GALNT9 gene expression is a prognostic marker in neuroblastoma patients
The enzymes encoded by the GALNT [UDP-N-acetyl-α-d-galactosamine:polypeptide N-acetylgalactosaminyltransferase (GALNAC-T)] gene family catalyze the first step of O-glycosylation. Little is known about the link between expression of the genes encoding GALNAC-T enzymes and tumor progression in neurobl...
Gespeichert in:
Veröffentlicht in: | Clinical chemistry (Baltimore, Md.) Md.), 2013-01, Vol.59 (1), p.225-233 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 233 |
---|---|
container_issue | 1 |
container_start_page | 225 |
container_title | Clinical chemistry (Baltimore, Md.) |
container_volume | 59 |
creator | Berois, Nora Gattolliat, Charles-Henry Barrios, Enrique Capandeguy, Laura Douc-Rasy, Sétha Valteau-Couanet, Dominique Bénard, Jean Osinaga, Eduardo |
description | The enzymes encoded by the GALNT [UDP-N-acetyl-α-d-galactosamine:polypeptide N-acetylgalactosaminyltransferase (GALNAC-T)] gene family catalyze the first step of O-glycosylation. Little is known about the link between expression of the genes encoding GALNAC-T enzymes and tumor progression in neuroblastoma, a pediatric cancer that can be classified as either low or high risk. We assessed the expression of genes in the GALNT family in a large cohort of neuroblastoma patients and characterized members of this family that might be used as new prognostic markers.
Reverse-transcription PCR analysis of 14 GALNT genes with a panel of neuroblastoma cell lines identified the GALNT9 gene as playing a potential role in disease progression. We used the log-rank test and the multivariable Cox proportional hazards model with a cohort of 122 neuroblastoma patients to analyze the relationship between GALNT9 expression and overall survival or disease-free survival.
In the high-risk neuroblastoma experimental model IGR-N-91, GALNT9 expression was present in neuroblasts derived from primary tumors but not in neuroblasts from metastatic bone marrow. Moreover, GALNT9 in neuroblastoma cell lines was expressed in substrate adherent (S)-type cell lines but not in neuronal (N)-type lines. In the tumor cohort, GALNT9 expression was associated with high overall survival, independent of the standard risk-stratification covariates. GALNT9 expression was significantly associated with disease-free survival for patients currently classified as at low risk (P < 0.0007).
GALNT9 expression correlates with both improved overall survival in low- and high-risk groups and an improved clinical outcome (overall and disease-free survival) in low-risk patients. Thus, the GALNT9 expression may be a prognostic marker for personalized therapy. |
doi_str_mv | 10.1373/clinchem.2012.192328 |
format | Article |
fullrecord | <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_pasteur_00845821v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1566834341</sourcerecordid><originalsourceid>FETCH-LOGICAL-c406t-b1c616ba5866558dafd1b06c0816c3b5ed0916417f066d87b2c5ec5a1d6345683</originalsourceid><addsrcrecordid>eNqNkU1P3DAQhi3UCrbAP6iqSL30ksXjj4lzXCFYkFZwoWfLcbxgmthbO6nKv8dogQMnTpalZ169Mw8h34EugTf8zA4-2Ac3LhkFtoSWcaYOyAIkp7WSCF_IglLa1i2I5oh8y_mxfEWj8JAcMQ4cmZALsl6vNjd3bXXvgqvc_11yOfsYKp8rU-1SvA8xT95Wo0l_XKp8qIKbU-wGk6c4FsRM3oUpn5CvWzNkd_r6HpPflxd351f15nZ9fb7a1FZQnOoOLAJ2RipEKVVvtj10FC1VgJZ30vW0BRTQbClir5qOWemsNNAjFxIVPyb1PvfBDHqXfOn1pKPx-mq10btSqrTTlCohFYN_UPhfe77s8nd2edKjz9YNgwkuzlmDxJIquPgEyhoO2ArKCvrzA_oY5xTK4rocFikqKWmhxJ6yKeac3Pa9MFD94lC_OdQvDvXeYRn78Ro-d6Pr34fepPFnFnWW9Q</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1366068550</pqid></control><display><type>article</type><title>GALNT9 gene expression is a prognostic marker in neuroblastoma patients</title><source>Oxford University Press Journals All Titles (1996-Current)</source><source>MEDLINE</source><creator>Berois, Nora ; Gattolliat, Charles-Henry ; Barrios, Enrique ; Capandeguy, Laura ; Douc-Rasy, Sétha ; Valteau-Couanet, Dominique ; Bénard, Jean ; Osinaga, Eduardo</creator><creatorcontrib>Berois, Nora ; Gattolliat, Charles-Henry ; Barrios, Enrique ; Capandeguy, Laura ; Douc-Rasy, Sétha ; Valteau-Couanet, Dominique ; Bénard, Jean ; Osinaga, Eduardo</creatorcontrib><description>The enzymes encoded by the GALNT [UDP-N-acetyl-α-d-galactosamine:polypeptide N-acetylgalactosaminyltransferase (GALNAC-T)] gene family catalyze the first step of O-glycosylation. Little is known about the link between expression of the genes encoding GALNAC-T enzymes and tumor progression in neuroblastoma, a pediatric cancer that can be classified as either low or high risk. We assessed the expression of genes in the GALNT family in a large cohort of neuroblastoma patients and characterized members of this family that might be used as new prognostic markers.
