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Quality assurance in RT-PCR-based BCR/ABL diagnostics: results of an interlaboratory test and a standardization approach

Identifieur interne : 000E80 ( PascalFrancis/Corpus ); précédent : 000E79; suivant : 000E81

Quality assurance in RT-PCR-based BCR/ABL diagnostics: results of an interlaboratory test and a standardization approach

Auteurs : T. Burmeister ; J. Maurer ; M. Aivado ; A. H. Elmaagacli ; F. Grünebach ; K. R. Held ; G. Hess ; A. Hochhaus ; W. Höppner ; K. U. Lentes ; M. Lübbert ; K. L. Sch Fer ; P. Schafhausen ; C. A. Schmidt ; F. Schüler ; K. Seeger ; R. Seelig ; C. Thiede ; S. Viehmann ; C. Weber ; S. Wilhelm ; A. Christmann ; J. H. Clement ; U. Ebener ; J. Enczmann ; R. Leo ; M. Schleuning ; R. Schoch ; E. Thiel

Source :

RBID : Pascal:01-0004051

Descripteurs français

English descriptors

Abstract

Here we describe the results of an interlaboratory test for RT-PCR-based BCR/ABL analysis. The test was organized in two parts. The number of participating laboratories in the first and second part was 27 and 20, respectively. In the first part samples containing various concentrations of plasmids with the ela2, b2a2 or b3a2 BCR/ABL transcripts were analyzed by PCR. In the second part of the test, cell samples containing various concentrations of BCR/ABL-positive cells were analyzed by RT-PCR. Overall PCR sensitivity was sufficient in approximately 90% of the tests, but a significant number of false positive results were obtained. There were significant differences in sensitivity in the cell-based analysis between the various participants. The results are discussed, and proposals are made regarding the choice of primers, controls, conditions for RNA extraction and reverse transcription.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 0887-6924
A02 01      @0 LEUKED
A03   1    @0 Leukemia
A05       @2 14
A06       @2 10
A08 01  1  ENG  @1 Quality assurance in RT-PCR-based BCR/ABL diagnostics: results of an interlaboratory test and a standardization approach
A11 01  1    @1 BURMEISTER (T.)
A11 02  1    @1 MAURER (J.)
A11 03  1    @1 AIVADO (M.)
A11 04  1    @1 ELMAAGACLI (A. H.)
A11 05  1    @1 GRÜNEBACH (F.)
A11 06  1    @1 HELD (K. R.)
A11 07  1    @1 HESS (G.)
A11 08  1    @1 HOCHHAUS (A.)
A11 09  1    @1 HÖPPNER (W.)
A11 10  1    @1 LENTES (K. U.)
A11 11  1    @1 LÜBBERT (M.)
A11 12  1    @1 SCHÄFER (K. L.)
A11 13  1    @1 SCHAFHAUSEN (P.)
A11 14  1    @1 SCHMIDT (C. A.)
A11 15  1    @1 SCHÜLER (F.)
A11 16  1    @1 SEEGER (K.)
A11 17  1    @1 SEELIG (R.)
A11 18  1    @1 THIEDE (C.)
A11 19  1    @1 VIEHMANN (S.)
A11 20  1    @1 WEBER (C.)
A11 21  1    @1 WILHELM (S.)
A11 22  1    @1 CHRISTMANN (A.)
A11 23  1    @1 CLEMENT (J. H.)
A11 24  1    @1 EBENER (U.)
A11 25  1    @1 ENCZMANN (J.)
A11 26  1    @1 LEO (R.)
A11 27  1    @1 SCHLEUNING (M.)
A11 28  1    @1 SCHOCH (R.)
A11 29  1    @1 THIEL (E.)
A14 01      @1 Freie Universitat Berlin, Med Klinik III @3 DEU @Z 1 aut. @Z 2 aut. @Z 29 aut.
A14 02      @1 Universität Düsseldorf, Klinik fur Hamatologie und Onkologie @3 DEU @Z 3 aut.
A14 03      @1 Universität-Gesamthochschule Essen, Klinik für Knochenmarktransplantation @3 DEU @Z 4 aut.
A14 04      @1 Universität Tübingen, Med, Klinik @3 DEU @Z 5 aut.
A14 05      @1 Praxis Held/Kesser/Arndt Hamburg @3 DEU @Z 6 aut.
A14 06      @1 Universität Mainz, III, Med, Klinik @3 DEU @Z 7 aut.
A14 07      @1 Universität Heidelberg, III, Med, Klinik, Klinikum Mannheim @3 DEU @Z 8 aut.
A14 08      @1 GLE medicon GmbH @2 Hamburg @3 DEU @Z 9 aut.
A14 09      @1 Universität Trier, Abt, Molekulare Neurogenetik @3 DEU @Z 10 aut.
A14 10      @1 Universität Freiburg, Med. Klinik I @3 DEU @Z 11 aut.
A14 11      @1 Universitat Münster, Institut fur Pathologie @3 DEU @Z 12 aut.
A14 12      @1 Universität Hamburg, Med. Klinik III @3 DEU @Z 13 aut.
A14 13      @1 113Humboldt-Universitat Berlin, Med. Klinik, Hamatologie/Onkologie @3 DEU @Z 14 aut.
A14 14      @1 Universität Greifswald, Klinik fur Innere Medizin C @3 DEU @Z 15 aut.
A14 15      @1 Humboldt-Universitat Berlin, Zentrum fur Kinderheilkunde @3 DEU @Z 16 aut.
A14 16      @1 Labor Prof Seelig und Partner @2 Karlsruhe @3 DEU @Z 17 aut.
A14 17      @1 Technische Universitat Dresden, Med, Klinik 1 @3 DEU @Z 18 aut.
A14 18      @1 Universität Giessen, Kinderklinik, Onkogenetisches Labor @3 DEU @Z 19 aut.
