Works matching DE "KELL blood group system"

Results: 56

A polymorphism in XKR4 is significantly associated with serum prolactin concentrations in beef cows grazing tall fescue.

Published in:

Animal Genetics, 2014, v. 45, n. 3, p. 439, doi. 10.1111/age.12134

By:

Bastin, B. C.;
Houser, A.;
Bagley, C. P.;
Ely, K. M.;
Payton, R. R.;
Saxton, A. M.;
Schrick, F. N.;
Waller, J. C.;
Kojima, C. J.

Publication type:

Article

Distribution of Clinically Relevant Erythrocyte Antigens among Blood Donors of the Republic of Srpska.

Published in:

Scripta Medica, 2015, v. 46, n. 1, p. 18, doi. 10.5937/scrimed1501018g

By:

Guzijan, Gordana;
Jukić, Biljana;
Mitrović, Sandra;
Ćejić, Veselka;
Bojanić, Janja;
Jojić, Dragica

Publication type:

Article

Kell Blood Group System Polymorphism in an Urban Tunisian Population.

Published in:

Biochemical Genetics, 2011, v. 49, n. 5/6, p. 323, doi. 10.1007/s10528-010-9410-8

By:

Bani, Meriem;
Kaabi, Houda;
Sellami, Mohamed;
Chaabane, Manel;
Cherif, Ghaya;
Bellali, Hedi;
Midouni, Brahim;
Chalfouh, Nejia;
Dridi, Amel;
Jeridi, Afef;
Hmida, Slama

Publication type:

Article

Free Communications 2.

Published in:: Transfusion Medicine, 2003, v. 13, p. 8
Publication type:: Article

A new murine monoclonal antibody against Kx protein.

Published in:

Transfusion Medicine, 2003, v. 13, n. 1, p. 43, doi. 10.1046/j.1365-3148.2003.00414.x

By:

Hattab, C.;
Blanchard, D.;
Gane, P.;
Verkarre, V.;
Petit-Leroux, Y.;
Loirat, M.-J.;
Cartron, J.-P.;
Bertrand, O.

Publication type:

Article

Kell Expression on Myeloid Progenitor Cells.

Published in:

Leukemia & Lymphoma, 2002, v. 43, n. 3, p. 479, doi. 10.1080/10428190290011949

By:

Wagner, T.;
Lanzer, G.;
Geissler, K.

Publication type:

Article

McLeod syndrome resulting from a novel XK mutation.

Published in:

British Journal of Haematology, 2003, v. 122, n. 4, p. 682, doi. 10.1046/j.1365-2141.2003.04474.x

By:

Singleton, Belinda K.;
Green, Carole A.;
Renaud, Susanne;
Fuhr, Peter;
Poole, Joyce;
Daniels, Geoff L.

Publication type:

Article

Heterozygosity for two novel null alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman.

Published in:

British Journal of Haematology, 2002, v. 117, n. 1, p. 220, doi. 10.1046/j.1365-2141.2002.03368.x

By:

Koda, Yoshiro;
Soejima, Mikiko;
Tsuneoka, Makoto;
Yasumoto, Kiyoshi;
Higashitani, Takanori;
Sagawa, Kimitaka;
Kimura, Hiroshi

Publication type:

Article

Clinical Potential of Effective Noninvasive Exclusion of KEL1-Positive Fetuses in KEL1-Negative Pregnant Women.

Published in:

2016

By:

Böhmova, Jana;
Vodicka, Radek;
Lubusky, Marek;
Holuskova, Iva;
Studnickova, Martina;
Kratochvilova, Romana;
Krejcirikova, Eva;
Janikova, Maria;
Durdová, Veronika;
Dolezalová, Tereza;
Filipová, Hana;
Dusek, Ladislav;
Dhaifalah, Ishraq;
Vomackova, Katherine;
Kacerovsky, Marian;
Prochazka, Martin;
Vrtel, Radek

Publication type:

journal article

Genomic association for sexual precocity in beef heifers using pre-selection of genes and haplotype reconstruction.

Published in:

PLoS ONE, 2018, v. 13, n. 1, p. 1, doi. 10.1371/journal.pone.0190197

By:

Takada, Luciana;
Barbero, Marina M. D.;
Oliveira, Henrique N.;
de Camargo, Gregório M. F.;
Fernandes Júnior, Gerardo A.;
Aspilcueta-Borquis, Rusbel R.;
Souza, Fabio R. P.;
Boligon, Arione A.;
Melo, Thaise P.;
Regatieri, Inaê C.;
Feitosa, Fabieli L. B.;
Fonseca, Larissa F. S.;
Magalhães, Ana F. B.;
Costa, Raphael B.;
Albuquerque, Lucia G.

