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Results: 1 to 20 of 141

Similar articles for PubMed (Select 22356522)

1.

Prevalence of RHD*DOL and RHCE*ce(818T) in two populations.

Halter Hipsky C, da Costa DC, Omoto R, Zanette A, Castilho L, Reid ME.

Immunohematology. 2011;27(2):66-7.

PMID:
22356522
2.

RHD*DOL1 and RHD*DOL2 encode a partial D antigen and are in cis with the rare RHCE*ceBI allele in people of African descent.

Roussel M, Poupel S, Nataf J, Juszczak G, Woimant G, Mailloux A, Menanteau C, Pham BN, Rouger P, Le Pennec PY, Peyrard T.

Transfusion. 2013 Feb;53(2):363-72. doi: 10.1111/j.1537-2995.2012.03743.x. Epub 2012 Jun 13.

PMID:
22690701
3.

The low-prevalence Rh antigen STEM (RH49) is encoded by two different RHCE*ce818T alleles that are often in cis to RHD*DOL.

Reid ME, Halter Hipsky C, Hue-Roye K, Coghlan G, Olsen C, Lomas-Francis C.

Transfusion. 2013 Mar;53(3):539-44. doi: 10.1111/j.1537-2995.2012.03754.x. Epub 2012 Jun 28.

4.

Molecular background of RH in Bastiaan, the RH:-31,-34 index case, and two novel RHD alleles.

Reid ME, Hipsky CH, Velliquette RW, Lomas-Francis C, Larimore K, Olsen C.

Immunohematology. 2012;28(3):97-103.

PMID:
23286557
5.

Red cells from the original JAL+ proband are also DAK+ and STEM+.

Hue-Roye K, Reid ME, Westhoff CM, Lomas-Francis C.

Vox Sang. 2011 Jul;101(1):61-4. doi: 10.1111/j.1423-0410.2010.01465.x. Epub 2011 Apr 8.

6.

Identification of RHCE and KEL alleles in large cohorts of Afro-Caribbean and Comorian donors by multiplex SNaPshot and fragment assays: a transfusion support for sickle cell disease patients.

Silvy M, Di Cristofaro J, Beley S, Papa K, Rits M, Richard P, Chiaroni J, Bailly P.

Br J Haematol. 2011 Jul;154(2):260-70. doi: 10.1111/j.1365-2141.2011.08691.x. Epub 2011 May 28.

PMID:
21623766
7.

RHCE*ceMO is frequently in cis to RHD*DAU0 and encodes a hr(S) -, hr(B) -, RH:-61 phenotype in black persons: clinical significance.

Westhoff CM, Vege S, Horn T, Hue-Roye K, Halter Hipsky C, Lomas-Francis C, Reid ME.

Transfusion. 2013 Nov;53(11 Suppl 2):2983-9. doi: 10.1111/trf.12271. Epub 2013 Jun 17.

8.

Weakened expression of 'e' owing to concomitant occurrence of Cys16 and Val245 (VS antigen).

Rodrigues A, Rios M, Costa FF, Saad ST, Pellegrino J Jr, Castilho L.

Vox Sang. 2004 Feb;86(2):136-40.

PMID:
15023184
9.

Molecular basis of the rare gene complex, DIVa(C)-, which encodes four low-prevalence antigens in the Rh blood group system.

Hipsky CH, Hue-Roye K, Lomas-Francis C, Huang CH, Reid ME.

Vox Sang. 2012 Feb;102(2):167-70. doi: 10.1111/j.1423-0410.2011.01519.x. Epub 2011 Jul 6.

PMID:
21729099
10.

A novel RHCE*ce 48C, 733G allele with Nucleotide 941C in Exon 7 encodes an altered red blood cell e antigen.

Hue-Roye K, Hipsky CH, Velliquette RW, Fuchisawa A, Lomas-Francis C, Hoppe C, Reid ME.

