The phosphatidylinositol polyphosphate 5-phosphatase SHIP1 associates with the dok1 phosphoprotein in bcr-Abl transformed cells (Q28144947)

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D Wisniewski

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A Strife

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B Clarkson

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M D Resh

A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia

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language of work or name

English

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publication date

May 2000

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published in

Cellular Signalling

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volume

12

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issue

5

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page(s)

317-26

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cites work

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Localization of the c-abl oncogene adjacent to a translocation break point in chronic myelocytic leukaemia

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Fused transcript of abl and bcr genes in chronic myelogenous leukaemia

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An alteration of the human c-abl protein in K562 leukemia cells unmasks associated tyrosine kinase activity.

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Activation of tyrosinase kinase and microfilament-binding functions of c-abl by bcr sequences in bcr/abl fusion proteins

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p62(dok): a constitutively tyrosine-phosphorylated, GAP-associated protein in chronic myelogenous leukemia progenitor cells

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Identification of the Abl- and rasGAP-associated 62 kDa protein as a docking protein, Dok

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Molecular cloning and characterization of p56dok-2 defines a new family of RasGAP-binding proteins

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The 145-kDa protein induced to associate with Shc by multiple cytokines is an inositol tetraphosphate and phosphatidylinositol 3,4,5-triphosphate 5-phosphatase

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p150Ship, a signal transduction molecule with inositol polyphosphate-5-phosphatase activity

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Multiple forms of an inositol polyphosphate 5-phosphatase form signaling complexes with Shc and Grb2

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Role of the inositol phosphatase SHIP in negative regulation of the immune system by the receptor Fc(gamma)RIIB.

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The emerging field of receptor-mediated inhibitory signaling: SHP or SHIP?

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The inositol polyphosphate 5-phosphatase ship is a crucial negative regulator of B cell antigen receptor signaling

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An SH2 domain-containing 5' inositolphosphatase inhibits insulin-induced GLUT4 translocation and growth factor-induced actin filament rearrangement

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SIP/SHIP inhibits Xenopus oocyte maturation induced by insulin and phosphatidylinositol 3-kinase

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SHIP modulates immune receptor responses by regulating membrane association of Btk.

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7 January 2021

Direct regulation of the Akt proto-oncogene product by phosphatidylinositol-3,4-bisphosphate

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A specific product of phosphatidylinositol 3-kinase directly activates the protein kinase Akt through its pleckstrin homology domain.

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7 January 2021

Shc interaction with Src homology 2 domain containing inositol phosphatase (SHIP) in vivo requires the Shc-phosphotyrosine binding domain and two specific phosphotyrosines on SHIP

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7 January 2021

The inositol 5'-phosphatase SHIP binds to immunoreceptor signaling motifs and responds to high affinity IgE receptor aggregation

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7 January 2021

Recruitment and phosphorylation of SH2-containing inositol phosphatase and Shc to the B-cell Fc gamma immunoreceptor tyrosine-based inhibition motif peptide motif

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7 January 2021

An alternative to SH2 domains for binding tyrosine-phosphorylated proteins

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7 January 2021

The Tek/Tie2 receptor signals through a novel Dok-related docking protein, Dok-R

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7 January 2021

The phosphatidylinositol polyphosphate 5-phosphatase SHIP and the protein tyrosine phosphatase SHP-2 form a complex in hematopoietic cells which can be regulated by BCR/ABL and growth factors

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FRIP, a hematopoietic cell-specific rasGAP-interacting protein phosphorylated in response to cytokine stimulation

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