Transfusion

Cover image for Vol. 53 Issue 11pt2

Special Issue: Twenty Years since the Cloning of the Blood Group Genes

November 2013

Volume 53, Issue 11pt2

Pages 2831–3024

  1. COMMENTARIES

    1. Top of page
    2. COMMENTARIES
    3. KEL
    4. NEW METHODS FOR BLOOD GROUP GENOTYPING
    5. ABO/P
    6. RH
    7. NEW ALLELES AND ANTIGENS
    1. PUBLICATION OF THIS SPECIAL ISSUE IS MADE POSSIBLE BY NOVARTIS DIAGNOSTICS.

    2. Noninvasive prenatal blood group and HPA-1a genotyping: the current European experience (pages 2834–2836)

      C. Ellen van der Schoot, Florentine F. Thurik, Barbera Veldhuisen and Masja de Haas

      Version of Record online: 4 SEP 2013 | DOI: 10.1111/trf.12411

  2. KEL

    1. Top of page
    2. COMMENTARIES
    3. KEL
    4. NEW METHODS FOR BLOOD GROUP GENOTYPING
    5. ABO/P
    6. RH
    7. NEW ALLELES AND ANTIGENS
    1. Identification of novel silent KEL alleles causing KEL:−5 (Ko) phenotype or discordance between KEL:1,−2 phenotype/KEL*01/02 genotype (pages 2859–2866)

      Stéphanie Martin-Blanc, Philippe Simon, Dominique Gien, Sandrine Kappler-Gratias, Pierre-Yves Le Pennec and Bach-Nga Pham

      Version of Record online: 14 APR 2013 | DOI: 10.1111/trf.12206

    2. Three novel alleles in the Kell blood group system resulting in the Knull phenotype and the first in a Native American (pages 2867–2871)

      Joann M. Moulds, Rosemary Persa, Darbi Rierson, Katrina L. Billingsley, Ghislain T. Noumsi, Kim Hue-Roye and Marion E. Reid

      Version of Record online: 14 APR 2013 | DOI: 10.1111/trf.12205

    3. Molecular basis of two novel and related high-prevalence antigens in the Kell blood group system, KUCI and KANT, and their serologic and spatial association with K11 and KETI (pages 2872–2881)

      Randall W. Velliquette, Kim Hue-Roye, Christine Lomas-Francis, Barbara Gillen, Jennifer Schierts, Kristie Gentzkow, Thierry Peyrard, Inge von Zabern, Willy A. Flegel, Karen Rodberg, Asim K. Debnath, Soohee Lee and Marion E. Reid

      Version of Record online: 8 APR 2013 | DOI: 10.1111/trf.12200

    4. Expansion of the Kell blood group system: two new high-prevalence antigens and two novel K0 (Kellnull) phenotypes (pages 2887–2891)

      Christine Lomas-Francis, Sunitha Vege, Randall W. Velliquette, Akiko Fuchisawa, Makoto Uchikawa, Yoshihiko Tani, Hiroko Moro, Asim K. Debnath and Connie M. Westhoff

      Version of Record online: 22 AUG 2013 | DOI: 10.1111/trf.12377

  3. NEW METHODS FOR BLOOD GROUP GENOTYPING

    1. Top of page
    2. COMMENTARIES
    3. KEL
    4. NEW METHODS FOR BLOOD GROUP GENOTYPING
    5. ABO/P
    6. RH
    7. NEW ALLELES AND ANTIGENS
    1. Next-generation sequencing: proof of concept for antenatal prediction of the fetal Kell blood group phenotype from cell-free fetal DNA in maternal plasma (pages 2892–2898)

      Klaus Rieneck, Mads Bak, Lars Jønson, Frederik Banch Clausen, Grethe Risum Krog, Niels Tommerup, Leif Kofoed Nielsen, Morten Hedegaard and Morten Hanefeld Dziegiel

      Version of Record online: 3 APR 2013 | DOI: 10.1111/trf.12172

  4. ABO/P

    1. Top of page
    2. COMMENTARIES
    3. KEL
    4. NEW METHODS FOR BLOOD GROUP GENOTYPING
    5. ABO/P
    6. RH
    7. NEW ALLELES AND ANTIGENS
    1. Molecular genetic analysis of ABO blood group variations reveals 29 novel ABO subgroup alleles (pages 2910–2916)

      Xiaohong Cai, Sha Jin, Xi Liu, Liangfeng Fan, Qiong Lu, Jianlian Wang, Wei Shen, Songsong Gong, Li Qiu and Dong Xiang

      Version of Record online: 21 MAR 2013 | DOI: 10.1111/trf.12168

    2. Mutation of the GATA site in the erythroid cell–specific regulatory element of the ABO gene in a Bm subgroup individual (pages 2917–2927)

      Tamiko Nakajima, Rie Sano, Yoichiro Takahashi, Rieko Kubo, Keiko Takahashi, Yoshihiko Kominato, Junichi Tsukada, Haruo Takeshita, Toshihiro Yasuda, Makoto Uchikawa, Kazumi Isa and Kenichi Ogasawara

