Lentiviral Vectors to Study the Differential Function of ERK1 and ERK2 MAP Kinases (Q42822951)

8 November 2017

title

Lentiviral vectors to study the differential function of ERK1 and ERK2 MAP kinases (English)

1 reference

8 November 2017

Lentiviral Vectors to Study the Differential Function of ERK1 and ERK2 MAP Kinases (English)

1 reference

https://api.crossref.org/works/10.1007/978-1-60761-795-2_12

5 July 2024

author name string

Marzia Indrigo

1

1 reference

8 November 2017

Alessandro Papale

2

1 reference

8 November 2017

Daniel Orellana

3

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8 November 2017

Riccardo Brambilla

4

1 reference

8 November 2017

language of work or name

English

0 references

publication date

1 January 2010

1 reference

full work available at URL

8 November 2017

number of pages

16

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based on heuristic

inferred from page(s)

http://link.springer.com/content/pdf/10.1007/978-1-60761-795-2_12

1 reference

https://api.crossref.org/works/10.1007/978-1-60761-795-2_12

Methods in Molecular Biology

5 July 2024

published in

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8 November 2017

volume

661

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8 November 2017

page(s)

205-220

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An essential function of the mitogen-activated protein kinase Erk2 in mouse trophoblast development

8 November 2017

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Extracellular signal-regulated kinase 2 (ERK2) knockdown mice show deficits in long-term memory; ERK2 has a specific function in learning and memory

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Mice lacking the ERK1 isoform of MAP kinase are unimpaired in emotional learning

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Knockout of ERK1 MAP kinase enhances synaptic plasticity in the striatum and facilitates striatal-mediated learning and memory

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ERK1 and ERK2 mitogen-activated protein kinases affect Ras-dependent cell signaling differentially.

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The Erk2 MAPK regulates CD8 T cell proliferation and survival

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MEK/ERK-dependent uPAR expression is required for motility via phosphorylation of P70S6K in human hepatocarcinoma cells

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RNAi-mediated ERK2 knockdown inhibits growth of tumor cells in vitro and in vivo

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ERK2 but not ERK1 plays a key role in hepatocyte replication: an RNAi-mediated ERK2 knockdown approach in wild-type and ERK1 null hepatocytes.

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MEK1-ERK2 signaling pathway protects myocardium from ischemic injury in vivo

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ERK2 is required for efficient terminal differentiation of skeletal myoblasts

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Multiple division cycles and long-term survival of hepatocytes are distinctly regulated by extracellular signal-regulated kinases ERK1 and ERK2.

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Regulated fast nucleocytoplasmic shuttling observed by reversible protein highlighting

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The N-terminal domain of ERK1 accounts for the functional differences with ERK2

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Single and combined silencing of ERK1 and ERK2 reveals their positive contribution to growth signaling depending on their expression levels

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Identifiers

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release_n4uok3uy6bapjbp2snpbwftc64

8 November 2017

Fatcat ID

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mapped directly with Wikidata item

24 November 2022

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