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Items: 10


Nuclear export of mRNA by TAP/NXF1 requires two nucleoporin-binding sites but not p15.

Braun IC, Herold A, Rode M, Izaurralde E.

Mol Cell Biol. 2002 Aug;22(15):5405-18.


The protein Mago provides a link between splicing and mRNA localization.

Le Hir H, Gatfield D, Braun IC, Forler D, Izaurralde E.

EMBO Rep. 2001 Dec;2(12):1119-24. Epub 2001 Nov 21.


The DExH/D box protein HEL/UAP56 is essential for mRNA nuclear export in Drosophila.

Gatfield D, Le Hir H, Schmitt C, Braun IC, Köcher T, Wilm M, Izaurralde E.

Curr Biol. 2001 Oct 30;11(21):1716-21.


Overexpression of TAP/p15 heterodimers bypasses nuclear retention and stimulates nuclear mRNA export.

Braun IC, Herold A, Rode M, Conti E, Izaurralde E.

J Biol Chem. 2001 Jun 8;276(23):20536-43. Epub 2001 Mar 19.


Prediction of structural domains of TAP reveals details of its interaction with p15 and nucleoporins.

Suyama M, Doerks T, Braun IC, Sattler M, Izaurralde E, Bork P.

EMBO Rep. 2000 Jul;1(1):53-8.


TAP (NXF1) belongs to a multigene family of putative RNA export factors with a conserved modular architecture.

Herold A, Suyama M, Rodrigues JP, Braun IC, Kutay U, Carmo-Fonseca M, Bork P, Izaurralde E.

Mol Cell Biol. 2000 Dec;20(23):8996-9008.


REF, an evolutionary conserved family of hnRNP-like proteins, interacts with TAP/Mex67p and participates in mRNA nuclear export.

Stutz F, Bachi A, Doerks T, Braun IC, Séraphin B, Wilm M, Bork P, Izaurralde E.

RNA. 2000 Apr;6(4):638-50.


The C-terminal domain of TAP interacts with the nuclear pore complex and promotes export of specific CTE-bearing RNA substrates.

Bachi A, Braun IC, Rodrigues JP, Panté N, Ribbeck K, von Kobbe C, Kutay U, Wilm M, Görlich D, Carmo-Fonseca M, Izaurralde E.

RNA. 2000 Jan;6(1):136-58.

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