      Version of Record online: 8 APR 2013 | DOI: 10.1111/trf.12181

    3. P1/P2 genotyping of known and novel null alleles in the P1PK and GLOB histo-blood group systems (pages 2928–2939)

      Julia S. Westman, Åsa Hellberg, Thierry Peyrard, Hein Hustinx, Britt Thuresson and Martin L. Olsson

      Version of Record online: 8 AUG 2013 | DOI: 10.1111/trf.12355

  5. RH

    1. Top of page
    2. COMMENTARIES
    3. KEL
    4. NEW METHODS FOR BLOOD GROUP GENOTYPING
    5. ABO/P
    6. RH
    7. NEW ALLELES AND ANTIGENS
    1. Combining serology and molecular typing of weak D role in improving D typing strategy in Egypt (pages 2940–2944)

      Abeer Mohamed Abdelrazik, Shahira Morsy Elshafie, Ghada M. Ezzat Ahmed and Hossam M. Abdelaziz

      Version of Record online: 30 JAN 2013 | DOI: 10.1111/trf.12100

    2. RHD variants in Polish blood donors routinely typed as D– (pages 2945–2953)

      Agnieszka Orzińska, Katarzyna Guz, Helene Polin, Monika Pelc-Kłopotowska, Justyna Bednarz, Agata Gieleżyńska, Beata Śliwa, Małgorzata Kowalewska, Elżbieta Pawłowska, Bogusława Włodarczyk, Małgorzata Malaga, Alicja Żmudzin, Magdalena Krzemienowska, Kshitij Srivastava, Bogumiła Michalewska, Christian Gabriel, Willy A. Flegel and Ewa Brojer

      Version of Record online: 1 MAY 2013 | DOI: 10.1111/trf.12230

    3. Novel RHD alleles with weak hemagglutination and genetic Exon 9 diversity: weak D Types 45.1, 75, and 76 (pages 2954–2959)

      Christoph Gassner, Irene Utz, Harald Schennach, Angela Ramoni, Hannes Steiner, Sabine Scholz, Ursula Kreklau and Günther F. Körmöczi

      Version of Record online: 3 APR 2013 | DOI: 10.1111/trf.12180

    4. D category IV: a group of clinically relevant and phylogenetically diverse partial D (pages 2960–2973)

      Inge von Zabern, Franz F. Wagner, Joann M. Moulds, John J. Moulds and Willy A. Flegel

      Version of Record online: 5 MAR 2013 | DOI: 10.1111/trf.12145

    5. A convenient qualitative and quantitative method to investigate RHD-RHCE hybrid genes (pages 2974–2982)

      Yann Fichou, Cédric Le Maréchal, Laurence Bryckaert, Isabelle Dupont, Déborah Jamet, Jian-Min Chen and Claude Férec

      Version of Record online: 3 APR 2013 | DOI: 10.1111/trf.12179

    6. RHCE*ceMO is frequently in cis to RHD*DAU0 and encodes a hrS–, hrB–, RH:–61 phenotype in black persons: clinical significance (pages 2983–2989)

      Connie M. Westhoff, Sunitha Vege, Trina Horn, Kim Hue-Roye, Christine Halter Hipsky, Christine Lomas-Francis and Marion E. Reid

      Version of Record online: 17 JUN 2013 | DOI: 10.1111/trf.12271

    7. Molecular background of novel silent RHCE alleles (pages 2990–2999)

      Bach-Nga Pham, Stéphanie Ramelet, Bénédicte Wibaut, Genevieve Juszczak, Chawki Loukil, Isabelle Dubeaux, Dominique Gien, Sandrine Kappler-Gratias, Philippe Rouger and Pierre-Yves Le Pennec

      Version of Record online: 17 DEC 2012 | DOI: 10.1111/trf.12023

    8. Serologic and molecular investigations of DAR1 (weak D Type 4.2), DAR1.2, DAR1.3, DAR2 (DARE), and DARA (pages 3000–3008)

      Sofia Lejon Crottet, Lonneke Haer-Wigman, Peter Gowland, Stefano Fontana, Christoph Niederhauser and Hein Hustinx

      Version of Record online: 31 JUL 2013 | DOI: 10.1111/trf.12363

    9. New RHCE variant alleles encoding the D– – phenotype (pages 3018–3023)

      Gorka Ochoa-Garay, Joann M. Moulds, Jacqueline Cote, Lesley Kresie, Adirane Garaizar, Mindy Goldman and Polly Wynn

      Version of Record online: 10 SEP 2013 | DOI: 10.1111/trf.12404

  6. NEW ALLELES AND ANTIGENS

    1. Top of page
    2. COMMENTARIES
    3. KEL
    4. NEW METHODS FOR BLOOD GROUP GENOTYPING
    5. ABO/P
    6. RH
    7. NEW ALLELES AND ANTIGENS
    1. A novel JK*02 allele in a French Canadian family (page 3024)

      Maryse St-Louis, Josée Lavoie, Samuel Caron, Mireille Paquet and Josée Perreault

      Version of Record online: 27 MAY 2013 | DOI: 10.1111/trf.12266

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