Publication type:

Article

Point mutations in KEL exon 8 determine a high-incidence (RAZ) and a low-incidence (KEL25, VLAN) antigen of the Kell blood group system.

Published in:

Vox Sanguinis, 2001, v. 81, n. 4, p. 259, doi. 10.1046/j.1423-0410.2001.00119.x

By:

Lee, S.;
Reid, M. E.;
Redman, C. M.

Publication type:

Article

Kell is not restricted to the erythropoietic lineage but is also expressed on myeloid progenitor cells.

Published in:

British Journal of Haematology, 2000, v. 110, n. 2, p. 409, doi. 10.1046/j.1365-2141.2000.02195.x

By:

Wagner, T.;
Berer, A.;
Lanzer, G.;
Geissler, K.

Publication type:

Article

Production and characterization of anti-Kell monoclonal antibodies using transfected cells as the immunogen.

Published in:

British Journal of Haematology, 1999, v. 106, n. 3, p. 817, doi. 10.1046/j.1365-2141.1999.01599.x

By:

Chu, Te-Hua Tearina;
Yazdanbakhsh, Karina;
Øyen, Ragnhild;
Smart, Elizabeth;
Reid, Marion E.

Publication type:

Article

A NEW EXPLANATION FOR THE REPRODUCTIVE WOES AND MIDLIFE DECLINE OF HENRY VIII.

Published in:

Historical Journal, 2010, v. 53, n. 4, p. 827, doi. 10.1017/S0018246X10000452

By:

WHITLEY, CATRINA BANKS;
KRAMER, KYRA

Publication type:

Article

A rare cause of jaundice in a newborn not predicted by maternal blood typing (Discussion and Diagnosis).

Published in:

Acta Paediatrica, 2009, v. 98, n. 7, p. 1221, doi. 10.1111/j.1651-2227.2009.01229.x

By:

Okulu, Emel;
Akin, Ilke Mungan;
Atasay, Begum;
Arsan, Saadet;
Ince, Elif Unal;
Turmen, Tomris

Publication type:

Article

Molecular basis of two novel high-prevalence antigens in the Kell blood group system, KALT and KTIM.

Published in:

Transfusion, 2006, v. 46, n. 8, p. 1323, doi. 10.1111/j.1537-2995.2006.00899.x

By:

Lee, Soohee;
Debnath, Asim K.;
Xu Wu;
Scofield, Terry;
George, Terry;
Kakaiya, Ram;
Yogore III, Mariano G.;
Sausais, Laima;
Yacob, Michelle;
Lomas-Francis, Christine;
Reid, Marion E.

Publication type:

Article

Onset of expression of the components of the Kell blood group complex.

Published in:

Transfusion, 2005, v. 45, n. 6, p. 969, doi. 10.1111/j.1537-2995.2005.04289.x

By:

Pu, Jeffrey J.;
Redman, Colvin M.;
Visser, Jan W. M.;
Soohee Lee

Publication type:

Article

Genetic basis of the K0 phenotype in the Swedish population.

Published in:

Transfusion, 2005, v. 45, n. 4, p. 545, doi. 10.1111/j.0041-1132.2005.04283.x

By:

Wester, Elisabet S.;
Storry, Jill R.;
Schneider, Karin;
Sojka, Birgitta Nilsson;
Poole, Joyce;
Olsson, Martin L.

Publication type:

Article

Mutations that diminish expression of Kell surface protein and lead to the Kmod RBC phenotype.

Published in:

2003

By:

Lee, Soohee;
Russo, David C.W.;
Reid, Marion E.;
Redman, Colvin M.

Publication type:

journal article

Successful Transfusion of Kp(a-b+) Red Cells Incompatible for Anti-Kp[sup b]Autoantibody.

Published in:: 2002
Publication type:: Abstract

Mutations Causing the Kell[sub mod] Red Cell Phenotype.

Published in:: 2002
Publication type:: Abstract

Kell sensitization can cause fetalanemia, too.

Published in:

Contemporary OB/GYN, 2008, v. 53, n. 9, p. 36

By:

Moise Jr., Kenneth J.

Publication type:

Article

Management of Kell isoimmunization — evaluation of a Doppler-guided approach.

