(Q44000418)

28 November 2017

title

Implications for the insulin signaling pathway in Snell dwarf mouse longevity: a similarity with the C. elegans longevity paradigm (English)

1 reference

28 November 2017

main subject

Caenorhabditis elegans

0 references

1 reference

Ching-Chyuan Hsieh

1

1 reference

28 November 2017

James H DeFord

2

1 reference

28 November 2017

Kevin Flurkey

3

1 reference

28 November 2017

David E Harrison

4

1 reference

28 November 2017

John Papaconstantinou

5

1 reference

28 November 2017

language of work or name

1 reference

1 May 2002

1 reference

Mechanisms of Ageing and Development

28 November 2017

published in

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28 November 2017

volume

123

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28 November 2017

issue

9

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28 November 2017

page(s)

1229-1244

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Neurosecretory control of aging in Caenorhabditis elegans

28 November 2017

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7 January 2021

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7 January 2021

A C. elegans mutant that lives twice as long as wild type

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Thermotolerance and extended life-span conferred by single-gene mutations and induced by thermal stress

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7 January 2021

The PTEN tumor suppressor homolog in Caenorhabditis elegans regulates longevity and dauer formation in an insulin receptor-like signaling pathway

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7 January 2021

A phosphatidylinositol-3-OH kinase family member regulating longevity and diapause in Caenorhabditis elegans

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7 January 2021

Insulin stimulates phosphorylation of the forkhead transcription factor FKHR on serine 253 through a Wortmannin-sensitive pathway

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7 January 2021

Role of binding proteins to IRS-1 in insulin signalling

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7 January 2021

The Fork head transcription factor DAF-16 transduces insulin-like metabolic and longevity signals in C. elegans

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7 January 2021

Caenorhabditis elegans Akt/PKB transduces insulin receptor-like signals from AGE-1 PI3 kinase to the DAF-16 transcription factor

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7 January 2021

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7 January 2021

The phosphatidylinositol 3-kinase alpha is required for DNA synthesis induced by some, but not all, growth factors

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Mutations in PROP1 cause familial combined pituitary hormone deficiency

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7 January 2021

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Identifiers

DOI

1 reference

28 November 2017

1 reference