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Items: 1 to 20 of 129

1.

Stimulation of NF-E2 DNA binding by CREB-binding protein (CBP)-mediated acetylation.

Hung HL, Kim AY, Hong W, Rakowski C, Blobel GA.

J Biol Chem. 2001 Apr 6;276(14):10715-21. Epub 2001 Jan 11.

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Human MafG is a functional partner for p45 NF-E2 in activating globin gene expression.

Blank V, Kim MJ, Andrews NC.

Blood. 1997 Jun 1;89(11):3925-35.

4.

Regulation of transcription by dimerization of erythroid factor NF-E2 p45 with small Maf proteins.

Igarashi K, Kataoka K, Itoh K, Hayashi N, Nishizawa M, Yamamoto M.

Nature. 1994 Feb 10;367(6463):568-72.

PMID:
8107826
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Human small Maf proteins form heterodimers with CNC family transcription factors and recognize the NF-E2 motif.

Toki T, Itoh J, Kitazawa J, Arai K, Hatakeyama K, Akasaka J, Igarashi K, Nomura N, Yokoyama M, Yamamoto M, Ito E.

Oncogene. 1997 Apr 24;14(16):1901-10.

7.

Activation of beta-major globin gene transcription is associated with recruitment of NF-E2 to the beta-globin LCR and gene promoter.

Sawado T, Igarashi K, Groudine M.

Proc Natl Acad Sci U S A. 2001 Aug 28;98(18):10226-31. Epub 2001 Aug 21.

8.

Characterization of the hematopoietic transcription factor NF-E2 in primary murine megakaryocytes.

Lecine P, Blank V, Shivdasani R.

J Biol Chem. 1998 Mar 27;273(13):7572-8.

9.

Functional characterization of the two alternative promoters of human p45 NF-E2 gene.

Toki T, Arai K, Terui K, Komatsu N, Yokoyama M, Katsuoka F, Yamamoto M, Ito E.

Exp Hematol. 2000 Oct;28(10):1113-9.

PMID:
11027829
10.

Ablation of Nrf2 function does not increase the erythroid or megakaryocytic cell lineage dysfunction caused by p45 NF-E2 gene disruption.

Kuroha T, Takahashi S, Komeno T, Itoh K, Nagasawa T, Yamamoto M.

J Biochem. 1998 Mar;123(3):376-9.

11.

Acetylation of cAMP-responsive element-binding protein (CREB) by CREB-binding protein enhances CREB-dependent transcription.

Lu Q, Hutchins AE, Doyle CM, Lundblad JR, Kwok RP.

J Biol Chem. 2003 May 2;278(18):15727-34. Epub 2003 Feb 20.

12.

Small Maf proteins heterodimerize with Fos and may act as competitive repressors of the NF-E2 transcription factor.

Kataoka K, Igarashi K, Itoh K, Fujiwara KT, Noda M, Yamamoto M, Nishizawa M.

Mol Cell Biol. 1995 Apr;15(4):2180-90. Erratum in: Mol Cell Biol 1995 Jun;15(6):3461.

13.

p45 NF-E2 regulates expression of thromboxane synthase in megakaryocytes.

Deveaux S, Cohen-Kaminsky S, Shivdasani RA, Andrews NC, Filipe A, Kuzniak I, Orkin SH, Roméo PH, Mignotte V.

EMBO J. 1997 Sep 15;16(18):5654-61.

14.

Bach proteins belong to a novel family of BTB-basic leucine zipper transcription factors that interact with MafK and regulate transcription through the NF-E2 site.

Oyake T, Itoh K, Motohashi H, Hayashi N, Hoshino H, Nishizawa M, Yamamoto M, Igarashi K.

Mol Cell Biol. 1996 Nov;16(11):6083-95.

15.

Regulation of the erythroid transcription factor NF-E2 by cyclic adenosine monophosphate-dependent protein kinase.

Casteel D, Suhasini M, Gudi T, Naima R, Pilz RB.

Blood. 1998 May 1;91(9):3193-201.

16.

Regulation of NF-E2 activity in erythroleukemia cell differentiation.

Nagai T, Igarashi K, Akasaka J, Furuyama K, Fujita H, Hayashi N, Yamamoto M, Sassa S.

J Biol Chem. 1998 Feb 27;273(9):5358-65.

17.

Small Maf proteins interact with the human transcription factor TCF11/Nrf1/LCR-F1.

Johnsen O, Skammelsrud N, Luna L, Nishizawa M, Prydz H, Kolstø AB.

Nucleic Acids Res. 1996 Nov 1;24(21):4289-97.

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