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au.\*:("AVENT, N. D")

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The Rh blood group system : a reviewAVENT, N. D; REID, M. E.Blood. 2000, Vol 95, Num 2, pp 375-387, issn 0006-4971Article

Antenatal genotyping of the blood groups of the fetusAVENT, N. D.Vox sanguinis (Basel. 1956). 1998, Vol 74, pp 365-374, issn 0042-9007, SUP2Conference Paper

Molecular genetic methods : Principles and feasibility in Transfusion MedicineAVENT, N. D.Vox sanguinis (Basel. 1956). 1998, Vol 74, pp 275-284, issn 0042-9007, SUP2Conference Paper

Effect of 1-β-D-arabino-furanosyl-cytosine (ara-C) induction of K562 cells on expression of Rh and other blood group active proteinsWIENER, E; SHIELS, A; WICKRAMASINGHE, S. N et al.British journal of haematology. 1998, Vol 103, Num 1, pp 259-267, issn 0007-1048Article

Prenatal determination of fetal blood group statusAVENT, N. D; FINNING, K. M; MARTIN, P. G et al.Vox sanguinis (Basel. 1956). 2000, Vol 78, pp 155-162, issn 0042-9007, SUP2Conference Paper

Site-directed mutagenesis of the human D antigen : definition of D epitopes on the sixth external domain of the D protein expressed on K562 cellsLIU, W; SMYTHE, J. S; SCOTT, M. L et al.Transfusion (Philadelphia, PA). 1999, Vol 39, Num 1, pp 17-25, issn 0041-1132Article

Translationally controlled tumour protein (TCTP) is a novel glucose-regulated protein that is important for survival of pancreatic beta cellsDIRAISON, F; HAYWARD, K; AVENT, N. D et al.Diabetologia (Berlin). 2011, Vol 54, Num 2, pp 368-379, issn 0012-186X, 12 p.Article

The Escherichia coli AmtB protein as a model system for understanding ammonium transport by Amt and Rh proteinsMERRICK, M; JAVELLE, A; DURAND, A et al.Transfusion clinique et biologique (Paris). 2006, Vol 13, Num 1-2, pp 97-102, issn 1246-7820, 6 p.Conference Paper

A clinically applicable method for determining the three major alleles at the Duffy (FY) blood group locus using polymerase chain reaction with allele-specific primersOLSSON, M. L; HANSSON, C; AVENT, N. D et al.Transfusion (Philadelphia, PA). 1998, Vol 38, Num 2, pp 168-173, issn 0041-1132Article

Molecular biology of partial D phenotypesAVENT, N. D; FINNING, K. M; LIU, W et al.Transfusion clinique et biologique (Paris). 1996, Vol 3, Num 6, pp 511-516, issn 1246-7820Conference Paper

Identification of functioning regulatory sites and a new myosin binding site in the C-terminal 288 amino acids of caldesmon expressed from a human cloneHUBER, P. A. J; REDWOOD, C. S; AVENT, N. D et al.Journal of muscle research and cell motility. 1993, Vol 14, Num 4, pp 385-391, issn 0142-4319Article

Prediction of fetal D status from maternal plasma: introduction of a new noninvasive fetal RHD genotyping serviceFINNING, Km; MARTIN, P. G; SOOTHILL, P. W et al.Transfusion (Philadelphia, PA). 2002, Vol 42, Num 8, pp 1079-1085, issn 0041-1132Article

Site directed mutagenesis of the human Rh D antigen : Molecular basis of D epitopesAVENT, N. D; LIU, W; SCOTT, M. L et al.Vox sanguinis (Basel. 1956). 2000, Vol 78, pp 83-89, issn 0042-9007, SUP2Conference Paper

Expression of RHD and RHCE gene products using retroviral transduction of K562 cells establishes the molecular basis of Rh blood group antigensSMYTHE, J. S; AVENT, N. D; JUDSON, P. A et al.Blood. 1996, Vol 87, Num 7, pp 2968-2973, issn 0006-4971Article

A point mutatin in the GYPC gene results in the expression of the blood group Ana antigen on glycophorin D but not on glycophorin C : further evidence that glycophorin D is a product of thz GYPC geneDANIELS, G; MAY-JEAN KING; AVENT, N. D et al.Blood. 1993, Vol 82, Num 10, pp 3198-3203, issn 0006-4971Article

cDNA cloning of a 30 kDa arythrocyte membrane protein associated with Rh (Rhesus)-blood-group-antigen expressionAVENT, N. D; RIDGWELL, K; TANNER, M. J. A et al.Biochemical journal (London. 1906). 1990, Vol 271, Num 3, pp 821-825, issn 0006-2936, 5 p.Article

Protein-sequence studies on Rh-related polypeptides suggest the presence of at least two groups of proteins which associate in the human red-cell membraneAVENT, N. D; RIDGWELL, K; MAWBY, W. J et al.Biochemical journal (London. 1906). 1988, Vol 256, Num 3, pp 1043-1046, issn 0006-2936Article

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 phenotypeSINGLETON, B. K; GREEN, C. A; AVENT, N. D et al.Blood. 2000, Vol 95, Num 1, pp 12-18, issn 0006-4971Article

Epitopes on Rh proteinsSCOTT, M. L; VOAK, D; LIU, W et al.Vox sanguinis (Basel. 1956). 2000, Vol 78, pp 117-120, issn 0042-9007, SUP2Conference Paper

Molecular configuration of Rh D epitopes as defined by site-directed mutagenesis and expression of mutant Rh constructs in K562 erythroleukemia cellsLIU, W; AVENT, N. D; JONES, J. W et al.Blood. 1999, Vol 94, Num 12, pp 3986-3996, issn 0006-4971Article

The Fyx phenotype is associated with a missense mutation in the Fyb allele predicting Arg89Cys in the Duffy glycoproteinOLSSON, M. L; SMYTHE, J. S; HANSSON, C et al.British journal of haematology. 1998, Vol 103, Num 4, pp 1184-1191, issn 0007-1048Article

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 geneAVENT, N. D; MARTIN, P. G; ARMSTRONG-FISHER, S. S et al.Blood. 1997, Vol 89, Num 7, pp 2568-2577, issn 0006-4971Article

Molecular analysis of Rh transcripts and polypeptides from individuals expressing the DVI variant phenotype: An RHD gene deletion event does not generate all DVIccEe phenotypesAVENT, N. D; LIU, W; JONES, J. W et al.Blood. 1997, Vol 89, Num 5, pp 1779-1786, issn 0006-4971Article

Molecular basis of the D variant phenotypes DNU and DII allows localization of critical amino acids required for expression of Rh D epitopes epD3, 4 and 9 to the sixth external domain of the Rh D proteinAVENT, N. D; JONES, J. W; LIU, W et al.British journal of haematology. 1997, Vol 97, Num 2, pp 366-371, issn 0007-1048Article

Point mutation in the glycophorin C gene results in the expression of the blood group antigen DhaKING, M. J; AVENT, N. D; MALLINSON, G et al.Vox sanguinis (Basel. 1956). 1992, Vol 63, Num 1, pp 56-58, issn 0042-9007Article

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