Transfusion. 2011 Jan;51(1):32-5. doi: 10.1111/j.1537-2995.2010.02765.x.

11.

Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety.

Noizat-Pirenne F, Lee K, Pennec PY, Simon P, Kazup P, Bachir D, Rouzaud AM, Roussel M, Juszczak G, Ménanteau C, Rouger P, Kotb R, Cartron JP, Ansart-Pirenne H.

Blood. 2002 Dec 1;100(12):4223-31. Epub 2002 Aug 1.

12.

Systematic RH genotyping and variant identification in French donors of African origin.

Kappler-Gratias S, Auxerre C, Dubeaux I, Beolet M, Ripaux M, Le Pennec PY, Pham BN.

Blood Transfus. 2014 Jan;12 Suppl 1:s264-72. doi: 10.2450/2013.0270-12. Epub 2013 Jun 17.

13.

RHD/CE typing by polymerase chain reaction using sequence-specific primers.

Gassner C, Schmarda A, Kilga-Nogler S, Jenny-Feldkircher B, Rainer E, Müller TH, Wagner FF, Flegel WA, Schönitzer D.

Transfusion. 1997 Oct;37(10):1020-6.

PMID:
9354819
14.

RHD*weak partial 4.0 is associated with an altered RHCE*ce(48C, 105T, 733G, 744C, 1025T) allele in the Tunisian population.

Ouchari M, Polin H, Romdhane H, Abdelkefi S, Houissa B, Chakroun T, Gabriel C, Hmida S, Jemni Yacoub S.

Transfus Med. 2013 Aug;23(4):245-9. doi: 10.1111/tme.12037. Epub 2013 Jun 7.

PMID:
23742316
15.

Alloanti-c/ce in a c+ceAR/Ce patient suggests that the rare RHCE ceAR allele (ceAR) encodes a partial c antigen.

Peyrard T, Pham BN, Poupel S, Martin-Blanc S, Auxerre C, Kappler-Gratias S, Bonin P, Rouger P, Le Pennec PY.

Transfusion. 2009 Nov;49(11):2406-11. doi: 10.1111/j.1537-2995.2009.02308.x. Epub 2009 Jul 14.

PMID:
19624489
16.

Presence of the RHD pseudogene and the hybrid RHD-CE-D(s) gene in Brazilians with the D-negative phenotype.

Rodrigues A, Rios M, Pellegrino J Jr, Costa FF, Castilho L.

Braz J Med Biol Res. 2002 Jul;35(7):767-73.

17.

Genomic analyses of RH alleles to improve transfusion therapy in patients with sickle cell disease.

Reid ME, Halter Hipsky C, Hue-Roye K, Hoppe C.

Blood Cells Mol Dis. 2014 Apr;52(4):195-202. doi: 10.1016/j.bcmd.2013.11.003. Epub 2013 Dec 2.

18.

Nucleotide deletion in RHCE*cE (907delC) is responsible for a D- - haplotype in Hispanics.

Westhoff CM, Vege S, Nickle P, Singh S, Hue-Roye K, Lomas-Francis C, Reid ME.

Transfusion. 2011 Oct;51(10):2142-7. doi: 10.1111/j.1537-2995.2011.03144.x. Epub 2011 Apr 22.

PMID:
21517889
19.

DIIIa and DIII Type 5 are encoded by the same allele and are associated with altered RHCE*ce alleles: clinical implications.

Westhoff CM, Vege S, Halter-Hipsky C, Whorley T, Hue-Roye K, Lomas-Francis C, Reid ME.

Transfusion. 2010 Jun;50(6):1303-11. doi: 10.1111/j.1537-2995.2009.02573.x. Epub 2010 Jan 15.

20.

The RHCE allele ceCF: the molecular basis of Crawford (RH43).

Flegel WA, Wagner FF, Chen Q, Schlanser G, Frame T, Westhoff CM, Moulds MK.

Transfusion. 2006 Aug;46(8):1334-42.

PMID:
16934069
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