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Investigation using an HER-2/neu transgenic mouse model of a newly developed MR contrast agent with the effect of an antitumor drug
Purpose To assess whether Gd‐DTPA‐Gel‐Cis, a conjugate of gadolinium (Gd), cis diamminedichloroplatinum (Cis), diethylenetriaminepentaacetic acid (DTPA)‐dianhydride, and bovine gelatin (Gel) can be used as an intravascular contrast agent at MRI and as an antitumor cell proliferation agent in vitro....
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Published in: | Journal of magnetic resonance imaging 2009-10, Vol.30 (4), p.907-910 |
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container_issue | 4 |
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container_title | Journal of magnetic resonance imaging |
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creator | Sonoda, Akinaga Nitta, Norihisa Ohta, Shinich Nitta-Seko, Ayumi Murata, Satoshi Jo, Jun-ichiro Tabata, Yasuhiko Takahashi, Masashi Tani, Toru Murata, Kiyoshi |
description | Purpose
To assess whether Gd‐DTPA‐Gel‐Cis, a conjugate of gadolinium (Gd), cis diamminedichloroplatinum (Cis), diethylenetriaminepentaacetic acid (DTPA)‐dianhydride, and bovine gelatin (Gel) can be used as an intravascular contrast agent at MRI and as an antitumor cell proliferation agent in vitro.
Materials and Methods
We injected Gd‐DTPA‐Gel‐Cis (200 mg/mL) into the caudal vein of female HER‐2/neu transgenic mice with spontaneous mammary tumors. The tumor signal intensity was measured with a 0.3 Tesla MRI scanner. HER‐2/neu‐expressing NT cells were treated with Gd‐DTPA‐Gel‐Cis (5 μM cisplatin, 200 mg/mL Gel), Cis alone (5 μM cisplatin), or Gel alone (200 mg/mL gelatin). Differences of P < 0.05 were considered to be statistically significant.
Results
On T1‐weighted MRI scans of mice injected with Gd‐DTPA‐Gel‐Cis we observed a 23% increase in signal intensity. The survival rates of cells exposed to Gd‐DTPA‐Gel‐Cis or Cis were 70.9% and 58.3%, respectively, of the survival rates observed after treatment with Gel alone. Gd‐DTPA‐Gel‐Cis showed significant toxicity (P < 0.05).
Conclusion
Gd‐DTPA‐Gel‐Cis shows promise for use as an MRI contrast medium and as an antitumor agent. J. Magn. Reson. Imaging 2009;30:907–910. © 2009 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/jmri.21911 |
format | article |
fullrecord | <record><control><sourceid>istex_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_jmri_21911</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_WNG_CDQRQ9V1_C</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3661-390fde74d72e8810560701089b032de6a08a104ada6aaf8d6010a27c377959243</originalsourceid><addsrcrecordid>eNp9kMtOAyEUhonReKlufADD2mQUmAvD0tRbTdXYeFkSHM5UdIZpgLF27YuL1svOhBxI-L4_OT9Cu5QcUELY4XPrzAGjgtIVtElzxhKWl8VqfJM8TWhJ-Aba8v6ZECJElq-jDSp4yXmWbaL3kX0FH8xUBdNZ3Htjp1hZfH4ySdihhR4Hp6yfgjUVbrveQ5waGtzVWGEL82aBNbxC081A48sJrjobDR-wik7AcxOecHgCDHUNVfjSbDzBhL7tHNaun26jtVo1Hna-7wG6Oz25HZ4n4-uz0fBonFRpUdAkFaTWwDPNGZRl3K0gnFBSikeSMg2FIqWiJFNaFUrVpS7ip2K8SjkXuWBZOkD7y9zKdd47qOXMmVa5haREfjYpP5uUX01GeG8Jz_rHFvQf-l1dBOgSmJsGFv9EyYvLyegnNFk6xgd4-3WUe5EFT3kuH67O5PD4ZnIj7qkcph8EaI4B</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Investigation using an HER-2/neu transgenic mouse model of a newly developed MR contrast agent with the effect of an antitumor drug</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Sonoda, Akinaga ; Nitta, Norihisa ; Ohta, Shinich ; Nitta-Seko, Ayumi ; Murata, Satoshi ; Jo, Jun-ichiro ; Tabata, Yasuhiko ; Takahashi, Masashi ; Tani, Toru ; Murata, Kiyoshi</creator><creatorcontrib>Sonoda, Akinaga ; Nitta, Norihisa ; Ohta, Shinich ; Nitta-Seko, Ayumi ; Murata, Satoshi ; Jo, Jun-ichiro ; Tabata, Yasuhiko ; Takahashi, Masashi ; Tani, Toru ; Murata, Kiyoshi</creatorcontrib><description>Purpose
To assess whether Gd‐DTPA‐Gel‐Cis, a conjugate of gadolinium (Gd), cis diamminedichloroplatinum (Cis), diethylenetriaminepentaacetic acid (DTPA)‐dianhydride, and bovine gelatin (Gel) can be used as an intravascular contrast agent at MRI and as an antitumor cell proliferation agent in vitro.