A14 19      @1 Universität Giessen, Abt, for Hamatologie @3 DEU @Z 20 aut.
A14 20      @1 Universität Rostock, Abt für Hämatologie/Onkologie @3 DEU @Z 21 aut.
A14 21      @1 Universität Homburg, Institut für Humangenetik @3 DEU @Z 22 aut.
A14 22      @1 Universität Jena, Innere Medizin II @3 DEU @Z 23 aut.
A14 23      @1 Universität Frankfurt, Zentrum für Kinderheilkunde @3 DEU @Z 24 aut.
A14 24      @1 Universität Düsseldorf, Knochenmarkspenderzentrale @3 DEU @Z 25 aut.
A14 25      @1 Universität Münster, Med, Klinik A @3 DEU @Z 26 aut.
A20       @1 1850-1856
A21       @1 2000
A23 01      @0 ENG
A43 01      @1 INIST @2 21129 @5 354000092220510160
A44       @0 0000 @1 © 2001 INIST-CNRS. All rights reserved.
A45       @0 19 ref.
A47 01  1    @0 01-0004051
A60       @1 P
A61       @0 A
A64 01  1    @0 Leukemia
A66 01      @0 GBR
C01 01    ENG  @0 Here we describe the results of an interlaboratory test for RT-PCR-based BCR/ABL analysis. The test was organized in two parts. The number of participating laboratories in the first and second part was 27 and 20, respectively. In the first part samples containing various concentrations of plasmids with the ela2, b2a2 or b3a2 BCR/ABL transcripts were analyzed by PCR. In the second part of the test, cell samples containing various concentrations of BCR/ABL-positive cells were analyzed by RT-PCR. Overall PCR sensitivity was sufficient in approximately 90% of the tests, but a significant number of false positive results were obtained. There were significant differences in sensitivity in the cell-based analysis between the various participants. The results are discussed, and proposals are made regarding the choice of primers, controls, conditions for RNA extraction and reverse transcription.
C02 01  X    @0 002B24O10
C03 01  X  FRE  @0 Translocation chromosomique @5 01
C03 01  X  ENG  @0 Chromosome translocation @5 01
C03 01  X  SPA  @0 Translocación cromosómica @5 01
C03 02  X  FRE  @0 Chromosome C9 anormal @5 02
C03 02  X  ENG  @0 Abnormal chromosome C9 @5 02
C03 02  X  SPA  @0 Cromosoma C9 anormal @5 02
C03 03  X  FRE  @0 Chromosome G22 anormal @5 03
C03 03  X  ENG  @0 Abnormal chromosome G22 @5 03
C03 03  X  SPA  @0 Cromosoma G22 anormal @5 03
C03 04  X  FRE  @0 Gène hybride @5 04
C03 04  X  ENG  @0 Hybrid gene @5 04
C03 04  X  SPA  @0 Gen híbrido @5 04
C03 05  X  FRE  @0 Technique @5 05
C03 05  X  ENG  @0 Technique @5 05
C03 05  X  SPA  @0 Técnica @5 05
C03 06  X  FRE  @0 Diagnostic @5 06
C03 06  X  ENG  @0 Diagnosis @5 06
C03 06  X  SPA  @0 Diagnóstico @5 06
C03 07  X  FRE  @0 Assurance qualité @5 08
C03 07  X  ENG  @0 Quality assurance @5 08
C03 07  X  SPA  @0 Aseguración calidad @5 08
C03 08  X  FRE  @0 Expression génique @5 09
C03 08  X  ENG  @0 Gene expression @5 09
C03 08  X  SPA  @0 Expresión genética @5 09
C03 09  X  FRE  @0 Réaction chaîne polymérase @5 10
C03 09  X  ENG  @0 Polymerase chain reaction @5 10
C03 09  X  SPA  @0 Reacción cadena polimerasa @5 10
C03 10  X  FRE  @0 RNA-directed DNA polymerase @2 FE @5 11
C03 10  X  ENG  @0 RNA-directed DNA polymerase @2 FE @5 11
C03 10  X  SPA  @0 RNA-directed DNA polymerase @2 FE @5 11
C03 11  X  FRE  @0 Normalisation @5 18
C03 11  X  ENG  @0 Standardization @5 18
C03 11  X  SPA  @0 Normalización @5 18
C03 12  X  FRE  @0 Homme @5 19
C03 12  X  ENG  @0 Human @5 19
C03 12  X  SPA  @0 Hombre @5 19
C03 13  X  FRE  @0 Etude multicentrique @5 20
C03 13  X  ENG  @0 Multicenter study @5 20
C03 13  X  SPA  @0 Estudio multicéntrico @5 20
C03 14  X  FRE  @0 Gène bcr @4 INC @5 86
C03 15  X  FRE  @0 Gène abl @4 INC @5 87
C07 01  X  FRE  @0 Chromosome anormal
C07 01  X  ENG  @0 Abnormal chromosome
C07 01  X  SPA  @0 Cromosoma anormal
C07 02  X  FRE  @0 Aberration chromosomique
C07 02  X  ENG  @0 Chromosomal aberration
C07 02  X  SPA  @0 Aberración cromosómica
C07 03  X  FRE  @0 Nucleotidyltransferases @2 FE
C07 03  X  ENG  @0 Nucleotidyltransferases @2 FE
C07 03  X  SPA  @0 Nucleotidyltransferases @2 FE
C07 04  X  FRE  @0 Transferases @2 FE
C07 04  X  ENG  @0 Transferases @2 FE
C07 04  X  SPA  @0 Transferases @2 FE
C07 05  X  FRE  @0 Enzyme
C07 05  X  ENG  @0 Enzyme
C07 05  X  SPA  @0 Enzima
C07 06  X  FRE  @0 Biologie moléculaire @5 61
C07 06  X  ENG  @0 Molecular biology @5 61
C07 06  X  SPA  @0 Biología molecular @5 61
N21       @1 001

Format Inist (serveur)