Published in:

Ultrasound in Obstetrics & Gynecology, 2006, v. 28, n. 6, p. 814, doi. 10.1002/uog.2837

By:

Rimon, E.;
Peltz, R.;
Gamzu, R.;
Yagel, S.;
Feldman, B.;
Chayen, B.;
Achiron, R.;
Lipitz, S.

Publication type:

Article

Kell alloimmünizasyonuna bağli hidrops fetalis: olgu sunumu.

Published in:

Gulhane Medical Journal, 2011, v. 53, n. 3, p. 219

By:

Bodur, Serkan;
Tütüncü, Levent;
Erdem, Galip

Publication type:

Article

An innovative test for non-invasive Kell genotyping on circulating fetal DNA by means of the allelic discrimination of K1 and K2 antigens.

Published in:

American Journal of Reproductive Immunology, 2016, v. 76, n. 6, p. 499, doi. 10.1111/aji.12593

By:

Cro', Fabiana;
Lapucci, Cristina;
Vicari, Emilio;
Salsi, Ginevra;
Rizzo, Nicola;
Farina, Antonio

Publication type:

Article

DNA-Based Typing of Kell, Kidd, MNS, Dombrock, Colton, and Yt Blood Group Systems in the French Basques.

Published in:

American Journal of Human Biology, 2008, v. 20, n. 3, p. 308, doi. 10.1002/ajhb.20720

By:

Touinssi, Mhammed;
Chiaroni, Jacques;
Degioanni, Anna;
Granter, Thomas;
Dutour, Olivier;
Bailly, Pascal;
Bauduer, Frederic

Publication type:

Article

Acanthocytes in the McLeod phenotype of X-linked chronic granulomatous disease.

Published in:

2017

By:

Beaulieu, Gregory P.;
Ward, Dawn C.;
Panch, Sandhya R.;
Flegel, Willy A.

Publication type:

journal article

A novel KEL silencing allele in a Brazilian patient with anti-Ku.

Published in:

2017

By:

Brunetta, Denise;
Carlos, Luciana M.B.;
Costa, Tiê B.;
Silva, Vilany F.P.;
Oliveira, Patrícia N.;
Gazito, Diana;
Arnoni, Carine;
Castilho, Lilian

Publication type:

journal article

Provision of KEL1-negative blood to obstetric patients: a 3-year single-institution retrospective review.

Published in:

Transfusion, 2015, v. 55, n. 3, p. 599, doi. 10.1111/trf.12814

By:

O'Brien, Kerry L.;
Kim, Yeowon A.;
Haspel, Richard L.;
Uhl, Lynne

Publication type:

Article

Novel alleles at the Kell blood group locus that lead to Kell variant phenotype in the Dutch population.

Published in:

Transfusion, 2015, v. 55, n. 2, p. 413, doi. 10.1111/trf.12838

By:

Ji, Yanli;
Veldhuisen, Barbera;
Ligthart, Peter;
Haer‐Wigman, Lonneke;
Jongerius, John;
Boujnan, Mohamed;
Ait Soussan, Aicha;
Luo, Guangping;
Fu, Yongshui;
Schoot, C. Ellen;
Haas, Masja

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

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

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

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

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

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

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

Generation of transgenic mice with antithetical KEL1 and KEL2 human blood group antigens on red blood cells.

Published in:

Transfusion, 2012, v. 52, n. 12, p. 2620, doi. 10.1111/j.1537-2995.2012.03641.x

By:

Smith, Nicole H.;
Henry, Kate L.;
Cadwell, Chantel M.;
Bennett, Ashley;
Hendrickson, Jeanne E.;
Frame, Tom;
Zimring, James C.

Publication type:

Article

The value of DNA analysis for antigens of the Kell and Kx blood group systems.

Published in:

Transfusion, 2007, v. 47, p. 32S, doi. 10.1111/j.1537-2995.2007.01308.x

By:

Soohee Lee

Publication type:

Article

A KEL gene encoding serine at position 193 of the Kell glycoprotein results in expression of KEL1 antigen.

Published in:

Transfusion, 2006, v. 46, n. 11, p. 1879, doi. 10.1111/j.1537-2995.2006.00993.x

By:

Poole, Joyce;
Warke, Nicole;
Hustinx, Hein;
Taleghani, Behrouz Mansouri;
Martin, Peter;
Finning, Kirstin;
Crew, Vanja Karamatic;
Green, Carole;
Bromilow, Imelda;
Daniels, Geoff

Publication type:

Article

Frequency of red cell alio- and autoimmunization in patients with transfusion-dependent beta thalassemia and affecting factors.

