van der Schoot CE - Search Results

1

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. Beckers EA, et al. Among authors: van rhenen dj, van der schoot ce. Br J Haematol. 1996 Jun;93(3):720-7. doi: 10.1046/j.1365-2141.1996.d01-1710.x. Br J Haematol. 1996. PMID: 8652401

2

Rapid Rh D genotyping by polymerase chain reaction-based amplification of DNA.

Simsek S, Faas BH, Bleeker PM, Overbeeke MA, Cuijpers HT, van der Schoot CE, von dem Borne AE. Simsek S, et al. Among authors: van der schoot ce. Blood. 1995 May 15;85(10):2975-80. Blood. 1995. PMID: 7742557 Free article.

3

Sequence analysis of cDNA derived from reticulocyte mRNAs coding for Rh polypeptides and demonstration of E/e and C/c polymorphisms.

Simsek S, de Jong CA, Cuijpers HT, Bleeker PM, Westers TM, Overbeeke MA, Goldschmeding R, van der Schoot CE, von dem Borne AE. Simsek S, et al. Among authors: van der schoot ce. Vox Sang. 1994;67(2):203-9. doi: 10.1111/j.1423-0410.1994.tb01661.x. Vox Sang. 1994. PMID: 7801613

4

Rh E/e genotyping by allele-specific primer amplification.

Faas BH, Simsek S, Bleeker PM, Overbeeke MA, Cuijpers HT, von dem Borne AE, van der Schoot CE. Faas BH, et al. Among authors: van der schoot ce. Blood. 1995 Feb 1;85(3):829-32. Blood. 1995. PMID: 7833484 Free article.

5

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. Beckers EA, et al. Among authors: van rhenen dj, van der schoot ce. Br J Haematol. 1996 Mar;92(3):751-7. doi: 10.1046/j.1365-2141.1996.382918.x. Br J Haematol. 1996. PMID: 8616049

6

Involvement of Ser103 of the Rh polypeptides in G epitope formation.

Faas BH, Beckers EA, Simsek S, Overbeeke MA, Pepper R, van Rhenen DJ, von dem Borne AE, van der Schoot CE. Faas BH, et al. Among authors: van rhenen dj, van der schoot ce. Transfusion. 1996 Jun;36(6):506-11. doi: 10.1046/j.1537-2995.1996.36696269508.x. Transfusion. 1996. PMID: 8669081

7

Characterization of the hybrid RHD gene leading to the partial D category IIIc phenotype.

Beckers EA, Faas BH, Ligthart P, Simsek S, Overbeeke MA, von dem Borne AE, van Rhenen DJ, van der Schoot CE. Beckers EA, et al. Among authors: van rhenen dj, van der schoot ce. Transfusion. 1996 Jun;36(6):567-74. doi: 10.1046/j.1537-2995.1996.36696269518.x. Transfusion. 1996. PMID: 8669091

8

Molecular background of VS and weak C expression in blacks.

Faas BH, Beckers EA, Wildoer P, Ligthart PC, Overbeeke MA, Zondervan HA, von dem Borne AE, van der Schoot CE. Faas BH, et al. Among authors: van der schoot ce. Transfusion. 1997 Jan;37(1):38-44. doi: 10.1046/j.1537-2995.1997.37197176949.x. Transfusion. 1997. PMID: 9024488

9

The Arg633His substitution responsible for the private platelet antigen Gro(a) unravelled by SSCP analysis and direct sequencing.

Simsek S, Folman C, van der Schoot CE, von dem Borne AE. Simsek S, et al. Among authors: van der schoot ce. Br J Haematol. 1997 May;97(2):330-5. doi: 10.1046/j.1365-2141.1997.502696.x. Br J Haematol. 1997. PMID: 9163597 Free article.

10

Lower antigen site density and weak D immunogenicity cannot be explained by structural genomic abnormalities or regulatory defects of the RHD gene.

Beckers EA, Faas BH, Ligthart P, Overbeeke MA, von dem Borne AE, van der Schoot CE, van Rhenen DJ. Beckers EA, et al. Among authors: van rhenen dj, van der schoot ce. Transfusion. 1997 Jun;37(6):616-23. doi: 10.1046/j.1537-2995.1997.37697335156.x. Transfusion. 1997. PMID: 9191822

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