NO : PASCAL 01-0004051 INIST
ET : Quality assurance in RT-PCR-based BCR/ABL diagnostics: results of an interlaboratory test and a standardization approach
AU : BURMEISTER (T.); MAURER (J.); AIVADO (M.); ELMAAGACLI (A. H.); GRÜNEBACH (F.); HELD (K. R.); HESS (G.); HOCHHAUS (A.); HÖPPNER (W.); LENTES (K. U.); LÜBBERT (M.); SCHÄFER (K. L.); SCHAFHAUSEN (P.); SCHMIDT (C. A.); SCHÜLER (F.); SEEGER (K.); SEELIG (R.); THIEDE (C.); VIEHMANN (S.); WEBER (C.); WILHELM (S.); CHRISTMANN (A.); CLEMENT (J. H.); EBENER (U.); ENCZMANN (J.); LEO (R.); SCHLEUNING (M.); SCHOCH (R.); THIEL (E.)
AF : Freie Universitat Berlin, Med Klinik III/Allemagne (1 aut., 2 aut., 29 aut.); Universität Düsseldorf, Klinik fur Hamatologie und Onkologie/Allemagne (3 aut.); Universität-Gesamthochschule Essen, Klinik für Knochenmarktransplantation/Allemagne (4 aut.); Universität Tübingen, Med, Klinik/Allemagne (5 aut.); Praxis Held/Kesser/Arndt Hamburg/Allemagne (6 aut.); Universität Mainz, III, Med, Klinik/Allemagne (7 aut.); Universität Heidelberg, III, Med, Klinik, Klinikum Mannheim/Allemagne (8 aut.); GLE medicon GmbH/Hamburg/Allemagne (9 aut.); Universität Trier, Abt, Molekulare Neurogenetik/Allemagne (10 aut.); Universität Freiburg, Med. Klinik I/Allemagne (11 aut.); Universitat Münster, Institut fur Pathologie/Allemagne (12 aut.); Universität Hamburg, Med. Klinik III/Allemagne (13 aut.); 113Humboldt-Universitat Berlin, Med. Klinik, Hamatologie/Onkologie/Allemagne (14 aut.); Universität Greifswald, Klinik fur Innere Medizin C/Allemagne (15 aut.); Humboldt-Universitat Berlin, Zentrum fur Kinderheilkunde/Allemagne (16 aut.); Labor Prof Seelig und Partner/Karlsruhe/Allemagne (17 aut.); Technische Universitat Dresden, Med, Klinik 1/Allemagne (18 aut.); Universität Giessen, Kinderklinik, Onkogenetisches Labor/Allemagne (19 aut.); Universität Giessen, Abt, for Hamatologie/Allemagne (20 aut.); Universität Rostock, Abt für Hämatologie/Onkologie/Allemagne (21 aut.); Universität Homburg, Institut für Humangenetik/Allemagne (22 aut.); Universität Jena, Innere Medizin II/Allemagne (23 aut.); Universität Frankfurt, Zentrum für Kinderheilkunde/Allemagne (24 aut.); Universität Düsseldorf, Knochenmarkspenderzentrale/Allemagne (25 aut.); Universität Münster, Med, Klinik A/Allemagne (26 aut.)
DT : Publication en série; Niveau analytique
SO : Leukemia; ISSN 0887-6924; Coden LEUKED; Royaume-Uni; Da. 2000; Vol. 14; No. 10; Pp. 1850-1856; Bibl. 19 ref.
LA : Anglais
EA : Here we describe the results of an interlaboratory test for RT-PCR-based BCR/ABL analysis. The test was organized in two parts. The number of participating laboratories in the first and second part was 27 and 20, respectively. In the first part samples containing various concentrations of plasmids with the ela2, b2a2 or b3a2 BCR/ABL transcripts were analyzed by PCR. In the second part of the test, cell samples containing various concentrations of BCR/ABL-positive cells were analyzed by RT-PCR. Overall PCR sensitivity was sufficient in approximately 90% of the tests, but a significant number of false positive results were obtained. There were significant differences in sensitivity in the cell-based analysis between the various participants. The results are discussed, and proposals are made regarding the choice of primers, controls, conditions for RNA extraction and reverse transcription.
CC : 002B24O10
FD : Translocation chromosomique; Chromosome C9 anormal; Chromosome G22 anormal; Gène hybride; Technique; Diagnostic; Assurance qualité; Expression génique; Réaction chaîne polymérase; RNA-directed DNA polymerase; Normalisation; Homme; Etude multicentrique; Gène bcr; Gène abl
FG : Chromosome anormal; Aberration chromosomique; Nucleotidyltransferases; Transferases; Enzyme; Biologie moléculaire
ED : Chromosome translocation; Abnormal chromosome C9; Abnormal chromosome G22; Hybrid gene; Technique; Diagnosis; Quality assurance; Gene expression; Polymerase chain reaction; RNA-directed DNA polymerase; Standardization; Human; Multicenter study
EG : Abnormal chromosome; Chromosomal aberration; Nucleotidyltransferases; Transferases; Enzyme; Molecular biology
SD : Translocación cromosómica; Cromosoma C9 anormal; Cromosoma G22 anormal; Gen híbrido; Técnica; Diagnóstico; Aseguración calidad; Expresión genética; Reacción cadena polimerasa; RNA-directed DNA polymerase; Normalización; Hombre; Estudio multicéntrico
LO : INIST-21129.354000092220510160
ID : 01-0004051

