News

    
Directory / Bottin
Contact Us
Directions / Maps
Steering Commitee
Events & Seminars
MDRC Core Facilities
Scientific Links
Education & Employment

    
Grants
Donations
Industrial Partners
    
JDRF
CDA
QDA
ADA
IDF
NIH / NIDDK
Alfediam
EASD


 Home / About Us > Dr. Alexey Pshezhetsky > Bibliography
Dr. Alexey Pshezhetsky - Bibliography (Last Five Years)

Articles in peer-reviewed journals
  • Ausseil J, Loredo-Osti JC, Verner A, Darmond-Zwaig C, Maire I, Poorthuis B, van Diggelen OP, Hudson TJ, Fujiwara TM, Morgan K, Pshezhetsky AV. Localisation of a gene for mucopolysaccharidosis IIIC to the pericentromeric region of chromosome 8.J Med Genet. 41:941-5 (2004). (download article)
  • 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. J Biol Chem. 279:40683-9 (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. J Biol Chem. 279:37021-9. (2004). (download article)
  • Raymond MA, Desormeaux A, Laplante P, Vigneault N, Filep JG, Landry K, Pshezhetsky AV, Hebert MJ. Apoptosis of endothelial cells triggers a caspase-dependent anti-apoptotic paracrine loop active on VSMC. FASEB J. 18:705-7 (2004).
  • Orlov SN, Pchejetski D, Taurin S, Thorin-Trescases N, Maximov GV, Pshezhetsky AV, Rubin AB, Hamet P. Apoptosis in serum-deprived vascular smooth muscle cells: evidence for cell volume-independent mechanism. Muscle. Apoptosis.9:55-66 (2004).
  • Seyrantepe V, Poupetova H, Froissart R, Zabot MT, Maire I, Pshezhetsky AV. Molecular pathology of NEU1 gene in sialidosis. Hum Mutat. 22:343-52 (2003). (download article)
  • Orlov SN, Pchejetski DV, Sarkissian SD, Adarichev V, Taurin S, Pshezhetsky AV, Tremblay J, Maximov GV, deBlois D, Bennett MR, Hamet P. [3H]-thymidine labelling of DNA triggers apoptosis potentiated by E1A-adenoviral protein. Apoptosis 8:199-208 (2003).
  • Pchejetski D, Taurin S, Der Sarkissian S, Lopina OD, Pshezhetsky AV, Tremblay J, deBlois D, Hamet P, Orlov SN. Inhibition of Na+,K+-ATPase by ouabain triggers epithelial cell death independently of the inversion of the [Na+]i/[K+]i ratio. Biochem.Biophys.Res.Commun. 301: 735-44 (2003).
  • Rodriguez Criado G, Pshezhetsky AV, Rodriguez Becerra A, Gomez de Terreros I. Clinical variability of type II sialidosis by C808T mutation. Amer. J. Med. Genet. 116: 368-71 (2003).
  • Taurin S, Seyrantepe V, Orlov SN, Tremblay T-L, 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. Circ. Res. 91:915-22 (2002). (download article)
  • 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 67: 254-9 (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. J. Hum. Genet. 47: 29-37 (2002).
  • Lukong KE, Seyrantepe V, Landry K, Trudel S, Ahmad A, Gahl WA, Lefrançois S, Morales CR, Pshezhetsky AV. Intracellular distribution of lysosomal sialidase is controlled by the internalization signal in its cytoplasmic tail. J. Biol. Chem. 276: 46172-81 (2001).
  • Thorin-Trescases N, Orlov SN, Taurin S, Dulin NO, Allen BG, deBlois D, Tremblay J, Pshezhetsky AV, Hamet P. Antiproliferative effect of brief exposure to cholera toxin in vascular smooth muscle cells : role of cAMP and protein kinase A. Can. J. Physiol. Pharmacol. 79: 471-80 (2001).
  • Lukong KE, Landry K, Elsliger M-A, Chang Y, Lefrancois S, Morales CR, Pshezhetsky AV. Mutations in sialidosis impair sialidase binding to the lysosomal multienzyme complex, J. Biol. Chem. 276:17286-90 (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. Eur. J. of Pediatrics 160: 26-30 (2001).
  • 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. J. Hum. Genet 45:241-9 (2000).
  • Lukong KE, Elsliger M-A, Chang Y, Richard C, Thomas G, Carey W, Tylki-Szymanska A, Czartoryska B, Buchholz T, Criado G, Palmeri S, Pshezhetsky AV. Characterization of the sialidase molecular defects in sialidosis patients suggests the structural organization of the lysosomal multienzyme complex. Hum. Mol. Genet. 9:1075-85 (2000).

 

Montreal Diabetes Research Center 2008
Home / About Us   News   Directory / Bottin   Contact Us