MYD88 mutated and wild-type Waldenström's Macroglobulinemia: characterization of chromosome 6q gene losses and their mutual exclusivity with mutations in CXCR4

Saved in:
Bibliographic Details
Published in:Haematologica (Roma) 2018-09, Vol.103 (9), p.e408-e411
Main Authors: Guerrera, Maria Luisa, Tsakmaklis, Nickolas, Xu, Lian, Yang, Guang, Demos, Maria, Kofides, Amanda, Chan, Gloria G, Manning, Robert J, Liu, Xia, Chen, Jiaji G, Munshi, Manit, Patterson, Christopher J, Castillo, Jorge J, Dubeau, Toni, Gustine, Joshua, Carrasco, Ruben D, Arcaini, Luca, Varettoni, Marzia, Cazzola, Mario, Treon, Steven P, Hunter, Zachary R
Format: Article
Language:English
Subjects:
Biomarkers
Chromosome Deletion
Genetic Association Studies
Humans
Mutation
Myeloid Differentiation Factor 88 - genetics
Online Only
Receptors, CXCR4 - genetics
Waldenstrom Macroglobulinemia - diagnosis
Waldenstrom Macroglobulinemia - genetics
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c474t-f9ef37f17b73c1d762c1ee434454bcb7c8e9b63d18ab22b2f954d7615e57b94b3
cites
container_end_page e411
container_issue 9
container_start_page e408
container_title Haematologica (Roma)
container_volume 103
creator Guerrera, Maria Luisa
Tsakmaklis, Nickolas
Xu, Lian
Yang, Guang
Demos, Maria
Kofides, Amanda
Chan, Gloria G
Manning, Robert J
Liu, Xia
Chen, Jiaji G
Munshi, Manit
Patterson, Christopher J
Castillo, Jorge J
Dubeau, Toni
Gustine, Joshua
Carrasco, Ruben D
Arcaini, Luca
Varettoni, Marzia
Cazzola, Mario
Treon, Steven P
Hunter, Zachary R
description
doi_str_mv 10.3324/haematol.2018.190181
format article
fullrecord <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_2dd51763f66444f692f0788be558c7a4</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_2dd51763f66444f692f0788be558c7a4</doaj_id><sourcerecordid>2020492911</sourcerecordid><originalsourceid>FETCH-LOGICAL-c474t-f9ef37f17b73c1d762c1ee434454bcb7c8e9b63d18ab22b2f954d7615e57b94b3</originalsourceid><addsrcrecordid>eNpVkt1u1DAQhSMEotvCGyDkO7jJYjtOHHOBVC1_lVohIRBwZdnOZOPKibe2U7o8DU_BC_BieLttRW9saXzmOyPPKYpnBC-rirJXg4JRJe-WFJN2SUQ-yYNiQWpBy5ZT8rBY4ErgssG8PSgOYzzHmGIh-OPigIpaCIrpovh99uNt26JxTipBh9TUoZ_WdWXabgB9U66DKabw98_4IqIzZYJfO69nZycYrXqNzKCCMgmC_aWS9RPyfa4FP_roR0DNBVrDBMj5GCFe09MANuz8ZuUQXBk3R3tp0zbbpmE_R-ZEZCe0-r76zJ4Uj3rlIjy9uY-Kr-_ffVl9LE8_fThZHZ-WhnGWyl5AX_GecM0rQzreUEMAWMVYzbTR3LQgdFN1pFWaUk17UbOsIjXUXAumq6PiZM_tvDqXm2BHFbbSKyuvCz6spQrJGgeSdl1NeFP1TcMY6xtB-_zHrYa6bg1XLLPe7FmbWY_QGZhSUO4e9P7LZAe59peyIUQQRjPg5Q0g-IsZYpKjjQacUxP4Ocq8OswEFYRkKdtL825iDNDf2RAsd0GRt0GRu6DIfVBy2_P_R7xruk1G9Q8AacBd</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2020492911</pqid></control><display><type>article</type><title>MYD88 mutated and wild-type Waldenström's Macroglobulinemia: characterization of chromosome 6q gene losses and their mutual exclusivity with mutations in CXCR4</title><source>NCBI_PubMed Central（免费）</source><source>Freely Accessible Science Journals - check A-Z of ejournals</source><creator>Guerrera, Maria Luisa ; Tsakmaklis, Nickolas ; Xu, Lian ; Yang, Guang ; Demos, Maria ; Kofides, Amanda ; Chan, Gloria G ; Manning, Robert J ; Liu, Xia ; Chen, Jiaji G ; Munshi, Manit ; Patterson, Christopher J ; Castillo, Jorge J ; Dubeau, Toni ; Gustine, Joshua ; Carrasco, Ruben