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Items: 8

1.

Single-molecule study of ribosome hierarchic dynamics at the peptidyl transferase center.

Altuntop ME, Ly CT, Wang Y.

Biophys J. 2010 Nov 3;99(9):3002-9. doi: 10.1016/j.bpj.2010.08.037.

2.

Single-molecule study of viomycin's inhibition mechanism on ribosome translocation.

Ly CT, Altuntop ME, Wang Y.

Biochemistry. 2010 Nov 16;49(45):9732-8. doi: 10.1021/bi101029g. Epub 2010 Oct 25.

PMID:
20886842
3.
4.

Differential requirement for individual sarcoglycans and dystrophin in the assembly and function of the dystrophin-glycoprotein complex.

Hack AA, Lam MY, Cordier L, Shoturma DI, Ly CT, Hadhazy MA, Hadhazy MR, Sweeney HL, McNally EM.

J Cell Sci. 2000 Jul;113 ( Pt 14):2535-44.

5.

Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammation.

McNally EM, Ly CT, Rosenmann H, Mitrani Rosenbaum S, Jiang W, Anderson LV, Soffer D, Argov Z.

Am J Med Genet. 2000 Apr 10;91(4):305-12.

PMID:
10766988
6.

Myoferlin, a candidate gene and potential modifier of muscular dystrophy.

Davis DB, Delmonte AJ, Ly CT, McNally EM.

Hum Mol Genet. 2000 Jan 22;9(2):217-26.

PMID:
10607832
7.

Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin.

Hack AA, Ly CT, Jiang F, Clendenin CJ, Sigrist KS, Wollmann RL, McNally EM.

J Cell Biol. 1998 Sep 7;142(5):1279-87.

8.

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