Works matching IS 00411132 AND DT 2015 AND VI 55 AND IP 6pt2

Results: 35

Red blood cell Thomsen- Friedenreich antigen expression and galectin-3 plasma concentrations in Streptococcus pneumoniae-associated hemolytic uremic syndrome and hemolytic anemia.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1563, doi. 10.1111/trf.12981

By:

Burin des Roziers, Nicolas;
Chadebech, Philippe;
Bodivit, Gwellaouen;
Guinchard, Emmanuelle;
Bruneel, Arnaud;
Dupré, Thierry;
Chevret, Laurent;
Jugie, Myriam;
Gallon, Philippe;
Bierling, Philippe;
Noizat‐Pirenne, France

Publication type:

Article

Training students in serologic reaction grading increased perceptions of self-efficacy and ability to recognize serologic reactions but decreased grading accuracy.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1572, doi. 10.1111/trf.12985

By:

Perry, Holly;
Henry, Stephen

Publication type:

Article

Changing practice: red blood cell typing by molecular methods for patients with sickle cell disease.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1388, doi. 10.1111/trf.12987

By:

Casas, Jessica;
Friedman, David F.;
Jackson, Tannoa;
Vege, Sunitha;
Westhoff, Connie M.;
Chou, Stella T.

Publication type:

Article

Short duplication within the RHCE gene associated with an in cis deleted RHD causing a Rhnull amorph phenotype in an immunized pregnant woman with anti- Rh29.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1407, doi. 10.1111/trf.12937

By:

Silvy, Monique;
Beley, Sophie;
Peyrard, Thierry;
Ouchari, Mouna;
Abdelkefi, Saadia;
Jemni Yacoub, Saloua;
Chiaroni, Jacques;
Bailly, Pascal

Publication type:

Article

A comparison of methods for the detection of the r′s haplotype.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1418, doi. 10.1111/trf.12956

By:

Moulds, Joann M.;
Noumsi, Ghislain T.;
Billingsley, Katrina L.

Publication type:

Article

CD44 antibody-mediated amelioration of murine immune thrombocytopenia (ITP): mouse background determines the effect of FcγRIIb genetic disruption.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1492, doi. 10.1111/trf.12957

By:

Crow, Andrew R.;
Amash, Alaa;
Lazarus, Alan H.

Publication type:

Article

Western immunoblotting as a new tool for investigating direct antiglobulin test-negative autoimmune hemolytic anemias.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1529, doi. 10.1111/trf.13082

By:

Bloch, Evgenia M.;
Sakac, Darinka;
Branch, Haley A.;
Cserti‐Gazdewich, Christine;
Pendergrast, Jacob;
Pavenski, Katerina;
Branch, Donald R.

Publication type:

Article

Routine non-ABO blood group antigen genotyping in sickle cell disease: the new frontier in pretransfusion testing?

Published in:

2015

By:

Tormey, Christopher A.;
Hendrickson, Jeanne E.

Publication type:

commentary

A new Rhnull allele in francophone Quebecers.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1580, doi. 10.1111/trf.12887

By:

St‐Louis, Maryse;
Éthier, Carole;
Perreault, Josée;
Lavoie, Josée

Publication type:

Article

A new low-frequency alloantigen ( Khab) located on platelet glycoprotein IIIa as a cause of maternal sensitization leading to neonatal alloimmune thrombocytopenia.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1584, doi. 10.1111/trf.12959

By:

Sullivan, Mia J.;
Peterson, Julie;
McFarland, Janice G.;
Bougie, Daniel;
Aster, Richard H.;
Curtis, Brian R.

Publication type:

Article

Resolving the daratumumab interference with blood compatibility testing.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1545, doi. 10.1111/trf.13069

By:

Chapuy, Claudia I.;
Nicholson, Rachel T.;
Aguad, Maria D.;
Chapuy, Bjoern;
Laubach, Jacob P.;
Richardson, Paul G.;
Doshi, Parul;
Kaufman, Richard M.