D ; Arcaini, Luca ; Varettoni, Marzia ; Cazzola, Mario ; Treon, Steven P ; Hunter, Zachary R</creator><creatorcontrib>Guerrera, Maria Luisa ; Tsakmaklis, Nickolas ; Xu, Lian ; Yang, Guang ; Demos, Maria ; Kofides, Amanda ; Chan, Gloria G ; Manning, Robert J ; Liu, Xia ; Chen, Jiaji G ; Munshi, Manit ; Patterson, Christopher J ; Castillo, Jorge J ; Dubeau, Toni ; Gustine, Joshua ; Carrasco, Ruben D ; Arcaini, Luca ; Varettoni, Marzia ; Cazzola, Mario ; Treon, Steven P ; Hunter, Zachary R</creatorcontrib><identifier>ISSN: 0390-6078</identifier><identifier>EISSN: 1592-8721</identifier><identifier>DOI: 10.3324/haematol.2018.190181</identifier><identifier>PMID: 29599202</identifier><language>eng</language><publisher>Italy: Ferrata Storti Foundation</publisher><subject>Biomarkers ; Chromosome Deletion ; Genetic Association Studies ; Humans ; Mutation ; Myeloid Differentiation Factor 88 - genetics ; Online Only ; Receptors, CXCR4 - genetics ; Waldenstrom Macroglobulinemia - diagnosis ; Waldenstrom Macroglobulinemia - genetics</subject><ispartof>Haematologica (Roma), 2018-09, Vol.103 (9), p.e408-e411</ispartof><rights>Copyright © 2018 Ferrata Storti Foundation 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-f9ef37f17b73c1d762c1ee434454bcb7c8e9b63d18ab22b2f954d7615e57b94b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6119142/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6119142/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29599202$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guerrera, Maria Luisa</creatorcontrib><creatorcontrib>Tsakmaklis, Nickolas</creatorcontrib><creatorcontrib>Xu, Lian</creatorcontrib><creatorcontrib>Yang, Guang</creatorcontrib><creatorcontrib>Demos, Maria</creatorcontrib><creatorcontrib>Kofides, Amanda</creatorcontrib><creatorcontrib>Chan, Gloria G</creatorcontrib><creatorcontrib>Manning, Robert J</creatorcontrib><creatorcontrib>Liu, Xia</creatorcontrib><creatorcontrib>Chen, Jiaji G</creatorcontrib><creatorcontrib>Munshi, Manit</creatorcontrib><creatorcontrib>Patterson, Christopher J</creatorcontrib><creatorcontrib>Castillo, Jorge J</creatorcontrib><creatorcontrib>Dubeau, Toni</creatorcontrib><creatorcontrib>Gustine, Joshua</creatorcontrib><creatorcontrib>Carrasco, Ruben D</creatorcontrib><creatorcontrib>Arcaini, Luca</creatorcontrib><creatorcontrib>Varettoni, Marzia</creatorcontrib><creatorcontrib>Cazzola, Mario</creatorcontrib><creatorcontrib>Treon, Steven P</creatorcontrib><creatorcontrib>Hunter, Zachary R</creatorcontrib><title>MYD88 mutated and wild-type Waldenström's Macroglobulinemia: characterization of chromosome 6q gene losses and their mutual exclusivity with mutations in CXCR4</title><title>Haematologica (Roma)</title><addtitle>Haematologica</addtitle><subject>Biomarkers</subject><subject>Chromosome Deletion</subject><subject>Genetic Association Studies</subject><subject>Humans</subject><subject>Mutation</subject><subject>Myeloid Differentiation Factor 88 - genetics</subject><subject>Online Only</subject><subject>Receptors, CXCR4 - genetics</subject><subject>Waldenstrom Macroglobulinemia - diagnosis</subject><subject>Waldenstrom Macroglobulinemia - genetics</subject><issn>0390-6078</issn><issn>1592-8721</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkt1u1DAQhSMEotvCGyDkO7jJYjtOHHOBVC1_lVohIRBwZdnOZOPKibe2U7o8DU_BC_BieLttRW9saXzmOyPPKYpnBC-rirJXg4JRJe-WFJN2SUQ-yYNiQWpBy5ZT8rBY4ErgssG8PSgOYzzHmGIh-OPigIpaCIrpovh99uNt26JxTipBh9TUoZ_WdWXabgB9U66DKabw98_4IqIzZYJfO69nZycYrXqNzKCCMgmC_aWS9RPyfa4FP_roR0DNBVrDBMj5GCFe09MANuz8ZuUQXBk3R3tp0zbbpmE_R-ZEZCe0-r76zJ4Uj3rlIjy9uY-Kr-_ffVl9LE8_fThZHZ-WhnGWyl5AX_GecM0rQzreUEMAWMVYzbTR3LQgdFN1pFWaUk17UbOsIjXUXAumq6PiZM_tvDqXm2BHFbbSKyuvCz6spQrJGgeSdl1NeFP1TcMY6xtB-_zHrYa6bg1XLLPe7FmbWY_QGZhSUO4e9P7LZAe59peyIUQQRjPg5Q0g-IsZYpKjjQacUxP4Ocq8OswEFYRkKdtL825iDNDf2RAsd0GRt0GRu6DIfVBy2_P_R7xruk1G9Q8AacBd</recordid><startdate>20180901</startdate><enddate>20180901</enddate><creator>Guerrera, Maria Luisa</creator><creator>Tsakmaklis, Nickolas</creator><creator>Xu, Lian</creator><creator>Yang, Guang</creator><creator>Demos, Maria</creator><creator>Kofides, Amanda</creator><creator>Chan, Gloria G</creator><creator>Manning, Robert J</creator><creator>Liu, Xia</creator><creator>Chen, Jiaji G</creator><creator>Munshi, Manit</creator><creator>Patterson, Christopher J</creator><creator>Castillo, Jorge J</creator><creator>Dubeau, Toni</creator><creator>Gustine, Joshua</creator><creator>Carrasco, Ruben D</creator><creator>Arcaini, Luca</creator><creator>Varettoni, Marzia</creator><creator>Cazzola, Mario</creator><creator>Treon, Steven P</creator><creator>Hunter, Zachary R</creator><general>Ferrata Storti Foundation</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>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20180901</creationdate><title>MYD88 mutated and wild-type Waldenström's Macroglobulinemia: characterization of chromosome 6q gene losses and their mutual exclusivity with mutations in CXCR4</title><author>Guerrera, Maria Luisa ; Tsakmaklis, Nickolas ; Xu, Lian ; Yang, Guang ; Demos, Maria ; Kofides, Amanda ; Chan, Gloria G ; Manning, Robert J ; Liu, Xia ; Chen, Jiaji G ; Munshi, Manit ; Patterson, Christopher J ; Castillo, Jorge J ; Dubeau, Toni ; Gustine, Joshua ; Carrasco, Ruben D ; Arcaini, Luca ; Varettoni, Marzia ; Cazzola, Mario ; Treon, Steven P ; Hunter, Zachary R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-f9ef37f17b73c1d762c1ee434454bcb7c8e9b63d18ab22b2f954d7615e57b94b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Biomarkers</topic><topic>Chromosome Deletion</topic><topic>Genetic Association Studies</topic><topic>Humans</topic><topic>Mutation</topic><topic>Myeloid Differentiation Factor 88 - genetics</topic><topic>Online Only</topic><topic>Receptors, CXCR4 - genetics</topic><topic>Waldenstrom Macroglobulinemia - diagnosis</topic><topic>Waldenstrom Macroglobulinemia - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guerrera, Maria Luisa</creatorcontrib><creatorcontrib>Tsakmaklis, Nickolas</creatorcontrib><creatorcontrib>Xu, Lian</creatorcontrib><creatorcontrib>Yang, Guang</creatorcontrib><creatorcontrib>Demos, Maria</creatorcontrib><creatorcontrib>Kofides, Amanda</creatorcontrib><creatorcontrib>Chan, Gloria G</creatorcontrib><creatorcontrib>Manning, Robert J</creatorcontrib><creatorcontrib>Liu, Xia</creatorcontrib><creatorcontrib>Chen, Jiaji G</creatorcontrib><creatorcontrib>Munshi, Manit</creatorcontrib><creatorcontrib>Patterson, Christopher