |
Martins C, Brunel-Guitton C, Lortie A, Gauvin F, Morales CR, Mitchell GA, Pshezhetsky AV. Atypical juvenile presentation of GM2 gangliosidosis AB in a patient compound-heterozygote for c.259G > T and c.164C > T mutations in the GM2A gene. Molecular Genetics and Metabolism Reports. 11: 24-29. PMID 28417072 DOI: 10.1016/J.Ymgmr.2017.01.017 |
0.384 |
|
| 2017 |
Pan X, Wang Y, Lübke T, Hinek A, Pshezhetsky AV. Mice, double deficient in lysosomal serine carboxypeptidases Scpep1 and Cathepsin A develop the hyperproliferative vesicular corneal dystrophy and hypertrophic skin thickenings. Plos One. 12: e0172854. PMID 28234994 DOI: 10.1371/Journal.Pone.0172854 |
0.316 |
|
| 2017 |
Martins C, Medeiros PFd, Leistner-Segal S, Elcioglu N, Behnam M, Lacerda L, Lefèbvre J, Giugliani R, Pshezhetsky AV. Mutation spectrum and haplotype study of mucopolysaccharidosis type IIIC patients reveal possible migration events and founder effects of HGSNAT mutations Molecular Genetics and Metabolism. 120. DOI: 10.1016/J.Ymgme.2016.11.227 |
0.334 |
|
| 2015 |
Katorcha E, Klimova N, Makarava N, Savtchenko R, Pan X, Annunziata I, Takahashi K, Miyagi T, Pshezhetsky AV, d'Azzo A, Baskakov IV. Loss of Cellular Sialidases Does Not Affect the Sialylation Status of the Prion Protein but Increases the Amounts of Its Proteolytic Fragment C1. Plos One. 10: e0143218. PMID 26569607 DOI: 10.1371/Journal.Pone.0143218 |
0.355 |
|
| 2015 |
Pshezhetsky AV. Lysosomal storage of heparan sulfate causes mitochondrial defects; altered autophagy and neuronal death in the mouse model of mucopolysaccharidosis III type C. Autophagy. 0. PMID 25998837 DOI: 10.1080/15548627.2015.1046671 |
0.329 |
|
| 2015 |
Martins C, H?lková H, Dridi L, Dormoy-Raclet V, Grigoryeva L, Choi Y, Langford-Smith A, Wilkinson FL, Ohmi K, DiCristo G, Hamel E, Ausseil J, Cheillan D, Moreau A, Svobodová E, ... ... Pshezhetsky AV, et al. Neuroinflammation, mitochondrial defects and neurodegeneration in mucopolysaccharidosis III type C mouse model. Brain : a Journal of Neurology. 138: 336-55. PMID 25567323 DOI: 10.1093/Brain/Awu355 |
0.369 |
|
| 2014 |
Morales CR, Grigoryeva LS, Pan X, Bruno L, Hickson G, Ngo MH, McMaster CR, Samuels ME, Pshezhetsky AV. Mitochondrial damage and cholesterol storage in human hepatocellular carcinoma cells with silencing of UBIAD1 gene expression. Molecular Genetics and Metabolism Reports. 1: 407-411. PMID 27896114 DOI: 10.1016/J.Ymgmr.2014.09.001 |
0.312 |
|
| 2014 |
Matos L, Canals I, Dridi L, Choi Y, Prata MJ, Jordan P, Desviat LR, Pérez B, Pshezhetsky AV, Grinberg D, Alves S, Vilageliu L. Therapeutic strategies based on modified U1 snRNAs and chaperones for Sanfilippo C splicing mutations. Orphanet Journal of Rare Diseases. 9: 180. PMID 25491247 DOI: 10.1186/S13023-014-0180-Y |
0.342 |
|
| 2014 |