Materials and Methods
We injected Gd‐DTPA‐Gel‐Cis (200 mg/mL) into the caudal vein of female HER‐2/neu transgenic mice with spontaneous mammary tumors. The tumor signal intensity was measured with a 0.3 Tesla MRI scanner. HER‐2/neu‐expressing NT cells were treated with Gd‐DTPA‐Gel‐Cis (5 μM cisplatin, 200 mg/mL Gel), Cis alone (5 μM cisplatin), or Gel alone (200 mg/mL gelatin). Differences of P < 0.05 were considered to be statistically significant.
Results
On T1‐weighted MRI scans of mice injected with Gd‐DTPA‐Gel‐Cis we observed a 23% increase in signal intensity. The survival rates of cells exposed to Gd‐DTPA‐Gel‐Cis or Cis were 70.9% and 58.3%, respectively, of the survival rates observed after treatment with Gel alone. Gd‐DTPA‐Gel‐Cis showed significant toxicity (P < 0.05).
Conclusion
Gd‐DTPA‐Gel‐Cis shows promise for use as an MRI contrast medium and as an antitumor agent. J. Magn. Reson. Imaging 2009;30:907–910. © 2009 Wiley‐Liss, Inc.</description><identifier>ISSN: 1053-1807</identifier><identifier>EISSN: 1522-2586</identifier><identifier>DOI: 10.1002/jmri.21911</identifier><identifier>PMID: 19787744</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject><![CDATA[Animals ; Antineoplastic Agents - administration & dosage ; Antineoplastic Agents - chemistry ; Antineoplastic Agents - pharmacology ; Cattle ; cis diamminedichloroplatinum ; Cisplatin - administration & dosage ; Cisplatin - chemical synthesis ; Cisplatin - pharmacology ; Contrast Media - administration & dosage ; Contrast Media - chemical synthesis ; Contrast Media - pharmacology ; Cross-Linking Reagents - administration & dosage ; Cross-Linking Reagents - chemical synthesis ; Cross-Linking Reagents - pharmacology ; diethylenetriaminepentaacetic acid ; Disease Models, Animal ; Female ; gadolinium ; Gadolinium DTPA - administration & dosage ; Gadolinium DTPA - analogs & derivatives ; Gadolinium DTPA - chemical synthesis ; Gadolinium DTPA - pharmacology ; gelatin ; Gelatin - administration & dosage ; Gelatin - chemical synthesis ; Gelatin - pharmacology ; Genes, erbB-2 ; HER-2/neu transgenic mice ; Magnetic Resonance Imaging - methods ; Mammary Neoplasms, Experimental - diagnosis ; Mammary Neoplasms, Experimental - drug therapy ; Mice ; Mice, Transgenic]]></subject><ispartof>Journal of magnetic resonance imaging, 2009-10, Vol.30 (4), p.907-910</ispartof><rights>Copyright © 2009 Wiley‐Liss, Inc.</rights><rights>(c) 2009 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3661-390fde74d72e8810560701089b032de6a08a104ada6aaf8d6010a27c377959243</citedby><cites>FETCH-LOGICAL-c3661-390fde74d72e8810560701089b032de6a08a104ada6aaf8d6010a27c377959243</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19787744$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sonoda, Akinaga</creatorcontrib><creatorcontrib>Nitta, Norihisa</creatorcontrib><creatorcontrib>Ohta, Shinich</creatorcontrib><creatorcontrib>Nitta-Seko, Ayumi</creatorcontrib><creatorcontrib>Murata, Satoshi</creatorcontrib><creatorcontrib>Jo, Jun-ichiro</creatorcontrib><creatorcontrib>Tabata, Yasuhiko</creatorcontrib><creatorcontrib>Takahashi, Masashi</creatorcontrib><creatorcontrib>Tani, Toru</creatorcontrib><creatorcontrib>Murata, Kiyoshi</creatorcontrib><title>Investigation using an HER-2/neu transgenic mouse model of a newly developed MR contrast agent with the effect of an antitumor drug</title><title>Journal of magnetic resonance imaging</title><addtitle>J. Magn. Reson. Imaging</addtitle><description>Purpose