Reverse-transcription PCR analysis of 14 GALNT genes with a panel of neuroblastoma cell lines identified the GALNT9 gene as playing a potential role in disease progression. We used the log-rank test and the multivariable Cox proportional hazards model with a cohort of 122 neuroblastoma patients to analyze the relationship between GALNT9 expression and overall survival or disease-free survival.
In the high-risk neuroblastoma experimental model IGR-N-91, GALNT9 expression was present in neuroblasts derived from primary tumors but not in neuroblasts from metastatic bone marrow. Moreover, GALNT9 in neuroblastoma cell lines was expressed in substrate adherent (S)-type cell lines but not in neuronal (N)-type lines. In the tumor cohort, GALNT9 expression was associated with high overall survival, independent of the standard risk-stratification covariates. GALNT9 expression was significantly associated with disease-free survival for patients currently classified as at low risk (P < 0.0007).
GALNT9 expression correlates with both improved overall survival in low- and high-risk groups and an improved clinical outcome (overall and disease-free survival) in low-risk patients. Thus, the GALNT9 expression may be a prognostic marker for personalized therapy.</description><identifier>ISSN: 0009-9147</identifier><identifier>EISSN: 1530-8561</identifier><identifier>DOI: 10.1373/clinchem.2012.192328</identifier><identifier>PMID: 23136245</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Age ; Apoptosis ; Biomarkers, Tumor - genetics ; Biomedical research ; Bone marrow ; Breast cancer ; Cell adhesion & migration ; Cell Line, Tumor ; Colorectal cancer ; Humans ; Infant ; Life Sciences ; Ligands ; N-Acetylgalactosaminyltransferases ; N-Acetylgalactosaminyltransferases - genetics ; Neuroblastoma ; Neuroblastoma - genetics ; Neuroblastoma - pathology ; Prognosis ; Proteins ; Reverse Transcriptase Polymerase Chain Reaction ; Survival ; Survival analysis ; Tumor Markers, Biological ; Tumors</subject><ispartof>Clinical chemistry (Baltimore, Md.), 2013-01, Vol.59 (1), p.225-233</ispartof><rights>2012 American Association for Clinical Chemistry</rights><rights>Copyright American Association for Clinical Chemistry Jan 2013</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c406t-b1c616ba5866558dafd1b06c0816c3b5ed0916417f066d87b2c5ec5a1d6345683</citedby><cites>FETCH-LOGICAL-c406t-b1c616ba5866558dafd1b06c0816c3b5ed0916417f066d87b2c5ec5a1d6345683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23136245$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://riip.hal.science/pasteur-00845821$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Berois, Nora</creatorcontrib><creatorcontrib>Gattolliat, Charles-Henry</creatorcontrib><creatorcontrib>Barrios, Enrique</creatorcontrib><creatorcontrib>Capandeguy, Laura</creatorcontrib><creatorcontrib>Douc-Rasy, Sétha</creatorcontrib><creatorcontrib>Valteau-Couanet, Dominique</creatorcontrib><creatorcontrib>Bénard, Jean</creatorcontrib><creatorcontrib>Osinaga, Eduardo</creatorcontrib><title>GALNT9 gene expression is a prognostic marker in neuroblastoma patients</title><title>Clinical chemistry (Baltimore, Md.)</title><addtitle>Clin Chem</addtitle><description>The enzymes encoded by the GALNT [UDP-N-acetyl-α-d-galactosamine:polypeptide N-acetylgalactosaminyltransferase (GALNAC-T)] gene family catalyze the first step of O-glycosylation. Little is known about the link between expression of the genes encoding GALNAC-T enzymes and tumor progression in neuroblastoma, a pediatric cancer that can be classified as either low or high risk. We assessed the expression of genes in the GALNT family in a large cohort of neuroblastoma patients and characterized members of this family that might be used as new prognostic markers.
Reverse-transcription PCR analysis of 14 GALNT genes with a panel of neuroblastoma cell lines identified the GALNT9 gene as playing a potential role in disease progression. We used the log-rank test and the multivariable Cox proportional hazards model with a cohort of 122 neuroblastoma patients to analyze the relationship between GALNT9 expression and overall survival or disease-free survival.
