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Kiven E. Lukong, Ph.D. - Publications

Affiliations: 
2002 Université de Montréal, Montréal, Canada 
Area:
Biochemistry, Pathology, Molecular Biology
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8 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
2008 Lukong KE, Richard S. Breast tumor kinase BRK requires kinesin-2 subunit KAP3A in modulation of cell migration. Cellular Signalling. 20: 432-42. PMID 18077133 DOI: 10.1016/J.Cellsig.2007.11.003  0.355
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  0.562
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  0.626
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  0.564
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  0.609
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  0.63
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  0.548
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  0.592
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