300 related articles for article (PubMed ID: 9116304)
1. 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]
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. Molecular basis of the altered antigenic expression of RhD in weak D(Du) and RhC/e in RN phenotypes.
Rouillac C; Gane P; Cartron J; Le Pennec PY; Cartron JP; Colin Y
Blood; 1996 Jun; 87(11):4853-61. PubMed ID: 8639859
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. RHD gene deletion occurred in the Rhesus box.
Wagner FF; Flegel WA
Blood; 2000 Jun; 95(12):3662-8. PubMed ID: 10845894
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. The RHD gene is highly detectable in RhD-negative Japanese donors.
Okuda H; Kawano M; Iwamoto S; Tanaka M; Seno T; Okubo Y; Kajii E
J Clin Invest; 1997 Jul; 100(2):373-9. PubMed ID: 9218514
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in africans with the Rh D-negative blood group phenotype.
Singleton BK; Green CA; Avent ND; Martin PG; Smart E; Daka A; Narter-Olaga EG; Hawthorne LM; Daniels G
Blood; 2000 Jan; 95(1):12-8. PubMed ID: 10607679
[TBL] [Abstract][Full Text] [Related]
11. Alteration of RH gene structure and expression in human dCCee and DCW-red blood cells: phenotypic homozygosity versus genotypic heterozygosity.
Huang CH
Blood; 1996 Sep; 88(6):2326-33. PubMed ID: 8822955
[TBL] [Abstract][Full Text] [Related]
12. RHD gene polymorphism among RhD-negative Han Chinese.
Xu Q; Zhang J; Wang Q; Zhang S; Si G
Chin Med J (Engl); 2003 Oct; 116(10):1539-43. PubMed ID: 14570619
[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. The genetic basis of a new partial D antigen: DDBT.
Beckers EA; Faas BH; Simsek S; Overbeeke MA; van Rhenen DJ; Wallace M; von dem Borne AE; van der Schoot CE
Br J Haematol; 1996 Jun; 93(3):720-7. PubMed ID: 8652401
[TBL] [Abstract][Full Text] [Related]
15. Comprehensive phenotypic and molecular investigation of RhD and RhCE variants in Moroccan blood donors.
El Housse H; El Wafi M; Ouabdelmoumene Z; Zarati F; Alid R; Nourichafi N; Bouisk K; Benajiba M; Férec C; Fichou Y; Habti N
Blood Transfus; 2019 Mar; 17(2):151-156. PubMed ID: 30418133
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Comprehensive analysis of RHD splicing transcripts reveals the molecular basis for the weak anti-D reactivity of Del -red blood cells.
Chen DP; Sun CF; Ning HC; Wang WT; Tseng CP
Transfus Med; 2016 Apr; 26(2):123-9. PubMed ID: 26774048
[TBL] [Abstract][Full Text] [Related]
19. Investigation of the RH locus in gorillas and chimpanzees.
Westhoff CM; Wylie DE
J Mol Evol; 1996 Jun; 42(6):658-68. PubMed ID: 8662018
[TBL] [Abstract][Full Text] [Related]
20. The STR polymorphisms in intron 8 may provide information about the molecular evolution of RH haplotypes.
Fujiwara H; Okuda H; Omi T; Iwamoto S; Tanaka Y; Takahashi J; Tani Y; Minakami H; Araki S; Sato I; Kajii E
Hum Genet; 1999 Apr; 104(4):301-6. PubMed ID: 10369159
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]