These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

120 related articles for article (PubMed ID: 7606008)

  • 1. Identification of a partial internal deletion in the RH locus causing the human erythrocyte D--phenotype.
    Huang CH; Reid ME; Chen Y
    Blood; 1995 Jul; 86(2):784-90. PubMed ID: 7606008
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. RH locus contraction in a novel Dc-/D-- genotype resulting from separate genetic recombination events.
    Huang CH; Peng J; Chen HC; Chen YX; Lin DT; Lin SW; Reid ME; Powell VI
    Transfusion; 2004 Jun; 44(6):853-9. PubMed ID: 15157251
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Molecular cloning and primary structure of the human blood group RhD polypeptide.
    Le van Kim C; Mouro I; Chérif-Zahar B; Raynal V; Cherrier C; Cartron JP; Colin Y
    Proc Natl Acad Sci U S A; 1992 Nov; 89(22):10925-9. PubMed ID: 1438298
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. Defining the Rh blood group antigens. Biochemistry and molecular genetics.
    Cartron JP
    Blood Rev; 1994 Dec; 8(4):199-212. PubMed ID: 7888828
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Multiple isoforms excluding normal RhD mRNA detected in Rh blood group Del phenotype with RHD 1227A allele.
    Shao CP; Xiong W; Zhou YY
    Transfus Apher Sci; 2006 Apr; 34(2):145-52. PubMed ID: 16510313
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic recombination at the human RH locus: a family study of the red-cell Evans phenotype reveals a transfer of exons 2-6 from the RHD to the RHCE gene.
    Huang CH; Chen Y; Reid M; Ghosh S
    Am J Hum Genet; 1996 Oct; 59(4):825-33. PubMed ID: 8808597
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rearrangements of the blood group RhD gene associated with the DVI category phenotype.
    Mouro I; Le Van Kim C; Rouillac C; van Rhenen DJ; Le Pennec PY; Bailly P; Cartron JP; Colin Y
    Blood; 1994 Feb; 83(4):1129-35. PubMed ID: 8111052
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Lack of RH C/E expression in the Rhesus D--phenotype is the result of a gene deletion.
    Blunt T; Steers F; Daniels G; Carritt B
    Ann Hum Genet; 1994 Jan; 58(1):19-24. PubMed ID: 7913307
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.