CIP4 is required for the hypertrophic growth of neonatal cardiac myocytes (Q28580563)

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English	CIP4 is required for the hypertrophic growth of neonatal cardiac myocytes	scientific journal article

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31 January 2017

CIP4 is required for the hypertrophic growth of neonatal cardiac myocytes (English)

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31 January 2017

Francesca Rusconi

1

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31 January 2017

Hrishikesh Thakur

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2

1 reference

31 January 2017

Jinliang Li

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3

1 reference

31 January 2017

Michael S. Kapiloff

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4

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31 January 2017

3 August 2013

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31 January 2017

Journal of Biomedical Science

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31 January 2017

20

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31 January 2017

56

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31 January 2017

The mAKAPbeta scaffold regulates cardiac myocyte hypertrophy via recruitment of activated calcineurin

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750294

retrieved

17 March 2017

The F-BAR protein CIP4 promotes GLUT4 endocytosis through bidirectional interactions with N-WASp and Dynamin-2

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750294

retrieved

17 March 2017

The mAKAP complex participates in the induction of cardiac myocyte hypertrophy by adrenergic receptor signaling

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750294

retrieved

17 March 2017

The TC10-interacting protein CIP4/2 is required for insulin-stimulated Glut4 translocation in 3T3L1 adipocytes

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750294

retrieved

17 March 2017

Identification and genetic analysis of human and mouse activated Cdc42 interacting protein-4 isoforms

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750294

retrieved

17 March 2017

Cdc42-interacting protein 4 mediates binding of the Wiskott-Aldrich syndrome protein to microtubules

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750294

retrieved

17 March 2017

Regulation of cardiac hypertrophy by intracellular signalling pathways

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750294

retrieved

7 April 2017

CIP4 coordinates with phospholipids and actin-associated proteins to localize to the protruding edge and produce actin ribs and veils.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750294

retrieved

29 September 2017

Cdc42-interacting protein 4 is a Src substrate that regulates invadopodia and invasiveness of breast tumors by promoting MT1-MMP endocytosis

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750294

retrieved

29 September 2017

Cdc42 interacting protein 4 (CIP4) is essential for integrin-dependent T-cell trafficking.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750294

retrieved

29 September 2017

The proposed functions of membrane curvatures mediated by the BAR domain superfamily proteins

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750294

retrieved

29 September 2017

The Cdc42-interacting protein-4 (CIP4) gene knock-out mouse reveals delayed and decreased endocytosis

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750294

retrieved

29 September 2017

Members of the CIP4 family of proteins participate in the regulation of platelet-derived growth factor receptor-beta-dependent actin reorganization and migration

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750294

retrieved

29 September 2017

F-BAR-containing adaptor CIP4 localizes to early endosomes and regulates Epidermal Growth Factor Receptor trafficking and downregulation.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750294

retrieved

29 September 2017

Signalosomes as Therapeutic Targets

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3750294

retrieved

29 September 2017

Cardiac hypertrophy is inhibited by antagonism of ADAM12 processing of HB-EGF: metalloproteinase inhibitors as a new therapy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1186%2F1423-0127-20-56

retrieved

21 January 2018

An angiotensin II type 1 receptor mutant lacking epidermal growth factor receptor transactivation does not induce angiotensin II-mediated cardiac hypertrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/23915320

retrieved

12 December 2020

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10.1186/1423-0127-20-56

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31 January 2017

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1 reference

31 January 2017

ResearchGate publication ID

255691841

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CIP4 is required for the hypertrophic growth of neonatal cardiac myocytes (Q28580563)

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CIP4 is required for the hypertrophic growth of neonatal cardiac myocytes (Q28580563)

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