Cell signaling under salt, water and cold stresses (Q34399362)

1 August 2017

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title

Cell signaling under salt, water and cold stresses (English)

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1 August 2017

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Zhu JK

1

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1 August 2017

1 October 2001

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Current Opinion in Plant Biology

1 August 2017

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1 August 2017

4

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1 August 2017

401-406

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1 August 2017

5

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Gene Expression and Signal Transduction in Water-Stress Response

1 August 2017

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

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7 January 2021

PLANT CELLULAR AND MOLECULAR RESPONSES TO HIGH SALINITY.

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Sodium transport in plant cells

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Genetic analysis of plant salt tolerance using Arabidopsis

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

SOS1, a Genetic Locus Essential for Salt Tolerance and Potassium Acquisition.

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Genetic analysis of salt tolerance in arabidopsis. Evidence for a critical role of potassium nutrition

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

The Arabidopsis thaliana salt tolerance gene SOS1 encodes a putative Na+/H+ antiporter.

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Molecular characterization of functional domains in the protein kinase SOS2 that is required for plant salt tolerance

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

A calcium sensor homolog required for plant salt tolerance

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

SOS3 function in plant salt tolerance requires N-myristoylation and calcium binding

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Genes that are uniquely stress regulated in salt overly sensitive (sos) mutants

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Calcium-independent activation of salicylic acid-induced protein kinase and a 40-kilodalton protein kinase by hyperosmotic stress

1 reference

https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Distinct osmo-sensing protein kinase pathways are involved in signalling moderate and severe hyper-osmotic stress

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Protein kinases induced by osmotic stresses and elicitor molecules in tobacco cell suspensions: two crossroad MAP kinases and one osmoregulation-specific protein kinase

1 reference

https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

SIMKK, a mitogen-activated protein kinase (MAPK) kinase, is a specific activator of the salt stress-induced MAPK, SIMK.

1 reference

https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Molecular cloning and characterization of a tobacco MAP kinase kinase that interacts with SIPK

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Various abiotic stresses rapidly activate Arabidopsis MAP kinases ATMPK4 and ATMPK6

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Tobacco MAP kinase: a possible mediator in wound signal transduction pathways.

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Stress signaling in plants: a mitogen-activated protein kinase pathway is activated by cold and drought

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

MAP kinase cascades in Arabidopsis: their roles in stress and hormone responses

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

So what's new in the field of plant cold acclimation? Lots!

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

A novel cis-acting element in an Arabidopsis gene is involved in responsiveness to drought, low-temperature, or high-salt stress

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Arabidopsis thaliana CBF1 encodes an AP2 domain-containing transcriptional activator that binds to the C-repeat/DRE, a cis-acting DNA regulatory element that stimulates transcription in response to low temperature and water deficit

1 reference

https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Two transcription factors, DREB1 and DREB2, with an EREBP/AP2 DNA binding domain separate two cellular signal transduction pathways in drought- and low-temperature-responsive gene expression, respectively, in Arabidopsis.

1 reference

https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Arabidopsis CBF1 overexpression induces COR genes and enhances freezing tolerance

1 reference

https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Monitoring the expression pattern of 1300 Arabidopsis genes under drought and cold stresses by using a full-length cDNA microarray

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Overexpression of the Arabidopsis CBF3 transcriptional activator mimics multiple biochemical changes associated with cold acclimation

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Transcriptional adaptor and histone acetyltransferase proteins in Arabidopsis and their interactions with CBF1, a transcriptional activator involved in cold-regulated gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

The Arabidopsis HOS1 gene negatively regulates cold signal transduction and encodes a RING finger protein that displays cold-regulated nucleo--cytoplasmic partitioning

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

HOS1, a genetic locus involved in cold-responsive gene expression in arabidopsis

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Eskimo1 mutants of Arabidopsis are constitutively freezing-tolerant.

1 reference

https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Cold-regulated gene expression and freezing tolerance in an Arabidopsis thaliana mutant

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

The sfr6 mutation in Arabidopsis suppresses low-temperature induction of genes dependent on the CRT/DRE sequence motif

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Cold calcium signaling in Arabidopsis involves two cellular pools and a change in calcium signature after acclimation

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Alteration of stimulus-specific guard cell calcium oscillations and stomatal closing in Arabidopsis det3 mutant.

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

Early steps in cold sensing by plant cells: the role of actin cytoskeleton and membrane fluidity

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https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

The pathway for perception and transduction of low-temperature signals in Synechocystis.

1 reference

https://api.crossref.org/works/10.1016%2FS1369-5266%2800%2900192-8

7 January 2021

10.1016/S1369-5266(00)00192-8

Identifiers

DOI

1 reference

1 August 2017

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PubMed ID

11597497