Hamdan FF, Srour M, Capo-Chichi JM, Daoud H, Nassif C, Patry L, Massicotte C, Ambalavanan A, Spiegelman D, Diallo O, Henrion E, Dionne-Laporte A, Fougerat A, Pshezhetsky AV, Venkateswaran S, et al. De novo mutations in moderate or severe intellectual disability. Plos Genetics. 10: e1004772. PMID 25356899 DOI: 10.1371/Journal.Pgen.1004772 |
0.361 |
|
| 2014 |
Smutova V, Albohy A, Pan X, Korchagina E, Miyagi T, Bovin N, Cairo CW, Pshezhetsky AV. Structural basis for substrate specificity of mammalian neuraminidases. Plos One. 9: e106320. PMID 25222608 DOI: 10.1371/Journal.Pone.0106320 |
0.362 |
|
| 2014 |
Pan X, Grigoryeva L, Seyrantepe V, Peng J, Kollmann K, Tremblay J, Lavoie JL, Hinek A, Lübke T, Pshezhetsky AV. Serine carboxypeptidase SCPEP1 and Cathepsin A play complementary roles in regulation of vasoconstriction via inactivation of endothelin-1. Plos Genetics. 10: e1004146. PMID 24586188 DOI: 10.1371/Journal.Pgen.1004146 |
0.303 |
|
| 2013 |
Albohy A, Zhang Y, Smutova V, Pshezhetsky AV, Cairo CW. Identification of Selective Nanomolar Inhibitors of the Human Neuraminidase, NEU4. Acs Medicinal Chemistry Letters. 4: 532-7. PMID 24900705 DOI: 10.1021/Ml400080T |
0.307 |
|
| 2013 |
Pshezhetsky AV, Ashmarina LI. Desialylation of surface receptors as a new dimension in cell signaling Biochemistry (Moscow). 78: 736-745. PMID 24010837 DOI: 10.1134/S0006297913070067 |
0.32 |
|
| 2013 |
Zhang Y, Albohy A, Zou Y, Smutova V, Pshezhetsky AV, Cairo CW. Identification of selective inhibitors for human neuraminidase isoenzymes using C4,C7-modified 2-deoxy-2,3-didehydro-N-acetylneuraminic acid (DANA) analogues. Journal of Medicinal Chemistry. 56: 2948-58. PMID 23530623 DOI: 10.1021/Jm301892F |
0.303 |
|
| 2013 |
Dridi L, Seyrantepe V, Fougerat A, Pan X, Bonneil E, Thibault P, Moreau A, Mitchell GA, Heveker N, Cairo CW, Issad T, Hinek A, Pshezhetsky AV. Positive regulation of insulin signaling by neuraminidase 1. Diabetes. 62: 2338-46. PMID 23520133 DOI: 10.2337/Db12-1825 |
0.304 |
|
| 2012 |
Sirois I, Groleau J, Pallet N, Brassard N, Hamelin K, Londono I, Pshezhetsky AV, Bendayan M, Hébert MJ. Caspase activation regulates the extracellular export of autophagic vacuoles. Autophagy. 8: 927-37. PMID 22692030 DOI: 10.4161/Auto.19768 |
0.312 |
|
| 2012 |
Gushulak L, Hemming R, Martin D, Seyrantepe V, Pshezhetsky A, Triggs-Raine B. Hyaluronidase 1 and β-Hexosaminidase Have Redundant Functions in Hyaluronan and Chondroitin Sulfate Degradation Journal of Biological Chemistry. 287: 16689-16697. PMID 22451654 DOI: 10.1074/Jbc.M112.350447 |
0.336 |
|
| 2011 |
Pshezhetsky AV, Hinek A. Where catabolism meets signalling: neuraminidase 1 as a modulator of cell receptors. Glycoconjugate Journal. 28: 441-52. PMID 21928149 DOI: 10.1007/S10719-011-9350-5 |
0.319 |
|
| 2010 |