Publication type:

Article

Impact of genetic variation in the SMIM1 gene on Vel expression levels.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1457, doi. 10.1111/trf.13014

By:

Haer‐Wigman, Lonneke;
Stegmann, Tamara C.;
Solati, Shabnam;
Ait Soussan, Aïcha;
Beckers, Erik;
van der Harst, Pim;
van Hulst‐Sundermeijer, Marga;
Ligthart, Peter;
van Rhenen, Dick;
Schepers, Hein;
de Haas, Masja;
van der Schoot, C. Ellen

Publication type:

Article

Evaluation of different testing methods for identification of RhIG in red blood cell antibody detection.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1444, doi. 10.1111/trf.13018

By:

Mikesell, Kael V.;
George, Melissa R.;
Castellani, William J.;
Domen, Ronald E.;
Gould, Joy M.;
Davis, Jerry W.;
Herman, Jay H.

Publication type:

Article

Extensive functional analyses of RHD splice site variants: Insights into the potential role of splicing in the physiology of Rh.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1432, doi. 10.1111/trf.13083

By:

Fichou, Yann;
Gehannin, Pierre;
Corre, Manon;
Le Guern, Alice;
Le Maréchal, Cédric;
Le Gac, Gérald;
Férec, Claude

Publication type:

Article

When blood transfusion medicine becomes complicated due to interference by monoclonal antibody therapy.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1555, doi. 10.1111/trf.13150

By:

Oostendorp, Marlies;
Lammerts van Bueren, Jeroen J.;
Doshi, Parul;
Khan, Imran;
Ahmadi, Tahamtan;
Parren, Paul W.H.I.;
van Solinge, Wouter W.;
De Vooght, Karen M.K.

Publication type:

Article

The prevalence of anti-K in Canadian prenatal patients.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1486, doi. 10.1111/trf.13151

By:

Goldman, Mindy;
Lane, Debra;
Webert, Kathryn;
Fallis, Robert

Publication type:

Article

A monoclonal antibody with anti-D-like activity in murine immune thrombocytopenia requires Fc domain function for immune thrombocytopenia ameliorative effects.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1501, doi. 10.1111/trf.13032

By:

Yu, Xiaojie;
Menard, Melissa;
Seabright, Gemma;
Crispin, Max;
Lazarus, Alan H.

Publication type:

Article

Barriers to using molecularly typed minority red blood cell donors in support of chronically transfused adult patients with sickle cell disease.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1399, doi. 10.1111/trf.13037

By:

Karafin, Matthew S.;
Field, Joshua J.;
Gottschall, Jerome L.;
Denomme, Gregory A.

Publication type:

Article

Noninvasive fetal genotyping of human platelet antigen-1a using targeted massively parallel sequencing.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1538, doi. 10.1111/trf.13102

By:

Wienzek‐Lischka, Sandra;
Krautwurst, Annika;
Fröhner, Vanessa;
Hackstein, Holger;
Gattenlöhner, Stefan;
Bräuninger, Andreas;
Axt‐Fliedner, Roland;
Degenhardt, Jan;
Deisting, Christina;
Santoso, Sentot;
Sachs, Ulrich J.;
Bein, Gregor

Publication type:

Article

RH diversity in Mali: characterization of a new haplotype RHDDIVa/RHCEceTI(D2).

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1423, doi. 10.1111/trf.13109

By:

Ba, Alhassane;
Beley, Sophie;
Chiaroni, Jacques;
Bailly, Pascal;
Silvy, Monique

Publication type:

Article

SARA: a 'new' low-frequency MNS antigen ( MNS47) provides further evidence of the extreme diversity of the MNS blood group system.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1451, doi. 10.1111/trf.12973

By:

McBean, Rhiannon S.;
Hyland, Catherine A.;
Hendry, Julia L.;
Shabani‐Rad, Meer‐Taher;
Flower, Robert L.