Links to Exploration step

Pascal:01-0004051

Le document en format XML

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<name sortKey="Weber, C" sort="Weber, C" uniqKey="Weber C" first="C." last="Weber">C. Weber</name>
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<inist:fA14 i1="19">
<s1>Universität Giessen, Abt, for Hamatologie</s1>
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</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Wilhelm, S" sort="Wilhelm, S" uniqKey="Wilhelm S" first="S." last="Wilhelm">S. Wilhelm</name>
<affiliation>
<inist:fA14 i1="20">
<s1>Universität Rostock, Abt für Hämatologie/Onkologie</s1>
<s3>DEU</s3>
<sZ>21 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Christmann, A" sort="Christmann, A" uniqKey="Christmann A" first="A." last="Christmann">A. Christmann</name>
<affiliation>
<inist:fA14 i1="21">
<s1>Universität Homburg, Institut für Humangenetik</s1>
<s3>DEU</s3>
<sZ>22 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Clement, J H" sort="Clement, J H" uniqKey="Clement J" first="J. H." last="Clement">J. H. Clement</name>
<affiliation>
<inist:fA14 i1="22">
<s1>Universität Jena, Innere Medizin II</s1>
<s3>DEU</s3>
<sZ>23 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Ebener, U" sort="Ebener, U" uniqKey="Ebener U" first="U." last="Ebener">U. Ebener</name>
<affiliation>
<inist:fA14 i1="23">
<s1>Universität Frankfurt, Zentrum für Kinderheilkunde</s1>
<s3>DEU</s3>
<sZ>24 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Enczmann, J" sort="Enczmann, J" uniqKey="Enczmann J" first="J." last="Enczmann">J. Enczmann</name>
<affiliation>
<inist:fA14 i1="24">
<s1>Universität Düsseldorf, Knochenmarkspenderzentrale</s1>
<s3>DEU</s3>
<sZ>25 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Leo, R" sort="Leo, R" uniqKey="Leo R" first="R." last="Leo">R. Leo</name>
<affiliation>
<inist:fA14 i1="25">
<s1>Universität Münster, Med, Klinik A</s1>
<s3>DEU</s3>
<sZ>26 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Schleuning, M" sort="Schleuning, M" uniqKey="Schleuning M" first="M." last="Schleuning">M. Schleuning</name>
</author>
<author>
<name sortKey="Schoch, R" sort="Schoch, R" uniqKey="Schoch R" first="R." last="Schoch">R. Schoch</name>
</author>
<author>
<name sortKey="Thiel, E" sort="Thiel, E" uniqKey="Thiel E" first="E." last="Thiel">E. Thiel</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Freie Universitat Berlin, Med Klinik III</s1>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>29 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
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<idno type="wicri:source">INIST</idno>
<idno type="inist">01-0004051</idno>
<date when="2000">2000</date>
<idno type="stanalyst">PASCAL 01-0004051 INIST</idno>
<idno type="RBID">Pascal:01-0004051</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000E80</idno>
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<analytic>
<title xml:lang="en" level="a">Quality assurance in RT-PCR-based BCR/ABL diagnostics: results of an interlaboratory test and a standardization approach</title>
<author>
<name sortKey="Burmeister, T" sort="Burmeister, T" uniqKey="Burmeister T" first="T." last="Burmeister">T. Burmeister</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Freie Universitat Berlin, Med Klinik III</s1>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>29 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Maurer, J" sort="Maurer, J" uniqKey="Maurer J" first="J." last="Maurer">J. Maurer</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Freie Universitat Berlin, Med Klinik III</s1>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>29 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Aivado, M" sort="Aivado, M" uniqKey="Aivado M" first="M." last="Aivado">M. Aivado</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Universität Düsseldorf, Klinik fur Hamatologie und Onkologie</s1>
<s3>DEU</s3>
<sZ>3 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Elmaagacli, A H" sort="Elmaagacli, A H" uniqKey="Elmaagacli A" first="A. H." last="Elmaagacli">A. H. Elmaagacli</name>
<affiliation>
<inist:fA14 i1="03">
<s1>Universität-Gesamthochschule Essen, Klinik für Knochenmarktransplantation</s1>
<s3>DEU</s3>
<sZ>4 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Grunebach, F" sort="Grunebach, F" uniqKey="Grunebach F" first="F." last="Grünebach">F. Grünebach</name>
<affiliation>
<inist:fA14 i1="04">
<s1>Universität Tübingen, Med, Klinik</s1>
<s3>DEU</s3>
<sZ>5 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Held, K R" sort="Held, K R" uniqKey="Held K" first="K. R." last="Held">K. R. Held</name>
<affiliation>
<inist:fA14 i1="05">
<s1>Praxis Held/Kesser/Arndt Hamburg</s1>
<s3>DEU</s3>
<sZ>6 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Hess, G" sort="Hess, G" uniqKey="Hess G" first="G." last="Hess">G. Hess</name>
<affiliation>
<inist:fA14 i1="06">
<s1>Universität Mainz, III, Med, Klinik</s1>
<s3>DEU</s3>
<sZ>7 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Hochhaus, A" sort="Hochhaus, A" uniqKey="Hochhaus A" first="A." last="Hochhaus">A. Hochhaus</name>
<affiliation>
<inist:fA14 i1="07">
<s1>Universität Heidelberg, III, Med, Klinik, Klinikum Mannheim</s1>
<s3>DEU</s3>
<sZ>8 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Hoppner, W" sort="Hoppner, W" uniqKey="Hoppner W" first="W." last="Höppner">W. Höppner</name>
<affiliation>
<inist:fA14 i1="08">
<s1>GLE medicon GmbH</s1>
<s2>Hamburg</s2>
<s3>DEU</s3>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Lentes, K U" sort="Lentes, K U" uniqKey="Lentes K" first="K. U." last="Lentes">K. U. Lentes</name>
<affiliation>
<inist:fA14 i1="09">