Seyrantepe V, Lema P, Caqueret A, Dridi L, Bel Hadj S, Carpentier S, Boucher F, Levade T, Carmant L, Gravel RA, Hamel E, Vachon P, Di Cristo G, Michaud JL, Morales CR, ... Pshezhetsky AV, et al. Mice doubly-deficient in lysosomal hexosaminidase A and neuraminidase 4 show epileptic crises and rapid neuronal loss. Plos Genetics. 6: e1001118. PMID 20862357 DOI: 10.1371/Journal.Pgen.1001118 |
0.322 |
|
| 2010 |
Durand S, Feldhammer M, Bonneil E, Thibault P, Pshezhetsky AV. Analysis of the biogenesis of heparan sulfate acetyl-CoA:alpha-glucosaminide N-acetyltransferase provides insights into the mechanism underlying its complete deficiency in mucopolysaccharidosis IIIC. The Journal of Biological Chemistry. 285: 31233-42. PMID 20650889 DOI: 10.1074/Jbc.M110.141150 |
0.425 |
|
| 2010 |
Seyrantepe V, Iannello A, Liang F, Kanshin E, Jayanth P, Samarani S, Szewczuk MR, Ahmad A, Pshezhetsky AV. Regulation of phagocytosis in macrophages by neuraminidase 1. The Journal of Biological Chemistry. 285: 206-15. PMID 19889639 DOI: 10.1074/Jbc.M109.055475 |
0.344 |
|
| 2010 |
Amith SR, Jayanth P, Franchuk S, Finlay T, Seyrantepe V, Beyaert R, Pshezhetsky AV, Szewczuk MR. Neu1 desialylation of sialyl alpha-2,3-linked beta-galactosyl residues of TOLL-like receptor 4 is essential for receptor activation and cellular signaling. Cellular Signalling. 22: 314-24. PMID 19796680 DOI: 10.1016/J.Cellsig.2009.09.038 |
0.306 |
|
| 2010 |
Laplante P, Sirois I, Raymond MA, Kokta V, Béliveau A, Prat A, Pshezhetsky AV, Hébert MJ. Caspase-3-mediated secretion of connective tissue growth factor by apoptotic endothelial cells promotes fibrosis. Cell Death and Differentiation. 17: 291-303. PMID 19730442 DOI: 10.1038/Cdd.2009.124 |
0.305 |
|
| 2009 |
Feldhammer M, Durand S, Pshezhetsky AV. Protein misfolding as an underlying molecular defect in mucopolysaccharidosis III type C. Plos One. 4: e7434. PMID 19823584 DOI: 10.1371/Journal.Pone.0007434 |
0.464 |
|
| 2009 |
Feldhammer M, Durand S, Mrázová L, Boucher RM, Laframboise R, Steinfeld R, Wraith JE, Michelakakis H, van Diggelen OP, Hrebícek M, Kmoch S, Pshezhetsky AV. Sanfilippo syndrome type C: mutation spectrum in the heparan sulfate acetyl-CoA: alpha-glucosaminide N-acetyltransferase (HGSNAT) gene. Human Mutation. 30: 918-25. PMID 19479962 DOI: 10.1002/Humu.20986 |
0.41 |
|
| 2009 |
Pshezhetsky AV, Hinek A. Serine carboxypeptidases in regulation of vasoconstriction and elastogenesis. Trends in Cardiovascular Medicine. 19: 11-7. PMID 19467448 DOI: 10.1016/J.Tcm.2009.03.002 |
0.39 |
|
| 2009 |
Amith SR, Jayanth P, Franchuk S, Siddiqui S, Seyrantepe V, Gee K, Basta S, Beyaert R, Pshezhetsky AV, Szewczuk MR. Dependence of pathogen molecule-induced toll-like receptor activation and cell function on Neu1 sialidase. Glycoconjugate Journal. 26: 1197-212. PMID 19430901 DOI: 10.1007/S10719-009-9239-8 |
0.316 |
|
| 2009 |
Feldhammer M, Durand S, Mrazova L, Diggelen OPv, Hrebicek M, Kmoch S, Pshezhetsky AV. 54. Sanfilippo syndrome type C: Novel mutations in the HGSNAT gene Molecular Genetics and Metabolism. 96. DOI: 10.1016/J.Ymgme.2008.11.055 |