Publication type:

Article

Anti- K formation is not associated with the storage time of transfused red blood cells.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1472, doi. 10.1111/trf.12974

By:

Hogervorst, Esther;
Middelburg, Rutger;
Brand, Anneke;
Watering, Leo;
Schonewille, Henk

Publication type:

Article

A multicenter study on the performance of a fully automated, walk-away high-throughput analyzer for pretransfusion testing in the US population.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1522, doi. 10.1111/trf.13053

By:

Roback, John D.;
Barclay, Sheilagh;
Moulds, JoAnn M.;
Denomme, Gregory A.

Publication type:

Article

Does recipient inflammation contribute to red blood cell alloimmunization?

Published in:

2015

By:

Shi, Patricia

Publication type:

commentary

A serologic weakly reactive RhD is caused by a RHD 374T>A (Ile125Asn).

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1586, doi. 10.1111/trf.13004

By:

Flesch, Brigitte K.;
Schottstedt, Volkmar;
Spallek, Heinrich;
Just, Burkhard

Publication type:

Article

Hyperhemolysis syndrome in patients with sickle cell anemia: report of three cases.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1394, doi. 10.1111/trf.12993

By:

Santos, Berta;
Portugal, Rodrigo;
Nogueira, Carmen;
Loureiro, Monique

Publication type:

Article

Alloimmunization in sickle cell disease: changing antibody specificities and association with chronic pain and decreased survival.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1378, doi. 10.1111/trf.12940

By:

Telen, Marilyn J.;
Afenyi‐Annan, Araba;
Garrett, Melanie E.;
Combs, Martha R.;
Orringer, Eugene P.;
Ashley‐Koch, Allison E.

Publication type:

Article

A novel B allele with c.502 C> G mutation identified in a Chinese individual.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1582, doi. 10.1111/trf.12942

By:

Chen, Qing;
Xiao, Jianyu;
Lu, Le;
Du, Leilei;
Huang, Chengyin;
Li, Min;
Li, Ping;
Yao, Genhong

Publication type:

Article

RHD variants in Flanders, Belgium.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1411, doi. 10.1111/trf.12947

By:

Van Sandt, Vicky S.T.;
Gassner, Christoph;
Emonds, Marie‐Paule;
Legler, Tobias J.;
Mahieu, Sarah;
Körmöczi, Günther F.

Publication type:

Article

Molecular genetic analysis of para-Bombay phenotype in Chinese persons: a novel FUT1 allele is identified.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1588, doi. 10.1111/trf.13022

By:

Liang, Wei;
Xu, Hong;
Liu, Yi‐yu;
Zhou, Shou‐rong;
Deng, Dan‐fei;
Yang, Liang;
Xu, De‐yi;
Deng, Gang;
Mei, Chuan‐liang;
He, Yun‐lei;
Zhang, Zhe

Publication type:

Article

Novel ABO gene variants caused by missense mutations in Exon 7 leading to discrepant ABO blood typing results.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1589, doi. 10.1111/trf.13025

By:

Matzhold, Eva M.;
Wagner, Andrea;
Drexler, Camilla;
Wagner, Thomas

Publication type:

Article

A new ABCG2 null allele with a 27-kb deletion including the promoter region causing the Jr(a−) phenotype.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1467, doi. 10.1111/trf.12969

By:

Ogasawara, Kenichi;
Osabe, Takahiro;
Suzuki, Yumi;
Tsuneyama, Hatsue;
Isa, Kazumi;
Kawai, Miho;
Obara, Kumi;
Ogiyama, Yoshiko;
Ito, Shoichi;
Uchikawa, Makoto;
Satake, Masahiro;
Tadokoro, Kenji

Publication type:

Article

Themed issue: immunohematology and blood group genomics.

Published in:

2015

By:

Westhoff, Connie M.;
Ness, Paul M.

Publication type:

Editorial

Female sex of older patients is an independent risk factor for red blood cell alloimmunization after transfusion.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1478, doi. 10.1111/trf.13111

By:

Verduin, Esther P.;
Brand, Anneke;
Middelburg, Rutger A.;
Schonewille, Henk

Publication type:

Article

Impact of priming on the response of neutrophils to human neutrophil alloantigen-3a antibodies.