<s1>Universität Trier, Abt, Molekulare Neurogenetik</s1>
<s3>DEU</s3>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Lubbert, M" sort="Lubbert, M" uniqKey="Lubbert M" first="M." last="Lübbert">M. Lübbert</name>
<affiliation>
<inist:fA14 i1="10">
<s1>Universität Freiburg, Med. Klinik I</s1>
<s3>DEU</s3>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Sch Fer, K L" sort="Sch Fer, K L" uniqKey="Sch Fer K" first="K. L." last="Sch Fer">K. L. Sch Fer</name>
<affiliation>
<inist:fA14 i1="11">
<s1>Universitat Münster, Institut fur Pathologie</s1>
<s3>DEU</s3>
<sZ>12 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Schafhausen, P" sort="Schafhausen, P" uniqKey="Schafhausen P" first="P." last="Schafhausen">P. Schafhausen</name>
<affiliation>
<inist:fA14 i1="12">
<s1>Universität Hamburg, Med. Klinik III</s1>
<s3>DEU</s3>
<sZ>13 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Schmidt, C A" sort="Schmidt, C A" uniqKey="Schmidt C" first="C. A." last="Schmidt">C. A. Schmidt</name>
<affiliation>
<inist:fA14 i1="13">
<s1>
<sup>113</sup>
Humboldt-Universitat Berlin, Med. Klinik, Hamatologie/Onkologie</s1>
<s3>DEU</s3>
<sZ>14 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Schuler, F" sort="Schuler, F" uniqKey="Schuler F" first="F." last="Schüler">F. Schüler</name>
<affiliation>
<inist:fA14 i1="14">
<s1>Universität Greifswald, Klinik fur Innere Medizin C</s1>
<s3>DEU</s3>
<sZ>15 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Seeger, K" sort="Seeger, K" uniqKey="Seeger K" first="K." last="Seeger">K. Seeger</name>
<affiliation>
<inist:fA14 i1="15">
<s1>Humboldt-Universitat Berlin, Zentrum fur Kinderheilkunde</s1>
<s3>DEU</s3>
<sZ>16 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Seelig, R" sort="Seelig, R" uniqKey="Seelig R" first="R." last="Seelig">R. Seelig</name>
<affiliation>
<inist:fA14 i1="16">
<s1>Labor Prof Seelig und Partner</s1>
<s2>Karlsruhe</s2>
<s3>DEU</s3>
<sZ>17 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Thiede, C" sort="Thiede, C" uniqKey="Thiede C" first="C." last="Thiede">C. Thiede</name>
<affiliation>
<inist:fA14 i1="17">
<s1>Technische Universitat Dresden, Med, Klinik 1</s1>
<s3>DEU</s3>
<sZ>18 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Viehmann, S" sort="Viehmann, S" uniqKey="Viehmann S" first="S." last="Viehmann">S. Viehmann</name>
<affiliation>
<inist:fA14 i1="18">
<s1>Universität Giessen, Kinderklinik, Onkogenetisches Labor</s1>
<s3>DEU</s3>
<sZ>19 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Weber, C" sort="Weber, C" uniqKey="Weber C" first="C." last="Weber">C. Weber</name>
<affiliation>
<inist:fA14 i1="19">
<s1>Universität Giessen, Abt, for Hamatologie</s1>
<s3>DEU</s3>
<sZ>20 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Wilhelm, S" sort="Wilhelm, S" uniqKey="Wilhelm S" first="S." last="Wilhelm">S. Wilhelm</name>
<affiliation>
<inist:fA14 i1="20">
<s1>Universität Rostock, Abt für Hämatologie/Onkologie</s1>
<s3>DEU</s3>
<sZ>21 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Christmann, A" sort="Christmann, A" uniqKey="Christmann A" first="A." last="Christmann">A. Christmann</name>
<affiliation>
<inist:fA14 i1="21">
<s1>Universität Homburg, Institut für Humangenetik</s1>
<s3>DEU</s3>
<sZ>22 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Clement, J H" sort="Clement, J H" uniqKey="Clement J" first="J. H." last="Clement">J. H. Clement</name>
<affiliation>
<inist:fA14 i1="22">
<s1>Universität Jena, Innere Medizin II</s1>
<s3>DEU</s3>
<sZ>23 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Ebener, U" sort="Ebener, U" uniqKey="Ebener U" first="U." last="Ebener">U. Ebener</name>
<affiliation>
<inist:fA14 i1="23">
<s1>Universität Frankfurt, Zentrum für Kinderheilkunde</s1>
<s3>DEU</s3>
<sZ>24 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Enczmann, J" sort="Enczmann, J" uniqKey="Enczmann J" first="J." last="Enczmann">J. Enczmann</name>
<affiliation>
<inist:fA14 i1="24">
<s1>Universität Düsseldorf, Knochenmarkspenderzentrale</s1>
<s3>DEU</s3>
<sZ>25 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Leo, R" sort="Leo, R" uniqKey="Leo R" first="R." last="Leo">R. Leo</name>
<affiliation>
<inist:fA14 i1="25">
<s1>Universität Münster, Med, Klinik A</s1>
<s3>DEU</s3>
<sZ>26 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Schleuning, M" sort="Schleuning, M" uniqKey="Schleuning M" first="M." last="Schleuning">M. Schleuning</name>
</author>
<author>
<name sortKey="Schoch, R" sort="Schoch, R" uniqKey="Schoch R" first="R." last="Schoch">R. Schoch</name>
</author>
<author>
<name sortKey="Thiel, E" sort="Thiel, E" uniqKey="Thiel E" first="E." last="Thiel">E. Thiel</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Freie Universitat Berlin, Med Klinik III</s1>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>29 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
</analytic>
<series>
<title level="j" type="main">Leukemia</title>
<title level="j" type="abbreviated">Leukemia</title>
<idno type="ISSN">0887-6924</idno>
<imprint>
<date when="2000">2000</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<title level="j" type="main">Leukemia</title>
<title level="j" type="abbreviated">Leukemia</title>
<idno type="ISSN">0887-6924</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Abnormal chromosome C9</term>
<term>Abnormal chromosome G22</term>
<term>Chromosome translocation</term>
<term>Diagnosis</term>
<term>Gene expression</term>
<term>Human</term>
<term>Hybrid gene</term>
<term>Multicenter study</term>
<term>Polymerase chain reaction</term>
<term>Quality assurance</term>
<term>RNA-directed DNA polymerase</term>
<term>Standardization</term>
<term>Technique</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Translocation chromosomique</term>
