196 related articles for article (PubMed ID: 9018818)
1. Molecular biology of partial D phenotypes.
Avent ND; Finning KM; Liu W; Scott ML
Transfus Clin Biol; 1996; 3(6):511-6. PubMed ID: 9018818
[TBL] [Abstract][Full Text] [Related]
2. Molecular analysis of Rh transcripts and polypeptides from individuals expressing the DVI variant phenotype: an RHD gene deletion event does not generate All DVIccEe phenotypes.
Avent ND; Liu W; Jones JW; Scott ML; Voak D; Pisacka M; Watt J; Fletcher A
Blood; 1997 Mar; 89(5):1779-86. PubMed ID: 9057663
[TBL] [Abstract][Full Text] [Related]
3. Evidence of genetic diversity underlying Rh D-, weak D (Du), and partial D phenotypes as determined by multiplex polymerase chain reaction analysis of the RHD gene.
Avent ND; Martin PG; Armstrong-Fisher SS; Liu W; Finning KM; Maddocks D; Urbaniak SJ
Blood; 1997 Apr; 89(7):2568-77. PubMed ID: 9116304
[TBL] [Abstract][Full Text] [Related]
4. Isolation, characterization, and family study of DTI, a novel partial D phenotype affecting the fourth external loop of D polypeptides.
Omi T; Takahashi J; Seno T; Tanaka M; Hirayama F; Matsuo M; Ueda N; Obara K; Okuda H; Iwamoto S; Tani Y; Kajii E
Transfusion; 2002 Apr; 42(4):481-9. PubMed ID: 12076297
[TBL] [Abstract][Full Text] [Related]
5. Whole exon 5 and intron 5 replaced by RHCE in DVa(Hus).
Shao C; Xiong W; Wang W
J Hum Genet; 2004; 49(2):106-108. PubMed ID: 14714195
[TBL] [Abstract][Full Text] [Related]
6. [System RH: screening of partials D with RHD/RHCE hybrid gene].
Ouchari M; Jemni Yacoub S; Houissa B; Abdelkefi S; Chakroun T; Bouslama M; Jerray I; Belhedi S; Hmida S
Transfus Clin Biol; 2013 Mar; 20(1):35-9. PubMed ID: 23523094
[TBL] [Abstract][Full Text] [Related]
7. Evidence for a separate genetic origin of the partial D phenotype DBT in a Japanese family.
Huang CH; Chen Y; Reid ME; Okubo Y
Transfusion; 1999; 39(11-12):1259-65. PubMed ID: 10604255
[TBL] [Abstract][Full Text] [Related]
8. Three molecular structures cause rhesus D category VI phenotypes with distinct immunohematologic features.
Wagner FF; Gassner C; Muller TH; Schonitzer D; Schunter F; Flegel WA
Blood; 1998 Mar; 91(6):2157-68. PubMed ID: 9490704
[TBL] [Abstract][Full Text] [Related]
9. The D category VI type 4 allele is prevalent in the Spanish population.
Esteban R; Montero R; Flegel WA; Wagner FF; Subirana L; Parra R; Ribera A; Nogués N
Transfusion; 2006 Apr; 46(4):616-23. PubMed ID: 16584438
[TBL] [Abstract][Full Text] [Related]
10. [Generation of RHD-CE(2-9)-D allele by gene conversion in cis].
Shao CP; Li Z; Xiong W; Zhou YY; Li XM
Yi Chuan; 2005 Jul; 27(4):561-5. PubMed ID: 16120578
[TBL] [Abstract][Full Text] [Related]
11. Transcript analysis of D category phenotypes predicts hybrid Rh D-CE-D proteins associated with alteration of D epitopes.
Rouillac C; Colin Y; Hughes-Jones NC; Beolet M; D'Ambrosio AM; Cartron JP; Le Van Kim C
Blood; 1995 May; 85(10):2937-44. PubMed ID: 7742554
[TBL] [Abstract][Full Text] [Related]
12. The genomic organization of the partial D category DVa: the presence of a new partial D associated with the DVa phenotype.
Omi T; Takahashi J; Tsudo N; Okuda H; Iwamoto S; Tanaka M; Seno T; Tani Y; Kajii E
Biochem Biophys Res Commun; 1999 Jan; 254(3):786-94. PubMed ID: 9920819
[TBL] [Abstract][Full Text] [Related]
13. Genotyping of RHD by multiplex polymerase chain reaction analysis of six RHD-specific exons.
Maaskant-van Wijk PA; Faas BH; de Ruijter JA; Overbeeke MA; von dem Borne AE; van Rhenen DJ; van der Schoot CE
Transfusion; 1998; 38(11-12):1015-21. PubMed ID: 9838930
[TBL] [Abstract][Full Text] [Related]
14. Characterization of the recombination hot spot involved in the genomic rearrangement leading to the hybrid D-CE-D gene in the D(VI) phenotype.
Matassi G; Chérif-Zahar B; Mouro I; Cartron JP
Am J Hum Genet; 1997 Apr; 60(4):808-17. PubMed ID: 9106526
[TBL] [Abstract][Full Text] [Related]
15. A D(V)-like phenotype is obliterated by A226P in the partial D DBS.
Wagner FF; Ernst M; Sonneborn HH; Flegel WA
Transfusion; 2001 Aug; 41(8):1052-8. PubMed ID: 11493738
[TBL] [Abstract][Full Text] [Related]
16. 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. PubMed ID: 9354819
[TBL] [Abstract][Full Text] [Related]
17. [Whole exon 5 and intron 5 replaced by RHD/CE in partial D phenotype DVa (Hus)].
Zhou YY; Xiong W; Shao CP
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2005 Feb; 13(1):140-2. PubMed ID: 15748454
[TBL] [Abstract][Full Text] [Related]
18. First description of a D-CE-D hybrid gene on a weak D Type 2 molecular background.
Granier T; Chiaroni J; Bailly P; Silvy M
Transfusion; 2017 May; 57(5):1248-1253. PubMed ID: 28164316
[TBL] [Abstract][Full Text] [Related]
19. RHD and RHCE variant and zygosity genotyping via multiplex ligation-dependent probe amplification.
Haer-Wigman L; Veldhuisen B; Jonkers R; Lodén M; Madgett TE; Avent ND; de Haas M; van der Schoot CE
Transfusion; 2013 Jul; 53(7):1559-74. PubMed ID: 23043317
[TBL] [Abstract][Full Text] [Related]
20. The R0Har RH:33 phenotype results from substitution of exon 5 of the RHCE gene by the corresponding exon of the RHD gene.
Beckers EA; Faas BH; von dem Borne AE; Overbeeke MA; van Rhenen DJ; van der Schoot CE
Br J Haematol; 1996 Mar; 92(3):751-7. PubMed ID: 8616049
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]