Works matching IS 00411132 AND DT 2013 AND VI 53 AND IP 11pt2

Results: 36

A comprehensive survey of both RHD and RHCE allele frequencies in sub-Saharan Africa.

Published in:

2013

By:

Granier, Thomas;
Beley, Sophie;
Chiaroni, Jacques;
Bailly, Pascal;
Silvy, Monique

Publication type:

Journal Article

P(1) /P(2) genotyping of known and novel null alleles in the P1PK and GLOB histo-blood group systems.

Published in:

2013

By:

Westman, Julia S;
Hellberg, Asa;
Peyrard, Thierry;
Hustinx, Hein;
Thuresson, Britt;
Olsson, Martin L

Publication type:

Journal Article

Serologic and molecular investigations of DAR1 (weak D Type 4.2), DAR1.2, DAR1.3, DAR2 (DARE), and DARA.

Published in:

2013

By:

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

Publication type:

Journal Article

RHCEceMO is frequently in cis to RHDDAU0 and encodes a hr(S) -, hr(B) -, RH:-61 phenotype in black persons: clinical significance.

Published in:

2013

By:

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

Publication type:

journal article

Identification of novel silent KEL alleles causing KEL:-5 (Ko) phenotype or discordance between KEL:1,-2 phenotype/KEL*01/02 genotype.

Published in:

2013

By:

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

Publication type:

Journal Article

Three novel alleles in the Kell blood group system resulting in the Knull phenotype and the first in a Native American.

Published in:

2013

By:

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

Publication type:

Journal Article

Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a Bm subgroup individual.

Published in:

2013

By:

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

Publication type:

Journal Article

A convenient qualitative and quantitative method to investigate RHD-RHCE hybrid genes.

Published in:

2013

By:

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

Publication type:

Journal Article

Molecular background of novel silent RHCE alleles.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2990, doi. 10.1111/trf.12023

By:

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

Publication type:

Article

Next-generation sequencing: proof of concept for antenatal prediction of the fetal Kell blood group phenotype from cell-free fetal DNA in maternal plasma.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2892, doi. 10.1111/trf.12172

By:

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

Publication type:

Article

Noninvasive prenatal blood group and HPA-1a genotyping: the current European experience.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2834, doi. 10.1111/trf.12411

By:

Schoot, C. Ellen;
Thurik, Florentine F.;
Veldhuisen, Barbera;
Haas, Masja

Publication type:

Article

Serologic and molecular investigations of DAR1 (weak D Type 4.2), DAR1.2, DAR1.3, DAR2 ( DARE), and DARA.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 3000, doi. 10.1111/trf.12363

By:

Lejon Crottet, Sofia;
Haer‐Wigman, Lonneke;
Gowland, Peter;
Fontana, Stefano;
Niederhauser, Christoph;
Hustinx, Hein

Publication type:

Article

Proficiency testing for blood group genotyping.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2847, doi. 10.1111/trf.12408

By:

Delaney, Meghan

Publication type:

Article

RHCEceMO is frequently in cis to RHDDAU0 and encodes a hrS-, hrB-, RH:-61 phenotype in black persons: clinical significance.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2983, doi. 10.1111/trf.12271

By:

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

Publication type:

Article

Identification of novel silent KEL alleles causing KEL:−5 ( Ko) phenotype or discordance between KEL:1,−2 phenotype/ KEL*01/02 genotype.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2859, doi. 10.1111/trf.12206

By:

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

Publication type:

Article

New RHCE variant alleles encoding the D- - phenotype.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 3018, doi. 10.1111/trf.12404

By:

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

Publication type:

Article

Three novel alleles in the Kell blood group system resulting in the Knull phenotype and the first in a Native American.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2867, doi. 10.1111/trf.12205

By:

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

Publication type:

Article

Comprehensive genotyping for 18 blood group systems using a multiplex ligation-dependent probe amplification assay shows a high degree of accuracy.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2899, doi. 10.1111/trf.12410

By:

Haer‐Wigman, Lonneke;
Ji, Yanli;
Lodén, Martin;
Haas, Masja;
Schoot, C. Ellen;
Veldhuisen, Barbera

Publication type:

Article

Molecular genetic analysis of ABO blood group variations reveals 29 novel ABO subgroup alleles.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2910, doi. 10.1111/trf.12168

By:

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

Publication type:

Article

Nomenclature for red blood cell blood group alleles.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2844, doi. 10.1111/trf.12407

By:

Storry, Jill R.

Publication type:

Article

P1/ P2 genotyping of known and novel null alleles in the P1 PK and GLOB histo-blood group systems.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2928, doi. 10.1111/trf.12355

By:

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

Publication type:

Article

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

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2887, doi. 10.1111/trf.12377

By:

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

Publication type:

Article

External quality assessment in molecular immunohematology: the INSTAND proficiency test program.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2850, doi. 10.1111/trf.12414

By:

Flegel, Willy A.;
Chiosea, Ion;
Sachs, Ulrich J.;
Bein, Gregor

Publication type:

Article

Resolution of translation start site for the human Kell glycoprotein.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2882, doi. 10.1111/trf.12267

By:

Blacken, Grady R.;
Zimring, James C.;
Fu, Xiaoyun

Publication type:

Article

RHD variants in Polish blood donors routinely typed as D-.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2945, doi. 10.1111/trf.12230

By:

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

Publication type:

Article

A convenient qualitative and quantitative method to investigate RHD- RHCE hybrid genes.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2974, doi. 10.1111/trf.12179

By:

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

Publication type:

Article

The concept of 'confirmatory testing' of donors for ABO and RhD.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2837, doi. 10.1111/trf.12413

By:

Westhoff, Connie M.