0.33 |
|
| 2008 |
Seyrantepe V, Hinek A, Peng J, Fedjaev M, Ernest S, Kadota Y, Canuel M, Itoh K, Morales CR, Lavoie J, Tremblay J, Pshezhetsky AV. Enzymatic activity of lysosomal carboxypeptidase (cathepsin) A is required for proper elastic fiber formation and inactivation of endothelin-1. Circulation. 117: 1973-81. PMID 18391110 DOI: 10.1161/Circulationaha.107.733212 |
0.42 |
|
| 2008 |
Seyrantepe V, Canuel M, Carpentier S, Landry K, Durand S, Liang F, Zeng J, Caqueret A, Gravel RA, Marchesini S, Zwingmann C, Michaud J, Morales CR, Levade T, Pshezhetsky AV. Mice deficient in Neu4 sialidase exhibit abnormal ganglioside catabolism and lysosomal storage. Human Molecular Genetics. 17: 1556-68. PMID 18270209 DOI: 10.1093/Hmg/Ddn043 |
0.354 |
|
| 2008 |
Ruijter GJ, Valstar MJ, van de Kamp JM, van der Helm RM, Durand S, van Diggelen OP, Wevers RA, Poorthuis BJ, Pshezhetsky AV, Wijburg FA. Clinical and genetic spectrum of Sanfilippo type C (MPS IIIC) disease in The Netherlands. Molecular Genetics and Metabolism. 93: 104-11. PMID 18024218 DOI: 10.1016/J.Ymgme.2007.09.011 |
0.375 |
|
| 2007 |
Pshezhetsky AV, Fedjaev M, Ashmarina L, Mazur A, Budman L, Sinnett D, Labuda D, Beaulieu JF, Ménard D, Nifant'ev I, Levy E. Subcellular proteomics of cell differentiation: quantitative analysis of the plasma membrane proteome of Caco-2 cells. Proteomics. 7: 2201-15. PMID 17549793 DOI: 10.1002/Pmic.200600956 |
0.305 |
|
| 2007 |
Bifsha P, Landry K, Ashmarina L, Durand S, Seyrantepe V, Trudel S, Quiniou C, Chemtob S, Xu Y, Gravel RA, Sladek R, Pshezhetsky AV. Altered gene expression in cells from patients with lysosomal storage disorders suggests impairment of the ubiquitin pathway. Cell Death and Differentiation. 14: 511-23. PMID 16888648 DOI: 10.1038/Sj.Cdd.4402013 |
0.357 |
|
| 2006 |
Hrebícek M, Mrázová L, Seyrantepe V, Durand S, Roslin NM, Nosková L, Hartmannová H, Ivánek R, Cízkova A, Poupetová H, Sikora J, Urinovská J, Stranecký V, Zeman J, Lepage P, ... ... Pshezhetsky AV, et al. Mutations in TMEM76* cause mucopolysaccharidosis IIIC (Sanfilippo C syndrome). American Journal of Human Genetics. 79: 807-19. PMID 17033958 DOI: 10.1086/508294 |
0.417 |
|
| 2006 |
Liang F, Seyrantepe V, Landry K, Ahmad R, Ahmad A, Stamatos NM, Pshezhetsky AV. Monocyte differentiation up-regulates the expression of the lysosomal sialidase, Neu1, and triggers its targeting to the plasma membrane via major histocompatibility complex class II-positive compartments. The Journal of Biological Chemistry. 281: 27526-38. PMID 16835219 DOI: 10.1074/Jbc.M605633200 |
0.341 |
|
| 2006 |
Seyrantepe V, Tihy F, Pshezhetsky AV. The microcell-mediated transfer of human chromosome 8 restores the deficient N-acetylytransferase activity in skin fibroblasts of Mucopolysaccharidosis type IIIC patients. Human Genetics. 120: 293-6. PMID 16783568 DOI: 10.1007/S00439-006-0211-4 |
