Comparative effects of various nitric oxide donors on ferritin regulation, programmed cell death, and cell redox state in plant cells
Past studies investigating the regulatory functions of nitric oxide (NO) in plant cells have utilized various NO-donors that release NO in different redox forms, which has lead to problems in the interpretation of data. In the present study, the effects of different NO-donors releasing NO with eithe...
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creator | Murgia, Irene Concetta de Pinto, Maria Delledonne, Massimo Soave, Carlo De Gara, Laura |
description | Past studies investigating the regulatory functions of nitric oxide (NO) in plant cells have utilized various NO-donors that release NO in different redox forms, which has lead to problems in the interpretation of data. In the present study, the effects of different NO-donors releasing NO with either NO
+ (SNP) or NO
(SNAP, GSNO, NOC-18) character have been compared in plant cells. In particular, ferritin regulation, programmed cell death, cellular redox state, and ROS-scavenging enzymes in
Arabidopsis thaliana and
Nicotiana tabacum cells were examined. The results show that SNP behaves differently than the other NO-donors tested; indeed, SNP induces accumulation of ferritin transcripts in
Arabidopsis, whereas SNAP inhibits its accumulation. Moreover, among the assortment of donors tested, only SNP caused programmed cell death and suppression of ROS-scavenging systems. |
doi_str_mv | 10.1016/j.jplph.2003.12.004 |
format | Article |
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+ (SNP) or NO
(SNAP, GSNO, NOC-18) character have been compared in plant cells. In particular, ferritin regulation, programmed cell death, cellular redox state, and ROS-scavenging enzymes in
Arabidopsis thaliana and
Nicotiana tabacum cells were examined. The results show that SNP behaves differently than the other NO-donors tested; indeed, SNP induces accumulation of ferritin transcripts in
Arabidopsis, whereas SNAP inhibits its accumulation. Moreover, among the assortment of donors tested, only SNP caused programmed cell death and suppression of ROS-scavenging systems.</description><identifier>ISSN: 0176-1617</identifier><identifier>EISSN: 1618-1328</identifier><identifier>DOI: 10.1016/j.jplph.2003.12.004</identifier><identifier>PMID: 15310066</identifier><identifier>CODEN: JPPHEY</identifier><language>eng</language><publisher>Jena: Elsevier GmbH</publisher><subject>3,3-bis(aminoethyl)-1-hydroxy-2-oxo-1-triazene ; antioxidant activity ; apoptosis ; Apoptosis - drug effects ; Arabidopsis - cytology ; Arabidopsis - drug effects ; Arabidopsis - metabolism ; Arabidopsis thaliana ; Ascorbate peroxidase ; ascorbic acid ; bioaccumulation ; Biological and medical sciences ; Catalase ; Cell physiology ; Cells, Cultured ; cultured cells ; Ferritin ; Ferritins - drug effects ; Ferritins - genetics ; Ferritins - metabolism ; Fundamental and applied biological sciences. Psychology ; Gene Expression Regulation - drug effects ; glutathione ; messenger RNA ; Molecular and cellular biology ; Nicotiana - cytology ; Nicotiana - drug effects ; Nicotiana - metabolism ; Nicotiana tabacum ; Nitric oxide ; Nitric Oxide - biosynthesis ; nitric oxide donors ; Nitric Oxide Donors - pharmacology ; Nitroprusside - pharmacology ; nitroso compounds ; Nitroso Compounds - pharmacology ; NO-donor ; Oxidation-Reduction - drug effects ; Penicillamine - analogs & derivatives ; Penicillamine - pharmacology ; Plant Cells ; Plants - drug effects ; Plants - metabolism ; Programmed cell death ; Reactive Oxygen Species ; Reactive Oxygen Species - antagonists & inhibitors ; Reactive Oxygen Species - metabolism ; redox reactions ; S-nitroso-N-acetylpenicillamine ; S-nitrosoglutathione ; S-Nitrosoglutathione - pharmacology ; Signal transduction ; sodium nitroprusside</subject><ispartof>Journal of plant physiology, 2004-07, Vol.161 (7), p.777-783</ispartof><rights>2004 Elsevier GmbH</rights><rights>2004 INIST-CNRS</rights><rights>Copyright Urban & Fischer Verlag Jul 2004</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c502t-6c284569cc04310e7642369c744ca6f430bfc7227a412f779d988060b3ad1ad23</citedby><cites>FETCH-LOGICAL-c502t-6c284569cc04310e7642369c744ca6f430bfc7227a412f779d988060b3ad1ad23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0176161704000173$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15954647$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15310066$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Murgia, Irene</creatorcontrib><creatorcontrib>Concetta de Pinto, Maria</creatorcontrib><creatorcontrib>Delledonne, Massimo</creatorcontrib><creatorcontrib>Soave, Carlo</creatorcontrib><creatorcontrib>De Gara, Laura</creatorcontrib><title>Comparative effects of various nitric oxide donors on ferritin regulation, programmed cell death, and cell redox state in plant cells</title><title>Journal of plant physiology</title><addtitle>J Plant Physiol</addtitle><description>Past studies investigating the regulatory functions of nitric oxide (NO) in plant cells have utilized various NO-donors that release NO in different redox forms, which has lead to problems in the interpretation of data. In the present study, the effects of different NO-donors releasing NO with either NO
+ (SNP) or NO
(SNAP, GSNO, NOC-18) character have been compared in plant cells. In particular, ferritin regulation, programmed cell death, cellular redox state, and ROS-scavenging enzymes in
Arabidopsis thaliana and
Nicotiana tabacum cells were examined. The results show that SNP behaves differently than the other NO-donors tested; indeed, SNP induces accumulation of ferritin transcripts in
Arabidopsis, whereas SNAP inhibits its accumulation. Moreover, among the assortment of donors tested, only SNP caused programmed cell death and suppression of ROS-scavenging systems.</description><subject>3,3-bis(aminoethyl)-1-hydroxy-2-oxo-1-triazene</subject><subject>antioxidant activity</subject><subject>apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Arabidopsis - cytology</subject><subject>Arabidopsis - drug effects</subject><subject>Arabidopsis - metabolism</subject><subject>Arabidopsis thaliana</subject><subject>Ascorbate peroxidase</subject><subject>ascorbic acid</subject><subject>bioaccumulation</subject><subject>Biological and medical sciences</subject><subject>Catalase</subject><subject>Cell physiology</subject><subject>Cells, Cultured</subject><subject>cultured cells</subject><subject>Ferritin</subject><subject>Ferritins - drug effects</subject><subject>Ferritins - genetics</subject><subject>Ferritins - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Regulation - drug effects</subject><subject>glutathione</subject><subject>messenger RNA</subject><subject>Molecular and cellular biology</subject><subject>Nicotiana - cytology</subject><subject>Nicotiana - drug effects</subject><subject>Nicotiana - metabolism</subject><subject>Nicotiana tabacum</subject><subject>Nitric oxide</subject><subject>Nitric Oxide - biosynthesis</subject><subject>nitric oxide donors</subject><subject>Nitric Oxide Donors - pharmacology</subject><subject>Nitroprusside - pharmacology</subject><subject>nitroso compounds</subject><subject>Nitroso Compounds - pharmacology</subject><subject>NO-donor</subject><subject>Oxidation-Reduction - drug effects</subject><subject>Penicillamine - analogs & derivatives</subject><subject>Penicillamine - pharmacology</subject><subject>Plant Cells</subject><subject>Plants - drug effects</subject><subject>Plants - metabolism</subject><subject>Programmed cell death</subject><subject>Reactive Oxygen Species</subject><subject>Reactive Oxygen Species - antagonists & inhibitors</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>redox reactions</subject><subject>S-nitroso-N-acetylpenicillamine</subject><subject>S-nitrosoglutathione</subject><subject>S-Nitrosoglutathione - pharmacology</subject><subject>Signal transduction</subject><subject>sodium nitroprusside</subject><issn>0176-1617</issn><issn>1618-1328</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kc1u1DAUhSMEotPCEyCBhcSuCdc_sZMFCzSigFSJBXRtefwzdZSJg-2MygPw3ng6kWDFyjq-37n3-riqXmFoMGD-fmiGeZzvGwJAG0waAPak2mCOuxpT0j2tNoAFr8uFuKguUxqg6Lajz6sL3FIMwPmm-r0Nh1lFlf3RIuuc1Tmh4NBRRR-WhCafo9coPHhjkQlTiKU8IWdj9NlPKNr9MhZ3mK7RHMM-qsPBGqTtOCJjVb6_RmpadbQmPKCUVbaoWOdRTfmxkl5Uz5wak325nlfV3c2nH9sv9e23z1-3H29r3QLJNdekYy3vtQZWHmAFZ4QWKRjTijtGYee0IEQohokTojd91wGHHVUGK0PoVfX23Les-nOxKcshLHEqIyUB3gnSsrZA9AzpGFKK1sk5-oOKvyQGeUpeDvIxeXlKXmIiS_LF9XptvexKAn89a9QFeLcCKmk1uqgm7dM_XN8yzkTh3pw5p4JU-1iYu-8EMAXoWxDdadSHM2FLVEdvo0za20lb42P5P2mC_--qfwCMzKxF</recordid><startdate>20040701</startdate><enddate>20040701</enddate><creator>Murgia, Irene</creator><creator>Concetta de Pinto, Maria</creator><creator>Delledonne, Massimo</creator><creator>Soave, Carlo</creator><creator>De Gara, Laura</creator><general>Elsevier GmbH</general><general>Elsevier</general><general>Elsevier Science Ltd</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7SS</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>S0X</scope></search><sort><creationdate>20040701</creationdate><title>Comparative effects of various nitric oxide donors on ferritin regulation, programmed cell death, and cell redox state in plant cells</title><author>Murgia, Irene ; Concetta de Pinto, Maria ; Delledonne, Massimo ; Soave, Carlo ; De Gara, Laura</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c502t-6c284569cc04310e7642369c744ca6f430bfc7227a412f779d988060b3ad1ad23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>3,3-bis(aminoethyl)-1-hydroxy-2-oxo-1-triazene</topic><topic>antioxidant activity</topic><topic>apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Arabidopsis - cytology</topic><topic>Arabidopsis - drug effects</topic><topic>Arabidopsis - metabolism</topic><topic>Arabidopsis thaliana</topic><topic>Ascorbate peroxidase</topic><topic>ascorbic acid</topic><topic>bioaccumulation</topic><topic>Biological and medical sciences</topic><topic>Catalase</topic><topic>Cell physiology</topic><topic>Cells, Cultured</topic><topic>cultured cells</topic><topic>Ferritin</topic><topic>Ferritins - drug effects</topic><topic>Ferritins - genetics</topic><topic>Ferritins - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression Regulation - drug effects</topic><topic>glutathione</topic><topic>messenger RNA</topic><topic>Molecular and cellular biology</topic><topic>Nicotiana - cytology</topic><topic>Nicotiana - drug effects</topic><topic>Nicotiana - metabolism</topic><topic>Nicotiana tabacum</topic><topic>Nitric oxide</topic><topic>Nitric Oxide - biosynthesis</topic><topic>nitric oxide donors</topic><topic>Nitric Oxide Donors - pharmacology</topic><topic>Nitroprusside - pharmacology</topic><topic>nitroso compounds</topic><topic>Nitroso Compounds - pharmacology</topic><topic>NO-donor</topic><topic>Oxidation-Reduction - drug effects</topic><topic>Penicillamine - analogs & derivatives</topic><topic>Penicillamine - pharmacology</topic><topic>Plant Cells</topic><topic>Plants - drug effects</topic><topic>Plants - metabolism</topic><topic>Programmed cell death</topic><topic>Reactive Oxygen Species</topic><topic>Reactive Oxygen Species - antagonists & inhibitors</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>redox