Pshezhetsky AV - Search Results

1

Glucosamine amends CNS pathology in mucopolysaccharidosis IIIC mouse expressing misfolded HGSNAT.

Pan X, Taherzadeh M, Bose P, Heon-Roberts R, Nguyen ALA, Xu T, Pará C, Yamanaka Y, Priestman DA, Platt FM, Khan S, Fnu N, Tomatsu S, Morales CR, Pshezhetsky AV. Pan X, et al. Among authors: pshezhetsky av. J Exp Med. 2022 Aug 1;219(8):e20211860. doi: 10.1084/jem.20211860. Epub 2022 Jun 15. J Exp Med. 2022. PMID: 35704026 Free PMC article.

2

Molecular mechanism of lysosomal sialidase deficiency in galactosialidosis involves its rapid degradation.

Vinogradova MV, Michaud L, Mezentsev AV, Lukong KE, El-Alfy M, Morales CR, Potier M, Pshezhetsky AV. Vinogradova MV, et al. Among authors: pshezhetsky av. Biochem J. 1998 Mar 1;330 ( Pt 2)(Pt 2):641-50. doi: 10.1042/bj3300641. Biochem J. 1998. PMID: 9480870 Free PMC article.

3

Purification, cDNA cloning, and expression of a new human blood plasma glutamate carboxypeptidase homologous to N-acetyl-aspartyl-alpha-glutamate carboxypeptidase/prostate-specific membrane antigen.

Gingras R, Richard C, El-Alfy M, Morales CR, Potier M, Pshezhetsky AV. Gingras R, et al. Among authors: pshezhetsky av. J Biol Chem. 1999 Apr 23;274(17):11742-50. doi: 10.1074/jbc.274.17.11742. J Biol Chem. 1999. PMID: 10206990 Free article.

4

Mutations in sialidosis impair sialidase binding to the lysosomal multienzyme complex.

Lukong KE, Landry K, Elsliger MA, Chang Y, Lefrancois S, Morales CR, Pshezhetsky AV. Lukong KE, et al. Among authors: pshezhetsky av. J Biol Chem. 2001 May 18;276(20):17286-90. doi: 10.1074/jbc.M100460200. Epub 2001 Feb 20. J Biol Chem. 2001. PMID: 11279074 Free article.

5

Neu4, a novel human lysosomal lumen sialidase, confers normal phenotype to sialidosis and galactosialidosis cells.

Seyrantepe V, Landry K, Trudel S, Hassan JA, Morales CR, Pshezhetsky AV. Seyrantepe V, et al. Among authors: pshezhetsky av. J Biol Chem. 2004 Aug 27;279(35):37021-9. doi: 10.1074/jbc.M404531200. Epub 2004 Jun 22. J Biol Chem. 2004. PMID: 15213228 Free article.

6

An acetylated 120-kDa lysosomal transmembrane protein is absent from mucopolysaccharidosis IIIC fibroblasts: a candidate molecule for MPS IIIC.

Ausseil J, Landry K, Seyrantepe V, Trudel S, Mazur A, Lapointe F, Pshezhetsky AV. Ausseil J, et al. Among authors: pshezhetsky av. Mol Genet Metab. 2006 Jan;87(1):22-31. doi: 10.1016/j.ymgme.2005.09.021. Epub 2005 Nov 15. Mol Genet Metab. 2006. PMID: 16293432

7

Mice deficient in Neu4 sialidase exhibit abnormal ganglioside catabolism and lysosomal storage.

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. Seyrantepe V, et al. Among authors: pshezhetsky av. Hum Mol Genet. 2008 Jun 1;17(11):1556-68. doi: 10.1093/hmg/ddn043. Epub 2008 Feb 11. Hum Mol Genet. 2008. PMID: 18270209

8

Enzymatic activity of lysosomal carboxypeptidase (cathepsin) A is required for proper elastic fiber formation and inactivation of endothelin-1.

Seyrantepe V, Hinek A, Peng J, Fedjaev M, Ernest S, Kadota Y, Canuel M, Itoh K, Morales CR, Lavoie J, Tremblay J, Pshezhetsky AV. Seyrantepe V, et al. Among authors: pshezhetsky av. Circulation. 2008 Apr 15;117(15):1973-81. doi: 10.1161/CIRCULATIONAHA.107.733212. Epub 2008 Apr 7. Circulation. 2008. PMID: 18391110

9

Sanfilippo syndrome type C: mutation spectrum in the heparan sulfate acetyl-CoA: alpha-glucosaminide N-acetyltransferase (HGSNAT) gene.

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. Feldhammer M, et al. Among authors: pshezhetsky av. Hum Mutat. 2009 Jun;30(6):918-25. doi: 10.1002/humu.20986. Hum Mutat. 2009. PMID: 19479962 Review.

10

Protein misfolding as an underlying molecular defect in mucopolysaccharidosis III type C.

Feldhammer M, Durand S, Pshezhetsky AV. Feldhammer M, et al. Among authors: pshezhetsky av. PLoS One. 2009 Oct 13;4(10):e7434. doi: 10.1371/journal.pone.0007434. PLoS One. 2009. PMID: 19823584 Free PMC article.

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