0.307 |
|
| 2006 |
Hinek A, Pshezhetsky AV, von Itzstein M, Starcher B. Lysosomal sialidase (neuraminidase-1) is targeted to the cell surface in a multiprotein complex that facilitates elastic fiber assembly. The Journal of Biological Chemistry. 281: 3698-710. PMID 16314420 DOI: 10.1074/Jbc.M508736200 |
0.354 |
|
| 2006 |
Ausseil J, Landry K, Seyrantepe V, Trudel S, Mazur A, Lapointe F, Pshezhetsky AV. An acetylated 120-kDa lysosomal transmembrane protein is absent from mucopolysaccharidosis IIIC fibroblasts: a candidate molecule for MPS IIIC. Molecular Genetics and Metabolism. 87: 22-31. PMID 16293432 DOI: 10.1016/J.Ymgme.2005.09.021 |
0.388 |
|
| 2005 |
Stamatos NM, Liang F, Nan X, Landry K, Cross AS, Wang LX, Pshezhetsky AV. Differential expression of endogenous sialidases of human monocytes during cellular differentiation into macrophages. The Febs Journal. 272: 2545-56. PMID 15885103 DOI: 10.1111/J.1742-4658.2005.04679.X |
0.35 |
|
| 2004 |
Soni KG, Lehner R, Metalnikov P, O'Donnell P, Semache M, Gao W, Ashman K, Pshezhetsky AV, Mitchell GA. Carboxylesterase 3 (EC 3.1.1.1) is a major adipocyte lipase. The Journal of Biological Chemistry. 279: 40683-9. PMID 15220344 DOI: 10.1074/Jbc.M400541200 |
0.347 |
|
| 2004 |
Seyrantepe V, Landry K, Trudel S, Hassan JA, Morales CR, Pshezhetsky AV. Neu4, a novel human lysosomal lumen sialidase, confers normal phenotype to sialidosis and galactosialidosis cells. The Journal of Biological Chemistry. 279: 37021-9. PMID 15213228 DOI: 10.1074/Jbc.M404531200 |
0.403 |
|
| 2003 |
Seyrantepe V, Poupetova H, Froissart R, Zabot MT, Maire I, Pshezhetsky AV. Molecular pathology of NEU1 gene in sialidosis. Human Mutation. 22: 343-52. PMID 14517945 DOI: 10.1002/Humu.10268 |
0.41 |
|
| 2003 |
Rodríguez Criado G, Pshezhetsky AV, Rodríguez Becerra A, Gómez de Terreros I. Clinical variability of type II sialidosis by C808T mutation American Journal of Medical Genetics. 116: 368-371. PMID 12522793 DOI: 10.1002/Ajmg.A.10710 |
0.363 |
|
| 2002 |
Taurin S, Seyrantepe V, Orlov SN, Tremblay TL, Thibault P, Bennett MR, Hamet P, Pshezhetsky AV. Proteome analysis and functional expression identify mortalin as an antiapoptotic gene induced by elevation of [Na+]i/[K+]i ratio in cultured vascular smooth muscle cells. Circulation Research. 91: 915-22. PMID 12433836 DOI: 10.1161/01.Res.0000043020.45534.3E |
0.315 |
|
| 2002 |
Taurin S, Ryazhsky GG, Maximova NV, Chuchalin AG, Hamet P, Pshezhetsky AV, Orlov SN. Suppression of programmed cell death by intracellular cAMP is not mediated by expression of genes encoding an inhibitor of apoptosis. Biochemistry. Biokhimii︠a︡. 67: 254-9. PMID 11952423 DOI: 10.1023/A:1014478417580 |
0.307 |
|
| 2002 |
Itoh K, Naganawa Y, Matsuzawa F, Aikawa S, Doi H, Sasagasako N, Yamada T, Kira J, Kobayashi T, Pshezhetsky AV, Sakuraba H. Novel missense mutations in the human lysosomal sialidase gene in sialidosis patients and prediction of structural alterations of mutant enzymes. Journal of Human Genetics. 47: 29-37. PMID 11829139 DOI: 10.1007/S10038-002-8652-7 |