reactions</topic><topic>S-nitroso-N-acetylpenicillamine</topic><topic>S-nitrosoglutathione</topic><topic>S-Nitrosoglutathione - pharmacology</topic><topic>Signal transduction</topic><topic>sodium nitroprusside</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Murgia, Irene</creatorcontrib><creatorcontrib>Concetta de Pinto, Maria</creatorcontrib><creatorcontrib>Delledonne, Massimo</creatorcontrib><creatorcontrib>Soave, Carlo</creatorcontrib><creatorcontrib>De Gara, Laura</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>SIRS Editorial</collection><jtitle>Journal of plant physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Murgia, Irene</au><au>Concetta de Pinto, Maria</au><au>Delledonne, Massimo</au><au>Soave, Carlo</au><au>De Gara, Laura</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative effects of various nitric oxide donors on ferritin regulation, programmed cell death, and cell redox state in plant cells</atitle><jtitle>Journal of plant physiology</jtitle><addtitle>J Plant Physiol</addtitle><date>2004-07-01</date><risdate>2004</risdate><volume>161</volume><issue>7</issue><spage>777</spage><epage>783</epage><pages>777-783</pages><issn>0176-1617</issn><eissn>1618-1328</eissn><coden>JPPHEY</coden><abstract>Past studies investigating the regulatory functions of nitric oxide (NO) in plant cells have utilized various NO-donors that release NO in different redox forms, which has lead to problems in the interpretation of data. In the present study, the effects of different NO-donors releasing NO with either NO
+ (SNP) or NO
(SNAP, GSNO, NOC-18) character have been compared in plant cells. In particular, ferritin regulation, programmed cell death, cellular redox state, and ROS-scavenging enzymes in
Arabidopsis thaliana and
Nicotiana tabacum cells were examined. The results show that SNP behaves differently than the other NO-donors tested; indeed, SNP induces accumulation of ferritin transcripts in
Arabidopsis, whereas SNAP inhibits its accumulation. Moreover, among the assortment of donors tested, only SNP caused programmed cell death and suppression of ROS-scavenging systems.</abstract><cop>Jena</cop><pub>Elsevier GmbH</pub><pmid>15310066</pmid><doi>10.1016/j.jplph.2003.12.004</doi><tpages>7</tpages></addata></record> |
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subjects | 3,3-bis(aminoethyl)-1-hydroxy-2-oxo-1-triazene antioxidant activity apoptosis Apoptosis - drug effects Arabidopsis - cytology Arabidopsis - drug effects Arabidopsis - metabolism Arabidopsis thaliana Ascorbate peroxidase ascorbic acid bioaccumulation Biological and medical sciences Catalase Cell physiology Cells, Cultured cultured cells Ferritin Ferritins - drug effects Ferritins - genetics Ferritins - metabolism Fundamental and applied biological sciences. Psychology Gene Expression Regulation - drug effects glutathione messenger RNA Molecular and cellular biology Nicotiana - cytology Nicotiana - drug effects Nicotiana - metabolism Nicotiana tabacum Nitric oxide Nitric Oxide - biosynthesis nitric oxide donors Nitric Oxide Donors - pharmacology Nitroprusside - pharmacology nitroso compounds Nitroso Compounds - pharmacology NO-donor Oxidation-Reduction - drug effects Penicillamine - analogs & derivatives Penicillamine - pharmacology Plant Cells Plants - drug effects Plants - metabolism Programmed cell death Reactive Oxygen Species Reactive Oxygen Species - antagonists & inhibitors Reactive Oxygen Species - metabolism redox reactions S-nitroso-N-acetylpenicillamine S-nitrosoglutathione S-Nitrosoglutathione - pharmacology Signal transduction sodium nitroprusside |
title | Comparative effects of various nitric oxide donors on ferritin regulation, programmed cell death, and cell redox state in plant cells |
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