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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).
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