<term>Chromosome C9 anormal</term>
<term>Chromosome G22 anormal</term>
<term>Gène hybride</term>
<term>Technique</term>
<term>Diagnostic</term>
<term>Assurance qualité</term>
<term>Expression génique</term>
<term>Réaction chaîne polymérase</term>
<term>RNA-directed DNA polymerase</term>
<term>Normalisation</term>
<term>Homme</term>
<term>Etude multicentrique</term>
<term>Gène bcr</term>
<term>Gène abl</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Here we describe the results of an interlaboratory test for RT-PCR-based BCR/ABL analysis. The test was organized in two parts. The number of participating laboratories in the first and second part was 27 and 20, respectively. In the first part samples containing various concentrations of plasmids with the ela2, b2a2 or b3a2 BCR/ABL transcripts were analyzed by PCR. In the second part of the test, cell samples containing various concentrations of BCR/ABL-positive cells were analyzed by RT-PCR. Overall PCR sensitivity was sufficient in approximately 90% of the tests, but a significant number of false positive results were obtained. There were significant differences in sensitivity in the cell-based analysis between the various participants. The results are discussed, and proposals are made regarding the choice of primers, controls, conditions for RNA extraction and reverse transcription.</div>
</front>
</TEI>
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<pA>
<fA01 i1="01" i2="1">
<s0>0887-6924</s0>
</fA01>
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<s0>LEUKED</s0>
</fA02>
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<s0>Leukemia</s0>
</fA03>
<fA05>
<s2>14</s2>
</fA05>
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<s2>10</s2>
</fA06>
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<s1>Quality assurance in RT-PCR-based BCR/ABL diagnostics: results of an interlaboratory test and a standardization approach</s1>
</fA08>
<fA11 i1="01" i2="1">
<s1>BURMEISTER (T.)</s1>
</fA11>
<fA11 i1="02" i2="1">
<s1>MAURER (J.)</s1>
</fA11>
<fA11 i1="03" i2="1">
<s1>AIVADO (M.)</s1>
</fA11>
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<s1>ELMAAGACLI (A. H.)</s1>
</fA11>
<fA11 i1="05" i2="1">
<s1>GRÜNEBACH (F.)</s1>
</fA11>
<fA11 i1="06" i2="1">
<s1>HELD (K. R.)</s1>
</fA11>
<fA11 i1="07" i2="1">
<s1>HESS (G.)</s1>
</fA11>
<fA11 i1="08" i2="1">
<s1>HOCHHAUS (A.)</s1>
</fA11>
<fA11 i1="09" i2="1">
<s1>HÖPPNER (W.)</s1>
</fA11>
<fA11 i1="10" i2="1">
<s1>LENTES (K. U.)</s1>
</fA11>
<fA11 i1="11" i2="1">
<s1>LÜBBERT (M.)</s1>
</fA11>
<fA11 i1="12" i2="1">
<s1>SCHÄFER (K. L.)</s1>
</fA11>
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<s1>SCHAFHAUSEN (P.)</s1>
</fA11>
<fA11 i1="14" i2="1">
<s1>SCHMIDT (C. A.)</s1>
</fA11>
<fA11 i1="15" i2="1">
<s1>SCHÜLER (F.)</s1>
</fA11>
<fA11 i1="16" i2="1">
<s1>SEEGER (K.)</s1>
</fA11>
<fA11 i1="17" i2="1">
<s1>SEELIG (R.)</s1>
</fA11>
<fA11 i1="18" i2="1">
<s1>THIEDE (C.)</s1>
</fA11>
<fA11 i1="19" i2="1">
<s1>VIEHMANN (S.)</s1>
</fA11>
<fA11 i1="20" i2="1">
<s1>WEBER (C.)</s1>
</fA11>
<fA11 i1="21" i2="1">
<s1>WILHELM (S.)</s1>
</fA11>
<fA11 i1="22" i2="1">
<s1>CHRISTMANN (A.)</s1>
</fA11>
<fA11 i1="23" i2="1">
<s1>CLEMENT (J. H.)</s1>
</fA11>
<fA11 i1="24" i2="1">
<s1>EBENER (U.)</s1>
</fA11>
<fA11 i1="25" i2="1">
<s1>ENCZMANN (J.)</s1>
</fA11>
<fA11 i1="26" i2="1">
<s1>LEO (R.)</s1>
</fA11>
<fA11 i1="27" i2="1">
<s1>SCHLEUNING (M.)</s1>
</fA11>
<fA11 i1="28" i2="1">
<s1>SCHOCH (R.)</s1>
</fA11>
<fA11 i1="29" i2="1">
<s1>THIEL (E.)</s1>
</fA11>
<fA14 i1="01">
<s1>Freie Universitat Berlin, Med Klinik III</s1>
<s3>DEU</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>29 aut.</sZ>
</fA14>
<fA14 i1="02">
<s1>Universität Düsseldorf, Klinik fur Hamatologie und Onkologie</s1>
<s3>DEU</s3>
<sZ>3 aut.</sZ>
</fA14>
<fA14 i1="03">
<s1>Universität-Gesamthochschule Essen, Klinik für Knochenmarktransplantation</s1>
<s3>DEU</s3>
<sZ>4 aut.</sZ>
</fA14>
<fA14 i1="04">
<s1>Universität Tübingen, Med, Klinik</s1>
<s3>DEU</s3>
<sZ>5 aut.</sZ>
</fA14>
<fA14 i1="05">
<s1>Praxis Held/Kesser/Arndt Hamburg</s1>
<s3>DEU</s3>
<sZ>6 aut.</sZ>
</fA14>
<fA14 i1="06">
<s1>Universität Mainz, III, Med, Klinik</s1>
<s3>DEU</s3>
<sZ>7 aut.</sZ>
</fA14>
<fA14 i1="07">
<s1>Universität Heidelberg, III, Med, Klinik, Klinikum Mannheim</s1>
<s3>DEU</s3>
<sZ>8 aut.</sZ>
</fA14>
<fA14 i1="08">
<s1>GLE medicon GmbH</s1>
<s2>Hamburg</s2>
<s3>DEU</s3>
<sZ>9 aut.</sZ>
</fA14>
<fA14 i1="09">
<s1>Universität Trier, Abt, Molekulare Neurogenetik</s1>
<s3>DEU</s3>
<sZ>10 aut.</sZ>
</fA14>
<fA14 i1="10">
<s1>Universität Freiburg, Med. Klinik I</s1>
<s3>DEU</s3>
<sZ>11 aut.</sZ>
</fA14>
<fA14 i1="11">
<s1>Universitat Münster, Institut fur Pathologie</s1>
<s3>DEU</s3>
<sZ>12 aut.</sZ>
</fA14>
<fA14 i1="12">
<s1>Universität Hamburg, Med. Klinik III</s1>
<s3>DEU</s3>
<sZ>13 aut.</sZ>
</fA14>
<fA14 i1="13">
<s1>
<sup>113</sup>
Humboldt-Universitat Berlin, Med. Klinik, Hamatologie/Onkologie</s1>
<s3>DEU</s3>
<sZ>14 aut.</sZ>
</fA14>
<fA14 i1="14">
<s1>Universität Greifswald, Klinik fur Innere Medizin C</s1>
<s3>DEU</s3>
<sZ>15 aut.</sZ>
</fA14>
<fA14 i1="15">
<s1>Humboldt-Universitat Berlin, Zentrum fur Kinderheilkunde</s1>
<s3>DEU</s3>
<sZ>16 aut.</sZ>
</fA14>
<fA14 i1="16">
<s1>Labor Prof Seelig und Partner</s1>
<s2>Karlsruhe</s2>
<s3>DEU</s3>
<sZ>17 aut.</sZ>
</fA14>
<fA14 i1="17">
<s1>Technische Universitat Dresden, Med, Klinik 1</s1>
<s3>DEU</s3>
<sZ>18 aut.</sZ>
</fA14>
<fA14 i1="18">
<s1>Universität Giessen, Kinderklinik, Onkogenetisches Labor</s1>
<s3>DEU</s3>
<sZ>19 aut.</sZ>
</fA14>
<fA14 i1="19">
<s1>Universität Giessen, Abt, for Hamatologie</s1>
<s3>DEU</s3>
<sZ>20 aut.</sZ>
</fA14>
<fA14 i1="20">