Published in:

Transfusion, 2015, v. 55, n. 6pt2, p. 1512, doi. 10.1111/trf.12898

By:

Berthold, Tom;
Muschter, Stefan;
Schubert, Nicole;
Wesche, Jan;
Ameling, Sabine;
Teumer, Alexander;
Reil, Angelika;
Bux, Jürgen;
Bakchoul, Tamam;
Greinacher, Andreas

Publication type:

Article

Works matching IS 00411132 AND DT 2015 AND VI 55 AND IP 6pt2

Red blood cell Thomsen- Friedenreich antigen expression and galectin-3 plasma concentrations in Streptococcus pneumoniae-associated hemolytic uremic syndrome and hemolytic anemia.

Training students in serologic reaction grading increased perceptions of self-efficacy and ability to recognize serologic reactions but decreased grading accuracy.

Changing practice: red blood cell typing by molecular methods for patients with sickle cell disease.

Short duplication within the RHCE gene associated with an in cis deleted RHD causing a Rh<sub>null</sub> amorph phenotype in an immunized pregnant woman with anti- Rh29.

A comparison of methods for the detection of the r′<sup>s</sup> haplotype.

CD44 antibody-mediated amelioration of murine immune thrombocytopenia (ITP): mouse background determines the effect of FcγRIIb genetic disruption.

Western immunoblotting as a new tool for investigating direct antiglobulin test-negative autoimmune hemolytic anemias.

Routine non-ABO blood group antigen genotyping in sickle cell disease: the new frontier in pretransfusion testing?

A new Rh<sub>null</sub> allele in francophone Quebecers.

A new low-frequency alloantigen ( Kha<sup>b</sup>) located on platelet glycoprotein IIIa as a cause of maternal sensitization leading to neonatal alloimmune thrombocytopenia.

Resolving the daratumumab interference with blood compatibility testing.

Impact of genetic variation in the SMIM1 gene on Vel expression levels.

Evaluation of different testing methods for identification of RhIG in red blood cell antibody detection.

Extensive functional analyses of RHD splice site variants: Insights into the potential role of splicing in the physiology of Rh.

When blood transfusion medicine becomes complicated due to interference by monoclonal antibody therapy.

The prevalence of anti-K in Canadian prenatal patients.

A monoclonal antibody with anti-D-like activity in murine immune thrombocytopenia requires Fc domain function for immune thrombocytopenia ameliorative effects.

Barriers to using molecularly typed minority red blood cell donors in support of chronically transfused adult patients with sickle cell disease.

Noninvasive fetal genotyping of human platelet antigen-1a using targeted massively parallel sequencing.

RH diversity in Mali: characterization of a new haplotype RHDDIVa/RHCEceTI(D2).

SARA: a 'new' low-frequency MNS antigen ( MNS47) provides further evidence of the extreme diversity of the MNS blood group system.

Anti- K formation is not associated with the storage time of transfused red blood cells.

A multicenter study on the performance of a fully automated, walk-away high-throughput analyzer for pretransfusion testing in the US population.

Does recipient inflammation contribute to red blood cell alloimmunization?

A serologic weakly reactive RhD is caused by a RHD 374T>A (Ile125Asn).

Hyperhemolysis syndrome in patients with sickle cell anemia: report of three cases.

Alloimmunization in sickle cell disease: changing antibody specificities and association with chronic pain and decreased survival.

A novel B allele with c.502 C> G mutation identified in a Chinese individual.

RHD variants in Flanders, Belgium.

Molecular genetic analysis of para-Bombay phenotype in Chinese persons: a novel FUT1 allele is identified.

Novel ABO gene variants caused by missense mutations in Exon 7 leading to discrepant ABO blood typing results.

A new ABCG2 null allele with a 27-kb deletion including the promoter region causing the Jr(a−) phenotype.

Themed issue: immunohematology and blood group genomics.

Female sex of older patients is an independent risk factor for red blood cell alloimmunization after transfusion.

Impact of priming on the response of neutrophils to human neutrophil alloantigen-3a antibodies.