Lukong KE - Search Results

1

Characterization of the sialidase molecular defects in sialidosis patients suggests the structural organization of the lysosomal multienzyme complex.

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. Lukong KE, et al. Hum Mol Genet. 2000 Apr 12;9(7):1075-85. doi: 10.1093/hmg/9.7.1075. Hum Mol Genet. 2000. PMID: 10767332

2

Identification of UDP-N-acetylglucosamine-phosphotransferase-binding sites on the lysosomal proteases, cathepsins A, B, and D.

Lukong KE, Elsliger MA, Mort JS, Potier M, Pshezhetsky AV. Lukong KE, et al. Biochemistry. 1999 Jan 5;38(1):73-80. doi: 10.1021/bi981324r. Biochemistry. 1999. PMID: 9890884

3

Molecular and structural studies of Japanese patients with sialidosis type 1.

Naganawa Y, Itoh K, Shimmoto M, Takiguchi K, Doi H, Nishizawa Y, Kobayashi T, Kamei S, Lukong KE, Pshezhetsky AV, Sakuraba H. Naganawa Y, et al. Among authors: lukong ke. J Hum Genet. 2000;45(4):241-9. doi: 10.1007/s100380070034. J Hum Genet. 2000. PMID: 10944856

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. 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

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: lukong ke. Biochem J. 1998 Mar 1;330 ( Pt 2)(Pt 2):641-50. doi: 10.1042/bj3300641. Biochem J. 1998. PMID: 9480870 Free PMC article.

6

Intracellular distribution of lysosomal sialidase is controlled by the internalization signal in its cytoplasmic tail.

Lukong KE, Seyrantepe V, Landry K, Trudel S, Ahmad A, Gahl WA, Lefrancois S, Morales CR, Pshezhetsky AV. Lukong KE, et al. J Biol Chem. 2001 Dec 7;276(49):46172-81. doi: 10.1074/jbc.M104547200. Epub 2001 Sep 24. J Biol Chem. 2001. PMID: 11571282 Free article.

7

Clinical presentation of congenital sialidosis in a patient with a neuraminidase gene frameshift mutation.

Buchholz T, Molitor G, Lukong KE, Praun M, Genzel-Boroviczény O, Freund M, Pshezhetsky AV, Schulze A. Buchholz T, et al. Among authors: lukong ke. Eur J Pediatr. 2001 Jan;160(1):26-30. doi: 10.1007/pl00008412. Eur J Pediatr. 2001. PMID: 11195014

8

Targeting the RNA-binding protein Sam68 as a treatment for cancer?

Lukong KE, Richard S. Lukong KE, et al. Future Oncol. 2007 Oct;3(5):539-44. doi: 10.2217/14796694.3.5.539. Future Oncol. 2007. PMID: 17927519 Review.

9

Tyrosine phosphorylation of sam68 by breast tumor kinase regulates intranuclear localization and cell cycle progression.

Lukong KE, Larocque D, Tyner AL, Richard S. Lukong KE, et al. J Biol Chem. 2005 Nov 18;280(46):38639-47. doi: 10.1074/jbc.M505802200. Epub 2005 Sep 22. J Biol Chem. 2005. PMID: 16179349 Free article.

10

The DEAD-box protein DDX43 (HAGE) is a dual RNA-DNA helicase and has a K-homology domain required for full nucleic acid unwinding activity.

Talwar T, Vidhyasagar V, Qing J, Guo M, Kariem A, Lu Y, Singh RS, Lukong KE, Wu Y. Talwar T, et al. Among authors: lukong ke. J Biol Chem. 2017 Jun 23;292(25):10429-10443. doi: 10.1074/jbc.M117.774950. Epub 2017 May 3. J Biol Chem. 2017. PMID: 28468824 Free PMC article.

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