To assess whether Gd‐DTPA‐Gel‐Cis, a conjugate of gadolinium (Gd), cis diamminedichloroplatinum (Cis), diethylenetriaminepentaacetic acid (DTPA)‐dianhydride, and bovine gelatin (Gel) can be used as an intravascular contrast agent at MRI and as an antitumor cell proliferation agent in vitro.
Materials and Methods
We injected Gd‐DTPA‐Gel‐Cis (200 mg/mL) into the caudal vein of female HER‐2/neu transgenic mice with spontaneous mammary tumors. The tumor signal intensity was measured with a 0.3 Tesla MRI scanner. HER‐2/neu‐expressing NT cells were treated with Gd‐DTPA‐Gel‐Cis (5 μM cisplatin, 200 mg/mL Gel), Cis alone (5 μM cisplatin), or Gel alone (200 mg/mL gelatin). Differences of P < 0.05 were considered to be statistically significant.
Results
On T1‐weighted MRI scans of mice injected with Gd‐DTPA‐Gel‐Cis we observed a 23% increase in signal intensity. The survival rates of cells exposed to Gd‐DTPA‐Gel‐Cis or Cis were 70.9% and 58.3%, respectively, of the survival rates observed after treatment with Gel alone. Gd‐DTPA‐Gel‐Cis showed significant toxicity (P < 0.05).
Conclusion
Gd‐DTPA‐Gel‐Cis shows promise for use as an MRI contrast medium and as an antitumor agent. J. Magn. Reson. Imaging 2009;30:907–910. © 2009 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>Antineoplastic Agents - administration & dosage</subject><subject>Antineoplastic Agents - chemistry</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Cattle</subject><subject>cis diamminedichloroplatinum</subject><subject>Cisplatin - administration & dosage</subject><subject>Cisplatin - chemical synthesis</subject><subject>Cisplatin - pharmacology</subject><subject>Contrast Media - administration & dosage</subject><subject>Contrast Media - chemical synthesis</subject><subject>Contrast Media - pharmacology</subject><subject>Cross-Linking Reagents - administration & dosage</subject><subject>Cross-Linking Reagents - chemical synthesis</subject><subject>Cross-Linking Reagents - pharmacology</subject><subject>diethylenetriaminepentaacetic acid</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>gadolinium</subject><subject>Gadolinium DTPA - administration & dosage</subject><subject>Gadolinium DTPA - analogs & derivatives</subject><subject>Gadolinium DTPA - chemical synthesis</subject><subject>Gadolinium DTPA - pharmacology</subject><subject>gelatin</subject><subject>Gelatin - administration & dosage</subject><subject>Gelatin - chemical synthesis</subject><subject>Gelatin - pharmacology</subject><subject>Genes, erbB-2</subject><subject>HER-2/neu transgenic mice</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Mammary Neoplasms, Experimental - diagnosis</subject><subject>Mammary Neoplasms, Experimental - drug