In the high-risk neuroblastoma experimental model IGR-N-91, GALNT9 expression was present in neuroblasts derived from primary tumors but not in neuroblasts from metastatic bone marrow. Moreover, GALNT9 in neuroblastoma cell lines was expressed in substrate adherent (S)-type cell lines but not in neuronal (N)-type lines. In the tumor cohort, GALNT9 expression was associated with high overall survival, independent of the standard risk-stratification covariates. GALNT9 expression was significantly associated with disease-free survival for patients currently classified as at low risk (P < 0.0007).
GALNT9 expression correlates with both improved overall survival in low- and high-risk groups and an improved clinical outcome (overall and disease-free survival) in low-risk patients. Thus, the GALNT9 expression may be a prognostic marker for personalized therapy.</description><subject>Age</subject><subject>Apoptosis</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Biomedical research</subject><subject>Bone marrow</subject><subject>Breast cancer</subject><subject>Cell adhesion & migration</subject><subject>Cell Line, Tumor</subject><subject>Colorectal cancer</subject><subject>Humans</subject><subject>Infant</subject><subject>Life Sciences</subject><subject>Ligands</subject><subject>N-Acetylgalactosaminyltransferases</subject><subject>N-Acetylgalactosaminyltransferases - genetics</subject><subject>Neuroblastoma</subject><subject>Neuroblastoma - genetics</subject><subject>Neuroblastoma - pathology</subject><subject>Prognosis</subject><subject>Proteins</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Survival</subject><subject>Survival analysis</subject><subject>Tumor Markers, Biological</subject><subject>Tumors</subject><issn>0009-9147</issn><issn>1530-8561</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNkU1P3DAQhi3UCrbAP6iqSL30ksXjj4lzXCFYkFZwoWfLcbxgmthbO6nKv8dogQMnTpalZ169Mw8h34EugTf8zA4-2Ac3LhkFtoSWcaYOyAIkp7WSCF_IglLa1i2I5oh8y_mxfEWj8JAcMQ4cmZALsl6vNjd3bXXvgqvc_11yOfsYKp8rU-1SvA8xT95Wo0l_XKp8qIKbU-wGk6c4FsRM3oUpn5CvWzNkd_r6HpPflxd351f15nZ9fb7a1FZQnOoOLAJ2RipEKVVvtj10FC1VgJZ30vW0BRTQbClir5qOWemsNNAjFxIVPyb1PvfBDHqXfOn1pKPx-mq10btSqrTTlCohFYN_UPhfe77s8nd2edKjz9YNgwkuzlmDxJIquPgEyhoO2ArKCvrzA_oY5xTK4rocFikqKWmhxJ6yKeac3Pa9MFD94lC_OdQvDvXeYRn78Ro-d6Pr34fepPFnFnWW9Q</recordid><startdate>201301</startdate><enddate>201301</enddate><creator>Berois, Nora</creator><creator>Gattolliat, Charles-Henry</creator><creator>Barrios, Enrique</creator><creator>Capandeguy, Laura</creator><creator>Douc-Rasy, Sétha</creator><creator>Valteau-Couanet, Dominique</creator><creator>Bénard, Jean</creator><creator>Osinaga, Eduardo</creator><general>Oxford University Press</general><general>American Association for Clinical Chemistry</general><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>4U-</scope><scope>7QO</scope><scope>7RV</scope><scope>7TM</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PCBAR</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>S0X</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope></search><sort><creationdate>201301</creationdate><title>GALNT9 gene expression is a prognostic marker in neuroblastoma patients</title><author>Berois, Nora ; Gattolliat, Charles-Henry ; Barrios, Enrique ; Capandeguy, Laura ; Douc-Rasy, Sétha ; Valteau-Couanet, Dominique ; Bénard, Jean ; Osinaga, Eduardo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c406t-b1c616ba5866558dafd1b06c0816c3b5ed0916417f066d87b2c5ec5a1d6345683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Age</topic><topic>Apoptosis</topic><topic>Biomarkers, Tumor - genetics</topic><topic>Biomedical research</topic><topic>Bone marrow</topic><topic>Breast cancer</topic><topic>Cell adhesion & migration</topic><topic>Cell Line, Tumor</topic><topic>Colorectal cancer</topic><topic>Humans</topic><topic>Infant</topic><topic>Life Sciences</topic><topic>Ligands</topic><topic>N-Acetylgalactosaminyltransferases</topic><topic>N-Acetylgalactosaminyltransferases - genetics</topic><topic>Neuroblastoma</topic><topic>Neuroblastoma - genetics</topic><topic>Neuroblastoma - pathology</topic><topic>Prognosis</topic><topic>Proteins</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Survival</topic><topic>Survival analysis</topic><topic>Tumor Markers, Biological</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Berois, Nora</creatorcontrib><creatorcontrib>Gattolliat, Charles-Henry</creatorcontrib><creatorcontrib>Barrios, Enrique</creatorcontrib><creatorcontrib>Capandeguy, Laura</creatorcontrib><creatorcontrib>Douc-Rasy, Sétha</creatorcontrib><creatorcontrib>Valteau-Couanet, Dominique</creatorcontrib><creatorcontrib>Bénard, Jean</creatorcontrib><creatorcontrib>Osinaga, Eduardo</creatorcontrib><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>University