Publication type:

Article

Where are we in efforts to unravel the complexity of Rh to guide transfusion decisions?

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2840, doi. 10.1111/trf.12406

By:

Nance, Sandra Taddie;
Lomas‐Francis, Christine

Publication type:

Article

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.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2872, doi. 10.1111/trf.12200

By:

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

Publication type:

Article

Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a Bm subgroup individual.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2917, doi. 10.1111/trf.12181

By:

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

Publication type:

Article

A novel JK*02 allele in a French Canadian family.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 3024, doi. 10.1111/trf.12266

By:

St‐Louis, Maryse;
Lavoie, Josée;
Caron, Samuel;
Paquet, Mireille;
Perreault, Josée

Publication type:

Article

A historical perspective on the discovery of the Kell blood group carriers.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2831, doi. 10.1111/trf.12405

By:

Redman, Colvin M.;
Lee, Soohee

Publication type:

Article

A comprehensive survey of both RHD and RHCE allele frequencies in sub- Saharan Africa.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 3009, doi. 10.1111/trf.12409

By:

Granier, Thomas;
Beley, Sophie;
Chiaroni, Jacques;
Bailly, Pascal;
Silvy, Monique

Publication type:

Article

Combining serology and molecular typing of weak D role in improving D typing strategy in Egypt.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2940, doi. 10.1111/trf.12100

By:

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

Publication type:

Article

Novel RHD alleles with weak hemagglutination and genetic Exon 9 diversity: weak D Types 45.1, 75, and 76.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2954, doi. 10.1111/trf.12180

By:

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

Publication type:

Article

D category IV: a group of clinically relevant and phylogenetically diverse partial D.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2960, doi. 10.1111/trf.12145

By:

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

Publication type:

Article

Works matching IS 00411132 AND DT 2013 AND VI 53 AND IP 11pt2

A comprehensive survey of both RHD and RHCE allele frequencies in sub-Saharan Africa.

P(1) /P(2) genotyping of known and novel null alleles in the P1PK and GLOB histo-blood group systems.

Serologic and molecular investigations of DAR1 (weak D Type 4.2), DAR1.2, DAR1.3, DAR2 (DARE), and DARA.

RHCEceMO is frequently in cis to RHDDAU0 and encodes a hr(S) -, hr(B) -, RH:-61 phenotype in black persons: clinical significance.

Identification of novel silent KEL alleles causing KEL:-5 (Ko) phenotype or discordance between KEL:1,-2 phenotype/KEL*01/02 genotype.

Three novel alleles in the Kell blood group system resulting in the Knull phenotype and the first in a Native American.

Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a Bm subgroup individual.

A convenient qualitative and quantitative method to investigate RHD-RHCE hybrid genes.

Molecular background of novel silent RHCE alleles.

Next-generation sequencing: proof of concept for antenatal prediction of the fetal Kell blood group phenotype from cell-free fetal DNA in maternal plasma.

Noninvasive prenatal blood group and HPA-1a genotyping: the current European experience.

Serologic and molecular investigations of DAR1 (weak D Type 4.2), DAR1.2, DAR1.3, DAR2 ( DARE), and DARA.

Proficiency testing for blood group genotyping.

RHCEceMO is frequently in cis to RHDDAU0 and encodes a hr<sup>S</sup>-, hr<sup>B</sup>-, RH:-61 phenotype in black persons: clinical significance.

Identification of novel silent KEL alleles causing KEL:−5 ( Ko) phenotype or discordance between KEL:1,−2 phenotype/ KEL*01/02 genotype.

New RHCE variant alleles encoding the D- - phenotype.

Three novel alleles in the Kell blood group system resulting in the K<sub>null</sub> phenotype and the first in a Native American.

Comprehensive genotyping for 18 blood group systems using a multiplex ligation-dependent probe amplification assay shows a high degree of accuracy.

Molecular genetic analysis of ABO blood group variations reveals 29 novel ABO subgroup alleles.

Nomenclature for red blood cell blood group alleles.

P<sup>1</sup>/ P<sup>2</sup> genotyping of known and novel null alleles in the P1 PK and GLOB histo-blood group systems.

Expansion of the Kell blood group system: two new high-prevalence antigens and two novel K<sub>0</sub> ( Kell<sub>null</sub>) phenotypes.

External quality assessment in molecular immunohematology: the INSTAND proficiency test program.

Resolution of translation start site for the human Kell glycoprotein.

RHD variants in Polish blood donors routinely typed as D-.

A convenient qualitative and quantitative method to investigate RHD- RHCE hybrid genes.

The concept of 'confirmatory testing' of donors for ABO and RhD.

Where are we in efforts to unravel the complexity of Rh to guide transfusion decisions?

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.

Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a B<sub>m</sub> subgroup individual.

A novel JK*02 allele in a French Canadian family.

A historical perspective on the discovery of the Kell blood group carriers.

A comprehensive survey of both RHD and RHCE allele frequencies in sub- Saharan Africa.

Combining serology and molecular typing of weak D role in improving D typing strategy in Egypt.

Novel RHD alleles with weak hemagglutination and genetic Exon 9 diversity: weak D Types 45.1, 75, and 76.

D category IV: a group of clinically relevant and phylogenetically diverse partial D.