Center for RNA Biology Publications

Publications by Tien-Hsien Chang since 2000

• Rosemary Hage, Luh Tung, Hansen Du, Leah Stands, Michael Rosbash, and Tien-Hsien Chang
  "A targeted bypass screen identifies Ynl187p, Prp42p, Snu71p, and Cbp80p for stable U1 snRNP/Pre-mRNA interaction."
  Mol. Cell. Biol. 29, 3941-52 (2009).

• Woan-Yuh Tarn and Tien-Hsien Chang
  "The current understanding of Ded1p/DDX3 homologs from yeast to human."
  RNA Biol 6, 17-20 (2009).

• Fehmida Kapadia, Anne Pryor, Tien-Hsien Chang, and Lee F Johnson
  "Nuclear localization of polyA mRNA following siRNA reduction of expression of the mammalian RNA helicases UAP56 and URH49."
  Gene 384, 37-44 (2006).

• Todd Burckin, Roland Nagel, Yael Mandel-Gutfreund, Lily Shiue, Tyson A Clark, Jean-Leon Chong, Tien-Hsien Chang, Sharon Squazzo, Grant Hartzog, and Manuel Ares
  "Exploring functional relationships between components of the gene expression machinery."
  Nat. Struct. Mol. Biol. 12, 175-82 (2005).

• Stephanie S Tseng-Rogenski and Tien-Hsien Chang
  "RNA unwinding assay for DExD/H-box RNA helicases."
  Methods Mol. Biol. 257, 93-102 (2004).

• Anne Pryor, Luh Tung, Zhe Yang, Fehmida Kapadia, Tien-Hsien Chang, and Lee F Johnson
  "Growth-regulated expression and G0-specific turnover of the mRNA that encodes URH49, a mammalian DExH/D box protein that is highly related to the mRNA export protein UAP56."
  Nucleic Acids Res. 32, 1857-65 (2004).

• Jean-Leon Chong, Ray-Yuan Chuang, Luh Tung, and Tien-Hsien Chang
  "Ded1p, a conserved DExD/H-box translation factor, can promote yeast L-A virus negative-strand RNA synthesis in vitro."
  Nucleic Acids Res. 32, 2031-8 (2004).

• Stephanie S-I Tseng-Rogenski, Jean-Leon Chong, Christopher B Thomas, Shinichiro Enomoto, Judith Berman, and Tien-Hsien Chang
  "Functional conservation of Dhh1p, a cytoplasmic DExD/H-box protein present in large complexes."
  Nucleic Acids Res. 31, 4995-5002 (2003).

• J Y Chen, L Stands, J P Staley, R R Jackups, L J Latus, and T H Chang
  "Specific alterations of U1-C protein or U1 small nuclear RNA can eliminate the requirement of Prp28p, an essential DEAD box splicing factor."
  Mol. Cell 7, 227-32 (2001).