therapy</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><issn>1053-1807</issn><issn>1522-2586</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9kMtOAyEUhonReKlufADD2mQUmAvD0tRbTdXYeFkSHM5UdIZpgLF27YuL1svOhBxI-L4_OT9Cu5QcUELY4XPrzAGjgtIVtElzxhKWl8VqfJM8TWhJ-Aba8v6ZECJElq-jDSp4yXmWbaL3kX0FH8xUBdNZ3Htjp1hZfH4ySdihhR4Hp6yfgjUVbrveQ5waGtzVWGEL82aBNbxC081A48sJrjobDR-wik7AcxOecHgCDHUNVfjSbDzBhL7tHNaun26jtVo1Hna-7wG6Oz25HZ4n4-uz0fBonFRpUdAkFaTWwDPNGZRl3K0gnFBSikeSMg2FIqWiJFNaFUrVpS7ip2K8SjkXuWBZOkD7y9zKdd47qOXMmVa5haREfjYpP5uUX01GeG8Jz_rHFvQf-l1dBOgSmJsGFv9EyYvLyegnNFk6xgd4-3WUe5EFT3kuH67O5PD4ZnIj7qkcph8EaI4B</recordid><startdate>200910</startdate><enddate>200910</enddate><creator>Sonoda, Akinaga</creator><creator>Nitta, Norihisa</creator><creator>Ohta, Shinich</creator><creator>Nitta-Seko, Ayumi</creator><creator>Murata, Satoshi</creator><creator>Jo, Jun-ichiro</creator><creator>Tabata, Yasuhiko</creator><creator>Takahashi, Masashi</creator><creator>Tani, Toru</creator><creator>Murata, Kiyoshi</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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></search><sort><creationdate>200910</creationdate><title>Investigation using an HER-2/neu transgenic mouse model of a newly developed MR contrast agent with the effect of an antitumor drug</title><author>Sonoda, Akinaga ; Nitta, Norihisa ; Ohta, Shinich ; Nitta-Seko, Ayumi ; Murata, Satoshi ; Jo, Jun-ichiro ; Tabata, Yasuhiko ; Takahashi, Masashi ; Tani, Toru ; Murata, Kiyoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3661-390fde74d72e8810560701089b032de6a08a104ada6aaf8d6010a27c377959243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Antineoplastic Agents - administration & dosage</topic><topic>Antineoplastic Agents - chemistry</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Cattle</topic><topic>cis diamminedichloroplatinum</topic><topic>Cisplatin - administration & dosage</topic><topic>Cisplatin - chemical synthesis</topic><topic>Cisplatin - pharmacology</topic><topic>Contrast Media - administration & dosage</topic><topic>Contrast Media - chemical synthesis</topic><topic>Contrast Media - pharmacology</topic><topic>Cross-Linking Reagents - administration & dosage</topic><topic>Cross-Linking Reagents - chemical synthesis</topic><topic>Cross-Linking Reagents - pharmacology</topic><topic>diethylenetriaminepentaacetic acid</topic><topic>Disease Models, Animal</topic><topic>Female</topic><topic>gadolinium</topic><topic>Gadolinium DTPA - administration & dosage</topic><topic>Gadolinium DTPA - analogs & derivatives</topic><topic>Gadolinium DTPA - chemical synthesis</topic><topic>Gadolinium DTPA - pharmacology</topic><topic>gelatin</topic><topic>Gelatin - administration & dosage</topic><topic>Gelatin - chemical synthesis</topic><topic>Gelatin - pharmacology</topic><topic>Genes, erbB-2</topic><topic>HER-2/neu transgenic mice</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Mammary Neoplasms, Experimental - diagnosis</topic><topic>Mammary Neoplasms, Experimental - drug therapy</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sonoda, Akinaga</creatorcontrib><creatorcontrib>Nitta, Norihisa</creatorcontrib><creatorcontrib>Ohta, Shinich</creatorcontrib><creatorcontrib>Nitta-Seko, Ayumi</creatorcontrib><creatorcontrib>Murata, Satoshi</creatorcontrib><creatorcontrib>Jo, Jun-ichiro</creatorcontrib><creatorcontrib>Tabata, Yasuhiko</creatorcontrib><creatorcontrib>Takahashi, Masashi</creatorcontrib><creatorcontrib>Tani, Toru</creatorcontrib><creatorcontrib>Murata, Kiyoshi</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of magnetic resonance