<s1>Universität Rostock, Abt für Hämatologie/Onkologie</s1>
<s3>DEU</s3>
<sZ>21 aut.</sZ>
</fA14>
<fA14 i1="21">
<s1>Universität Homburg, Institut für Humangenetik</s1>
<s3>DEU</s3>
<sZ>22 aut.</sZ>
</fA14>
<fA14 i1="22">
<s1>Universität Jena, Innere Medizin II</s1>
<s3>DEU</s3>
<sZ>23 aut.</sZ>
</fA14>
<fA14 i1="23">
<s1>Universität Frankfurt, Zentrum für Kinderheilkunde</s1>
<s3>DEU</s3>
<sZ>24 aut.</sZ>
</fA14>
<fA14 i1="24">
<s1>Universität Düsseldorf, Knochenmarkspenderzentrale</s1>
<s3>DEU</s3>
<sZ>25 aut.</sZ>
</fA14>
<fA14 i1="25">
<s1>Universität Münster, Med, Klinik A</s1>
<s3>DEU</s3>
<sZ>26 aut.</sZ>
</fA14>
<fA20>
<s1>1850-1856</s1>
</fA20>
<fA21>
<s1>2000</s1>
</fA21>
<fA23 i1="01">
<s0>ENG</s0>
</fA23>
<fA43 i1="01">
<s1>INIST</s1>
<s2>21129</s2>
<s5>354000092220510160</s5>
</fA43>
<fA44>
<s0>0000</s0>
<s1>© 2001 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45>
<s0>19 ref.</s0>
</fA45>
<fA47 i1="01" i2="1">
<s0>01-0004051</s0>
</fA47>
<fA60>
<s1>P</s1>
</fA60>
<fA61>
<s0>A</s0>
</fA61>
<fA64 i1="01" i2="1">
<s0>Leukemia</s0>
</fA64>
<fA66 i1="01">
<s0>GBR</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>Here we describe the results of an interlaboratory test for RT-PCR-based BCR/ABL analysis. The test was organized in two parts. The number of participating laboratories in the first and second part was 27 and 20, respectively. In the first part samples containing various concentrations of plasmids with the ela2, b2a2 or b3a2 BCR/ABL transcripts were analyzed by PCR. In the second part of the test, cell samples containing various concentrations of BCR/ABL-positive cells were analyzed by RT-PCR. Overall PCR sensitivity was sufficient in approximately 90% of the tests, but a significant number of false positive results were obtained. There were significant differences in sensitivity in the cell-based analysis between the various participants. The results are discussed, and proposals are made regarding the choice of primers, controls, conditions for RNA extraction and reverse transcription.</s0>
</fC01>
<fC02 i1="01" i2="X">
<s0>002B24O10</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE">
<s0>Translocation chromosomique</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>Chromosome translocation</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Translocación cromosómica</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Chromosome C9 anormal</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Abnormal chromosome C9</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Cromosoma C9 anormal</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Chromosome G22 anormal</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Abnormal chromosome G22</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Cromosoma G22 anormal</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Gène hybride</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Hybrid gene</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Gen híbrido</s0>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Technique</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Technique</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Técnica</s0>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Diagnostic</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Diagnosis</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Diagnóstico</s0>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Assurance qualité</s0>
<s5>08</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Quality assurance</s0>
<s5>08</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA">
<s0>Aseguración calidad</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE">
<s0>Expression génique</s0>
<s5>09</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
<s0>Gene expression</s0>
<s5>09</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Expresión genética</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE">
<s0>Réaction chaîne polymérase</s0>
<s5>10</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG">
<s0>Polymerase chain reaction</s0>
<s5>10</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA">
<s0>Reacción cadena polimerasa</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE">
<s0>RNA-directed DNA polymerase</s0>
<s2>FE</s2>
<s5>11</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG">
<s0>RNA-directed DNA polymerase</s0>
<s2>FE</s2>
<s5>11</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA">
<s0>RNA-directed DNA polymerase</s0>
<s2>FE</s2>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE">
<s0>Normalisation</s0>
<s5>18</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG">
<s0>Standardization</s0>
<s5>18</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA">
<s0>Normalización</s0>
<s5>18</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE">
<s0>Homme</s0>
<s5>19</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG">
<s0>Human</s0>
<s5>19</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA">
<s0>Hombre</s0>
<s5>19</s5>
</fC03>
<fC03 i1="13" i2="X" l="FRE">
<s0>Etude multicentrique</s0>
<s5>20</s5>
</fC03>
<fC03 i1="13" i2="X" l="ENG">
<s0>Multicenter study</s0>
<s5>20</s5>
</fC03>
<fC03 i1="13" i2="X" l="SPA">
<s0>Estudio multicéntrico</s0>
<s5>20</s5>
</fC03>
<fC03 i1="14" i2="X" l="FRE">
<s0>Gène bcr</s0>
<s4>INC</s4>
<s5>86</s5>
</fC03>
<fC03 i1="15" i2="X" l="FRE">
<s0>Gène abl</s0>
<s4>INC</s4>
