Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 61

1.

Physical interaction between hepatitis C virus NS4B protein and CREB-RP/ATF6beta.

Tong WY, Nagano-Fujii M, Hidajat R, Deng L, Takigawa Y, Hotta H.

Biochem Biophys Res Commun. 2002 Dec 6;299(3):366-72.

PMID:
12445808
2.

Structural and functional comparison of the non-structural protein 4B in flaviviridae.

Welsch C, Albrecht M, Maydt J, Herrmann E, Welker MW, Sarrazin C, Scheidig A, Lengauer T, Zeuzem S.

J Mol Graph Model. 2007 Sep;26(2):546-57. Epub 2007 Apr 4.

PMID:
17507273
4.

Opposing roles for ATF6alpha and ATF6beta in endoplasmic reticulum stress response gene induction.

Thuerauf DJ, Morrison L, Glembotski CC.

J Biol Chem. 2004 May 14;279(20):21078-84. Epub 2004 Feb 18.

5.
6.
8.

Dimerization of the hepatitis C virus nonstructural protein 4B depends on the integrity of an aminoterminal basic leucine zipper.

Welker MW, Welsch C, Meyer A, Antes I, Albrecht M, Forestier N, Kronenberger B, Lengauer T, Piiper A, Zeuzem S, Sarrazin C.

Protein Sci. 2010 Jul;19(7):1327-36. doi: 10.1002/pro.409.

9.

The minimal transactivation domain of the basic motif-leucine zipper transcription factor NRL interacts with TATA-binding protein.

Friedman JS, Khanna H, Swain PK, Denicola R, Cheng H, Mitton KP, Weber CH, Hicks D, Swaroop A.

J Biol Chem. 2004 Nov 5;279(45):47233-41. Epub 2004 Aug 24.

10.

Inhibition of protein synthesis by the nonstructural proteins NS4A and NS4B of hepatitis C virus.

Florese RH, Nagano-Fujii M, Iwanaga Y, Hidajat R, Hotta H.

Virus Res. 2002 Dec;90(1-2):119-31.

PMID:
12457968
11.

N-glycosylation of ATF6beta is essential for its proteolytic cleavage and transcriptional repressor function to ATF6alpha.

Guan D, Wang H, Li VE, Xu Y, Yang M, Shen Z.

J Cell Biochem. 2009 Nov 1;108(4):825-31. doi: 10.1002/jcb.22310.

PMID:
19693772
12.
13.
14.
15.

The liver-enriched transcription factor CREB-H is a growth suppressor protein underexpressed in hepatocellular carcinoma.

Chin KT, Zhou HJ, Wong CM, Lee JM, Chan CP, Qiang BQ, Yuan JG, Ng IO, Jin DY.

Nucleic Acids Res. 2005 Mar 30;33(6):1859-73. Print 2005.

16.

Luman, the cellular counterpart of herpes simplex virus VP16, is processed by regulated intramembrane proteolysis.

Raggo C, Rapin N, Stirling J, Gobeil P, Smith-Windsor E, O'Hare P, Misra V.

Mol Cell Biol. 2002 Aug;22(16):5639-49.

17.

Regulation of GTP cyclohydrolase I gene transcription by basic region leucine zipper transcription factors.

Al Sarraj J, Vinson C, Han J, Thiel G.

J Cell Biochem. 2005 Dec 1;96(5):1003-20.

PMID:
16149046
18.

Monomeric and dimeric bZIP transcription factor GCN4 bind at the same rate to their target DNA site.

Cranz S, Berger C, Baici A, Jelesarov I, Bosshard HR.

Biochemistry. 2004 Jan 27;43(3):718-27.

PMID:
14730976
19.

Hepatitis C virus NS4B carboxy terminal domain is a membrane binding domain.

Liefhebber JM, Brandt BW, Broer R, Spaan WJ, van Leeuwen HC.

Virol J. 2009 May 25;6:62. doi: 10.1186/1743-422X-6-62.

20.

Dengue virus NS4B interacts with NS3 and dissociates it from single-stranded RNA.

Umareddy I, Chao A, Sampath A, Gu F, Vasudevan SG.

J Gen Virol. 2006 Sep;87(Pt 9):2605-14.

PMID:
16894199

Supplemental Content

Support Center