imaging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sonoda, Akinaga</au><au>Nitta, Norihisa</au><au>Ohta, Shinich</au><au>Nitta-Seko, Ayumi</au><au>Murata, Satoshi</au><au>Jo, Jun-ichiro</au><au>Tabata, Yasuhiko</au><au>Takahashi, Masashi</au><au>Tani, Toru</au><au>Murata, Kiyoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigation using an HER-2/neu transgenic mouse model of a newly developed MR contrast agent with the effect of an antitumor drug</atitle><jtitle>Journal of magnetic resonance imaging</jtitle><addtitle>J. Magn. Reson. Imaging</addtitle><date>2009-10</date><risdate>2009</risdate><volume>30</volume><issue>4</issue><spage>907</spage><epage>910</epage><pages>907-910</pages><issn>1053-1807</issn><eissn>1522-2586</eissn><abstract>Purpose
To assess whether Gd‐DTPA‐Gel‐Cis, a conjugate of gadolinium (Gd), cis diamminedichloroplatinum (Cis), diethylenetriaminepentaacetic acid (DTPA)‐dianhydride, and bovine gelatin (Gel) can be used as an intravascular contrast agent at MRI and as an antitumor cell proliferation agent in vitro.
Materials and Methods
We injected Gd‐DTPA‐Gel‐Cis (200 mg/mL) into the caudal vein of female HER‐2/neu transgenic mice with spontaneous mammary tumors. The tumor signal intensity was measured with a 0.3 Tesla MRI scanner. HER‐2/neu‐expressing NT cells were treated with Gd‐DTPA‐Gel‐Cis (5 μM cisplatin, 200 mg/mL Gel), Cis alone (5 μM cisplatin), or Gel alone (200 mg/mL gelatin). Differences of P < 0.05 were considered to be statistically significant.
Results
On T1‐weighted MRI scans of mice injected with Gd‐DTPA‐Gel‐Cis we observed a 23% increase in signal intensity. The survival rates of cells exposed to Gd‐DTPA‐Gel‐Cis or Cis were 70.9% and 58.3%, respectively, of the survival rates observed after treatment with Gel alone. Gd‐DTPA‐Gel‐Cis showed significant toxicity (P < 0.05).
Conclusion
Gd‐DTPA‐Gel‐Cis shows promise for use as an MRI contrast medium and as an antitumor agent. J. Magn. Reson. Imaging 2009;30:907–910. © 2009 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>19787744</pmid><doi>10.1002/jmri.21911</doi><tpages>4</tpages></addata></record> |
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subjects | Animals Antineoplastic Agents - administration & dosage Antineoplastic Agents - chemistry Antineoplastic Agents - pharmacology Cattle cis diamminedichloroplatinum Cisplatin - administration & dosage Cisplatin - chemical synthesis Cisplatin - pharmacology Contrast Media - administration & dosage Contrast Media - chemical synthesis Contrast Media - pharmacology Cross-Linking Reagents - administration & dosage Cross-Linking Reagents - chemical synthesis Cross-Linking Reagents - pharmacology diethylenetriaminepentaacetic acid Disease Models, Animal Female gadolinium Gadolinium DTPA - administration & dosage Gadolinium DTPA - analogs & derivatives Gadolinium DTPA - chemical synthesis Gadolinium DTPA - pharmacology gelatin Gelatin - administration & dosage Gelatin - chemical synthesis Gelatin - pharmacology Genes, erbB-2 HER-2/neu transgenic mice Magnetic Resonance Imaging - methods Mammary Neoplasms, Experimental - diagnosis Mammary Neoplasms, Experimental - drug therapy Mice Mice, Transgenic |
title | Investigation using an HER-2/neu transgenic mouse model of a newly developed MR contrast agent with the effect of an antitumor drug |
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