Readers</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</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>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Earth, Atmospheric & Aquatic Science Database</collection><collection>Materials Science Collection</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 Basic</collection><collection>Genetics Abstracts</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Clinical chemistry (Baltimore, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Berois, Nora</au><au>Gattolliat, Charles-Henry</au><au>Barrios, Enrique</au><au>Capandeguy, Laura</au><au>Douc-Rasy, Sétha</au><au>Valteau-Couanet, Dominique</au><au>Bénard, Jean</au><au>Osinaga, Eduardo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>GALNT9 gene expression is a prognostic marker in neuroblastoma patients</atitle><jtitle>Clinical chemistry (Baltimore, Md.)</jtitle><addtitle>Clin Chem</addtitle><date>2013-01</date><risdate>2013</risdate><volume>59</volume><issue>1</issue><spage>225</spage><epage>233</epage><pages>225-233</pages><issn>0009-9147</issn><eissn>1530-8561</eissn><abstract>The enzymes encoded by the GALNT [UDP-N-acetyl-α-d-galactosamine:polypeptide N-acetylgalactosaminyltransferase (GALNAC-T)] gene family catalyze the first step of O-glycosylation. Little is known about the link between expression of the genes encoding GALNAC-T enzymes and tumor progression in neuroblastoma, a pediatric cancer that can be classified as either low or high risk. We assessed the expression of genes in the GALNT family in a large cohort of neuroblastoma patients and characterized members of this family that might be used as new prognostic markers.
Reverse-transcription PCR analysis of 14 GALNT genes with a panel of neuroblastoma cell lines identified the GALNT9 gene as playing a potential role in disease progression. We used the log-rank test and the multivariable Cox proportional hazards model with a cohort of 122 neuroblastoma patients to analyze the relationship between GALNT9 expression and overall survival or disease-free survival.
In the high-risk neuroblastoma experimental model IGR-N-91, GALNT9 expression was present in neuroblasts derived from primary tumors but not in neuroblasts from metastatic bone marrow. Moreover, GALNT9 in neuroblastoma cell lines was expressed in substrate adherent (S)-type cell lines but not in neuronal (N)-type lines. In the tumor cohort, GALNT9 expression was associated with high overall survival, independent of the standard risk-stratification covariates. GALNT9 expression was significantly associated with disease-free survival for patients currently classified as at low risk (P < 0.0007).
GALNT9 expression correlates with both improved overall survival in low- and high-risk groups and an improved clinical outcome (overall and disease-free survival) in low-risk patients. Thus, the GALNT9 expression may be a prognostic marker for personalized therapy.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>23136245</pmid><doi>10.1373/clinchem.2012.192328</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0009-9147 |
ispartof | Clinical chemistry (Baltimore, Md.), 2013-01, Vol.59 (1), p.225-233 |
issn | 0009-9147 1530-8561 |
language | eng |
recordid | cdi_hal_primary_oai_HAL_pasteur_00845821v1 |
source | Oxford University Press Journals All Titles (1996-Current); MEDLINE |
subjects | Age Apoptosis Biomarkers, Tumor - genetics Biomedical research Bone marrow Breast cancer Cell adhesion & migration Cell Line, Tumor Colorectal cancer Humans Infant Life Sciences Ligands N-Acetylgalactosaminyltransferases N-Acetylgalactosaminyltransferases - genetics Neuroblastoma Neuroblastoma - genetics Neuroblastoma - pathology Prognosis Proteins Reverse Transcriptase Polymerase Chain Reaction Survival Survival analysis Tumor Markers, Biological Tumors |
title | GALNT9 gene expression is a prognostic marker in neuroblastoma patients |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T17%3A34%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=GALNT9%20gene%20expression%20is%20a%20prognostic%20marker%20in%20neuroblastoma%20patients&rft.jtitle=Clinical%20chemistry%20(Baltimore,%20Md.)&rft.au=Berois,%20Nora&rft.date=2013-01&rft.volume=59&rft.issue=1&rft.spage=225&rft.epage=233&rft.pages=225-233&rft.issn=0009-9147&rft.eissn=1530-8561&rft_id=info:doi/10.1373/clinchem.2012.192328&rft_dat=%3Cproquest_hal_p%3E1566834341%3C/proquest_hal_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1366068550&rft_id=info:pmid/23136245&rfr_iscdi=true |