Deletion of the COOH-terminal domain of CXC chemokine receptor 4 leads to the down-regulation of cell-to-cell contact, enhanced motility and proliferation in breast carcinoma cells (Q37147052)

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scientific article published on June 2006

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English	Deletion of the COOH-terminal domain of CXC chemokine receptor 4 leads to the down-regulation of cell-to-cell contact, enhanced motility and proliferation in breast carcinoma cells	scientific article published on June 2006

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Deletion of the COOH-terminal domain of CXC chemokine receptor 4 leads to the down-regulation of cell-to-cell contact, enhanced motility and proliferation in breast carcinoma cells (English)

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

breast carcinoma

1 reference

based on heuristic

inferred from title

5

object named as

Ann Richmond

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

author name string

Yukiko Ueda

1

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Nicole F Neel

2

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Evemie Schutyser

3

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Dayanidhi Raman

4

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Europe PubMed Central

PMC publication ID

18 August 2017

language of work or name

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publication date

1 June 2006

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Europe PubMed Central

PMC publication ID

18 August 2017

Cancer Research

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Europe PubMed Central

PMC publication ID

18 August 2017

66

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

11

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

5665-5675

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Role of beta-arrestin 1 in the metastatic progression of colorectal cancer

1 reference

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CXCR4 mutations in WHIM syndrome: a misguided immune system?

1 reference

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The C-terminal domain LLKIL motif of CXCR2 is required for ligand-mediated polarization of early signals during chemotaxis

1 reference

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GPCR interacting proteins (GIP).

1 reference

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1 reference

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The significance of cancer cell expression of the chemokine receptor CXCR4.

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Lipid raft-dependent glucagon-like peptide-2 receptor trafficking occurs independently of agonist-induced desensitization.

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The role of beta-arrestins in the termination and transduction of G-protein-coupled receptor signals

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Involvement of chemokine receptors in breast cancer metastasis

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Signal transduction by CXC chemokine receptor 4. Stromal cell-derived factor 1 stimulates prolonged protein kinase B and extracellular signal-regulated kinase 2 activation in T lymphocytes.

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beta-arrestin differentially regulates the chemokine receptor CXCR4-mediated signaling and receptor internalization, and this implicates multiple interaction sites between beta-arrestin and CXCR4

1 reference

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Point mutation causing constitutive signaling of CXCR2 leads to transforming activity similar to Kaposi's sarcoma herpesvirus-G protein-coupled receptor

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Function of the chemokine receptor CXCR4 in haematopoiesis and in cerebellar development

1 reference

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The chemokine receptor CXCR4 is essential for vascularization of the gastrointestinal tract

1 reference

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Spontaneous and ligand-induced trafficking of CXC-chemokine receptor 4.

1 reference

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The many faces of G protein signaling

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In vivo evolution of HIV-1 co-receptor usage and sensitivity to chemokine-mediated suppression.

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The HIV coreceptors CXCR4 and CCR5 are differentially expressed and regulated on human T lymphocytes

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Identifiers

10.1158/0008-5472.CAN-05-3579

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

ResearchGate publication ID

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