0.425 |
|
| 2001 |
Lukong KE, Seyrantepe V, Landry K, Trudel S, Ahmad A, Gahl WA, Lefrancois S, Morales CR, Pshezhetsky AV. Intracellular distribution of lysosomal sialidase is controlled by the internalization signal in its cytoplasmic tail. The Journal of Biological Chemistry. 276: 46172-81. PMID 11571282 DOI: 10.1074/Jbc.M104547200 |
0.681 |
|
| 2001 |
Pshezhetsky AV, Ashmarina M. Lysosomal multienzyme complex: Biochemistry, genetics, and molecular pathophysiology Progress in Nucleic Acid Research and Molecular Biology. 69. PMID 11550799 DOI: 10.1016/S0079-6603(01)69045-7 |
0.421 |
|
| 2001 |
Lukong KE, Landry K, Elsliger MA, Chang Y, Lefrancois S, Morales CR, Pshezhetsky AV. Mutations in sialidosis impair sialidase binding to the lysosomal multienzyme complex. The Journal of Biological Chemistry. 276: 17286-90. PMID 11279074 DOI: 10.1074/Jbc.M100460200 |
0.705 |
|
| 2001 |
Buchholz T, Molitor G, Lukong KE, Praun M, Genzel-Boroviczény O, Freund M, Pshezhetsky AV, Schulze A. Clinical presentation of congenital sialidosis in a patient with a neuraminidase gene frameshift mutation. European Journal of Pediatrics. 160: 26-30. PMID 11195014 DOI: 10.1007/Pl00008412 |
0.672 |
|
| 2000 |
Naganawa Y, Itoh K, Shimmoto M, Takiguchi K, Doi H, Nishizawa Y, Kobayashi T, Kamei S, Lukong KE, Pshezhetsky AV, Sakuraba H. Molecular and structural studies of Japanese patients with sialidosis type 1. Journal of Human Genetics. 45: 241-9. PMID 10944856 DOI: 10.1007/S100380070034 |
0.696 |
|
| 2000 |
Lukong KE, Elsliger MA, Chang Y, Richard C, Thomas G, Carey W, Tylki-Szymanska A, Czartoryska B, Buchholz T, Criado GR, Palmeri S, Pshezhetsky AV. Characterization of the sialidase molecular defects in sialidosis patients suggests the structural organization of the lysosomal multienzyme complex. Human Molecular Genetics. 9: 1075-85. PMID 10767332 DOI: 10.1093/Hmg/9.7.1075 |
0.704 |
|
| 1999 |
Gingras R, Richard C, El-Alfy M, Morales CR, Potier M, Pshezhetsky AV. Purification, cDNA cloning, and expression of a new human blood plasma glutamate carboxypeptidase homologous to N-acetyl-aspartyl-α-glutamate carboxypeptidase/prostate-specific membrane antigen Journal of Biological Chemistry. 274: 11742-11750. PMID 10206990 DOI: 10.1074/Jbc.274.17.11742 |
0.329 |
|
| 1999 |
Lukong KE, Elsliger MA, Mort JS, Potier M, Pshezhetsky AV. Identification of UDP-N-acetylglucosamine-phosphotransferase-binding sites on the lysosomal proteases, cathepsins A, B, and D. Biochemistry. 38: 73-80. PMID 9890884 DOI: 10.1021/Bi981324R |
0.659 |
|
| 1998 |
Richard C, Tranchemontagne J, Elsliger MA, Mitchell GA, Potier M, Pshezhetsky AV. Molecular pathology of galactosialidosis in a patient affected with two new frameshift mutations in the cathepsin A/protective protein gene Human Mutation. 11: 461-469. PMID 9603439 DOI: 10.1002/(Sici)1098-1004(1998)11:6<461::Aid-Humu7>3.0.Co;2-F |