Published in:

Turkish Journal of Pediatrics, 2014, v. 56, n. 5, p. 487

By:

Koçyiğit, Cemil;
Eliaçik, Kayı;
Kanık, Ali;
Atabay, Berna;
Türker, Meral

Publication type:

Article

The Outcome of Pregnancy in Kell Allo-immunisation.

Published in:: Journal of Obstetrics & Gynaecology, 1998, v. 18, p. S35
Publication type:: Article

Silent <italic>KEL</italic> alleles identified from Japanese individuals with the Ko phenotype.

Published in:

Vox Sanguinis, 2018, v. 113, n. 3, p. 290, doi. 10.1111/vox.12628

By:

Onodera, T.;
Kawai, M.;
Obara, K.;
Enomoto, T.;
Sasaki, K.;
Osabe, T.;
Ogasawara, K.;
Toyoda, C.;
Tsuneyama, H.;
Uchikawa, M.;
Inaba, S.;
Satake, M.

Publication type:

Article

Three uncommon KEL alleles in one family with unusual Kell phenotypes explain a 35-year old conundrum.

Published in:

Vox Sanguinis, 2014, v. 106, n. 3, p. 242, doi. 10.1111/vox.12094

By:

Karamatic Crew, V.;
Poole, J.;
Burton, N.;
Daniels, G.

Publication type:

Article

KEL*02 alleles with alterations in and around exon 8 in individuals with apparent KEL:1,−2 phenotypes.

Published in:

Vox Sanguinis, 2010, v. 99, n. 2, p. 150, doi. 10.1111/j.1423-0410.2010.01334.x

By:

Wester, E. S.;
Steffensen, R.;
Ligthart, P. C.;
Vad, J.;
de Haas, M.;
Storry, J. R.;
Olsson, M. L.

Publication type:

Article

Kell alloimmunization in pregnancy: associated with fetal thrombocytopenia?

Published in:

Vox Sanguinis, 2008, v. 95, n. 1, p. 66, doi. 10.1111/j.1423-0410.2008.01061.x

By:

van den Akker, E. S. A.;
Klumper, F. J. C. M.;
Brand, A.;
Kanhai, H. H. H.;
Oepkes, D.

Publication type:

Article

Transfusion support for a patient with McLeod phenotype without chronic granulomatous disease and with antibodies to Kx and Km.

Published in:

Vox Sanguinis, 2008, v. 94, n. 3, p. 216, doi. 10.1111/j.1423-0410.2007.01021.x

By:

Bansal, I.;
Jeon, H.-R.;
Hui, S. R.;
Calhoun, B. W.;
Manning, D. W.;
Kelly, T. J.;
Lee, S.;
Baron, B. W.

Publication type:

Article

International Society of Blood Transfusion Committee on Terminology for Red Cell Surface Antigens: Cape Town report.

Published in:

Vox Sanguinis, 2007, v. 92, n. 3, p. 250, doi. 10.1111/j.1423-0410.2007.00887.x

By:

Daniels, G.;
Flegel, W. A.;
Fletcher, A.;
Garratty, G.;
Levene, C.;
Lomas-Francis, C.;
Moulds, J. M.;
Moulds, J. J.;
Olsson, M. L.;
Overbeeke, M. A. M.;
Poole, J.;
Reid, M. E.;
Rouger, P.;
van der Schoot, C. E.;
Scott, M.;
Sistonen, P.;
Smart, E.;
Storry, J. R.;
Tani, Y.;
Yu, L.-C.

Publication type:

Article

The human Kell blood group binds the erythroid 4.1R protein: new insights into the 4.1R-dependent red cell membrane complex.

Published in:

British Journal of Haematology, 2015, v. 171, n. 5, p. 862, doi. 10.1111/bjh.13778

By:

Azouzi, Slim;
Collec, Emmanuel;
Mohandas, Narla;
An, Xiuli;
Colin, Yves;
Le Van Kim, Caroline

Publication type:

Article

The mouse Kell blood group gene (Kel): cDNA sequence, genomic organization, expression, and enzymatic function.

Published in:

Immunogenetics, 2000, v. 52, n. 1/2, p. 53, doi. 10.1007/s002510000251

By:

Lee, Soohee;
Russo, David C.W.;
Pu, Jeffrey;
Ho, Mengfatt;
Redman, Colvin M.

Publication type:

Article