T. Chang

发表

RNA11 protein is associated with the yeast spliceosome and is localized in the periphery of the cell nucleus

M. Cusick, M. W. Clark, J. Abelson, 1988, Molecular and cellular biology.

Mapping the putative RNA helicase genes by sequence overlaping

B. Baum, T. Chang, 1992, Yeast.

Four yeast spliceosomal proteins (PRP5, PRP9, PRP11, and PRP21) interact to promote U2 snRNP binding to pre-mRNA.

J. Abelson, S. Ruby, T. Chang, 1993, Genes & development.

Specific alterations of U1-C protein or U1 small nuclear RNA can eliminate the requirement of Prp28p, an essential DEAD box splicing factor.

R. Jackups, J. Chen, L. Latus, 2001, Molecular cell.

Dbp3p, a putative RNA helicase in Saccharomyces cerevisiae, is required for efficient pre-rRNA processing predominantly at site A3

C. Sun, T. Chang, P. L. Weaver, 1997, Molecular and cellular biology.

Dbp5p, a cytosolic RNA helicase, is required for poly(A)+ RNA export

Yan Liu, A. Tartakoff, M. Hitomi, 1998, The EMBO journal.

Identification of five putative yeast RNA helicase genes.

J. Abelson, J Abelson, T H Chang, 1990, Proceedings of the National Academy of Sciences of the United States of America.

site A 3 . efficient pre-rRNA processing predominantly at Saccharomyces cerevisiae , is required for Dbp 3 p , a putative RNA helicase in

C. Sun, T. Chang, P. L. Weaver, 1997 .

Modular long-range regulation of Myf5 reveals unexpected heterogeneity between skeletal muscles in the mouse embryo.

M. Primig, S. Tajbakhsh, M. Buckingham, 2000, Development.

Identification of a putative amidase gene in yeast Saccharomyces cerevisiae.

J. Abelson, T. Chang, 1990, Nucleic acids research.

Genetic interactions of conserved regions in the DEAD-box protein Prp28p.

L. Latus, J. Abbott, Z. Liu, 1997, Nucleic acids research.

A novel GFPneo vector designed for the isolation and analysis of enhancer elements in transfected mammalian cells.

M. Primig, M. Buckingham, T. Chang, 1998, Gene.