SHIP-mediated inhibition of K562 erythroid differentiation requires an intact catalytic domain and Shc binding site (Q38317552)

2 September 2017

SHIP-mediated inhibition of K562 erythroid differentiation requires an intact catalytic domain and Shc binding site (English)

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2 September 2017

J Siegel

1

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2 September 2017

Y Li

series ordinal

2

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2 September 2017

P Whyte

series ordinal

3

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2 September 2017

language of work or name

English

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publication date

1 November 1999

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2 September 2017

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2 September 2017

18

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2 September 2017

50

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2 September 2017

7135-7148

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https://scigraph.springernature.com/pub.10.1038/sj.onc.1203212

2 September 2017

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cites work

The primary structure of the human ε-globin gene

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

21 January 2018

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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

21 January 2018

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Selective in vivo recruitment of the phosphatidylinositol phosphatase SHIP by phosphorylated FcγRIIB during negative regulation of IgE-dependent mouse mast cell activation

21 January 2018

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The chronic myelocytic cell line K562 contains a breakpoint in bcr and produces a chimeric bcr/c-abl transcript

21 January 2018

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Isolation and characterization of full-length cDNA clones for human alpha-, beta-, and gamma-actin mRNAs: skeletal but not cytoplasmic actins have an amino-terminal cysteine that is subsequently removed

21 January 2018

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Association of adenovirus early-region 1A proteins with cellular polypeptides

21 January 2018

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Targeted disruption of SHIP leads to hemopoietic perturbations, lung pathology, and a shortened life span

21 January 2018

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Targeted disruption of SHIP leads to Steel factor-induced degranulation of mast cells.

21 January 2018

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Signaling inositol polyphosphate-5-phosphatase. Characterization of activity and effect of GRB2 association.

21 January 2018

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Mutation of the conserved domains of two inositol polyphosphate 5-phosphatases

21 January 2018

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

21 January 2018

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An alternative to SH2 domains for binding tyrosine-phosphorylated proteins

21 January 2018

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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

21 January 2018

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ABL oncogene expression during erythroleukemia cell differentiation

21 January 2018

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

21 January 2018

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Multiple Cytokines Stimulate the Binding of a Common 145-Kilodalton Protein to Shc at the Grb2 Recognition Site of Shc

21 January 2018

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The Src homology 2 (SH2) domain of SH2-containing inositol phosphatase (SHIP) is essential for tyrosine phosphorylation of SHIP, its association with Shc, and its induction of apoptosis

21 January 2018

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

21 January 2018

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

21 January 2018

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Deletion of SHIP or SHP-1 reveals two distinct pathways for inhibitory signaling

21 January 2018

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

21 January 2018

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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

21 January 2018

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Signalling mechanisms in erythropoiesis: the enigmatic role of calcium

21 January 2018

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Phosphatidylinositol-3,4,5-trisphosphate (PtdIns-3,4,5-P3)/Tec kinase-dependent calcium signaling pathway: a target for SHIP-mediated inhibitory signals

21 January 2018

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Disrupted signaling in a mutant J2E cell line that shows enhanced viability, but does not proliferate or differentiate, with erythropoietin

21 January 2018

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

21 January 2018

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Negative signaling in B cells: SHIP Grbs Shc.

21 January 2018

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Megakaryocytic differentiation induced by constitutive activation of mitogen-activated protein kinase kinase

21 January 2018

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Generation of committed erythroid BFU-E and CFU-E progenitors does not require erythropoietin or the erythropoietin receptor

21 January 2018

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Transcriptional regulation of globin gene expression in the human erythroid cell line K562

21 January 2018

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Inositol 1,3,4,5-tetrakisphosphate activates an endothelial Ca2+-permeable channel

21 January 2018

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The SHIP phosphatase becomes associated with Fc gammaRIIB1 and is tyrosine phosphorylated during 'negative' signaling

21 January 2018

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7 January 2021

The scanning model for translation: an update

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1203212

7 January 2021

A strategy tinged with chauvinism

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1203212

7 January 2021

Regulation of biosynthesis and phosphorylation of P210bcr/abl protein during differentiation induction of K 562 cells

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1203212

7 January 2021

High-Efficiency Cloning of Full-Length cDNA

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1203212

7 January 2021

Sustained activation of the extracellular signal-regulated kinase/mitogen-activated protein kinase pathway is required for megakaryocytic differentiation of K562 cells

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1203212

7 January 2021

Sodium butyrate induces tyrosine phosphorylation and activation of MAP kinase (ERK-1) in human K562 cells

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1203212

7 January 2021

Identifiers

DOI

10.1038/SJ.ONC.1203212

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Dimensions Publication ID

2 September 2017

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1 reference