<s5>87</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Chromosome anormal</s0>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Abnormal chromosome</s0>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Cromosoma anormal</s0>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Aberration chromosomique</s0>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Chromosomal aberration</s0>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Aberración cromosómica</s0>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Nucleotidyltransferases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Nucleotidyltransferases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Nucleotidyltransferases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Transferases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Transferases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Transferases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Enzyme</s0>
</fC07>
<fC07 i1="05" i2="X" l="ENG">
<s0>Enzyme</s0>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Enzima</s0>
</fC07>
<fC07 i1="06" i2="X" l="FRE">
<s0>Biologie moléculaire</s0>
<s5>61</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>Molecular biology</s0>
<s5>61</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Biología molecular</s0>
<s5>61</s5>
</fC07>
<fN21>
<s1>001</s1>
</fN21>
</pA>
</standard>
<server>
<NO>PASCAL 01-0004051 INIST</NO>
<ET>Quality assurance in RT-PCR-based BCR/ABL diagnostics: results of an interlaboratory test and a standardization approach</ET>
<AU>BURMEISTER (T.); MAURER (J.); AIVADO (M.); ELMAAGACLI (A. H.); GRÜNEBACH (F.); HELD (K. R.); HESS (G.); HOCHHAUS (A.); HÖPPNER (W.); LENTES (K. U.); LÜBBERT (M.); SCHÄFER (K. L.); SCHAFHAUSEN (P.); SCHMIDT (C. A.); SCHÜLER (F.); SEEGER (K.); SEELIG (R.); THIEDE (C.); VIEHMANN (S.); WEBER (C.); WILHELM (S.); CHRISTMANN (A.); CLEMENT (J. H.); EBENER (U.); ENCZMANN (J.); LEO (R.); SCHLEUNING (M.); SCHOCH (R.); THIEL (E.)</AU>
<AF>Freie Universitat Berlin, Med Klinik III/Allemagne (1 aut., 2 aut., 29 aut.); Universität Düsseldorf, Klinik fur Hamatologie und Onkologie/Allemagne (3 aut.); Universität-Gesamthochschule Essen, Klinik für Knochenmarktransplantation/Allemagne (4 aut.); Universität Tübingen, Med, Klinik/Allemagne (5 aut.); Praxis Held/Kesser/Arndt Hamburg/Allemagne (6 aut.); Universität Mainz, III, Med, Klinik/Allemagne (7 aut.); Universität Heidelberg, III, Med, Klinik, Klinikum Mannheim/Allemagne (8 aut.); GLE medicon GmbH/Hamburg/Allemagne (9 aut.); Universität Trier, Abt, Molekulare Neurogenetik/Allemagne (10 aut.); Universität Freiburg, Med. Klinik I/Allemagne (11 aut.); Universitat Münster, Institut fur Pathologie/Allemagne (12 aut.); Universität Hamburg, Med. Klinik III/Allemagne (13 aut.);
<sup>113</sup>
Humboldt-Universitat Berlin, Med. Klinik, Hamatologie/Onkologie/Allemagne (14 aut.); Universität Greifswald, Klinik fur Innere Medizin C/Allemagne (15 aut.); Humboldt-Universitat Berlin, Zentrum fur Kinderheilkunde/Allemagne (16 aut.); Labor Prof Seelig und Partner/Karlsruhe/Allemagne (17 aut.); Technische Universitat Dresden, Med, Klinik 1/Allemagne (18 aut.); Universität Giessen, Kinderklinik, Onkogenetisches Labor/Allemagne (19 aut.); Universität Giessen, Abt, for Hamatologie/Allemagne (20 aut.); Universität Rostock, Abt für Hämatologie/Onkologie/Allemagne (21 aut.); Universität Homburg, Institut für Humangenetik/Allemagne (22 aut.); Universität Jena, Innere Medizin II/Allemagne (23 aut.); Universität Frankfurt, Zentrum für Kinderheilkunde/Allemagne (24 aut.); Universität Düsseldorf, Knochenmarkspenderzentrale/Allemagne (25 aut.); Universität Münster, Med, Klinik A/Allemagne (26 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Leukemia; ISSN 0887-6924; Coden LEUKED; Royaume-Uni; Da. 2000; Vol. 14; No. 10; Pp. 1850-1856; Bibl. 19 ref.</SO>
<LA>Anglais</LA>
<EA>Here we describe the results of an interlaboratory test for RT-PCR-based BCR/ABL analysis. The test was organized in two parts. The number of participating laboratories in the first and second part was 27 and 20, respectively. In the first part samples containing various concentrations of plasmids with the ela2, b2a2 or b3a2 BCR/ABL transcripts were analyzed by PCR. In the second part of the test, cell samples containing various concentrations of BCR/ABL-positive cells were analyzed by RT-PCR. Overall PCR sensitivity was sufficient in approximately 90% of the tests, but a significant number of false positive results were obtained. There were significant differences in sensitivity in the cell-based analysis between the various participants. The results are discussed, and proposals are made regarding the choice of primers, controls, conditions for RNA extraction and reverse transcription.</EA>
<CC>002B24O10</CC>
<FD>Translocation chromosomique; Chromosome C9 anormal; Chromosome G22 anormal; Gène hybride; Technique; Diagnostic; Assurance qualité; Expression génique; Réaction chaîne polymérase; RNA-directed DNA polymerase; Normalisation; Homme; Etude multicentrique; Gène bcr; Gène abl</FD>
<FG>Chromosome anormal; Aberration chromosomique; Nucleotidyltransferases; Transferases; Enzyme; Biologie moléculaire</FG>
<ED>Chromosome translocation; Abnormal chromosome C9; Abnormal chromosome G22; Hybrid gene; Technique; Diagnosis; Quality assurance; Gene expression; Polymerase chain reaction; RNA-directed DNA polymerase; Standardization; Human; Multicenter study</ED>
<EG>Abnormal chromosome; Chromosomal aberration; Nucleotidyltransferases; Transferases; Enzyme; Molecular biology</EG>
<SD>Translocación cromosómica; Cromosoma C9 anormal; Cromosoma G22 anormal; Gen híbrido; Técnica; Diagnóstico; Aseguración calidad; Expresión genética; Reacción cadena polimerasa; RNA-directed DNA polymerase; Normalización; Hombre; Estudio multicéntrico</SD>
<LO>INIST-21129.354000092220510160</LO>
<ID>01-0004051</ID>
</server>
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