J</creatorcontrib><creatorcontrib>Castillo, Jorge J</creatorcontrib><creatorcontrib>Dubeau, Toni</creatorcontrib><creatorcontrib>Gustine, Joshua</creatorcontrib><creatorcontrib>Carrasco, Ruben D</creatorcontrib><creatorcontrib>Arcaini, Luca</creatorcontrib><creatorcontrib>Varettoni, Marzia</creatorcontrib><creatorcontrib>Cazzola, Mario</creatorcontrib><creatorcontrib>Treon, Steven P</creatorcontrib><creatorcontrib>Hunter, Zachary R</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Haematologica (Roma)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guerrera, Maria Luisa</au><au>Tsakmaklis, Nickolas</au><au>Xu, Lian</au><au>Yang, Guang</au><au>Demos, Maria</au><au>Kofides, Amanda</au><au>Chan, Gloria G</au><au>Manning, Robert J</au><au>Liu, Xia</au><au>Chen, Jiaji G</au><au>Munshi, Manit</au><au>Patterson, Christopher J</au><au>Castillo, Jorge J</au><au>Dubeau, Toni</au><au>Gustine, Joshua</au><au>Carrasco, Ruben D</au><au>Arcaini, Luca</au><au>Varettoni, Marzia</au><au>Cazzola, Mario</au><au>Treon, Steven P</au><au>Hunter, Zachary R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MYD88 mutated and wild-type Waldenström's Macroglobulinemia: characterization of chromosome 6q gene losses and their mutual exclusivity with mutations in CXCR4</atitle><jtitle>Haematologica (Roma)</jtitle><addtitle>Haematologica</addtitle><date>2018-09-01</date><risdate>2018</risdate><volume>103</volume><issue>9</issue><spage>e408</spage><epage>e411</epage><pages>e408-e411</pages><issn>0390-6078</issn><eissn>1592-8721</eissn><cop>Italy</cop><pub>Ferrata Storti Foundation</pub><pmid>29599202</pmid><doi>10.3324/haematol.2018.190181</doi><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0390-6078
ispartof Haematologica (Roma), 2018-09, Vol.103 (9), p.e408-e411
issn 0390-6078
1592-8721
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_2dd51763f66444f692f0788be558c7a4
source NCBI_PubMed Central（免费）; Freely Accessible Science Journals - check A-Z of ejournals
subjects Biomarkers
Chromosome Deletion
Genetic Association Studies
Humans
Mutation
Myeloid Differentiation Factor 88 - genetics
Online Only
Receptors, CXCR4 - genetics
Waldenstrom Macroglobulinemia - diagnosis
Waldenstrom Macroglobulinemia - genetics
title MYD88 mutated and wild-type Waldenström's Macroglobulinemia: characterization of chromosome 6q gene losses and their mutual exclusivity with mutations in CXCR4
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T08%3A53%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=MYD88%20mutated%20and%20wild-type%20Waldenstr%C3%B6m's%20Macroglobulinemia:%20characterization%20of%20chromosome%206q%20gene%20losses%20and%20their%20mutual%20exclusivity%20with%20mutations%20in%20CXCR4&rft.jtitle=Haematologica%20(Roma)&rft.au=Guerrera,%20Maria%20Luisa&rft.date=2018-09-01&rft.volume=103&rft.issue=9&rft.spage=e408&rft.epage=e411&rft.pages=e408-e411&rft.issn=0390-6078&rft.eissn=1592-8721&rft_id=info:doi/10.3324/haematol.2018.190181&rft_dat=%3Cproquest_doaj_%3E2020492911%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c474t-f9ef37f17b73c1d762c1ee434454bcb7c8e9b63d18ab22b2f954d7615e57b94b3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2020492911&rft_id=info:pmid/29599202&rfr_iscdi=true