0.435 |
|
| 1998 |
Vinogradova MV, Michaud L, Mezentsev AV, Lukong KE, El-Alfy M, Morales CR, Potier M, Pshezhetsky AV. Molecular mechanism of lysosomal sialidase deficiency in galactosialidosis involves its rapid degradation. The Biochemical Journal. 330: 641-50. PMID 9480870 DOI: 10.1042/Bj3300641 |
0.687 |
|
| 1997 |
Pshezhetsky AV, Richard C, Michaud L, Igdoura S, Wang S, Elsliger MA, Qu J, Leclerc D, Gravel R, Dallaire L, Potier M. Cloning, expression and chromosomal mapping of human lysosomal sialidase and characterization of mutations in sialidosis Nature Genetics. 15: 316-320. PMID 9054950 DOI: 10.1038/Ng0397-316 |
0.388 |
|
| 1996 |
Elsliger MA, Pshezhetsky AV, Vinogradova MV, Švedas VK, Potier M. Comparative modeling of substrate binding in the S1′ subsite of serine carboxypeptidases from yeast, wheat, and human Biochemistry. 35: 14899-14909. PMID 8942654 DOI: 10.1021/Bi952833L |
0.335 |
|
| 1996 |
Pshezhetsky AV, Potier M. Association of N-acetylgalactosamine-6-sulfate sulfatase with the multienzyme lysosomal complex of β-galactosidase, cathepsin A, and neuraminidase: Possible implication for intralysosomal catabolism of keratan sulfate Journal of Biological Chemistry. 271: 28359-28365. PMID 8910459 DOI: 10.1074/Jbc.271.45.28359 |
0.323 |
|
| 1995 |
Pshezhetsky AV, Vinogradova MV, Elsliger MA, Elzein F. Continuous Spectrophotometric Assay of Human Lysosomal Cathepsin A/Protective Protein in Normal and Galactosialidosis Cells Analytical Biochemistry. 230: 303-307. PMID 7503422 DOI: 10.1006/Abio.1995.1478 |
0.387 |
|
| 1994 |
Ashmarina LI, Pshezhetsky AV, Spivey HO, Potier M. Demonstration of enzyme associations by countermigration electrophoresis in agarose gel. Analytical Biochemistry. 219: 349-55. PMID 8080091 DOI: 10.1006/Abio.1994.1275 |
0.341 |
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| 1994 |
Pshezhetsky AV, Potier M. Direct Affinity Purification and Supramolecular Organization of Human Lysosomal Cathepsin A Archives of Biochemistry and Biophysics. 313: 64-70. PMID 8053688 DOI: 10.1006/Abbi.1994.1359 |
0.31 |
|
| 1992 |
Pshezhetsky AV, Levashow AV, Wiederschain GY. Regulation of the GM1-galactosidase supramolecular structure and catalytic activity in vitro Biochimica Et Biophysica Acta (Bba)/Protein Structure and Molecular. 1122: 154-160. PMID 1643088 DOI: 10.1016/0167-4838(92)90318-8 |
0.347 |
|
| 1988 |
Kabanov AV, Levashov AV, Klyachko NL, Namyotkin SN, Pshezhetsky AV, Martinek K. Enzymes entrapped in reversed micelles of surfactants in organic solvents: A theoretical treatment of the catalytic activity regulation Journal of Theoretical Biology. 133: 327-343. DOI: 10.1016/S0022-5193(88)80325-4 |
0.302 |
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